Genetic Determinants of Fatty Acid Composition in Subcutaneous and Visceral Adipose Tissue.

Altayeb Ahmed, Afreen Naz, Marjola Thanaj, Elena P Sorokin, Brandon Whitcher, Jimmy D Bell, E Louise Thomas, Madeleine Cule, Hanieh Yaghootkar
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Abstract

Objective: Fatty acids in adipose tissue are key structural and metabolic regulators of cardiometabolic health, but the genetic architecture governing depot-specific composition in subcutaneous (SAT) and visceral adipose tissue (VAT) is not well defined.

Methods: We used MRI-derived estimates of fatty acid composition in SAT and VAT from 33,583 UK Biobank participants to perform genome-wide association studies. Functional annotation, fine mapping, colocalization, and expression QTL analyses were conducted to prioritize likely causal variants and explore mechanisms.

Results: We identified six loci associated with adipose tissue fatty acid composition, including both shared (PKD2L1, INSIG1) and depot-specific associations (LEKR1 and KLF14 for SAT; CDCA2 for VAT). The strongest association, rs603424-G (near PKD2L1), was linked to higher monounsaturated and polyunsaturated fatty acids, lower saturated fatty acids, and increased SCD1 expression in SAT and VAT, suggesting a role in desaturation and lipid remodeling. Several loci were linked to cardiometabolic outcomes including type 2 diabetes, hypertension, and cholelithiasis, with functional evidence supporting gene-diet interactions at the PKD2L1 locus.

Conclusions: Our findings uncover genetic determinants of human adipose tissue fatty acid composition, highlight depot-specific regulation, and point to SCD1 as a potential metabolic regulator. These results deepen understanding of lipid metabolism and its links to cardiometabolic risk.

皮下和内脏脂肪组织中脂肪酸组成的遗传决定因素。
目的:脂肪组织中的脂肪酸是心脏代谢健康的关键结构和代谢调节剂,但控制皮下(SAT)和内脏脂肪组织(VAT)中储存特异性成分的遗传结构尚不明确。方法:我们使用来自33,583名英国生物银行参与者的SAT和VAT脂肪酸组成的mri估计来进行全基因组关联研究。通过功能注释、精细映射、共定位和表达QTL分析来确定可能的因果变异并探索其机制。结果:我们确定了6个与脂肪组织脂肪酸组成相关的位点,包括共享的(PKD2L1, INSIG1)和仓库特异性关联(SAT的LEKR1和KLF14; VAT的CDCA2)。最强关联rs603424-G(靠近PKD2L1)与较高的单不饱和和多不饱和脂肪酸、较低的饱和脂肪酸以及SAT和VAT中SCD1表达增加有关,表明其在去饱和和脂质重塑中起作用。几个基因座与心脏代谢结果相关,包括2型糖尿病、高血压和胆石症,功能证据支持PKD2L1位点的基因-饮食相互作用。结论:我们的研究结果揭示了人类脂肪组织脂肪酸组成的遗传决定因素,强调了储存特异性调节,并指出SCD1是一种潜在的代谢调节因子。这些结果加深了对脂质代谢及其与心脏代谢风险的联系的理解。
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