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Linking obesity-associated genotype to child language development: the role of early-life neurology-related proteomics and brain myelination

Linking obesity-associated genotype to child language development: the role of early-life neurology-related proteomics and brain myelination
Linking obesity-associated genotype to child language development: the role of early-life neurology-related proteomics and brain myelination
Background: the association between childhood obesity and language development may be confounded by socio-environmental factors and attributed to comorbid pathways.

Methods: in a longitudinal Singaporean mother-offspring cohort, we leveraged trans-ancestry polygenic predictions of body mass index (BMI) to interrogate the causal effects of early-life BMI on child language development and its effects on molecular and neuroimaging measures. Leveraging large genome-wide association studies, we examined whether the link between obesity and language development is causal or due to a shared genetic basis.

Findings: we found an inverse association between polygenic risk for obesity, which is less susceptible to confounding, and language ability assessed at age 9. Our findings suggested a shared genetic basis between obesity and language development rather than a causal effect of obesity on language development. Interrogating early-life mechanisms including neurology-related proteomics and language-related white matter microstructure, we found that EFNA4 and VWC2 expressions were associated with language ability as well as fractional anisotropy of language-related white matter tracts, suggesting a role in brain myelination. Additionally, the expression of the EPH-Ephrin signalling pathway in the hippocampus might contribute to language development. Polygenic risk for obesity was nominally associated with EFNA4 and VWC2 expression. However, we did not find support for mediating mechanisms via these proteins.

Interpretation: this study demonstrates the potential of examining early-life proteomics in conjunction with deep genotyping and phenotyping and provides biological insights into the shared genomic links between obesity and language development.

Funding: Singapore National Research Foundation and Agency for Science, Technology and Research.
Language development, Neurology-related protein, Obesity, Polygenic risk score
2352-3964
Huang, Jian
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Che, Jinyi
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Kee, Michelle Z.L.
b10a1ed0-e2ab-40bf-bba0-471e5f7ae601
Tan, Ai Peng
aa74aa67-3429-4b8b-9782-fa3925eaa59b
Law, Evelyn C.
49ba55c6-ffc3-40a4-9ac4-6c05b5fd7f85
Pelufo Silveira, Patricia
a7d97f02-967f-410f-9a18-eab0cd17dfc7
Pokhvisneva, Irina
58960728-d6fe-40cd-9c87-454bef8b062d
Patel, Sachin
d257fe28-c25c-4ff0-bf9c-3cb0e7e0e289
Godfrey, Keith M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Daniel, Lourdes Mary
8092af24-31fe-42e5-be16-eda563047752
Tan, Kok Hian
4714c94d-334a-42ad-b879-f3aa3a931def
Chong, Yap-Seng
7043124b-e892-4d4b-8bb7-6d35ed94e136
Chan, Shiao-Yng
3c9d8970-2cc4-430a-86a7-96f6029a5293
Eriksson, Johan G.
eb96b1c5-af07-4a52-8a73-7541451d32cd
Wang, Dennis
118a3400-592b-44c4-afa1-f6da24c4da3d
Huang, Jonathan Y.
35e14404-4a04-49f6-822a-65ec0ac4f50c
Huang, Jian
583a2bd9-a83b-4446-89aa-1b6ff6ac2418
Che, Jinyi
55986313-1f0f-45ae-beed-ccb803a57f47
Kee, Michelle Z.L.
b10a1ed0-e2ab-40bf-bba0-471e5f7ae601
Tan, Ai Peng
aa74aa67-3429-4b8b-9782-fa3925eaa59b
Law, Evelyn C.
49ba55c6-ffc3-40a4-9ac4-6c05b5fd7f85
Pelufo Silveira, Patricia
a7d97f02-967f-410f-9a18-eab0cd17dfc7
Pokhvisneva, Irina
58960728-d6fe-40cd-9c87-454bef8b062d
Patel, Sachin
d257fe28-c25c-4ff0-bf9c-3cb0e7e0e289
Godfrey, Keith M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Daniel, Lourdes Mary
8092af24-31fe-42e5-be16-eda563047752
Tan, Kok Hian
4714c94d-334a-42ad-b879-f3aa3a931def
Chong, Yap-Seng
7043124b-e892-4d4b-8bb7-6d35ed94e136
Chan, Shiao-Yng
3c9d8970-2cc4-430a-86a7-96f6029a5293
Eriksson, Johan G.
eb96b1c5-af07-4a52-8a73-7541451d32cd
Wang, Dennis
118a3400-592b-44c4-afa1-f6da24c4da3d
Huang, Jonathan Y.
35e14404-4a04-49f6-822a-65ec0ac4f50c

Huang, Jian, Che, Jinyi, Kee, Michelle Z.L., Tan, Ai Peng, Law, Evelyn C., Pelufo Silveira, Patricia, Pokhvisneva, Irina, Patel, Sachin, Godfrey, Keith M., Daniel, Lourdes Mary, Tan, Kok Hian, Chong, Yap-Seng, Chan, Shiao-Yng, Eriksson, Johan G., Wang, Dennis and Huang, Jonathan Y. (2025) Linking obesity-associated genotype to child language development: the role of early-life neurology-related proteomics and brain myelination. EBioMedicine, 113, [105579]. (doi:10.1016/j.ebiom.2025.105579).

Record type: Article

Abstract

Background: the association between childhood obesity and language development may be confounded by socio-environmental factors and attributed to comorbid pathways.

Methods: in a longitudinal Singaporean mother-offspring cohort, we leveraged trans-ancestry polygenic predictions of body mass index (BMI) to interrogate the causal effects of early-life BMI on child language development and its effects on molecular and neuroimaging measures. Leveraging large genome-wide association studies, we examined whether the link between obesity and language development is causal or due to a shared genetic basis.

Findings: we found an inverse association between polygenic risk for obesity, which is less susceptible to confounding, and language ability assessed at age 9. Our findings suggested a shared genetic basis between obesity and language development rather than a causal effect of obesity on language development. Interrogating early-life mechanisms including neurology-related proteomics and language-related white matter microstructure, we found that EFNA4 and VWC2 expressions were associated with language ability as well as fractional anisotropy of language-related white matter tracts, suggesting a role in brain myelination. Additionally, the expression of the EPH-Ephrin signalling pathway in the hippocampus might contribute to language development. Polygenic risk for obesity was nominally associated with EFNA4 and VWC2 expression. However, we did not find support for mediating mechanisms via these proteins.

Interpretation: this study demonstrates the potential of examining early-life proteomics in conjunction with deep genotyping and phenotyping and provides biological insights into the shared genomic links between obesity and language development.

Funding: Singapore National Research Foundation and Agency for Science, Technology and Research.

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More information

Accepted/In Press date: 17 January 2025
e-pub ahead of print date: 11 February 2025
Published date: 11 February 2025
Keywords: Language development, Neurology-related protein, Obesity, Polygenic risk score

Identifiers

Local EPrints ID: 499006
URI: http://eprints.soton.ac.uk/id/eprint/499006
ISSN: 2352-3964
PURE UUID: cab9e034-9a05-4ec4-b75c-a766e948c9dc
ORCID for Keith M. Godfrey: ORCID iD orcid.org/0000-0002-4643-0618

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Date deposited: 06 Mar 2025 17:56
Last modified: 27 Aug 2025 01:34

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Contributors

Author: Jian Huang
Author: Jinyi Che
Author: Michelle Z.L. Kee
Author: Ai Peng Tan
Author: Evelyn C. Law
Author: Patricia Pelufo Silveira
Author: Irina Pokhvisneva
Author: Sachin Patel
Author: Lourdes Mary Daniel
Author: Kok Hian Tan
Author: Yap-Seng Chong
Author: Shiao-Yng Chan
Author: Johan G. Eriksson
Author: Dennis Wang
Author: Jonathan Y. Huang

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