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HGG advances · 2026

Multi-omic characterization of the Hispanic/Latino blood lipidome reveals an additional locus and attenuated genetic prediction.

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Zhu Wanying, Chen Hung-Hsin, Highland Heather M, Giles Corey, Meikle Peter J, Lin Phillip, Petty Lauren E, Polikowsky Hannah G, Petty Alex S, Anwar Mohammad Y, Zhang Xinruo, Curran Joanne E, Frankel Elizabeth G, Roshani Rashedeh, Landman Joshua M, Castrodad-Rivera Gabriela S, Herndon Caroline, McCormick Joseph B, Fisher-Hoch Susan P, Gordon-Larsen Penny, Gamazon Eric R, North Kari E, Below Jennifer E

Аннотация

While lipids have been extensively investigated, genetic regulation of the circulating lipidome in diverse populations remains poorly understood. We conducted a lipidome-wide genome-wide association study (GWAS) of 830 lipid species in 2,287 Hispanic/Latino participants and performed predictive modeling across omics layers. We identified 7,593 genome-wide significant SNPs mapping to 208 genes. Conditional analysis disentangled the long-range linkage disequilibrium artifacts from the pleiotropic FADS1/2/3 cluster. Separately, we discovered an association at the GPLD1 locus for a circulating ceramide. Colocalization revealed shared genetic architecture with conventional lipids alongside distinct, species-specific pathways. Incorporating Native/Indigenous American expression quantitative trait loci (eQTLs) within a multi-omic framework uncovered 62 likely regulatory genes missed by European-centric gene expression models. Finally, genetically regulated predictive models demonstrated performance declining from transcriptomics to proteomics to lipidomics, reflecting increased distance from gene action along the molecular cascade. Our study provides a genetic landscape of lipid metabolism in a highly burdened population and highlights the challenges in predicting lipid abundance.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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