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本文引用的文献

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Atomistic Insights into Structural Differences between E3 and E4 Isoforms of Apolipoprotein E.载脂蛋白E的E3和E4亚型结构差异的原子水平见解。
Biophys J. 2017 Dec 19;113(12):2682-2694. doi: 10.1016/j.bpj.2017.10.006.
2
Association of APOE gene polymorphism with lipid profile and coronary artery disease in Afro-Caribbeans.非裔加勒比人中APOE基因多态性与血脂谱及冠状动脉疾病的关联
PLoS One. 2017 Jul 20;12(7):e0181620. doi: 10.1371/journal.pone.0181620. eCollection 2017.
3
Coronary artery disease-associated genetic variants and biomarkers of inflammation.冠状动脉疾病相关的基因变异与炎症生物标志物。
PLoS One. 2017 Jul 7;12(7):e0180365. doi: 10.1371/journal.pone.0180365. eCollection 2017.
4
Evolution of human apolipoprotein E (APOE) isoforms: Gene structure, protein function and interaction with dietary factors.人类载脂蛋白 E(APOE)同工型的演变:基因结构、蛋白质功能以及与膳食因素的相互作用。
Ageing Res Rev. 2017 Aug;37:146-161. doi: 10.1016/j.arr.2017.06.002. Epub 2017 Jun 21.
5
Coronary Artery Calcium and Risk of Dementia in MESA (Multi-Ethnic Study of Atherosclerosis).动脉粥样硬化多民族研究(MESA)中的冠状动脉钙化与痴呆风险
Circ Cardiovasc Imaging. 2017 May;10(5). doi: 10.1161/CIRCIMAGING.116.005349.
6
Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico.墨西哥梅斯蒂索人和不同美洲印第安人群体中MTHFR基因变异的异质性分布。
PLoS One. 2016 Sep 20;11(9):e0163248. doi: 10.1371/journal.pone.0163248. eCollection 2016.
7
Cosegregation of serum cholesterol with cholesterol intestinal absorption markers in families with primary hypercholesterolemia without mutations in LDLR, APOB, PCSK9 and APOE genes.在低密度脂蛋白受体(LDLR)、载脂蛋白B(APOB)、前蛋白转化酶枯草溶菌素9(PCSK9)和载脂蛋白E(APOE)基因无突变的原发性高胆固醇血症家族中,血清胆固醇与胆固醇肠道吸收标志物的共分离情况。
Atherosclerosis. 2016 Mar;246:202-7. doi: 10.1016/j.atherosclerosis.2016.01.005. Epub 2016 Jan 6.
8
Influence of Abdominal Obesity on the Lipid-Lipoprotein Profile in Apoprotein E2/4 Carriers: The Effect of an Apparent Duality.腹部肥胖对载脂蛋白E2/4携带者脂质-脂蛋白谱的影响:一种明显双重性的效应
J Lipids. 2015;2015:742408. doi: 10.1155/2015/742408. Epub 2015 Oct 28.
9
The Relationship between Native American Ancestry, Body Mass Index and Diabetes Risk among Mexican-Americans.墨西哥裔美国人中美洲原住民血统、体重指数与糖尿病风险之间的关系。
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10
Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children.SORT1和APOE附近变异对儿童低密度脂蛋白胆固醇的遗传贡献:独立于肥胖因素
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载脂蛋白 E 多态性与墨西哥美洲印第安人群脂质谱的关联。

Association between APOE polymorphisms and lipid profile in Mexican Amerindian population.

机构信息

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.

出版信息

Mol Genet Genomic Med. 2019 Nov;7(11):e958. doi: 10.1002/mgg3.958. Epub 2019 Sep 26.

DOI:10.1002/mgg3.958
PMID:31557780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6825948/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

Our results suggest that APOE gene genotypes play an important role in the differential modulation of lipid profiles in the MA population with obesity.

摘要

背景

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。

方法

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。

结果

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。

结论

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。