Khankari Nikhil K, Su Timothy, Cai Qiuyin, Liu Lili, Jasper Elizabeth A, Hellwege Jacklyn N, Murff Harvey J, Shrubsole Martha J, Long Jirong, Edwards Todd L, Zheng Wei
Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, USA.
Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, USA.
Genet Epidemiol. 2025 Jan;49(1):e22613. doi: 10.1002/gepi.22613.
Polyunsaturated fatty acids (PUFAs) including omega-3 and omega-6 are obtained from diet and can be measured objectively in plasma or red blood cells (RBCs) membrane biomarkers, representing different dietary exposure windows. In vivo conversion of omega-3 and omega-6 PUFAs from short- to long-chain counterparts occurs via a shared metabolic pathway involving fatty acid desaturases and elongase. This analysis leveraged genome-wide association study (GWAS) summary statistics for RBC and plasma PUFAs, along with expression quantitative trait loci (eQTL) to estimate tissue-specific genetically predicted gene expression effects for delta-5 desaturase (FADS1), delta-6 desaturase (FADS2), and elongase (ELOVL2) on changes in RBC and plasma biomarkers. Using colocalization, we identified shared variants associated with both increased gene expression and changes in RBC PUFA levels in relevant PUFA metabolism tissues (i.e., adipose, liver, muscle, and whole blood). We observed differences in RBC versus plasma PUFA levels for genetically predicted increase in FADS1 and FADS2 gene expression, primarily for omega-6 PUFAs linoleic acid (LA) and arachidonic acid (AA). The colocalization analysis identified rs102275 to be significantly associated with a 0.69% increase in total RBC membrane-bound LA levels (p = 5.4 × 10). Future PUFA genetic studies examining long-term PUFA biomarkers are needed to confirm our results.
包括ω-3和ω-6在内的多不饱和脂肪酸(PUFA)可从饮食中获取,并可在血浆或红细胞(RBC)膜生物标志物中进行客观测量,这些生物标志物代表了不同的饮食暴露窗口。ω-3和ω-6多不饱和脂肪酸在体内从短链向长链对应物的转化是通过一条涉及脂肪酸去饱和酶和延长酶的共同代谢途径进行的。本分析利用了红细胞和血浆多不饱和脂肪酸的全基因组关联研究(GWAS)汇总统计数据,以及表达定量性状位点(eQTL),以估计组织特异性基因预测的δ-5去饱和酶(FADS1)、δ-6去饱和酶(FADS2)和延长酶(ELOVL2)对红细胞和血浆生物标志物变化的基因表达效应。通过共定位,我们在相关多不饱和脂肪酸代谢组织(即脂肪、肝脏、肌肉和全血)中确定了与基因表达增加和红细胞多不饱和脂肪酸水平变化相关的共同变体。我们观察到,在基因预测的FADS1和FADS2基因表达增加时,红细胞与血浆多不饱和脂肪酸水平存在差异,主要是针对ω-6多不饱和脂肪酸亚油酸(LA)和花生四烯酸(AA)。共定位分析确定rs102275与红细胞膜结合总LA水平显著增加0.69%相关(p = 5.4×10)。未来需要进行多不饱和脂肪酸基因研究,以检查长期多不饱和脂肪酸生物标志物,以证实我们的结果。