Forager and farmer evolutionary adaptations to malaria evidenced by 7000 years of thalassemia in Southeast Asia

Abstract

Thalassemias are inherited blood disorders that are found in high prevalences in the Mediterranean, Southeast Asia and the Pacific. These diseases provide varying levels of resistance to malaria and are proposed to have emerged as an adaptive response to malaria in these regions. The transition to agriculture in the Holocene has been suggested to have influenced the selection for thalassemia in the Mediterranean as land clearance for farming encouraged interaction between Anopheles mosquitos, the vectors for malaria, and human groups. Here we document macroscopic and microscopic skeletal evidence for the presence of thalassemia in both hunter-gatherer (Con Co Ngua) and early agricultural (Man Bac) populations in northern Vietnam. Firstly, our findings demonstrate that thalassemia emerged prior to the transition to agriculture in Mainland Southeast Asia, from at least the early seventh millennium BP, contradicting a long-held assumption that agriculture was the main driver for an increase in malaria in Southeast Asia. Secondly, we describe evidence for significant malarial burden in the region during early agriculture. We argue that the introduction of farming into the region was not the initial driver of the selection for thalassemia, as it may have been in other regions of the world.

Full text

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
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Forager and farmer evolutionary
adaptations to malaria evidenced
by 7000 years of thalassemia
in Southeast Asia
Melandri Vlok1*, Hallie R. Buckley1, Justyna J. Miszkiewicz2, Meg M. Walker2, Kate Domett3,
Anna Willis7, Hiep H. Trinh4, Tran T. Minh4, Mai Huong T. Nguyen4, Lan Cuong Nguyen4,
Hirofumi Matsumura5, Tianyi Wang6, Huu T. Nghia4 & Marc F. Oxenham2*
Thalassemias are inherited blood disorders that are found in high prevalences in the Mediterranean,
Southeast Asia and the Pacic. These diseases provide varying levels of resistance to malaria and
are proposed to have emerged as an adaptive response to malaria in these regions. The transition to
agriculture in the Holocene has been suggested to have inuenced the selection for thalassemia in the
Mediterranean as land clearance for farming encouraged interaction between Anopheles mosquitos,
the vectors for malaria, and human groups. Here we document macroscopic and microscopic skeletal
evidence for the presence of thalassemia in both hunter-gatherer (Con Co Ngua) and early agricultural
(Man Bac) populations in northern Vietnam. Firstly, our ndings demonstrate that thalassemia
emerged prior to the transition to agriculture in Mainland Southeast Asia, from at least the early
seventh millennium BP, contradicting a long-held assumption that agriculture was the main driver
for an increase in malaria in Southeast Asia. Secondly, we describe evidence for signicant malarial
burden in the region during early agriculture. We argue that the introduction of farming into the region
was not the initial driver of the selection for thalassemia, as it may have been in other regions of the
world.
alassemias, a group of inherited hemoglobin blood disorders1, are highly prevalent in present day Southeast
Asia and the Pacic. ese diseases stand testament to a deep history of genetic adaptation to the parasitic disease
malaria2,3. However, it is unknown when thalassemias or malaria originated in the region. e two forms of the
disease, alpha and beta thalassemia, cause disruptions to the synthesis of the alpha or beta hemoglobin chains
respectively. Malformation of hemoglobin results in an excess of the opposing hemoglobin chain which is the
cause of disease in the body4,5. Today, malaria aicts approximately 8 million people in Southeast Asia. Eradica-
tion eorts are sporadic and reliant on access to treatment at a community level to be eective6. alassemias,
like other hemoglobin disorders, disrupt the mechanism for malarial parasite-binding to red blood cells2. In
Southeast Asia where thalassemia genes are observed in high frequencies, in as much as over 75% of the popula-
tion, malaria is also highly endemic, particularly the most lethal form Plasmodium falciparum3.
Although most variants of alpha thalassemia provide resistance to malaria with little clinical complication,
most homozygous beta thalassemia variants (thalassemia major and intermedia) can have signicant eects on
health. Complications of beta thalassemia include gross changes to the skeleton and death from infection or iron
overload3,7,8. In Southeast Asia specically, a milder form of beta thalassemia, the hemoglobin-E (HbE) variant,
is also present in high frequencies, with the gene present in up to 30–50% of the population in some geographi-
cal areas9. Homozygous HbE is not associated with clinical symptoms. However, complications can occur with
co-inheritance of HbE and classical beta thalassemia variants (HbE beta thalassemia)7,10. HbE beta and classic
beta thalassemias are frequently found co-inherited with alpha thalassemia in Southeast Asia and result in a wide
OPEN
Department of Anatomy, University of Otago, Dunedin, New Zealand. School of Archaeology and Anthropology,
The Australian National University, Canberra, Australia. College of Medicine and Dentistry, James Cook University,
Townsville, Australia. Institute of Archaeology, Hanoi, Vietnam. School of Health Sciences, Sapporo Medical
University, Sapporo, Japan. Department of Archaeology, University of Cambridge, Cambridge, UK. College of
Arts, Society & Education, James Cook University, Townsville, Australia. *email: Melandri.vlok@otago.ac.nz;
marc.oxenham@anu.edu
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spectrum of symptoms and severity11. Modern day research demonstrates that variants within Southeast Asia
and the Pacic can vary across short distances, and relate to the ecological ranges of Anopheles mosquitos, the
vectors for malarial parasites3. Given the co-evolutionary relationship that continues to drive high frequencies
of thalassemia in the Southeast Asian region today, it can be hypothesized that the identication of thalassemia
in the prehistoric record can be, at least in part, related to a prior selection pressure of malaria.
To date, the only archaeological evidence for hereditary anemia in the region dates from approximately
4000–3500 BP from Khok Phanom Di, a Neolithic site in central ailand (Fig.1)12. In the Mediterranean
region, where beta thalassemia is similarly frequent, skeletal evidence in prehistoric assemblages supports the
emergence of the disease with the transition to agriculture (the Neolithic) from approximately 7000years ago13.
It is hypothesized that agricultural practices such as land clearance encouraged contact between human groups
and Anopheles mosquitos13,14. Did these conditions then emerge alongside the spread of agriculture in Southeast
Asia as is proposed to be the case in the Mediterranean?
e emergence of farming in Mainland Southeast Asia (MSEA) occurred much later than the Mediter-
ranean, from only aer 4500years ago15, with most Neolithic sites post-dating 4,000 BP. Prior to this time the
region was occupied by indigenous Pre-Neolithic foragers descended from the rst people out of Africa and
into Asia16. By the early seventh millennium BP some forager groups in northern Vietnam and southern China
developed large sedentary settlements, at the same time as agriculture was practiced to the north in China17. e
Figure1. Map of Southeast Asia with sites important for this study. Khok Phanom Di in ailand provides
the only prehistoric evidence of thalassemia in the region. Our study includes research from Man Bac and Con
Co Ngua in northern Vietnam. Modied from image by Koba-chan (https ://uploa d.wikim edia.org/wikip edia/
commo ns/1/15/Topog raphi c30de g_N0E90 .png) created from DEMIS Mapserver (http://www2.demis .nl/world
map/mappe r.asp). Published under CC BY-SA 3.0 (https ://creat iveco mmons .org/licen ses/by-sa/3.0/deed.en).
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subsequent adoption of agriculture in MSEA during the Neolithic (4500–3100 BP) was associated with multiple
migration events of farmers from what is now geo-politically southern China, coming into contact with these
forager groups15,18,19. ese subsistence transition and migration events signicantly altered the demography
and genetics of this region from this point forward. e aim of this research is to investigate, for the rst time,
whether thalassemia, as a proxy for malaria burden, was present prior to agriculture in northern Vietnam, and
to what degree the transition to agriculture may have contributed to the emergence of thalassemia in Southeast
Asia. Additionally, if thalassemia is observed we aim to further investigate which variants may have been present.
We applied a diagnostic protocol based on macroscopically observed dry bone lesions for thalassemia to
two archaeological human skeletal assemblages. e Pre-Neolithic site of Con Co Ngua radiocarbon dated to at
minimum 6200–6700cal BP17,18 represented a pre-agricultural but sedentary forager community (n = 155; Fig.1).
e Man Bac site dating to 3,906–3,523cal BP was occupied during the agricultural transition of Southeast Asia
(n = 70). is site captures co-habitation of indigenous forager and migrant farmers during the early stages of
the agricultural transition18. To support the strength of the disease diagnosis using the macroscopic methods,
we also conducted histological analysis on three Con Co Ngua individuals to assess microscopic pathological
changes in aected bone.
Results
Macroscopic results present strong evidence for thalassemia at Man Bac. Five children aged
between 6months and 12years and one adult presented with skeletal changes that are strongly diagnostic
(pathognomonic) for thalassemia (Table1, Supplementary Text S1; Supplementary TableS1; Figs.2, 3). ese
changes included rodent facies, a skeletal condition specic to thalassemia, where expansion of the marrow
results in a bulbous face and mandible. Radiographs conrm marrow expansion, a clinical consequence of severe
thalassemia (Fig.2). Radiographic ‘rib-within-a-rib sign’, again pathognomonic for thalassemia, was identied
in three individuals. is condition results from extensive marrow expansion within the shas of the ribs. Fur-
ther evidence for thalassemia included a lack of the development of facial and cranial sinuses, commonly caused
by extensive marrow expansion of the face since infancy. Two children also presented with severe porosity of
the orbits and the endocranium, likely due to marrow expansion through the cortical margins of the skull, as a
result of thalassemia. Additionally, a newborn with multiple lesions suggestive of possible thalassemia, including
evidence of marrow expansion throughout the skeleton was identied (Table1, Figs.2, 3).
Macroscopic results present evidence suggestive but not diagnostic for thalassemia at Con Co
Ngua. We identied seven adults and adolescents at Con Co Ngua presenting with macroscopic and radio-
graphic ‘bone-within-a-bone’ changes of the limb bones (Supplementary Fig.S1; Supplementary TableS1). We
observed a mixture of enlargement and restriction of the medullary canal areas in these individuals. In thalas-
semia, this skeletal change is caused by marrow expansion within the long bones perforating the outer cortex.
As such, these pathologies are suggestive of thalassemia but alone are not diagnostic for thalassemia, as they
can also be found in a number of other chronic conditions20 (Supplementary text S1). However, these skeletal
changes were similar to those with strong diagnostic evidence of thalassemia at Man Bac. We extracted bone
samples from three of the CCN individuals for further microscopic analysis.
Table 1. Macroscopic and radiographic diagnosis of thalassemia in Man Bac individuals. P = present,
A = absent, N/A = skeletal element missing/unobservable. *MB07H1M12 presented with multiple suggestive
lesions, but no diagnostic (D)or strongly diagnostic (SD)lesions (see Supplementary TableS1). **Frontal
sinuses were not preserved, absence of pneumatization based on preservation of maxillary sinuses only.
Individual ID MB07H1M8 MB07H1M12* MB07H2M26 MB05M12 MB05M3 MB07H1M1
Age (years) 30–39 0 1.5 2 0.5 12
Sex Male N/A N/A N/A N/A N/A
Diagnostic criteria
Marrow hyperplasia of the facial bones: maxillae-leading to ventral displacement of
central incisors, zygomatic bones-leading to orbital displacement, and/or mandible
(rodent facies deformity) (SD) A N/A P P P P
Radiographic: “rib-within-a-rib” appearance. Radiographically dened sclerotic
bands within the ribs due to extramedullary hematopoiesis (SD) PA P P A
Poor or lack of pneumatization of the paranasal and cranial sinuses sparing the
ethmoid sinuses (D) A N/A P A** A P
Enlarged tubular bones of the hands and feet due to marrow hyperplasia (infants)
sometimes associated with enlarged nutrient foramina or Radiographic: coarse
trabecular patterns of the hands or feet, sometimes associated with cyst-like lucencies
due to focal collection of hyperplasic marrow (D)
P N/A N/A N/A A N/A
Premature fusion of epiphyseal plates particularly of the proximal humerus and distal
femur, oen causing short long bone maximum length (D) A A A A A N/A
Widening of entire rib, or widening of the rib head and neck with pronounced bul-
bous appearance posteriorly (costal osteomas). Associated with radiograph appear-
ance of erosion of the inner cortex (D) P A A A P A
Diagnosis Probable Possible Probable Probable Probable Probable
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Figure2. Cranial evidence for thalassemia at Man Bac. (a) Anterior protrusion of the zygomatic bones
consistent with rodent facies (MB05M3, approx. 6months old, antero-lateral aspect). (b) and (c) Diploic
expansion of the cranial vault. ere is no porosity on the ectocranium but hair-on-end formations are present
on the endocranium (MB05M12, approx. 2years, lateral aspect). (d) Marrow hyperplasia of the zygomatic
bones (MB05M12, antero-posterior view). (e) Lack of pneumatization of the frontal sinus (MB07H1M1, approx.
12years, antero-posterior view). (f) Rodent facies of the maxilla, mandible and zygoma (MB07H2M26, approx.
1.5years, antero-superior aspect). (g) Severe cribra orbitalia (white circle) and diploic expansion of the crania
(black arrow, antero-lateral aspect) (MB07H1M1). (h) Marrow hyperplasia of the le zygoma (MB07H1M1,
lateral aspect). (i) and (j) Marrow hyperplasia of the maxilla (MB07H1M1, superior-inferior view). e expanse
of the marrow hyperplasia is indicated by the white arrows.
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Figure3. Postcranial evidence for thalassemia at Man Bac. (a) Enlarged rib (MB05M3, approx. 6months old,
superior aspect). (b) and (d) Expanded foramina of the phalanges (yellow arrows) with marrow hyperplasia
(white arrow, MB07H1M8, middle aged adult, antero-posterior view). (c) “Rib-within-a-rib” sign (yellow
arrows, MB07H1M8, supero-inferior view). (e) Alteration of the trabecular structure of the ilia. Note the
radiating pattern (MB07H1M12, neonate, antero-posterior view). (f) “Rib-within-a-rib” sign (yellow arrow,
MB07H2M26, approx. 1.5years, supero-inferior view). (g) Enlargement of the scapular spines (MB07H1M12,
neonate, posterior aspect). (h) Marrow hyperplasia of the humerus (white arrow, MB05M12, approx. 2years,
antero-posterior view).
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Combined microscopic and macroscopic results strongly suggest thalassemia at Con Co
Ngua. We assessed bone samples of one adolescent (> 16years) of unknown sex (CCN13M67a), and two
adults: CCN13M40a (young adult female), CCN13M59a (old adult male) (Fig.4). We focused specically on the
endocortex (cortical bone located on the inner third portion of the cross-section) as preliminary macroscopic
assessment of the samples prior to microscopy determined this region to be particularly important (Fig.4).
Widespread pores were evident on the endocortical surfaces of samples from the old adult male (CCN13M59a).
e porosity consists of ‘giant’ pores that appear to have been created as a result of adjacent coalescing pores
(Figs.4, 5). All three bones of this individual showed a “trabecularization eect”, which essentially transformed
cortical bone into a trabeculae-like matrix of bone as a result of prolonged resorption, and possibly marrow
expansion.
In contrast, the bone samples in the young adult female (CCN13M40a), showed denser and enlarged endo-
cortical surfaces. e adolescent (CCN13M67a) presented with a mix of large porous regions of the endocortex
(right humerus) and regions of increased cortical density (femur). Possible beginnings of the ‘trabecularization
eect’ such as those observed in the old adult male (CCN13M59a) were found in the right humerus of the old
adult. e extent of medullary bone size reduction can be seen, particularly in the adolescent femur section where
the cortical wall is unusually enlarged (Fig.4d). is femur showed evidence for secondary bone remodeling
conrming cyclical replacement of old bone with new bone tissue, possibly driven by increased metabolic bone
needs (Fig.6). ere was a clear pattern whereby samples from the femur did not show evidence for widespread
porosity and coalescing of bone pores, but were observed in the bones of the upper limb (ulna, humerus, and
radius) (Fig.6).
We compared the microscopic results to various diseases of infectious and metabolic etiologies known to
cause the macroscopic ‘bone-within-a-bone’ sign (Supplementary text S1). e microscopic outcomes of Con
Co Ngua are only consistent with clinical bone histological observations in cases of beta thalassemia. Increased
osteoclast-mediated resorptive activity, and decreased osteoblastic activity have both been described as under-
lying processes that increase porosity of the endocortical margins of the long bones in beta thalassemia21. In
thalassemia, skeletal changes can be localized, due to focal deposits of iron during iron overload which is con-
sistent with the variation between the upper and lower limbs we observed across the samples21–23. e overall
histological bone pattern observed in the Con Co Ngua individuals therefore supports localized metabolic
changes consistent with thalassemia.
Figure4. Cross section of microscopic samples from Con Co Ngua. (a) Femora sections from CCN13M40a.
ere is increased cortical thickness, and the cortical width of right femur is asymmetrically wider than the le.
(b) Upper limb sections from CCN13M40a. Large endocortical pores are evident. Medullary canal widening is
most distinct on the humerus. (c) Upper and lower limb sections from CCN13M67a. While the femur presents
with extreme cortical thickness and restriction of the medullary canal area, the upper limb sections present with
severe porosity of the endocortical surfaces. (d) Asymmetry of the medullary canals of the humeri and femora
of CCN13M67a.
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Discussion
What hemoglobinopathy variants were present in prehistoric Vietnam? Our results demonstrate
skeletal evidence for thalassemia from the early seventh millennium BP in northern Vietnam. e gross skeletal
changes in all but one Man Bac individual are consistent with beta thalassemia4. e clinical consequences,
including bone changes, of beta thalassemia only develop following replacement of fetal gamma hemoglobin
with adult beta hemoglobin in the months following birth. However, the possible case diagnosed in a Man Bac
Figure5. Macroporosity observed in the arm bones of CCN13M59a. e porosity is large and coalescing.
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Figure6. Regions of bone captured from the endocortical surface in the adolescent (CCN13M67a), allowing to examine the
degree of bone modelling and remodeling. (a–d) e femur: Secondary osteons (SO), primary osteons (PO), Haversian canals
(HC), and osteocyte lacunae (OL) can be seen. (a) White arrows point to endosteal lamellar layers which are typical for this bone
region. (c) White arrows point to a cement line of a secondary osteon that indicates a remodeling event of a fragmentary osteon
(FO) underneath, conrming cyclical replacement of old bone with new bone tissue, possibly driven by increased metabolic bone
needs. (e) White arrows point to primary lamellar bone layers and an isolated HC. (f) A SO amongst primary bone.
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newborn may be consistent with alpha thalassemia major (Bart’s hydrops fetalis)24. Alpha thalassemia major,
caused by deletion of all of the four alpha alleles, is a common variant in Southeast Asia today25. ere is little
clinical description of the skeletal complications of alpha thalassemia major due to its fatal outcome. However,
severe bone marrow expansions occur in utero during growth detected as early as 18 fetal weeks7, and skeletal
complications similar to beta thalassemia major can be expected24. Severe growth stunting is a common out-
come of alpha thalassemia major, and skeletal deformities have been clinically documented, but not described5,7.
Evidence for co-occurrence of both alpha and beta thalassemia variants at Man Bac is of evolutionary sig-
nicance. e gross skeletal pathologies of Man Bac post-birth individuals are commonly observed in patients
with beta thalassemia major, a severe form that requires removal of excess iron and blood transfusions in order
to survive past infancy26. However, 57% (4/7) of individuals macroscopically diagnosed with thalassemia at
Man Bac were older than 1-year of age, having survived infancy without treatment. Alpha and beta thalassemia
co-inheritance is known to result in a milder form of disease than beta thalassemia major due to a balance of
depleted alpha and beta hemoglobins27. Additionally, the Southeast Asian variant HbE beta thalassemia com-
monly results in severe forms of thalassemia that do not require blood transfusions to survive (known clinically
as thalassemia intermedia)28. It is possible that co-inheritance of beta thalassemia with alpha and/or HbE may
account for the severe skeletal changes in individuals at Man Bac who survived past infancy.
It is not possible to determine whether the Con Co Ngua individuals had beta or alpha thalassemia. While
there is clear clinical recognition of the skeletal changes of beta thalassemia29, HbH alpha thalassemia caused
by deletion of three of the four alpha alleles are reported to cause mild to moderate skeletal deformities in some
patients5. Signicant facial deformity was not recorded at Con Co Ngua. However, infants at this site were very
poorly preserved, so more severe forms of thalassemia at Con Co Ngua cannot be ruled out.
Evidence for deep antiquity of thalassemia and malaria in Mainland Southeast Asia. Based on
our macroscopic and microscopic observations we suggest that thalassemia was potentially a considerable bur-
den for Southeast Asian populations prior to the adoption of farming. is contrasts with our current knowledge
on the emergence of thalassemias in the Mediterranean and demonstrates that the agricultural transition was
not the dening factor in the emergence of this disease in Southeast Asia. We note here that the one adult with
probable thalassemia from Man Bac had dental and skeletal anity to Australo-Papuan populations, such as
those from Con Co Ngua (and all foraging groups from Vietnam prior to agriculture). e inhabitants from the
Neolithic central ailand site of Khok Phanom Di where thalassemia was previously reported represent mixed
Australo-Papuan and East Asian dental anities30. erefore, a deep antiquity for thalassemia in the region prior
to the Neolithic appears highly probable. However, the complexity of gene ow and stabilizing selection in the
region exceeds the capabilities of skeletal morphometric data.
e heterogeneity of mutations that cause beta, HbE beta and alpha thalassemia in Southeast Asia support
multiple instances of independent emergence within the region likely tied to a consistent threat of malaria
within MSEA31,32. Alpha thalassemia variants in Southeast Asia populations have similarly been identied in
modern indigenous Papuan and Austroasiatic (modern Southeast Asian) speaking populations33. e widespread
geography of these variants today, and the compounded eect of multiple migration and genetic admixture
events since prehistory, mean it is not possible to determine the origins of these variants from the distribution
in modern populations. However, dierent haplotypes do indicate separate founder eects in Australo-Papuan
(indigenousAustralian and New Guinean Highlanders) and Austroasiatic (ai) groups33. At least in the case of
alpha thalassemia, a pre-agricultural deep history of this disease in MSEA is consistent with present day genetic
data. In contrast, selection models of one HbE variant from a ai population indicates an emergence between
4400 and 1240years ago, consistent with agricultural intensication between the Neolithic to Iron Age periods
(4500–1500 BP) in MSEA34. HbE emergence is consistent with the time period of the Man Bac individuals with
thalassemia. Multiple independent events of thalassemia emergence may have occurred due to dierent social
transitions in Southeast Asia’s prehistory.
e presence of thalassemia in prehistoric MSEA, as is the case today, indicates a constant selection pressure
of malaria stemming from deep antiquity. It is expected that the gene frequencies of thalassemias in the absence
of malaria would not have been maintained given its mortal cost when inherited in its severe forms14. While P.
falciparum has a considerably higher mortality rate than P. vivax, thereby incurring a stronger selection pressure,
both Plasmodium species are endemic to the region and thought to have had possible selection eects on thalas-
semia in Southeast Asia35. Both P. falciparum and P. vivax malarias share African origins. It is thought that P.
vivax emerged out of Africa with human groups prior to 30,000years ago36 consistent with the rst anatomically
modern humans who inhabited MSEA as early as 60,000years ago16. P. falciparum is thought to have emerged
in Africa approximately 60,000–40,000years ago, and estimated to have undergone a bottle neck approximately
6,000–4,000years ago that likely favored human infection37. is proposed bottle neck event post-dates the
skeletal evidence for thalassemia at Con Co Ngua and pre-dates that of Man Bac. Rather than provide resist-
ance, alpha thalassemia has been proposed to increase susceptibility to infection by P. vivax35. is susceptibility
may be an adaptive mechanism to cross vaccinate against P. falciparum35 which signals the complex connection
between Plasmodium infections and the emergence of thalassemia. e association between thalassemias and P.
vivax morbidity and mortality, however, remains unknown and is a necessary component to understanding the
relationship between malarial types and the emergence of thalassemias in the region38. Rarer still, Plasmodium
variants commonly found in Southeast Asian forest macaques have also been known to transfer to humans39,
an important local reservoir in communities in Vietnam40. Potential human to non-human primate interactions
may also factor into the relationship between malaria and thalassemia in the prehistory of the region. Both Man
Bac and Con Co Ngua inhabitants exploited non-human primates as a food source17,41.
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Lowland ood plains in Vietnam, such as where Man Bac and Con Co Ngua are located have low reported
malarial cases and primary vectors today, as is the case with coastal and estuarine environments42. However,
the original ecology of the region surrounding these sites in antiquity included movement within fringe forests,
brackish water, and riverine areas that may have placed the inhabitants at risk of a number of dierent Anopheles
mosquito species that carry both human and simian Plasmodium species42. In tropical forested areas of MSEA,
malarial vectors are common. Tropical forested regions expanded substantially from approximately 14,000years
ago following the Last Glacial Maximum, which would have been opportunistic for the spread of species A. dirus
and A. minimus, the primary mosquito vectors of malaria in MSEA42. e tropical climate would have enabled
year-round transmission even in seasonal areas such as northern Vietnam that experience dry and wet seasons43.
While pre-agricultural, the complex hunter-gathers of Con Co Ngua existed in large sedentary populations,
thereby encompassing a suite of factors that have been argued to be associated with the emergence of malaria
and thalassemia in the Mediterranean44. Sedentary residential mobility would have enabled completion of the
cycle of the disease within one host population42, increasing the selection pressure on these populations. In
Southeast Asia today, an increased risk is observed in people who live in villages but actively exploit the forest
for resources45. is risk appears to be related to the early night feeding times of these vectors. e exposure
to forest Anopheles mosquitos and sedentary residence alone would likely have been sucient to increase the
probability of contracting malaria in the absence of agricultural land clearing.
The agricultural transition and gene ow variation. While Con Co Ngua individuals were less well
preserved than those from Man Bac, 10% (7/70) of the latter assemblage presented evidence for thalassemia.
Man Bac is contemporaneous with Khok Phanom Di indicating these alleles were widespread through the region
at this point in time. erefore, the transition to agriculture may have considerably altered the gene ow or
increased the selection pressure of thalassemia mutations, and shaped the relationship between human groups
and malarial vectors in the region. Wet rice agriculture (irrigation) was only developed during the Iron Age
(2500–1500 BP) in Southeast Asia46. is form of agriculture has been previously, erroneously, argued to be
linked to increased malarial vectors compared to dry rice agriculture in MSEA47. Our results indicate a strong
relationship between human groups and malaria prior to wet rice farming. Present day reports of dierences
in malarial vector prevalence in irrigated versus non-irrigated farming localities vary and depends on other
ecological dynamics such as seasonality48. In Mainland Southeast Asia, A. dirus is found in signicantly higher
densities in forested areas than in villages, and reside in shallow pools42 rather than in deep waters. erefore,
the moated settlements of the Iron Age in ailand may have made the ecology around villages less attractive
to primary malarial vectors or attracted dierent Anopheles mosquitos such as A. barbirostris with signicantly
lower vector potential49. Instead, the reliance of dry rice farming on mild seasonal ooding may have increased
the exposure of Neolithic inhabitants to malarial vectors42, particularly as they continued to exploit forested
areas through mixed farmer-foraging practices50. While Pre-Neolithic foragers in northern Vietnam and south-
ern China were arguably primarily sedentary, an increase in sedentism and signicant population growth dur-
ing the transition to agriculture in MSEA51,52 would have increased the transmission potential within human
populations.
Possible interaction between Man Bac inhabitants and other nearby contemporaneous sites further inland,
where higher vector densities have been reported42, may have also contributed to the presence of thalassemia at
Man Bac. Alternatively, we also recognize that gene ow of thalassemia alleles from other inland Neolithic sites
may be responsible, and a direct relationship between thalassemia and malaria presence at Man Bac cannot be
determined. A similar argument can be made for Con Co Ngua, as contemporaneous forager sites of northern
Vietnam are also archaeologically documented to have maintained interactions through exchange53. Nevertheless,
it is apparent that mobility and interactions within and between groups were essential for the spread of thalas-
semia variants in the prehistory of MSEA, and the prevalence of this disease can be tied directly or indirectly to
malarial endemicity in prehistoric MSEA.
Conclusion
rough a combined macroscopic and microscopic approach we demonstrate that thalassemia has been present
in northern Vietnam from at least the early seventh millennium BP. is nding indicates that agriculture was
not a crucial factor in the emergence of thalassemia in response to malaria in Southeast Asia as appears to be the
case in the Mediterranean. In the context of large sedentary forager populations exploiting forested resources,
such as the inhabitants of Con Co Ngua, we propose a pre-agricultural origin for the emergence of thalassemia
in MSEA as an adaptive response to the threat of malaria. However, the agricultural transition approximately
4500–3500years ago likely encouraged the spread of malarial vectors, increasing the gene frequencies of thalas-
semias. e outcomes of our research indicate a deep history of thalassemias which are endemic in MSEA today.
Methods and materials
Ethics and approvals. Paleopathological observation and collection and analysis of samples for histologi-
cal investigation was approved by the Vietnam Institute of Archaeology in Hanoi, Vietnam on October 12, 2018.
Bone samples were exported to the Australian National University in Canberra under approval by Dr. Nguyen
Gia Doi (Director), and are currently housed at this institution until further notice. As the samples are of an
archaeological nature, no ethical approvals were required for this study.
The sample. We macroscopically assessed 70 individuals from Man Bac and 155 individuals from Con Co
Ngua for pathology. All skeletal elements with pathological change with the potential for diagnosis were radio-
graphed. ree individuals from Con Co Ngua were sampled for histological analysis.
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e skeletal assemblage of Man Bac was well preserved. While post-mortem breaks were frequent, the skel-
etons were easily reconstructed. Surfaces were excellently preserved. For most skeletons both adult and subadult
were either complete or near complete54. In contrast, the individuals from Con Co Ngua presented with erosion
of the cortical surfaces, but not to the degree that pathologies could not be observed. Post-mortem breakage
was common, and a large proportion of the assemblage was at most partially complete. Subadults were com-
monly poorly preserved, with infants highly fragmented. Methods for age and sex of the individuals from Man
Bac and Con Co Ngua were previously reported and briey summarized here50,55,56. Non-metric traits of the
os coxae, cranial morphology, and sample-specic post-cranial functions were used to estimate adult sex57–60.
Adult age-at-death was estimated by way of pubic symphyseal morphology61 and/or sample-specic molar wear
functions developed by Oxenham60. Subadult age-at-death was estimated using dental eruption and calcication
standards62,63, and/or skeletal maturity schedules64.
Paleopathological dierential diagnosis. e paleopathological diagnosis of thalassemia was based on
macroscopic and radiographic observations of pathologies in dry bone. A standardized ‘threshold’ diagnostic
protocol for thalassemia was produced following clinical diagnostic standards (Table2). A possible case was
diagnosed when an individual exhibited one diagnostic or two suggestive lesions. A probable case was diagnosed
when an individual exhibited one strongly diagnostic or two diagnostic lesions. Such recording methods are
consistent with a number of previously published diagnostic protocols in paleopathology, and ensure diagnostic
rigour18,65.
Gross skeletal manifestations of thalassemia are restricted to beta thalassemia only, except in the case of
alpha thalassemia major (also called Bart’s hydrops fetalis) a fatal form, where infants die prior to or immedi-
ately following birth7. Severe porotic hyperostosis leading to a ‘hair-on-end’ appearance is a common skeletal
manifestation of thalassemia (as is the case in other anemias) and has been reported particularly in cases of
thalassemia major68,77.
Extensive marrow hyperplasia of the medullary canal and within cancellous bone regions cause consider-
able thinning of the bone cortex, and expansion of the area of the medullary canal68. e extent of the marrow
Table 2. Criteria for diagnosis of thalassemia in dry bone (SD = strongly diagnostic, D = diagnostic, and
S = suggestive). A probable case is dened as an individual exhibiting at minimum one strongly diagnostic
pathology or two diagnostic pathologies. A possible case is dened as an individual exhibiting at minimum
one diagnostic or two suggestive pathologies. *A strongly diagnostic lesion is one that is considered
pathognomonic for that disease and alone stands as evidence of probable disease. In extremely rare instances
these pathologies can occur in other diseases which are listed here in the dierential diagnosis.
Pathology Diagnostic strength Dierential diagnosis References
Marrow hyperplasia of the facial bones: maxillae- leading to ventral
displacement of central incisors, zygomatic bones-leading to orbital
displacement, and/ or mandible (rodent facies deformity) SD 29,66–70
Radiographic: “rib-within-a-rib” appearance. Radiographically dened
sclerotic bands within the ribs due to extramedullary hematopoiesis SD Sickle cell anemia, osteomyelitis, leukemia* 29,66,68,71
Poor or lack of pneumatization of the paranasal and cranial sinuses
sparing the ethmoid sinuses DNeoplasms, Paget’s disease, trauma, hypopituitarism, hypothyroidism,
osteopetrosis, sickle cell anemia 29,68
Widening of entire rib, or widening of the rib head and neck with pro-
nounced bulbous appearance posteriorly (costal osteomas). Associated
with radiograph appearance of erosion of the inner cortex D Neuroblastoma, Nieman-Pick disease, Leukemia 29,66,68,71
Enlarged tubular bones of the hands and feet due to marrow hyper-
plasia (infants) sometimes associated with enlarged nutrient foramina
or Radiographic: coarse trabecular patterns of the hands or feet,
sometimes associated with cyst-like lucencies due to focal collection of
hyperplasic marrow
D Treponemal disease, leprosy, tuberculosis 12,29,66,68
Premature fusion of epiphyseal plates particularly of the proximal
humerus and distal femur, oen causing short long bone maximum
length DScurvy, hypervitaminosis A, trauma, achondroplasia, Morquio’s
disease, Ellis-van Creveld disease, peripheral dysostosis, poliomyelitis,
mucopolysaccharidosis, rickets, osteomalacia
12,29,66,68,72
Extensive marrow proliferation of the long bones leading to expansion
of the medullary canal, associated with thin cortices (and in extreme
circumstances honeycomb-like porosity) resulting in swollen appear-
ance or metaphyseal asked shaped deformities
SOther hemolytic anemia, scurvy, rickets, metaphyseal dysplasia,
Gaucher’s disease, osteomyelitis 66,68,73
Severe porotic hyperostosis/ diploic expansions of vault and maxilla
with “hair-on-end” appearance and/ or cribra orbitalia S
Aer Lagia74: hemolytic anemias and red cell enzyme disorders
(including sickle cell disease, iron deciency anemia and G-6-PD de-
ciency), cancers (including leukemia, multiple myeloma, meningioma,
metastases and secondary to kidney cancers), and polycythemia
29,66,68,74
Wide dental spacing S Skeletal dysplasias, normal variation 66
Spiculated or scalloped proliferation of subperiosteal reactive new
bone on the shas of the limb bones and the clavicles SInfectious diseases, rickets, scurvy, hypertrophic osteoarthropathy,
Gaucher’s diseases, Paget’s disease 12,69,75
Marked osteoporosis and cortical thinning of the vertebrae, with
compression fractures in severe cases S Age related osteoporosis, osteomalacia, scurvy, trauma 29
Bone infarction S Osteomyelitis, sickle cell anemia, osteosarcoma 76
Enlargement and alteration of the trabecular pattern in at bones
(pelvis and scapula) S Other hemolytic anemia, leukemia 70
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hyperplasia causes thinning trabeculae. However, subperiosteal new bone response to the trabecular destruction
instigates the coarsening of trabeculae which is observed radiographically68. In extreme circumstances cortical
thinning can progress to destruction of the cortex and subsequent honeycomb appearance of the bone surface70.
A distinct facial deformity called rodent facies occurs in severe cases particularly in thalassemia major
whereby extensive marrow proliferation of the maxillae and zygomatic bones creates anterior bulging of the
face, oen associated with anterior displacement of the central incisors, and lack of pneumatization of the
maxillary, sphenoidal and frontal sinuses29,66–68. is pathological lesion is strongly diagnostic for thalassemia,
particularly of thalassemia major (Table2)29,68. e marrow proliferation also causes anterior teeth protrusion
and malocclusion of the remaining teeth66. A strongly diagnostic radiographic feature of this disorder is the ‘rib-
within-in-a-rib’ sign. is feature is produced by extensive marrow hypertrophy perforating the thin cortex of the
rib associated with a radiodense line in the middle of the medullary canal29,66,69,78. Hypertrophic changes to the
hands and feet of infants (with associated expanded foramina in the phalanges) is also characteristic of the dis-
ease, as this lesion indicates an extreme form of anemia unlikely to be associated with non-genetic etiologies12,68.
Marrow perforation of the cortex known as extramedullary hematopoiesis occurs. In certain circumstances
subperiosteal new bone response similar to the “hair-on-end” appearance of the skull, surrounding thin cortices
of postcranial bones, can result as a consequence of marrow perforation69,75. is skeletal response has been
documented to lead to premature fusion of the epiphyses of long bones particularly of the proximal humerus
and distal femur68,75. e extent of prematurity is dependent on the individual. is lesion is more common in
cases of thalassemia intermedia75. Bone infarction, while less common in thalassemia than sickle cell anemia,
hasalso been reported. In this pathological condition, bone death occurs followed by inammatory new bone
response around the region of necrosis, and has a distinct appearance on radiographs76.
Histological sectioning. All sectioning procedures followed standard protocols79,80 and were completed
at the Institute of Archaeology, Hanoi, Vietnam. A Dremel Variable-Speed Rotary Tool 3000 with associated
Dremel blades was used to cut into the bone shas. is involved making two longitudinally oriented parallel
(along the long bone axis) cuts, followed by a transversely oriented (perpendicular to the longitudinal cuts) cut,
so that sections freely detached themselves from the bone. Permissions obtained from the collection curators
strictly stipulated that sections were onlyto beremoved from the bone regions already aected by post-mortem
breaks to avoid further damage to the specimens. For example, where the long bone was broken in half or
had epiphyseal ends missing due to taphonomic issues. Sampling in those regions avoided further damage to
the specimens. However, we ensured that the bone sections still derived from the long bone shas so that we
could assess the histological changes on the endocortical surfaces. e three individuals sampled for histological
analysis met these criteria. We sampled the le and right femur of CCN13M40a (Fig.4). e right humerus, le
ulna and le radius of CCN13M59a were sampled as they were the only available long bones for this individual
(the lower limb only consisted of a fragmented right bula). e right humerus, le radius, and le femur of the
subadult CCN13M67a were sectioned as both the upper and lower limb bones showed a degree of endocortical
thickening. e lower (distal direction) third of the le femoral sha, approximately 4cm below the linea aspera,
and the midsha of the right femur, were sampled in CCN13M40a. e upper limb bones of CCN13M59a were
sectioned at the distal end of the le ulna and the right radius, and the midsha of the right humerus. e le
femur of CCN13M67a was sectioned at the middle of the upper (proximal direction) third of sha, the distal
third of the sha in the le radius, and the upper (proximal direction) third sha of the right humerus. We note
that the le radius in this individual shows a well remodeled and healed fracture at midsha (Supplementary
Fig.S2), which clearly resulted in a deformation of the bone. is will need to be borne in mind when interpret-
ing the appearance of histology in thin section. A total of eight, approximately 1cm thick, roughly C-shaped,
sections of bone from the posterior aspect were removed for the entire sample (Fig.4).
Prior to histological preparation, external size measurements of the bones and sections were recorded using
standard digital calipers and a so measuring tape. All measurements were repeated at least two times from
which an average was computed and reported here. e measurements79 were: sha circumference (Circ) at point
of sectioning (mm), anterior–posterior diameter in mm (AP dm), medial–lateral diameter in mm (ML dm),
cortical width (Ct.W) of the extracted sample measured from both the proximal and distal surfaces in the lateral
direction (from the endosteal, referring to the endosteum lining the medullary cavity, to the periosteal surfaces).
Histopathology. No prior information on age, sex or macropathology was provided for the samples to
ensure an objective observation. All samples were processed into thin sections following standard methods
applicable for histological analysis of archaeological human bone81,82. e processing was completed at the Hard
Tissue Histology laboratory in the School of Archaeology and Anthropology at the Australian National Univer-
sity (Canberra, Australia), which is also where the resulting thin sections are curated until further notice. Each
sample was embedded in Buehler epoxy resin, cut on a low-speed saw equipped with a diamond wafering blade,
and attached to microscope glass slides using Stuck epoxy glue. e attached samples were further trimmed on
a cutting saw, and later lapped on a series of grinding pads of various grit sizes that increased from 400 to 1200
in coarseness. e thickness of each section was controlled using a handheld Buehler 28 × 48mm target holder,
allowing to produce sections of approximately 90–100μm thickness. e sections were polished using a Buehler
MicroPolish powder, 0.05µm, until all scratches created during grinding were removed. is was followed by
cleaning the sections in an ultrasonic bath, dehydrating them in a series of ethanol baths, and clearing using
xylene for histopathology. e samples were nally covered with glass cover slips glued to the bone surface with
DPX.
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Imaging and histomorphological analysis. Each thin section was imaged using transmitted and polar-
ized light under a high powered Olympus BX53 microscope equipped with a DP74 high resolution camera81.
We used a series of objective lenses, ranging from 4 × to 40 × (40 × to 400 × total magnication), to examine his-
tological features82. Each section was rst examined for any overall diagenetic damage, and second for patterns
in, and areas of, abnormal bone matrices and micro-organization. is was followed by a targeted examination
of bone regions on the endocortical surfaces, which is where we hypothesized abnormal changes would occur as
per the macroscopic manifestation (Fig.4). As the border between intra-cortical and endocortical bone relies on
a somewhat arbitrary division, the endocortical area examined in our samples was, on average, 1.5–1.7cm once
the entire section surface was sub-divided into four equal segments (one sub-periosteal, two intra-cortically,
and one endocortically). We captured individual regions of interest (ROIs) from within the endocortical areas.
It is also where we recorded a full endocortical strip of bone using an automated stitching tool of the Olympus
CellSens soware.
e microscopic examination revealed an overall moderately good preservation of the samples83. Our histo-
logical examination was based on inspecting bone regions for: bone matrix type (woven, lamellar)84; bone growth
stage (primary, secondary/ Haversian)85; bone remodeling indicators (poorly remodeled with singular secondary
osteon units, well remodeled with several generations of fragmentary and intact secondary osteons)80,85, ‘giant’
resorption canals (porosity eect indicating prolonged osteoclast-mediated resorption, tabularization eect)86,87.
Where necessary, we also undertook histomorphometric measurements using ImageJ ‘straight line’ tool to obtain
maximum diameter of pores in cases of abnormal porosity.
Received: 10 November 2020; Accepted: 8 February 2021
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Acknowledgements
We would like to thank Dr. Ngo Anh Son, Mr. Bui Van Khanh and Ms. Nellissa Ling for their assistance with the
radiographs. We are grateful to Dr. Nguyen Gia Doi for permission to extract histological samples. is work
was supported by a National Geographic Early Career Grant (EC-54332R-18); Royal Society of New Zealand
Skinner Fund Grant; University of Otago Doctoral Scholarship; Australian Research Council DP110101097 and
FT120100299. Histological processing was funded by the Australian Research Council DE190100068.
Author contributions
M.F.O. directed the excavation of MB. M.F.O. and H.H.T. jointly directed the excavation of CCN. Initial osteo-
logical analyses, including sex, age, and pathologywere performed by MF.O. and K.D. for MB and M.F.O., H.B.,
K.D. and A.W. for CCN. M.V. and H.B. designed thehydatid disease study. M.V., H.B., T.M. and M.W. collected
the data. M.V., H.B., J.M. and M.W. analyzed the data. All authors contributed input to the manuscript including
contextualization of the data and draing of the manuscript. M.V. prepared Figs.1, 2, 3 and S1. J.M. prepared
Figs.4, 5 and S2.
Competing interests
e authors declare no competing interests.
Additional information
Supplementary Information e online version contains supplementary material available at https ://doi.
org/10.1038/s4159 8-021-83978 -4.
Correspondence and requests for materials should be addressed to M.V.orM.F.O.
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