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Improvement of stuttering with use of methylphenidate in a child who was diagnosed with concomitant stuttering and ADHD

Authors:
Bozatlı et al. 71
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Case report / Olgu sunumu
Improvement of stuttering with use of methylphenidate in a child
who was diagnosed with concomitant stuttering and ADHD
Leyla BOZATLI,1 Kıvanç Kudret BERBEROĞLU,1 Cansın CEYLAN,1 Işık GÖRKER1
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ABSTRACT
Stuttering is a psychological, neurological and neurophysiological rhythmic disorder in an understandable speech
that is characterized by hesitation in speech flow, standstill with repeating a word or a sound, extension of a sound.
Etiology of stuttering is not exactly known. In this case presentation, it is aimed to discuss the disappearance of
stuttering in an 11 year old child who was diagnosed with stuttering and ADHD after treating with methylphenidate
extended release. (Anatolian Journal of Psychiatry 2016; 17(Suppl.3):71-73)
Keywords: stuttering, stuttering treatment, methylphenidate, ADHD
DEHB ile birlikte kekemeliği olan bir çocukta
metilfenidatla kekemeliğin düzelmesi
ÖZ
Kekemelik, konuşma akışında tutukluk, bir sözcük ya da sesi tekrarlayarak duraklama, sesi uzatma, anlamlı bir
konuşmada psikolojik, nörolojik ve fizyolojik bir ritim bozukluğu olarak tanımlanmaktadır. Kekemeliğin etyolojisi
kesin olarak bilinmemektedir. Bu olgu sunumunda 11 yaşındaki vakamıza Kekemelik ve DEHB tanılarının konma
üzerine başlanan uzun etkili metilfenidat sonrasında ortadan kalkan kekemeliğin tartışılması amaçlanmıştır. (Ana-
dolu Psikiyatri Derg 2016; 17(Ek.3):71-73)
Anahtar sözcükler: Kekemelik, kekemelik tedavisi, metilfenidat, DEHB
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INTRODUCTION
Stuttering is a rhythmic disorder in an under-
standable speech that is characterized by hesi-
tation in speech flow, standstill with repeating a
word or a sound, extension of a sound. It occurs
commonly between ages of 2-7 years old.1 Etio-
logy of stuttering is not exactly known. In the etio-
logy; genetical, neurophsyiological and psycho-
logical factors which lead liability to disturbing
the flow of speech are considered.2
A transient instability in basal ganglia can be
seen due to dysfunction of realizing of dopamine
from substantia nigra to nigrostriatal pathway
during emotional states that occur in stressful
events. In this case, there can be stuttering and
other involuntary movement disorders due to
disinhibition. The all states that trigger stuttering
reinforce and increase stuttering; this condition
is called as feed-forward state.3,4
There have been several studies that demon-
strated hyperdopaminergic states caused stut-
tering. However, the roles of D1-D2 receptors in
the development of stuttering are still unclear.
Beside beneficial effects of methylphenidate in
stuttering, in some cases it worsens the stut-
tering. It has been demonstrated that methyl-
phenidate stimulated D1 receptors and reduced
the D2 receptors in prefrontal cortex by indirect
stimulation.4
In this case presentation, it is aimed to discuss
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1 Department of Child and Adolescent Psychiatry, Trakya University Faculty of Medicine, Edirne
Correspondence address / Yazışma adresi:
Uzm. Dr., Leyla BOZATLI, Department of Child and Adolescent Psychiatry, Trakya University Faculty of Medicine, Edirne, Turkey
E-mail: leylyabozatli@gmail.com
Received: 17.03.2016, Accepted: 11.07.2016, doi: 10.5455/apd.222279
Anadolu Psikiyatri Dergisi 2016; 17(Ek.3):71-73
72 Improvement of stuttering with use of methylphenidate in a child who was diagnosed …
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the disappearance of stuttering in a child who
was diagnosed with stuttering and ADHD after
treating with methylphenidate extended release.
CASE
An 11 year old boy admitted to outpatient clinic
with complaint of hesitation of speech. He had
tonsillectomy and ear tube surgeries when he
was 3 years old, the ear tube was extracted
when he was 4 years old and after this second
surgical intervention, it was reported that hesita-
tion in speech initiated. The family reported that
the hesitation of speech reduced sometimes
however it never disappeared and when he
started to the primary school, the hesitation of
speech worsened. In history, it was reported that
patient was diagnosed with ADHD at the second
and third years of primary school, he was treated
with methylphenidate and imipramine for one
year and he was treated with methylphenidate
extended release after the first year of treatment.
The family reported that patient benefited parti-
ally from treatment and stopped treatment. It was
considered that there have been hesitations in
speech during the clinical examination and it was
noted this hesitation commonly appeared at
initiating of speech and it was also noted that
frequency of hesitations were at the beginnings
of every 2-3 words. After taking information from
family and teacher and clinical examination,
case was diagnosed as ADHD according to DSM
5. At the second assessment, patient was
started on methylphenidate treatment and he
was referred to speech therapist. When patient
came to outpatient control, it was considered that
the hesitations in speech disappeared. The
family reported that hesitations in speech disap-
peared after 2-3 week of methylphenidate ex-
tended release treatment and they did not admit
to speech therapist.
DISCUSSION
There is not a specific drug treatment for stut-
tering according to literature data. Because there
are movement symptoms concomitant with stut-
tering, there are similarities between tic disor-
ders and stuttering, and there is worsening of
stuttering during stressful events, the dopamine
type 2 (D2) receptor antagonists were tried in the
treatment of stuttering. In this aspect, haloperidol
and risperidone were reported to be effective in
the treatment of stuttering in the case of ac-
companying movement disorders. While avoid-
ant behaviors and anxiety are intensive, patients
are reported to be benefited from serotonin re-
uptake inhibitors (SSRIs).2
In our case, it was noted that stuttering ameli-
orated after starting on methylphenidate ex-
tended release for treatment of ADHD. Re-
garding this case, it was found that there have
been studies that investigated the role of D-
amphetamine, non-selective beta blocker oxpre-
nolol, methylphenidate and methylphenidate ex-
tended release in the treatment of stuttering and
there has been also placebo controlled studies
that mentioned this issue in literature.
Ginn and Hohman were the first authors who
were aware of the beneficial effects of ampheta-
mine in stuttering; they also reported 4 cases
with stuttering who were treated with ampheta-
mine for behavior disorder and in 2 cases stut-
tering were improved after treatment.5 In a
double blind placebo controlled study, there was
a significant improvement in D-amphetamine
group compared with placebo group in terms of
stuttering; however there was not any improve-
ment in other speech disorders.6,7 In another
study that compared methylphenidate and pla-
cebo in patients with stuttering, the patients were
assessed in terms of reading and speech; there
have been statistically significant decrease in
hesitation in methylphenidate group compared
with placebo group4
Although D-amphetamine demonstrated signifi-
cant effects in the treatment of stuttering, they
were not used in clinical practice due to their side
effects. Methylphenidate which is an analogous
of D-amphetamine is known to have no side
effects like D-amphetamine, further randomized
controlled studies are needed for providing the
use of methylphenidate in the treatment of stut-
tering.7
There have been another agents that were in-
vestigated in the treatment of stuttering. Olanza-
pine was reported to have superiority to placebo
in terms of ameliorating the stuttering; however
only a few study confirmed this effect due to
possible intolerable side effects of olanzapine8
Pimozide has been reported to have a significant
role in providing the flow of speech. However,
when considering the dopamine antagonists in
the treatment of stuttering, potential side effects
should be mentioned.9 In a randomized study,
risperidone was reported to be effective in the
treatment of developmental stuttering and also
reported to be tolerable.10
SSRIs such as citalopram, escitalopram, tricyclic
antidepressants such as clomipramine and
benzodiazepines such as alprazolam were in-
Anatolian Journal of Psychiatry 2016; 17(Suppl.3):71-73
Bozatlı et al. 73
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vestigated in the treatment of stuttering and beneficial effects were reported.11,12 In our literature
research, we considered that the agents that were investigated in the treatment of stuttering are limited
to studies which were not confirmed or case reports. Regarding the amelioration of stuttering with
methylphenidate in our case, it is emphasized that further studies are needed to clarify the place of
methylphenidate extended release in the treatment of stuttering.
Authors’ contributions: L.B.: Konuyu bulma, planlama, literatür, makaleyi yazma; K.K.B.: Konuyu bulma, literatür;
C.C.: Literatür; I.G.: Literatür.
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Anadolu Psikiyatri Dergisi 2016; 17(Ek.3):71-73
... In the literature review conducted regarding the association between methylphenidate and stuttering, we found a study testing methylphenidate as a treatment option for stuttering, suggesting that methylphenidate is suitable for treating the condition (3). Similar results were established by two case reports indicating improvement in stuttering symptoms when treated with methylphenidate (11-and 18-year-old patients) (4,5). ...
Article
Full-text available
Recently, a case report described a decrease in frequency of stuttering after intake of methylphenidate (MPH). This study was undertaken to investigate if this effect could again be reproduced in a population of young healthy male adult persons with developmental stuttering. A double-blind randomized crossover trial, with a 2-week washout period, including 15 Dutch-speaking young healthy persons with developmental stuttering, assessed the effects of a single dose of 20 mg MPH compared with placebo on stuttering. Dependent and 1-sample t tests were used to detect significant differences. The end point was the number of stutter moments and self-perceived improvement. MPH yielded a significant decrease in the number of stutter moments when reading and speaking (P = 0.002), which was not the case with placebo (P = 0.090). There was a significant improvement from baseline after intake of MPH as compared with placebo (P = 0.003). Self-perceived improvement with MPH was not significantly better as compared with placebo (P = 0.28). This study showed that the participants had an objective statistically significant decrease in the frequency of stuttering with MPH, and this was not the case with placebo. This was also the case for a reduction in stutter moments when reading out loud and speaking spontaneously. However, this result was not subjectively perceived by the participants. © The Author(s) 2015.
Article
Introduction: A randomized placebo controlled trial with methylphenidate (MPH) was set up to identify the effects of MPH on cognition in healthy young adults (ea. without attention deficit hyperactivity disorder, ADHD). Subjects repeatedly performed tests of the immediate and delayed memory and vigilance tasks after administration of placebo or 20 mg MPH. Case presentation: We report the case of an 18 year old man who participated in the study. He suffered from stuttering since childhood. During the study phase he reported a remarkable relief of the stuttering after the intake of 20 mg MPH. Conclusions: For D-amphetamine the beneficial effect on stuttering has been demonstrated but it was never implemented in clinical practice because of important adverse events. MPH, an amphetamine analogue, doesn't present these side effects. For this reason, MPH seems to merit further investigation in a randomized-controlled trial as a possible agent in the treatment of stuttering.Methylphenidate, Stuttering.
Article
A randomized, double-blind, placebo-controlled study was conducted to assess the efficacy of risperidone in the treatment of developmental stuttering in 16 adults. Eight subjects received placebo and eight received risperidone at 0.5 mg once daily at night, increased to a maximum of 2 mg/day. After 6 weeks of treatment, decreases in all measures of stuttering severity were greater in the risperidone group than in the placebo group; the between-treatment difference was significant (p < 0.05) on the most important measure, the percentage of syllables stuttered. In the risperidone group, reductions from baseline in scores for the percentage of syllables stuttered, time stuttering as a percentage of total time speaking, and overall stuttering severity were significant (p < 0.01); changes in scores on the fourth measure of stuttering, duration, were not significant. No significant decreases occurred in the placebo group. Among the eight patients in the risperidone group, five responded best to 0.5 mg/day, with stuttering recurring at higher doses. The remaining three patients responded better with increasing doses of risperidone. Risperidone was generally well tolerated. The results of this small study indicate that risperidone may be effective in the treatment of developmental stuttering. This finding needs to be confirmed in a larger trial.
Article
In a double-blind study, 106 mentally retarded patients with speech defects were given 15 mg. of d-Amphetamine daily, or a placebo, for a three-month period. Speech defect types were: Stuttering, immature production, oral inaccuracy, lisp, psychotic, mongoloid, aphasia, deafness, and cleft palate. Only the stutterers showed obvious improvement in comparison with the placebo group. Three severe, long-term stutterers showed such dramatic improvement that their whole course in life has been changed.
Article
Stuttering is a speech disorder that affects one-percent of all adults and much has been learned recently of its neurologic correlates. Stuttering has been associated with excessive cerebral activity of the neurotransmitter, dopamine. Pharmacologic research has suggested that older generation dopamine antagonist (i.e. "typical antipsychotic") medications improve stuttering symptoms, but are associated with poorly tolerated adverse effects. The purpose of this study was to compare the efficacy and tolerability of olanzapine, a novel dopamine antagonist (or "atypical antipsychotic"), versus placebo in the treatment of adult developmental stuttering. Twenty-four adults who stutter participated in a twelve-week, randomized, double-blind, placebo-controlled trial conducted at two separate sites. Subjects received either olanzapine (2.5 mg titrated to 5 mg) or matching placebo. Subjects were rated on an objective measure of stuttering severity (SSI-3), a clinician based global impression (CGI), and a subject-rated self-assessment of stuttering (SSS). Subjects were also monitored for potential side-effects. Twenty-three of the twenty-four subjects enrolled in the trial successfully completed the full course of the study. Olanzapine was statistically superior to placebo on the three ratings of stuttering severity, the SSI-3, the CGI and SSS (p < .05). Olanzapine is a promising medication for the treatment of stuttering and further research is warranted.
Article
Unlabelled: Medications with dopamine antagonist properties, such as haloperidol, and those with serotonin reuptake inhibitor properties, such as clomipramine, have been shown to improve fluency. To examine the degree to which each of these two pharmacological mechanisms might independently affect fluency, a selective serotonin reuptake inhibitor, paroxetine, and a selective dopamine (D-2) antagonist, pimozide, were evaluated. Both types of medications also affect mood and anxiety, factors that could influence fluency levels. Therefore, we also evaluated the medications' effects on generalized and speech-related anxiety and the relationships between changes in anxiety and changes in fluency in 11 subjects with a history of developmental stuttering. The randomized, double blind, placebo-controlled crossover study that was designed had to be terminated prior to completion due to severe side effects following withdrawal from paroxetine. Even with a reduced sample size (n=6), significant improvement in percent fluent speaking time (p=0.02) was found using a telephone task between baseline and pimozide (n=6), with average duration of dysfluencies significantly shorter (p=0.04) but no significant difference in the estimated number of dysfluencies per minute. This significant improvement was associated with non-significant increases in generalized anxiety, but non-significant decreases in speech-related anxiety. No significant differences were found in fluency between baseline and paroxetine (n=5). These preliminary results suggest that fluency improvement is more likely to be mediated by dopaminergic rather than serotonergic mechanisms. Due to its side effects, however, pimozide may be considered a risk for treatment of stuttering. Educational objectives: As a result of reading this paper the reader will describe and explain: (1) how medications may affect fluency and the rationale for selecting medications for treatment trials; (2) the interrelationship between fluency and anxiety; and (3) factors important in developing clinical trials using medications.
Çocuklarda kekemelik: Karşılaştırmalı bir izleme çalışması
  • A Avcı
  • Ş Uğuz
  • F Toros
Avcı A, Uğuz Ş, Toros F. Çocuklarda kekemelik: Karşılaştırmalı bir izleme çalışması. Klinik Psikiyatri 2002; 5:16-21.