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Speech perception in dyslexia is characterized by a categorical perception (CP) deficit, demonstrated by weaker discrimination of acoustic differences between phonemic categories in conjunction with better discrimination of acoustic differences within phonemic categories. We performed a meta-analysis of studies that examined the reliability of the CP deficit in dyslexia. The results show a reliable CP deficit in individuals with dyslexia compared to both chronological-age and reading-level controls. The CP deficit is stronger for discrimination than for identification, suggesting that the latter may only reveal between-category differences that do not fully reflect the CP deficit. The implications of these findings for the allophonic theory of dyslexia are discussed.
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Scientific Studies of Reading,00:120,2015
Copyright © 2015 Society for the Scientific Study of Reading
ISSN: 1088-8438 print/1532-799X online
DOI: 10.1080/10888438.2015.1052455
The Categorical Perception Deficit in Dyslexia:
AMeta-Analysis
Mark W. Noordenbos
Radboud University Nijmegen
Willy Serniclaes
Université Libre de Bruxelles, CNRS & Université Paris Descartes
Speech perception in dyslexia is characterized by a categorical perception (CP) deficit, demonstrated
by weaker discrimination of acoustic differences between phonemic categories in conjunction with
better discrimination of acoustic differences within phonemic categories. We performed a meta-anal-
ysis of studies that examined the reliability of the CP deficit in dyslexia. The results show a reliable
CP deficit in individuals with dyslexia compared to both chronological-age and reading-level con-
trols. The CP deficit is stronger for discrimination than for identification, suggesting that the latter
may only reveal between-category differences that do not fully reflect the CP deficit. The implications
of these findings for the allophonic theory of dyslexia are discussed.
Developmental dyslexia, a specific impairment of written language acquisition (Lyon, Shaywitz,
&Shaywitz,2003), has important implications for education. Many studies have attempted to
determine its nature and origin, producing evidence of many different correlates of dyslexia
(Sprenger-Charolles, Colé, & Serniclaes, 2013). Dyslexia is basically a failure to relate written
symbols to phonological segments, that is, to relate graphemes to phonemes in alphabetic writ-
ing systems. A review of different sources of evidence (behavioral, neural, and genetic) points
to three broad categories of core deficits in dyslexia (Serniclaes & Sprenger-Charolles, 2015):
aphonologicaldecit,whichisclassicallyattributedtoalesserdegreeofphonemicawareness
(I. Y. Liberman, Shankweiler, Fischer, & Carter, 1974;Melby-Lervåg,Lyster,&Hulme,2012);
agraphemicdecit,duetoafailuretocombinegraphemesintowordrepresentations(Dehaene,
2014;Vogel,Petersen,&Schlaggar,2014); and a grapho-phonemic deficit, due to a specific fail-
ure to establish grapheme–phoneme correspondences despite the absence of either phonemic or
graphemic impairments (Blomert, 2011).
The study of dyslexia is further complicated by the fact that there are several possible causes
for each of these core deficits. Here we focus on the perceptual determinants of the phonological
deficit in dyslexia. Although this deficit is often ascribed to an underlying deficit in phonemic
awareness, it may instead be caused by a more remote deficit in the perception of phoneme
Correspondence should be sent to Mark W. Noordenbos, Centre for Language Studies, Radboud University Nijmegen,
Nijmegen, P.O. Box 9103, 6500 HD Nijmegen, The Netherlands. E-mail: m.noordenbos@let.ru.nl
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2 NOORDENBOS AND SERNICLAES
categories, which can either lead to a deficit in phonemic awareness and thus in turn to sound-
letter matching difficulties, or lead more directly to such difficulties.
THE CATEGORICAL PERCEPTION DEFICIT
Although dyslexia is now thought to be a multifactorial disorder, with a range of associated
behavioral symptoms that cannot be explained by a single cognitive deficit, a number of studies
have demonstrated that at least part of the dyslexic population has a deficit in the “categorical
perception” of phonemes (e.g., Godfrey, Syrdal-Lasky, Millay, & Knox, 1981;Werker&Tees,
1987). Categorical perception ( CP) of phonemes is an important phenomenon wherein segrega-
tion between speech sounds is constrained by their phonemic labels, that is, where only acoustic
differences between phonemic categories can be discriminated, whereas within-category differ-
ences cannot (A. M. Liberman, Harris, Hoffman, & Griffith, 1957). Consequently, a deficit in CP
means that discrimination responses are less constrained by category labels, so that in principle
not only discrimination data but also identification data are needed to evidence a CP deficit, with
the latter indicating whether two different speech sounds belong to different categories. However,
discrimination data are sufficient for stimuli varying along some acoustic continuum, and CP can
be assessed by comparing between-category discrimination (for acoustic contrasts straddling the
phonemic boundary) and within-category discrimination (for acoustic contrasts located within
each phonemic category).
The most common manifestation of the CP deficit in dyslexia is weaker discrimination of
acoustic differences between phonemic categories in conjunction with better discrimination
of acoustic differences within phonemic categories (Serniclaes, Sprenger-Charolles, Carré, &
Démonet, 2001;Werker&Tees,1987; see Figure 1A). Finally, more recent studies have shown
that the enhanced discrimination of acoustic differences within phoneme categories observed in
1 2 3 4 5 6 7
25
50
75
100
Pair
% Correct Discrimination
Controls
Dyslexics
1 2 3 4 5 6 7
25
50
75
100
Pair
% Correct Discrimination
Controls
Dyslexics
AB
FIGURE 1 Schematic representations of the categorical perception (CP)
deficit in dyslexia. Note. The left panel represents the CP deficit, which
is characterized by a smaller between-category discrimination peak,
and increased within-category discrimination. The right panel represents
allophonic perception, which is characterized by a smaller between-
category discrimination peak and enhanced sensitivity to allophonic
features.
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 3
individuals with dyslexia is in fact due to enhanced sensitivity to allophonic features, that is, the
different universal acoustic features that are normally combined to perceive a given phonemic
feature (for a review, see Serniclaes & Sprenger-Charolles, 2015;seeFigure 1B).
THEORETICAL ACCOUNTS OF THE CP DEFICIT
This enhanced sensitivity to allophonic features suggests that the CP deficit in dyslexia might be
due to another mode of speech perception that is characterized by the use of allophones instead
of phonemes (Serniclaes, Van Heghe, Mousty, Carré, & Sprenger-Charolles, 2004). Allophonic
perception is also found in prelinguistic children, but this ability is normally reorganized during
the 1st year of life according to the contrasts present in the ambient language (Hoonhorst et al.,
2009). In addition, typically developing preschool children’s sensitivity to allophonic contrasts
has been shown to partly depend on school experience (Horlyck, Reid, & Burnham, 2012), sug-
gesting that school experience might enhance the use of top-down strategies to focus on relevant
contrasts and ignore irrelevant ones. However, allophonic perception may persist until later in life
in some part of the population: particularly, this reorganization of phonological representations
may not occur to the same extent in individuals with dyslexia for genetic reasons and is prob-
ably one of the causes of dyslexia. In these cases, allophonic perception blurs the relationships
between phonemes and graphemes, even in perfectly transparent alphabetic writing systems, and
is thus highly disruptive of reading acquisition.
Interpretations of the CP deficit other than the allophonic theory have been advanced. Auditory
explanations are mainly based on data evidencing a shallower slope of the phonemic identification
curve for stimuli varying along some continuum (e.g., Vandermosten et al., 2010;seeFigure 2).
1 2 3 4 5 6 7 8
0
25
50
75
100
Stimulus
% Category Labelling
Controls
Dyslexics
A
FIGURE 2 Schematic representation of the identification deficit in
dyslexia, which is characterized by a shallower slope of the identification
function and lower asymptotic floors and ceilings.
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4 NOORDENBOS AND SERNICLAES
Ashalloweridenticationslopehasmuchthesamemeaningasaweakerbetween-categorydis-
crimination peak: Both indicate lesser precision in the perception of a phonemic distinction.
However, as just explained, the observed CP deficit in dyslexia is characterized not only by
weaker sensitivity to phonemic contrasts but also by enhanced sensitivity to allophonic contrasts.
Therefore, it remains to be seen whether such differential sensitivity to different contrasts can be
explained solely on auditory grounds.
The CP deficit’s comorbidity with attention problems has also been questioned (Breier
et al., 2001). A CP deficit has been found in children both with and without attention
deficit/hyperactivity disorder (ADHD). This puts the attentional interpretation into question and
suggests that ADHD is unlikely to be a determinant of the CP deficit. Furthermore, correlations
between the CP deficit and reading performance were only found for children without ADHD.
In summary, allophonic perception provides a comprehensive explanation of the CP deficit
and has straightforward implications for learning to read. However, a possible contribution of
auditory factors cannot be entirely dismissed.
RELIABILITY OF THE CP DEFICIT
Despite the potential implications of the CP deficit for the understanding of dyslexia, its reliability
remains in question. Some studies claim to evidence a CP deficit (see above), whereas others con-
clude to the absence of such a deficit (e.g., Blomert & Mitterer, 2004;Hazan,Messaoud-Galusi,
Rosen, Nouwens, & Shakespeare, 2009;Messaoud-Galusi,Hazan,&Rosen,2011); the issue
thus remains uncertain. A problem for establishing the reliability of the CP deficit in dyslexia is
that most studies claiming to investigate the CP deficit have only collected either identification
or discrimination data. As just mentioned, it is possible to estimate a CP deficit with discrim-
ination data. However, doing so with identification data only is less straightforward. Typical
differences in the identification of speech sounds varying along some acoustic continuum are
presented in Figure 2. When compared to controls, individuals with dyslexia usually display
both a shallower slope around the phonemic boundary and less extreme asymptotic floors and
ceilings at the continuum endpoints. A shallower slope indicates less precise phonemic cate-
gorisation, a difference that is comparable to the lower between-category peak evidenced with
discrimination data. However, the difference in asymptotic floors and ceilings is more difficult to
interpret in a CP framework. Such asymptotic differences might simply be another manifestation
of lesser categorical precision, which thus bear no obvious relationship to enhanced sensivity to
within-category differences. However, it is also possible that the difference in asymptotic floors
and ceilings might somehow be due to the conflicting use of phonemic labels when reporting
within-category differences. In short, it is clear that identification data can reveal differences
in the perception of between-category differences, but they might not reveal differences in the
perception of within-category differences, which is also needed to demonstrate a CP deficit.
Finally, it is worth mentioning that if an identification function has weaker asymptotic floors
and ceilings at the endpoints of some acoustic continuum, this is roughly equivalent to a deficit in
the identification of pairs of stimuli differing in a single phonological feature (i.e., minimal pairs
for voicing, place-of-articulation, etc.). However, data collected with minimal pairs can reveal
only differences that are roughly equivalent to those present at the continuum endpoints, not
those that might also be present around the phonological boundary.
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 5
THE PRESENT STUDY
In the present meta-analysis, we examine the general reliability of the CP deficit in studies that
compared individuals with dyslexia with both chronological-age (CA) and reading-level (RL)
controls, and investigate whether the CP deficit depends on the type of task used. We also compare
the reliability of the CP deficit to that of classical indicators of dyslexia such as pseudoword read-
ing (e.g., van IJzendoorn & Bus, 1994), pseudoword repetition (Melby-Lervåg & Lervåg, 2012),
and the phonological short-term memory deficit (Swanson, Zheng, & Jerman, 2009). As previ-
ously explained, the CP deficit is more readily evidenced with a discrimination task than with
an identification task because the latter may reveal only between-category differences that do not
fully reflect the CP deficit. Therefore, we hypothesized that effect sizes based on discrimination
tasks would be larger than effect sizes based on identification tasks.
METHODS
This meta-analysis was conducted in accordance with the MOOSE guidelines for the meta-
analysis of observational studies in epidemiology (Stroup et al., 2000).
Data Collection, Inclusion, and Extraction
The data collection and inclusion process is summarized in Figure 3.Studieswereidentied
by searching electronic databases (Medline, PubMed, PsycINFO, Google Scholar) up to and
including 2014, using the following keywords: categorical perception and speech perception,
combined with terms related to dyslexia (dyslexia, reading disorder, specific reading disorder,
poor readers, poor reading, reading impairment and poor decoders). Our search was limited to
original research published as a full article in English, that is, not a review, abstract, editorial,
letter, or commentary. We also manually searched the reference lists of published studies in order
to locate other relevant studies. The authors independently screened the retrieved studies on the
basis of titles and abstracts, and where necessary the full article, to determine suitability for
inclusion or exclusion.
Studies were eligible for inclusion in the meta-analysis if they assessed CP in individuals
diagnosed with dyslexia for speech stimuli along a continuum using identification and/or dis-
crimination tasks. Studies that reported data based on minimal pairs were excluded, as there was
no stimulus continuum making the minimal pairs equivalent to continuum endpoints, making only
rough estimation of the CP deficit possible. Studies that reported data based on nonspeech stim-
uli or speech-in-noise perception were excluded. Multiple studies published by the same author
were carefully examined in order to prevent the inclusion of data from the same sample more
than once.
The authors independently extracted the data using an electronic form. The intercoder reliabil-
ity for the extracted data related to identification and discrimination ranged from 95% to 100%.
Any disagreements were resolved by discussion or consulting the original paper.
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6 NOORDENBOS AND SERNICLAES
FIGURE 3 Flow diagram for the study selection process.
Data Synthesis
As not all studies reported both identification and discrimination data, effect sizes were calculated
from either identification or discrimination results, or both. Effect sizes were mainly estimated
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 7
from reported F-ort-test values. When statistical information was not reported, but mean and
standard deviations were available for each group, we used these values to estimate the effect size.
For identification data, effect sizes were calculated from group effects for slope when av ail-
able. Results based directly on identification scores were avoided as far as possible, because
Stimulus × Group interactions can be significant in an analysis of variance even with two strictly
parallel identification curves with different 50% crossover points as a result of the S-shaped form
of the curves. Nevertheless, for studies that did not report group effects for slope (or did not
report exact test values for group effects for slope) we based the effect size on Stimulus × Group
interactions (this was the case in four studies; see also Supplementary Table 1). This approach
was appropriate, because the 50% crossover points of the identification curves were fairly similar
between the groups in these studies (based on visual inspection of the curves). For discrimination
data, effect sizes were calculated from Between-/Within-Category Difference × Group interac-
tions whenever available, and otherwise on Stimulus Pair × Group interactions. When possible
we used test statistics based on observed discrimination scores, not those based on the differ-
ence between observed discrimination scores and those predicted from identification data (see
Supplementary Table 1). The precise references of the data that were selected to calculate the
effect sizes of the included studies are reported in Supplementary Table 1.
We made an a priori decision to include all reported speech continua, in order to draw conclu-
sions about the CP deficit in general rather than for a limited or selected set of stimulus continua.
The lexical tone continua of the studies under scope were characterized by syllables differing in
fundamental frequency (F0) patterns (a continuum of Cantonese /si/ syllables varying between
ahigh-levelF0andamid-levelF0:Cheungetal.,2009;acontinuumofMandarin/pa/ syllables
varying between a high rising F0 and a falling F0: Zhang et al., 2012)makingthemcompa-
rable to consonant and vowel features, such as voicing and place-of-articulation, which also
have acoustic correlates extending over several phonemic segments (Mattock, Molnar, Polka,
&Burnham,2008). If data were collected on several stimulus continua within the same study,
asingleweightedmeaneffectsizewascalculatedforthedifferentcontinuainordertoavoid
assigning more weight to studies with more than one stimulus continuum.
For studies reporting statistical tests that were not significant (e.g., F < 1) and where means
and standard deviations, p values, or any other measures needed to estimate an effect size were
not available, we contacted the authors to request further information. Of the ve authors we
contacted, three responded and one provided numerical data to calculate the effect size. If the
information was still not available, we conservatively assumed an F value of 0.5 (halfway
between 0 and 1; this assumption was made for four studies). All analyses were repeated
excluding the assumed F values and yielded essentially identical results.
Meta-Analytic Methods
For each outcome measure, effect sizes were computed using Cohen’s d (Cohen, 1988)andcor-
rected for bias from small sample sizes (Hedges, 1981). Cohen’s d is calculated as the difference
between the means of the control and dyslexic groups divided by their pooled standard deviation
(d = [M
ctl
M
dys
]/σ ,whereσ
2
= within-group variance). A positive d indicates that the control
group had a higher group mean on average, whereas a negative d indicates a group difference in
favor of individuals with dyslexia. According to Cohen’s classification, values between 0.2 and
0.5 can be interpreted as small effects, values between 0.5 and 0.8 as moderate effects, and values
greater than 0.8 as large effects.
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TA B L E 1
Characteristics of Studies Comparing Individuals With Dyslexia and Controls on Categorical Perception for Identification and Discrimination Tasks
Sample Characteristics Effect Size (d)
Native Age (Years) N Discrimination Identification Continua
Study Language Dys CA RL Dys CA RL CA RL CA RL Place Voicing Tones
Godfrey et al. (1981) English 10.4 10.4 17 17 0.78 0.61 ba-da
0.78 0.63 da-ga
Werker and Tees (1987) English 10.3 10.5 14 14 1.14 0.52 ba-da
De Weirdt (1988) Dutch 6.6 6.4 18 18 0.63 p@-t@
Reed (1989) English 9.0 8.9 23 23 0.49 0.62 ba-da
Steffens, Eilers, Gross-Glenn, and
Jallad (1992)
English 39.6 33.3 18 18 0.24 0.71 sta-sa
0.63 0.61 a-e
0.24 0.66 b-d
Manis et al. (1997) English 13.3 12.0 8.5 25 25 24 0.64 0.20 bath-path
Adlard and Hazan (1998) English 10.3 10.1 8.2 13 12 12 0.51 0.28 sue-zoo
0.28 0.28 date-gate
de Gelder and Vroomen (1998)Dutch11.411.48.1141414 0.74 0.74 ba-da
Nittrouer (1999) English 9.0 9.0 17 93 0.43 da-ta
0.30 sei-stei
0.74 sa-sha
0.94 su-shu
Joanisse et al. (2000) English 8.6 8.4 6.9 61 52 37 0.21 0.17 spy-sky
0.15 0.09 dug-tug
Breier et al. (2001) English 10.5 10.6 47 48 0.77 ga-ka
Chiappe et al. (2001) English 7.0 6.8 26 36 1.86 bif-pif
1.34 bis-pis
Maassen, Groenen, Crul,
Assman-Hulsmans, and Gabreëls
(2001)
Dutch 8.8 8.8 7.0 8 12 8 1.03 1.13 0.16 0.16 bak-dak
1.07 1.17 1.01 1.11 bak-pak
Rosen and Manganari (2001)English13.013.0 88 0.69 ba-da
0.77 ab-ad
Serniclaes et al. (2001) French 12.9 13.0 19 17 0.57 ba-da
8
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Blomert and Mitterer (2004) Dutch 9.0 9.3 10 12 0.88 ba-da
0.54 tart-kart
Blomert, Mitterer, and Paffen (2004) Dutch 9.1 8.5 14 18 0.38 tart-kart
Chiappe, Chiappe, and Gottardo
(2004)
English 7.8 7.6 13 49 0.66 bath-path
Serniclaes et al. (2004) French 9.1 9.2 18 23 0.65 ba-pa/ga-ka
a
van Beinum, Schwippert, Been, van
Leeuwen, and Kuijpers (2005)
Dutch 25.0 25.0 12 12 1.55 1.55 bak-dak
Boada and Pennington (2006)English12.312.18.4202020 0.92 0.94 sa-sha/su-shu
White et al. (2006) English 10.5 10.3 23 22 0.00 ba-da
0.40 coat-goat
Veu i l l et , M a gn a n , E c al l e , Th a i- Va n ,
and Collet (2007)
French 10.9 10.8 23 23 0.36 ba-pa
Bogliotti, Serniclaes,
Messaoud-Galusi, and
Sprenger-Charolles (2008)
French 9.6 9.8 7.6 10 11 10 0.93 0.69 1.12 0.26 do-to
Cheung et al. (2009) Chinese 10.4 10.4 8.9 24 25 24 0.65 0.02 si
55
-si
33
30 30 30 0.73 0.01 gi
55
-ki
55
Hazan et al. (2009) English 22.8 23.4 17 20 0.70 0.46 pea-bee
Liu, Shu, and Yang (2009) Chinese 10.4 10.2 25 25 0.45 pa-p
h
a
Robertson, Joanisse, Desroches, and
Ng (2009)
English 10.5 9.7 8.0 14 14 14 0.77 0.00 0.12 0.51 ball-doll
Van d e r mo s t e n e t a l . (2010) Dutch 21.4 21.5 31 31 1.04 bak-dak
0.18 u-y
Boets et al. (2011) Dutch 5.3 5.3 16 46 0.78 bak-dak
Johnson, Pennington, Lowenstein,
and Nittrouer (2011)
English 10.9 11.2 16 16 0.29 da-ta
0.78 sue-shoe
Messaoud-Galusi et al. (2011)English11.310.56251 2.03 0.64 bee-pea
Van d e r mo s t e n e t a l . (2011) Dutch 11.6 11.7 13 25 1.32 bak-dak
0.62 u-y
Baart, de Boer-Schellekens, and
Vroomen (2012)
Dutch 20.0 20.0 22 22 0.66 aba-ada
Zhang et al. (2012) Chinese 10.3 10.3 18 18 1.64 pa
2
-pa
4
Noordenbos et al. (2013) Dutch 20.9 21.4 19 19 0.27 0.68 b@-d@
Note. Dys = individuals with dyslexia; CA = chronological-age controls; RL = reading-level controls.
a
Results of continua were combined as no differences between continua were observed irrespective of the group.
9
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10 NOORDENBOS AND SERNICLAES
Ameta-analysiswasperformedtoobtainaglobalassessmentoftheCPdecitbycalculating
an inverse variance-weighted overall effect size. A normal distribution test was used to test the
null hypothesis of a zero mean effect size, as well as differences in overall effect size between
identification and discrimination tasks. As it is unlikely that any variables which might have an
effect on the outcome of a study are identical across all of the studies included in the analysis, a
random effects model, which takes both within-study and between-study variability into account,
was used to calculate the overall effect sizes with corresponding 95% confidence intervals (CIs).
Between-study variance was estimated using a restricted maximum likelihood (REML) model.
Amajoradvantageofarandomeffectsmodelisthattheresultsarenotrestrictedtotheidenti-
fied population but can be generalized to the whole population (Borenstein, Hedges, Higgins, &
Rothstein, 2009).
Heterogeneity—that is, whether variation in effect sizes between studies was greater than
would be expected by chance alone—was estimated using Cochran’s Q and quantified with the
Higgins I
2
statistic (Higgins & Thompson, 2002). The latter describes the percentage of true
heterogeneity across the sample of studies (Higgins, Thompson, Deeks, & Altman, 2003). Note
that I
2
is not directly affected by the number of studies in the analysis and that values of 25%,
50%, and 75% are considered as low, moderate, and high levels of heterogeneity, respectively.
To further explore heterogeneity, sensitivity analyses were performed to evaluate the stability of
the overall effect size and to determine the impact of possible outliers (Viechtbauer & Cheung,
2010). All statistical analyses were carried out in the statistical software R (version 3.1.2) using
the metafor package (Viechtbauer, 2010). All reported p values were two-sided, and p < .05 was
considered statistically significant.
Publication Bias
Potential publication bias was examined using a funnel plot (Egger, Smith, Schneider, & Minder,
1997). A funnel plot is obtained by plotting a sample size-related measure (y-axis) as a function of
effect size (x-axis). Publication bias is indicated by an imbalance of variance between small and
large sample results. Typically, effect sizes are more variable for small versus large samples, but
mean effect sizes should not be larger with larger samples if there is no selection bias. If there is
no publication bias, the scatter plot should be symmetrical, resembling an inverse funnel. When
multiplied by some precision coefficient (i.e., a value inversely related to sample size), effect
sizes for very small samples should tend toward zero, because small samples have almost zero
precision. This implies that the regression line between the Effect Size × Precision interaction
and Precision should run through the origin. The intercept of that regression line provides a test
of asymmetry (Egger et al., 1997): the larger the deviation from zero, the higher the proportion
of small sample results with small effect sizes that are missing from the survey.
RESULTS
Characteristics of the Included Studies
Of the 632 studies retrieved by the literature search, 36 studies were found to meet the inclusion
criteria. The main reasons for exclusion were the use of minimal pairs rather than a stimulus
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 11
continuum, or participants who were not (yet) diagnosed with dyslexia (e.g., at-risk children).
The seminal study of Brandt and Rosen (1980)wasnotincludedinthemeta-analysisbecause
it did not contain appropriate results to calculate an effect size. We contacted the authors for
further information, but records of this study were no longer available (J. Brandt, personal com-
munication, February 14, 2015). The included studies were mainly published in journals, most
frequently in the Journal of Experimental Child Psychology (10 publications out of 36); fol-
lowed by Journal of Speech, Language, and Hearing Research (7 publications); Research in
Developmental Disabilities; Brain and Language; Journal of Child Psychology and Psychiatry;
and Developmental Science (2 publications each). The remainder (11 publications) were pub-
lished in 11 different journals. Half of the studies (18 publications) were conducted with English-
speaking participants. The remainder were conducted with Dutch-speaking (11 publications),
French-speaking (4 publications), and Chinese-speaking (3 publications) participants.
Effect sizes as a function of stimulus characteristics (continua) and group characteristics (age
and language) are listed in Table 1.The36relevantstudiesincluded754individualswithdyslexia
(M = 20.94, SD = 12.42, range = 8–62) and 914 CA controls (M = 25.39, SD = 16.73,
range = 8–93). Most of these studies ensured that the individuals with dyslexia had average or
above-average nonverbal intelligence scores, showed difficulties on standardized reading and/or
spelling tasks and had no other neurological or psychological disorders. Three studies included
participants regardless of any comorbid ADHD diagnosis (Boada & Pennington, 2006;Breier
et al., 2001; White et al., 2006). Nine of the 36 studies also included RL controls, a total of
169 individuals (M = 18.78, SD = 9.82, range = 8–37).
Most studies (20 of 36) used only one stimulus continuum. Place-of-articulation continua were
more frequently used (62%) than voicing continua (35%), and two studies (4%) used a lexical
tone continuum. A large majority of the studies (34 of 36) collected identification data, about
one third of the studies (13 of 36) collected discrimination data, and only 11 of the 36 studies
collected both identification and discrimination data.
Comparisons of Individuals With Dyslexia and Chronological-Age Controls
As expected, CP was systematically weaker in individuals with dyslexia compared to CA con-
trols. For identification data, the overall mean effect size was d = 0.66, 95% CI [0.54, 0.77],
and was significantly different from zero (z = 10.89, p < .001). Heterogeneity was s mall and
not significant, Q(33) = 43.78, p = .10, I
2
= 27%, indicating no statistical evidence for differ-
ences between the studies. In the sensitivity analyses, two studies were identified as influential
(Chiappe, Chiappe, & Siegel, 2001;Joanisse,Manis,Keating,&Seidenberg,2000). The study by
Joanisse et al. (2000)hadthelargestweightintheanalysis,whereasthestudybyChiappeetal.
(2001)hadoneofthelargesteffectsizesintheanalysis.Weexaminedthesestudiestodetermine
whether they had any characteristics that set them apart from the other studies besides extreme
values, but no other complicating factors were clearly evident. Excluding these two studies did
not significantly change the overall mean effect size (p = .89).
For discrimination data, the overall mean effect size was d = 0.86, 95% CI [0.56, 1.16], and
was also significantly dif ferent from zero (z = 5.68, p < .001). Heterogeneity was moderate
and significant, Q(12) = 40.29, p < .001, I
2
= 65%. In the sensitivity analyses, one study was
identified as influential with respect to between-study variance (Messaoud-Galusi et al., 2011).
We examined this study to determine whether any characteristics set this study apart from the
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12 NOORDENBOS AND SERNICLAES
other studies, but besides a large sample size (> 50 participants per group) no other factors were
clearly evident. Excluding this study did not significantly change the overall mean effect size
(p = .33), but the study had an effect on between-study variance, as between-study variance
among the remaining 12 studies was small, and did not significantly differ from chance. Effect
sizes with CIs for each study are displayed in Figures 4 and 5 for identification and discrimination
data, respectively.
To test whether the extent of evidence for a CP decit depended on the type of task used, we
compared the effect sizes based on discrimination tasks with the effect sizes based on identifica-
tion tasks. The difference in overall mean effect size between identification and discrimination
data was significant in both an independent group comparison including all 36 studies (z = 2.52,
p = .01) and in a pairwise comparison including only the 11 studies in which both identification
and discrimination data were available (d = 0.64 vs. 0.97; z = 2.37, p = .02), with a larger effect
size for discrimination data.
To check for potential publication bias, we used funnel plots in which identication or dis-
crimination effect sizes were plotted on the x-axis and the weight of each study was plotted on
the y-axis. The resulting funnel plots are shown in Supplementary Figure 1. Examination of the
funnel plots revealed no indication of publication bias (i.e., no decrease in either identification
or discrimination effect size variability at higher weights). Egger’s asymmetry test (Egger et al.,
1997)fortheidenticationordiscriminationeffectsizesshowedthattheinterceptoftheregres-
sion lines between the Effect Size × Precision interaction and Precision did not significantly
differ from zero in either case (both p > .05). According to Egger’s asymmetry tests, there seems
to have been no publication bias in the studies within the scope of the present meta-analysis.
However, a closer visual inspection of the funnel plot with discrimination data reveals a slight
asymmetry, suggesting potential publication bias.
Comparisons of Individuals With Dyslexia and Reading-Level Controls
The CP of individuals with dyslexia was weaker than that of RL controls in all nine studies
examined here. The overall mean effect size for differences in identification between individuals
with dyslexia and RL controls was d = 0.32, 95% CI [0.10, 0.53], and was significantly different
from zero (z = 2.91, p < .01). Heterogeneity was small and not significant, Q(8) = 8.36, p = .40,
I
2
= 14%, indicating no statistical evidence for differences between the studies. In the sensitivity
analyses, one study was identified as an influential study (Boada & Pennington, 2006). Other
than the fact that this study had the largest effect size in the analysis, no other factors were clearly
evident, which set this study apart from the other studies in the analysis. Excluding this study did
not significantly change the overall mean effect size (p = .58). The number of studies reporting
discrimination results with RL controls was too small (only three) to draw any conclusions.
DISCUSSION
The results of the 36 studies that were eligible for the present meta-analysis give a fairly clear
picture of the CP deficit in dyslexia. The results of the meta-analysis show that the CP deficit is
indeed reliable overall, with large and significant effects for both identification and discrimination
tasks. Although no significant publication bias was identified statistically, visual inspection of the
discrimination data suggests possible publication bias.
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 13
FIGURE 4 Forest plot for group differences in categorical perception
between individuals with dyslexia and chronological-age controls, based
on identification data. Note. The effect sizes of the individual studies are
indicated by squares and the 95% confidence intervals by horizontal lines.
The size of each square is proportional to the weight of the corresponding
study. The diamond indicates the overall mean effect size, and the width
of the diamond represents the overall confidence interval.
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14 NOORDENBOS AND SERNICLAES
FIGURE 5 Forest plot for group differences in categorical perception
between individuals with dyslexia and chronological-age controls, based
on discrimination data. Note. The effect sizes of the individual studies are
indicated by squares and the 95% confidence intervals by horizontal lines.
The size of each square is proportional to the weight of the corresponding
study. The diamond indicates the overall mean effect size and the width of
the diamond represents the overall confidence interval.
In comparisons between individuals with dyslexia and CA controls, the CP deficit was highly
significant for both tasks, identification and discrimination, although effect sizes were signifi-
cantly larger for the discrimination task. The overall mean effect size for the discrimination task
was d = 0.86 (13 studies, more than 250 participants per group), which is a large effect size
according to Cohen’s (1988) classification. The overall mean effect size for the identification
task was d = 0.66 (34 studies, more than 700 participants per group), an effect size that falls
between moderate (0.50) and large (0.80) in Cohen’s classification.
In comparisons of individuals with dyslexia to RL controls—that is, to younger individuals
of the same reading age—a significant difference in overall mean effect size was also found.
However, only the effect sizes for identification could be estimated here, an analysis that yielded
a d value of only 0.32 (nine studies, about 170 participants per group), which falls between small
(0.20) and moderate (0.50) in Cohen’s classification.
Comparing the CP Deficit With Other Deficits in Dyslexia
There is ample evidence that the majority of individuals with dyslexia have a phonological deficit
and that pseudoword reading is one of the best indicators of this phonological deficit. Therefore,
pseudoword reading can be used as a benchmark to assess the reliability of the CP deficit. Given
the importance of reading development, most studies on pseudoword reading have used a design
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 15
in which individuals with dyslexia are compared to RL controls rather than CA controls, to ensure
that observed group differences could not be explained by reading level differences between
groups. Meta-analytic studies comparing individuals with dyslexia to RL controls have shown
that the mean effect size for the deficit in pseudoword reading was about d = 0.48 (van IJzendoorn
&Bus,1994), or, in a more recent meta-analysis, d = 0.65 (Herrmann, Matyas, & Pratt, 2006).
For similar comparisons with RL controls, the mean effect size for the CP deficit (d = 0.32) was a
bit smaller than this pseudoword reading deficit. However, the latter effect size is based on identi-
fication data and is probably much smaller than what would be obtained with discrimination data.
Recall that the number of comparisons between individuals with dyslexia and RL controls with
discrimination data within the scope of the present meta-analysis was too small (three studies) to
allow reliable assessment. But based on the results obtained with CA controls, the discrimination
effect size should be much larger than the identification effect size (d = 0.86 vs. 0.66). An esti-
mate of the effect size of the CP deficit based on discrimination data would therefore probably
reach much the same level as in pseudoword reading. This is not to say that pseudoword reading
and CP stand in the same relationship to dyslexia. It may be that the pseudoword reading deficit
is related to different core deficits in dyslexia, whereas the CP deficit is specifically related to
the phonological deficit. The fact that, despite such limitations, the effect size of the CP deficit is
comparable to that of the deficit in pseudoword reading is impressive.
Another meta-analytic study investigated the deficit in pseudoword repetition that is also asso-
ciated with dyslexia (Melby-Lervåg & Lervåg, 2012). This study showed a mean effect size
of d = 0.92 in comparisons of pseudoword repetition performance between individuals with
dyslexia and CA controls, which is close to the mean effect size obtained here for the CP deficit
with discrimination data (d = 0.86). Also, the mean effect size in pseudoword repetition was
d = 0.36 for comparisons between individuals with dyslexia and RL controls, a value not far
above the one obtained here for the CP deficit in nonoptimal conditions (with identification data:
d = 0.32).
Other meta-analyses have investigated possible determinants of dyslexia and evidenced large
effect sizes for phonological skills, well above those obtained here for the CP deficit (d = 1.37 for
CA controls, d = 0.57 for RL controls in Melby-Lervåg et al., 2012; d = 1.20 for CA controls,
d = 0.52 for RL controls in Melby-Lervåg & Lervåg, 2012). However, the effect sizes found here
for the CP deficit are similar to those obtained elsewhere for oral language skills (d = 0.82 for
CA controls, d = 0.32 for RL controls in Melby-Lervåg & Lervåg, 2012)andforphonological
short-term memory (d = 0.83 for CA controls in Swanson et al., 2009). Apart from phonemic
awareness, which is assessed with tasks that are very close to the processes involved in reading,
the CP deficit is certainly not less reliable than the other possible determinants of dyslexia. This
is a noteworthy result, recalling that there are different possible sources of dyslexia, and that
therefore no deficit can be completely reliable.
Explaining the Variability of the CP Deficit
Although the overall CP deficit in dyslexia is reliable, the magnitude of this deficit is variable
across studies. Studies comparing individuals with dyslexia to typically developing readers dif-
fer in sample characteristics, experimental design, language, and selection criteria, among other
factors. Because it is unlikely that all factors which may account for v ariation in effect sizes of
the included studies are identical, we used a random effects model, which also takes into account
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16 NOORDENBOS AND SERNICLAES
the factors that differ between studies. The advantage of this approach is that the results allow for
generalization beyond the particular set of studies included in the meta-analysis.
Our meta-analysis focused on the extent to which the CP deficit depends on the type of task
used. The mean effect size of the CP deficit was significantly larger for discrimination data
than for identification data (d = 0.86 vs. 0.66). As explained in the Introduction, identification
responses might be adequate only to establish sensitivity to differences between categories but
not to those within phonemic categories. As both (decreased) sensitivity to between-category dif-
ferences and (increased) sensitivity to within-category differences contribute to the CP deficit in
dyslexia, this might explain why a weaker CP deficit was obtained here with identification data.
Implications of the CP Deficit for Explaining Dyslexia
Concerning the causal role of the CP deficit in dyslexia, there is no doubt that reading instruction
exerts a strong influence on CP, and more specifically on the perception of allophonic contrasts.
This raises an important issue, because it bears on the direction of the causal relationship between
CP and reading difficulties. A study with Australian children suggested that the perception of
allophonic contrasts was negatively related to school experience but had no relationship with
age (Horlyck et al., 2012). In this study, a group of 5-year-old children with 6 months of school
experience were found to be less sensitive to an allophonic contrast than children of the same
age without school experience. Although the children in this Australian study were not at risk
for dyslexia, they exhibited some allophonic sensitivity, the degree of which was modulated by
school experience. The effect of school experience on allophonic sensitivity was confirmed in a
longitudinal study with Dutch children at risk for dyslexia. These children exhibited a strong CP
deficit when they were in kindergarten, characterized by both a weaker phonemic discrimination
peak and a stronger allophonic peak; but this CP deficit was completely absent when they were
in the first grade, after 6 months of formal reading instruction (Noordenbos, Segers, Serniclaes,
Mitterer, & Verhoeven, 2012a). These findings might suggest that allophonic perception is not
entirely specific to dyslexia and that it decreases with reading experience. However, these conclu-
sions have been called into question by neurophysiological data, which point to the persistence of
allophonic percepts in dyslexia, irrespective of reading experience. Even though allophonic sensi-
tivity was no longer apparent in the behavioral responses of the Dutch children at risk f or dyslexia
in first grade, it was still present in neurophysiological recordings performed on the same chil-
dren (Noordenbos, Segers, Serniclaes, Mitterer, & Verhoeven, 2012b). Similar results have been
obtained for adults with dyslexia (Noordenbos, Segers, Serniclaes, & Verhoeven, 2013). These
apparently conflicting results might be explained by differences in sensitivity between behav-
ioral and neural measures. Neural measures accurately reflect the temporal development of the
underlying processes, whereas overt behavioral responses only reflect the endpoint of process-
ing and may abstract away from subtle underlying processing deficits. In summary, although the
behavioral manifestations of allophonic perception and the related CP deficit may disappear with
reading experience, this sensitivity may still be present in the form of neural activation.
CONCLUSIONS
The results of this meta-analysis demonstrate that the finding of a CP deficit in individuals with
dyslexia is highly reliable, although the magnitude of the effect is quite variable across studies.
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CATEGORICAL PERCEPTION DEFICIT IN DYSLEXIA 17
Part of this variability is due to random variations between groups, but it is also due to the type
of task used, the CP deficit being more easily evidenced with a discrimination task than with an
identification task.
SUPPLEMENTAL MATERIAL
Supplemental data for this article can be accessed at www.tandfonline.com/hssr.
ACKNOWLEDGMENTS
We thank Sunjing Ji for providing assistance on tone perception in Chinese. Many thanks to Paul
Reeve for proofreading the manuscript.
FUNDING
The research reported in this meta-analysis was supported by a public grant overseen by the
French National Research Agency (ANR) as part of the “Investissements d’Avenir” program
(reference: ANR-10-LABX-0083) to Willy Serniclaes.
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... In order to define the inter-category boundary between these phonemes and to consistently classify the same ambiguous stimuli into the same phoneme category, fine-tuned auditory spectro-temporal processing skills are essential. Thus, multiple processes are necessary for this task, i.e., sensitive auditory spectro-temporal processing, neglecting the variance within-speech sound category and linking the speech sound to phoneme representations in the brain (via interaction with long-term memory) [74][75][76] . ...
... Given the current data set, we cannot say whether an impairment in consistently identifying phonemes may be due to inefficient auditory spectro-temporal processing, or rather due to difficulties with neglecting withinphoneme category variance or with linking the sound to the correct phoneme representation [74][75][76] . Administering a phoneme discrimination task in addition to the phoneme identification task may be useful to disentangle the underlying processes in the future. ...
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Acoustic and phonemic processing are understudied in aphasia, a language disorder that can affect different levels and modalities of language processing. For successful speech comprehension, processing of the speech envelope is necessary, which relates to amplitude changes over time (e.g., the rise times). Moreover, to identify speech sounds (i.e., phonemes), efficient processing of spectro-temporal changes as reflected in formant transitions is essential. Given the underrepresentation of aphasia studies on these aspects, we tested rise time processing and phoneme identification in 29 individuals with post-stroke aphasia and 23 healthy age-matched controls. We found significantly lower performance in the aphasia group than in the control group on both tasks, even when controlling for individual differences in hearing levels and cognitive functioning. Further, by conducting an individual deviance analysis, we found a low-level acoustic or phonemic processing impairment in 76% of individuals with aphasia. Additionally, we investigated whether this impairment would propagate to higher-level language processing and found that rise time processing predicts phonological processing performance in individuals with aphasia. These findings show that it is important to develop diagnostic and treatment tools that target low-level language processing mechanisms.
... Plusieurs théories ont ainsi exploré le lien entre les troubles pho nologiques et les troubles développementaux du langage (pour une revue, voir Parisse & Maillart [7]). L'existence d'un déficit de perception catégorielle en cas de dyslexie a également été étudiée à maintes reprises [8]. Évaluer les capacités phonologiques réceptives dans le cadre de troubles langagiers a donc un intérêt diagnostique, mais permet également d'ajuster la prise en charge orthopho nique. ...
... There is substantial evidence to suggest that speech-processing difficulties are associated with childhood language disorders. In categorical perception studies, children with dyslexia are often less consistent at matching unambiguous stimuli to appropriate phonemic categories, and show shallower labeling functions (Godfrey et al., 1981;Joanisse et al., 2000;Manis et al., 1997;Messaoud-Galusi et al., 2007;Noordenbos & Serniclaes, 2015). Furthermore, discrimination of speech sounds at 5½ years predicts phoneme awareness and reading abilities at 6½ years (Snowling, Lervåg, et al., 2019;. ...
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Poor performance on phonological tasks is characteristic of neurodevelopmental language disorders (dyslexia and/or developmental language disorder). Perceptual deficit accounts attribute phonological dysfunction to lower-level deficits in speech-sound processing. However, a causal pathway from speech perception to phonological performance has not been established. We assessed this relationship in typical adults by experimentally disrupting speech-sound discrimination in a phonological short-term memory (pSTM) task. We used an automated audio-morphing method (Rogers & Davis, 2017) to create ambiguous intermediate syllables between 16 letter name–letter name (“B”–“P”) and letter name–word (“B”–“we”) pairs. High- and low-ambiguity syllables were used in a pSTM task in which participants (N = 36) recalled six- and eight-letter name sequences. Low-ambiguity sequences were better recalled than high-ambiguity sequences, for letter name–letter name but not letter name–word morphed syllables. A further experiment replicated this ambiguity cost (N = 26), but failed to show retroactive or prospective effects for mixed high- and low-ambiguity sequences, in contrast to pSTM findings for speech-in-noise (SiN; Guang et al., 2020; Rabbitt, 1968). These experiments show that ambiguous speech sounds impair pSTM, via a different mechanism to SiN recall. We further show that the effect of ambiguous speech on recall is context-specific, limited, and does not transfer to recall of nonconfusable items. This indicates that speech perception deficits are not a plausible cause of pSTM difficulties in language disorders.
... Cross-linguistic studies have demonstrated that cortical processing is modulated by experience with phonotactic patterns (Dehaene-Lambertz et al., 2000;Wagner et al., 2012Wagner et al., , 2013Wagner et al., , 2022 and these modulatory influences are established during childhood (Jusczyk et al., 1993;Ortiz-Mantilla et al., 2016;Werker and Hensch, 2015). Sensory processing that is selective to native-language phonotactic patterns is streamlined and may facilitate language comprehension (Hisagi et al., 2010;Noordenbos and Serniclaes, 2015;Strange, 2011;Wagner et al., 2012). ...
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The phonotactic patterns of one's native language are established within cortical network processing during development. Sensory processing of native language phonotactic patterns established in memory may be modulated by top-down signals within the alpha and beta frequency bands. To explore sensory processing of phonotactic patterns in the alpha and beta frequency bands, electroencephalograms (EEGs) were recorded from native Polish and native English-speaking adults as they listened to spoken nonwords within same and different nonword pairs. The nonwords contained three phonological sequence onsets that occur in the Polish and English languages (/pət/,/st/,/sət/) and one onset sequence/pt/, which occurs in Polish but not in English onsets. Source localization modeling was used to transform 64-channel EEGs into brain source-level channels. Spectral power values in the low frequencies (2-29 Hz) were analyzed in response to the first nonword in nonword pairs within the context of counterbalanced listening-task conditions, which were presented on separate testing days. For the with-task listening condition, participants performed a behavioral task to the second nonword in the pairs. For the without-task condition participants were only instructed to listen to the stimuli. Thus, in the with-task condition, the first nonword served as a cue for the second nonword, the target stimulus. The results revealed decreased spectral power in the beta frequency band for the with-task condition compared to the without-task condition in response to native language phonotactic patterns. In contrast, the task-related suppression effects in response to the non-native phonotactic pattern/pt/for the English listeners extended into the alpha frequency band. These effects were localized to source channels in left auditory cortex, the left anterior temporal cortex and the occipital pole. This exploratory study revealed a pattern of results that, if replicated, suggests that native language speech perception is supported by modulations in the alpha and beta frequency bands.
... Although dyslexia is primarily defined as a reading disorder, it is also characterized by phonological deficits, manifested in assessments of phonological awareness, phonological short-term judgement, and rapid retrieval of phonological forms (Noordenbos & Serniclaes, 2015). Indeed, deficits in phonological skills are found in the majority of children, adolescents and adults with dyslexia (Ramus et al., 2003). ...
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With the use of ICT, in general in special education and in particular in dyslexia, there are tangible results that allow the development of the student. New technologies, therefore, give the possibility to create a digital environment that will enhance the use of the senses on the part of the student, which is not always easy in the case of conventional education for the student diagnosed with dyslexia.
... Another common task used to assess speech perception is the categorical perception task. A previous meta-analysis found a robust defect of categorical perception in DD (Noordenbos & Serniclaes, 2015). Although both SPIN and categorical perception tasks can represent speech perception, no correlations were found between them in either typical or dyslexic readers (Calcus et al., 2016), suggesting that the two tasks may represent different aspects of speech perception. ...
Article
Purpose Developmental dyslexia is a specific learning disorder that affects 5–17% children, and persists into adulthood. Speech perception in noise (SPIN) ability in dyslexia has been largely examined in previous studies. However, the available literature remains controversial and it is unclear under which conditions the deficits occur. The present meta-analysis explored the reliability of the SPIN deficit in dyslexia and examined possible moderators of the variability across studies. Method A robust variation estimation model was used based on 19 studies comprising 69 effect sizes. Results Individuals with dyslexia showed a reliable SPIN deficit (Hedges’ g = 0.64, 95% CI [0.41, 0.87], p < .001) compared to chronological age-matched controls, with the presence of moderate inter-study variability. Moderation analyses showed that the SPIN deficit in dyslexia was moderated by performance measure, manifesting a larger effect size measured by accuracy than by speech reception threshold. Nevertheless, comparable medium SPIN effect sizes were found for background noises inducing energetic masking and informational masking, as well as for children and adults with dyslexia. Conclusion The present meta-analysis for the first time provides a comprehensive understanding of the SPIN deficit and its underlying cognitive mechanisms in individuals with dyslexia.
... However, in the absence of a continuum from one phoneme to another, the present paradigm should not be considered a measure of categorical phoneme processing. Nevertheless, our results are in line with behavioral evidence of deficient categorical phoneme processing associated with DD (Noordenbos and Serniclaes, 2015). A phoneme categorization deficit in infants could lead to language learning dysfunctions, since efficient acquisition of native language phonemes during infancy was proposed to be vital for good language development (Kuhl, 2010) and for eventually mapping the phonemes with their written input, i.e., literacy acquisition (Serniclaes, 2018). ...
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A crucial skill in infant language acquisition is learning of the native language phonemes. This requires the ability to group complex sounds into distinct auditory categories based on their shared features. Problems in phonetic learning have been suggested to underlie language learning difficulties in dyslexia, a developmental reading-skill deficit. We investigated auditory abilities important for language acquisition in newborns with or without a familial risk for dyslexia with electrophysiological mismatch responses (MMRs). We presented vowel changes in a sequence of acoustically varying vowels, requiring grouping of the stimuli to two phoneme categories. The vowel changes elicited an MMR which was significantly diminished in infants whose parents had the most severe dyslexia in our sample. Phoneme-MMR amplitude and its hemispheric lateralization were associated with language test outcomes assessed at 28 months, an age at which it becomes possible to behaviourally test children and several standardized tests are available. In addition, statistically significant MMRs to violations of a complex sound-order rule were only found in infants without dyslexia risk, but these results are very preliminary due to small sample size. The results demonstrate the relevance of the newborn infants' readiness for phonetic learning for their emerging language skills. Phoneme extraction difficulties in infants at familial risk may contribute to the phonological deficits observed in dyslexia.
Preprint
Both Developmental Language Disorder (DLD) and Reading Disorder (RD or dyslexia) have been proposed to derive in part from low-level speech perception deficits which may affect downstream language/reading processes. However, DLD and RD are comorbid, raising questions of whether the deficits in one group are driven by the other. Moreover, methodological limits of traditional forced-choice categorizations create uncertainty regarding the nature of the deficits. We examined speech categorization in children with language/reading disabilities, using a visual analog scaling task that overcomes these limits. Participants hear tokens from a speech continuum and indicate the degree of correspondence between the stimulus and each word by selecting a point on a continuous rating scale. Results revealed that children with poor language/reading exhibited similar long-term category structure to their peers with better abilities, but greater trial-to-trial categorization inconsistency. The categorization inconsistency has a unique effect on language/reading abilities, even after controlling for the potential mediating effect of phonological processing on language/reading. Importantly, children with poor reading showed high inconsistency specifically for vowels. These suggest that children’s language/reading abilities are more associated with the consistency of the perceptual processes.
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Learning to read is a middle-distance race for children worldwide. Most of them succeed in this acquisition with “normal” difficulties that ensue from the progressive (re)structuring of the phonological and orthographic systems. Evidence accumulated on reading difficulties in children with developmental dyslexia (DYS children, henceforth) shows a pervasive phonological deficit. However, the phonological deficit may not be due to degraded phonological representations but rather due to impaired access to them. This study focused on how and to what extent phonological syllables, which are essential reading units in French, were accessible to DYS children to segment and access words. We tested the assumption that DYS children did not strictly have pervasive degraded phonological representations but also have impaired access to phonological and orthographic representations. We administered a visually adapted word-spotting paradigm, engaging both sublexical processing and lexical access, with French native-speaking DYS children (N = 25; Mage in months = 121.6, SD = 3.0) compared with chronological age-matched peers (N = 25; Mage in months = 121.8, SD = 2.7; CA peers henceforth) and reading level-matched peers (N = 25; Mage in months = 94.0, SD = 4.6; RL peers henceforth). Although DYS children were slower and less accurate than CA and RL peers, we found that they used phonological syllables to access and segment words. However, they exhibit neither the classical inhibitory syllable frequency effect nor the lexical frequency effect, which is generally observed in typically developing children. Surprisingly, DYS children did not show strictly degraded phonological representations because they demonstrated phonological syllable-based segmentation abilities, particularly with high-frequency syllables. Their difficulties are rather interpreted in terms of impaired access to orthographic and phonological representations, which could be a direct effect of difficulties in generalizing and consolidating low-frequency syllables. We discuss these results regarding reading acquisition and the specificities of the French linguistic system.
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The perception of phonological categories in dyslexia is less refined than in typically developing (TD) individuals. Traditionally, this characteristic was considered unique to phonology, yet many studies showed non-phonological perceptual difficulties. Importantly, measuring the dynamics of cortical adaptation, associated with category acquisition, revealed a broadly distributed faster decay of cortical adaptation. Taken together, these observations suggest that the acquisition of perceptual categories in dyslexia may be slower across modalities. To test this, we tested adult individuals with developmental dyslexia (IDDs) and TDs on learning of two unknown faces, yielding face-specific categorization. Initial accuracy was similar in the two groups, yet practice-induced increase in accuracy was significantly larger in TDs. Modeling the learning process (using Drift Diffusion Model) revealed that TDs' steeper learning results from a larger increase in their effective face-specific signal. We propose that IDDs' slower item-specific categorical learning of unknown faces indicates that slower categorical learning in dyslexia is a core, domain-general difficulty.
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Reading is an important but phylogenetically new skill. While neuroimaging studies have identified brain regions used in reading, it is unclear to what extent these regions become specialized for use predominantly in reading vs. other tasks. Over the past several years, our group has published three studies addressing this question, particularly focusing on whether the putative visual word form area (VWFA) is used predominantly in reading, or whether it is used more generally in a number of tasks. Our three studies utilize a range of neuroimaging techniques, including task based fMRI experiments, a seed based resting state functional connectivity (RSFC) experiment, and a network based RSFC experiment. Overall, our studies indicate that the VWFA is not used specifically or even predominantly for reading. Rather the VWFA is a general use region that has processing properties making it particularly useful for reading, though it continues to be used in any task that requires its general processing properties. Our network based RSFC analysis extends this finding to other regions typically thought to be used predominantly for reading. Here, we review these findings and describe how the three studies complement each other. Then, we argue that conceptualizing the VWFA as a brain region with specific processing characteristics rather than a brain region devoted to a specific stimulus class, allows us to better explain the activity seen in this region during a variety of tasks. Having this type of conceptualization not only provides a better understanding of the VWFA but also provides a framework for understanding other brain regions, as it affords an explanation of function that is in keeping with the long history of studying the brain in terms of the type of information processing performed (Posner, 1978).
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This study examined the interaction between speech perception and sentential context among 13 poor readers and 49 good readers in grades one to three. Children's performance was examined on tasks assessing expressive and receptive vocabulary, reading skill, phonological awareness, pseudoword repetition, and phoneme identification. Good readers showed clearly defined categorical perception in the phoneme identification task for both sentence frames biased to the identification of the /b/ or /p/ phoneme. The /b/–/p/ category boundary for the BATH frame was at longer voice onset times (VOTs) than the boundary for PATH frame. Poor readers showed less sharply defined categorical perception with both sentence frames. Although poor readers did not show a shift in the /b/–/p/ category boundary, sentential context did affect the overall rate with which phonemes were identified as /b/ or /p/ at each VOT. These findings suggest that semantic information may operate as a compensatory mechanism for resolving ambiguities in speech perception. Furthermore, expressive vocabulary was more closely related than receptive vocabulary to individual differences in reading and phonological processing, providing support for the phonological distinctness hypothesis.
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In a recent narrative review, Rack, Snowling, and Olson (1992) evaluated the hypothesis that dyslexic children have a specific deficit in phonological reading processes. To replicate, test, and extend their findings and speculations, the authors performed a quantitative meta-analysis with the same hypothesis and on the same database. Clear evidence for a modest difference (d=.48; N=1183) between dyslexics and reading-level-matched normal readers on nonword reading tasks was found. The nonword reading deficit in developmental dyslexia should be considered an established fact, although its contribution to the explanation of dyslexia is not large (less than 6% of the variance). Contrary to Rack et al. (1992), the major weaknesses of studies not finding a significant deficit did not appear to be the type of nonword reading test, the age of the normal readers, or the dyslexics' participation in special remediation programs. The adequacy of the matching procedure in terms of differences in age and intelligence and in word recognition ability was more important. /// [French] Dans une récente revue de question de type narratif, Rack, Snowling et Olson (1992) ont évalué l'hypothèse que les enfants dyslexiques ont un déficit spécifique dans les processus de lecture phonologique. Pour répliquer, tester et étendre ces conclusions et ces réflexions, les auteurs du présent texte ont réalisé une méta-analyse quantitative avec la même hypothèse et la même base de données. Ils ont clairement établi l'existence d'une différence modeste (d=.48; N=1183) entre des dyslexiques et des lecteurs normaux qui avaient été appariés selon l'âge de lecture dans des tâches de lecture de non mots. On devrait donc considérer comme un fait établi l'existence du déficit des enfants dyslexiques dans la lecture de non mots, quoique sa contribution à l'éxplication de la dyslexie ne soit pas grande: moins de 6% de la variance. Contrairement à Rack et al. (1992), les faiblesses majeures des études qui ne trouvent pas de différence significative n'apparaissent pas être le type de test de lecture de non mots, l'âge des lecteurs normaux, ou la participation des dyslexiques à des programmes particuliers de rééducation. Ce qui est apparu plus important est l'adéquation de la procédure d'appariement des enfants en termes de différences d'âge et d'intelligence, et en capacité de reconnaissance des mots. /// [Spanish] En una revisión reciente, Rack, Snowling y Olson (1992) evaluaron la hipótesis de que los niños disléxicos tienen un déficit específico en los procesos fonológicos de la lectura. Para replicar, probar y extender estos hallazgos y especulaciones, los autores hicieron un meta-análisis cuantitativo con la misma hipótesis y la misma base de datos. Se encontró evidencia clara de una leve diferencia (d=.48; N=1183) entre disléxicos y lectores normales, apareados por nivel de lectura, en tareas de lectura de pseudopalabras. El déficit en lectura de pseudopalabras en la dislexia evolutiva debe ser considerado un hecho establecido, si bien la contribución de este hecho a la explicación de la dislexia no es grande (menos del 6% de la varianza). Contrariamente a lo propuesto por Rack et al. (1992), la debilidad principal de los estudios que no hallaron un déficit significativo, no fue el tipo de prueba de lectura de pseudopalabras, la edad de los lectores normales o la participación de los disléxicos en programas especiales de recuperación. La adecuación del procedimiento de apareamiento en términos de diferencias de edad e inteligencia y en habilidades de reconocimiento de palabras fue más importante. /// [German] In einer neueren Überblicksdarstellung evaluierten Rack, Snowling und Olson (1992) die Hypothese, daß lesegestörte Kinder einen spezifischen Mangel auf der phonologischen Ebene des Leseprozesses aufweisen. Um ihre Ergebnisse und Beobachtungen einschätzen, testen und erweitern zu können, unternahmen die Autoren eine quantitative Meta-Analyse mit derselben Hypothese und auf derselben Datenbasis. Es konnten deutliche Hinweise auf einen kleinen Unterschied (d=.48; N=1183) zwischen dem erreichten Level von Lesegestörten und dem normaler Leser von Texten gefunden werden. Das Textlesedefizit bei Leseentwicklungsstörung kann als Faktum angenommen werden, obwohl sein Erklärungsumfang nicht allzu weit reicht (weniger als 6% der Abweichung). Im Unterschied zu Rack u. a. (1992) schien die Hauptschwäche der Studien, die keinen signifikanten Mangel fanden, darin zu liegen, daß sie nicht den Textlesetest beinhalteten, das Alter der normalen Leser oder die Teilnahme lesegestörter Personen an speziellen Verbesserungsprogrammen. Die Adäquanz der Erfolgsprozedur, gemessen an Alter, Intelligenz und Wortlernfähigkeit, war vorher wichtiger.
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IntroductionIndividual studiesThe summary effectHeterogeneity of effect sizesSummary points
Article
Reading in the Brain (Les neurones de la lecture, 2007) examined the origins of human reading abilities in the light of contemporary cognitive neuroscience. It argued that reading acquisition, in all cultures, recycles preexisting cortical circuits dedicated to invariant visual recognition, and that the organization of these circuits imposes strong constraints on the invention and cultural evolution of writing systems. In this article, seven years later, I briefly review new experimental evidence, particularly from brain imaging studies of illiterate adults, which indicates that reading acquisition invades culturally universal cortical circuits and competes with their prior function, including mirror-invariant visual recognition and face processing. In response to my critics, I emphasize how brain plasticity and brain constraints can be reconciled within the Bayesian perspective on learning. I also discuss the importance of a newly discovered gesture system in reading and writing. Finally, I argue that there is consistent evidence for deep cross-cultural universals in writing systems, as well as for the multiple subtypes of dyslexia that are expected given the broad set of areas recruited by the reading task.
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Does the intensification of what can be called “language-specific speech perception” around reading onset occur as a function of maturation or experience? Preschool 5-year-olds with no school experience, 5-year-olds with 6 months' schooling, 6-year-olds with 6 months' schooling, and 6-year-olds with 18 months' schooling were tested on native and nonnative speech contrasts, phonological awareness, and letter identification. Native speech perception was predicted by phonological awareness, but not school experience or age, whereas nonnative speech perception was negatively related to school experience and had no relationship with age or phonological awareness. Over and above any limitation of a possible selection bias associated with parents' choice of school entry age, the results suggest that intensified language-specific speech perception is due to more robust phoneme categories: increased phonological awareness facilitates judgments of native phoneme membership, whereas increased experience with phoneme-to-grapheme mapping assists in the process of disregarding allophonic variations within native phoneme classes.
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Glass's estimator of effect size, the sample mean difference divided by the sample standard deviation, is studied in the context of an explicit statistical model. The exact distribution of Glass's estimator is obtained and the estimator is shown to have a small sample bias. The minimum variance unbiased estimator is obtained and shown to have uniformly smaller variance than Glass's (biased) estimator. Measurement error is shown to attenuate estimates of effect size and a correction is given. The effects of measurement invalidity are discussed. Expressions for weights that yield the most precise weighted estimate of effect size are also derived.