Evidence map›Paper›PMID 41081938›Full record

ArticleHuman genetics2025

Diet as a source of the non-direct genetic effects in metabolic traits: evidence from a family-based GWAS study.

Han Xiao, Zechen Zhou, Yujia Ma, Xiaoyi Li, Kexin Ding, Yiqun Wu, Tao Wu, Yonghua Hu, Dafang Chen

Abstract read
In one paragraph

Article in Human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Han XiaoDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-6108-2789
Zechen ZhouDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Yujia MaDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Xiaoyi LiDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Kexin DingDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Yiqun WuDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Tao WuDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Yonghua HuDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Dafang ChenDepartment of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China. dafangchen@bjmu.edu.cn.

Funding

National Key Research and Development Program of China 2023YFF1104203National Natural Science Foundation of China 82073642
6 · The paper itself

Abstract

Within-family genome-wide association studies (GWAS) can separate direct genetic effects from non-direct genetic biases introduced by analyses based on unrelated individuals, yet evidence regarding metabolic phenotypes remains sparse. Here, we aim to uncover non-direct genetic effects for metabolic traits and the role of diet in the non-direct genetic mechanism. We conducted family-based GWAS studies on six metabolic traits using data from full siblings (N = 777) and parent-offspring trios (N = 386). We calculated and compared within-family and population-based polygenic score (PGS) associations to identify non-direct genetic effects. Additionally, we assessed the parental indirect genetic effects of diet on offspring's metabolic traits. Within-sibship GWAS analyses were also conducted to evaluate the impact of non-direct genetic effects at the individual variant level. On average, the magnitudes of within-family PGS associations for metabolic traits showed a 35.2% reduction compared to population-based estimates, suggesting the presence of non-direct genetic effects. This discrepancy diminished after accounting for dietary score, indicating that diet is a major source of non-direct genetic effects. Additionally, parental indirect genetic effects of diet were revealed in parent-offspring models. For instance, PGS of parental fat consumption was positively related to the child's blood glucose levels (β: 0.44, 95% CI 0.21-0.67). After excluding non-direct genetic effects, within-sibship GWAS models are more effective at identifying functional genes associated with metabolic traits. Our study showed significant contributions of non-direct genetic effects on metabolic traits and also identified diet as a major source of non-direct genetic effects. These findings underlined the importance of family-based GWAS data in disentangling the genetic effects and gene-environment correlations underlying metabolic traits.

Indexed as

DietGenome-Wide Association StudyAdultFemaleHumansMaleMiddle AgedMultifactorial InheritancePhenotypePolymorphism, Single NucleotideSiblings

Identifiers

PMID41081938
PMCPMC12689802

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.