National Institute of Genomic Medicine (Instituto Nacional de Medicina Genómica INMEGEN), Laboratory of Genomics of Psychiatric Diseases, Neurodegenerative and Addictions, Ministry of Health, Mexico City, Mexico.
Comalcalco Multidisciplinary Academic Division, Autonomous Juárez University of Tabasco (Universidad Juárez Autónoma de Tabasco), Comalcalco, Tabasco, Mexico.
Mol Genet Genomic Med. 2019 Nov;7(11):e958. doi: 10.1002/mgg3.958. Epub 2019 Sep 26.
Apolipoprotein E (ApoE) is a glycoprotein that plays an important role in lipid homeostasis at both cerebral and systemic levels. Moreover, the differential distribution of APOE gene alleles among different populations, means that ApoE isoforms could have different effects on lipids metabolism. The present study aims to evaluate the relationship between APOE gene alleles and the lipid profile in a Mexican Amerindian (MA) population.
This study included 1997 MA individuals of different ethnicities distributed throughout different states of Mexico. All individuals underwent anthropometric measurements as well as laboratory tests including fasting glucose (FG), total cholesterol (TC), triglycerides, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C). TaqMan probe genotyping assays were used to genotype APOE. The Kruskal-Wallis test was performed to determine the correlation between APOE gene alleles and genotypes and the biochemical variables measured.
Among the biochemical variables analyzed, only the HDL-C and LDL-C levels showed statistical differences (p-value < .05) between individuals carrying different APOE alleles. For HDL-C, individuals carrying the E2 allele had higher HDL-C levels, followed by individuals carrying the E3 allele and carriers of the E4 allele presented the lowest levels of HDL-C (E2 > E3 > E4). This relationship was inversed for LDL-C levels (E2 < E3 < E4). Nevertheless, the difference of HDL-C levels between APOE-E3 and APOE-E4 carriers remained only in obese individuals.
Our results suggest that APOE gene genotypes play an important role in the differential modulation of lipid profiles in the MA population with obesity.
载脂蛋白 E(ApoE)是一种糖蛋白,在大脑和全身水平的脂质平衡中发挥重要作用。此外,不同人群中 APOE 基因等位基因的差异分布意味着 ApoE 异构体可能对脂质代谢有不同的影响。本研究旨在评估墨西哥裔美国人(MA)人群中 APOE 基因等位基因与血脂谱之间的关系。
本研究包括来自墨西哥不同州的 1997 名不同种族的 MA 个体。所有个体均进行了人体测量学测量和实验室检查,包括空腹血糖(FG)、总胆固醇(TC)、甘油三酯、低密度脂蛋白胆固醇(LDL-C)和高密度脂蛋白胆固醇(HDL-C)。使用 TaqMan 探针基因分型检测法对 APOE 进行基因分型。采用 Kruskal-Wallis 检验分析 APOE 基因等位基因和基因型与所测生化变量之间的相关性。
在所分析的生化变量中,只有 HDL-C 和 LDL-C 水平在携带不同 APOE 等位基因的个体之间存在统计学差异(p 值<.05)。对于 HDL-C,携带 E2 等位基因的个体 HDL-C 水平较高,其次是携带 E3 等位基因的个体,携带 E4 等位基因的个体 HDL-C 水平最低(E2>E3>E4)。这种关系与 LDL-C 水平相反(E2<E3<E4)。然而,APOE-E3 和 APOE-E4 携带者的 HDL-C 水平之间的差异仅在肥胖个体中存在。
我们的结果表明,APOE 基因基因型在肥胖的 MA 人群中对血脂谱的差异调节中起重要作用。