Author
Listed:
- Chengran Yang
(Washington University School of Medicine
Washington University School of Medicine)
- Priyanka Gorijala
(Washington University School of Medicine
Washington University School of Medicine)
- Jigyasha Timsina
(Washington University School of Medicine
Washington University School of Medicine)
- Lihua Wang
(Washington University School of Medicine
Washington University School of Medicine)
- Menghan Liu
(Washington University School of Medicine
Washington University School of Medicine)
- Ciyang Wang
(Washington University School of Medicine
Washington University School of Medicine)
- William Brock
(Washington University School of Medicine
Washington University School of Medicine)
- Yueyao Wang
(Washington University School of Medicine
Washington University School of Medicine)
- Fumihiko Urano
(MSC 8127-0021-09
Washington University School of Medicine)
- Yun Ju Sung
(Washington University School of Medicine
Washington University School of Medicine
Washington University School of Medicine)
- Carlos Cruchaga
(Washington University School of Medicine
Washington University School of Medicine
Washington University School of Medicine
Washington University School of Medicine)
Abstract
In this study, we generated and integrated plasma proteomics and metabolomics with the genotype datasets of over 2300 European (EUR) and 400 African (AFR) ancestries to identify ancestry-specific multi-omics quantitative trait loci (QTLs). In total, we mapped 954 AFR pQTLs, 2848 EUR pQTLs, 65 AFR mQTLs, and 490 EUR mQTLs. We further applied these QTLs to ancestry-stratified type-2 diabetes (T2D) risk to pinpoint key proteins and metabolites underlying the disease-associated genetic loci. Using INTACT that combined trait-imputation and colocalization results, we nominated 270 proteins and 72 metabolites from the EUR set; seven proteins and one metabolite from the AFR set as molecular effectors of T2D risk in an ancestry-stratified manner. Here, we show that the integration of genetic and omic studies of different ancestries can be used to identify distinct effector molecular traits underlying the same disease across diverse ancestral groups.
Suggested Citation
Chengran Yang & Priyanka Gorijala & Jigyasha Timsina & Lihua Wang & Menghan Liu & Ciyang Wang & William Brock & Yueyao Wang & Fumihiko Urano & Yun Ju Sung & Carlos Cruchaga, 2025.
"European and African ancestry-specific plasma protein-QTL and metabolite-QTL analyses identify ancestry-specific T2D effector proteins and metabolites,"
Nature Communications, Nature, vol. 16(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62463-w
DOI: 10.1038/s41467-025-62463-w
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