Lemaitre Rozenn N, King Irena B, Kabagambe Edmond K, Wu Jason H Y, McKnight Barbara, Manichaikul Ani, Guan Weihua, Sun Qi, Chasman Daniel I, Foy Millennia, Wang Lu, Zhu Jingwen, Siscovick David S, Tsai Michael Y, Arnett Donna K, Psaty Bruce M, Djousse Luc, Chen Yii-Der I, Tang Weihong, Weng Lu-Chen, Wu Hongyu, Jensen Majken K, Chu Audrey Y, Jacobs David R, Rich Stephen S, Mozaffarian Dariush, Steffen Lyn, Rimm Eric B, Hu Frank B, Ridker Paul M, Fornage Myriam, Friedlander Yechiel
Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA.
Department of Internal Medicine, University of New Mexico, Albuquerque, NM.
J Lipid Res. 2015 Jan;56(1):176-84. doi: 10.1194/jlr.M052456. Epub 2014 Nov 6.
Very long-chain saturated fatty acids (VLSFAs) are saturated fatty acids with 20 or more carbons. In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influence circulating levels of VLSFAs is not known. We investigated the association of common genetic variation with plasma phospholipid/erythrocyte levels of three VLSFAs by performing genome-wide association studies in seven population-based cohorts comprising 10,129 subjects of European ancestry. We observed associations of circulating VLSFA concentrations with common variants in two genes, serine palmitoyl-transferase long-chain base subunit 3 (SPTLC3), a gene involved in the rate-limiting step of de novo sphingolipid synthesis, and ceramide synthase 4 (CERS4). The SPTLC3 variant at rs680379 was associated with higher arachidic acid (20:0 , P = 5.81 × 10(-13)). The CERS4 variant at rs2100944 was associated with higher levels of 20:0 (P = 2.65 × 10(-40)) and in analyses that adjusted for 20:0, with lower levels of behenic acid (P = 4.22 × 10(-26)) and lignoceric acid (P = 3.20 × 10(-21)). These novel associations suggest an inter-relationship of circulating VLSFAs and sphingolipid synthesis.
极长链饱和脂肪酸(VLSFAs)是含有20个或更多碳原子的饱和脂肪酸。与更为常见的饱和脂肪酸(如棕榈酸)不同,越来越多的证据表明,循环中的VLSFAs可能具有有益的生物学特性。目前尚不清楚遗传因素是否会影响VLSFAs的循环水平。我们通过在七个基于人群的队列中对10129名欧洲血统受试者进行全基因组关联研究,调查了常见基因变异与三种VLSFAs的血浆磷脂/红细胞水平之间的关联。我们观察到循环VLSFA浓度与两个基因中的常见变异有关,这两个基因分别是丝氨酸棕榈酰转移酶长链碱亚基3(SPTLC3),该基因参与鞘脂从头合成的限速步骤,以及神经酰胺合酶4(CERS4)。rs680379处的SPTLC3变异与更高的花生酸水平(20:0,P = 5.81×10⁻¹³)相关。rs2100944处的CERS4变异与更高的20:0水平(P = 2.65×10⁻⁴⁰)相关,并且在对20:0进行校正的分析中,与更低的山嵛酸水平(P = 4.22×10⁻²⁶)和木蜡酸水平(P = 3.20×10⁻²¹)相关。这些新发现的关联表明循环VLSFAs与鞘脂合成之间存在相互关系。