糖尿病相关脂肪因子血清水平的基因测定

Q3 Medicine Review of Diabetic Studies Pub Date : 2015-09-01 Epub Date: 2016-01-28 DOI:10.1900/RDS.2015.12.277
Dorit Schleinitz
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引用次数: 0

摘要

脂肪组织会分泌大量蛋白质。其中一些蛋白质被称为脂肪因子和脂肪衍生激素,它们与代谢紊乱(包括 2 型糖尿病)甚至癌症都有关联。血清脂肪因子浓度的变化通常与脂肪组织质量的增加(肥胖)或减少(脂肪营养不良)密切相关,并受年龄、性别和脂肪组织位置的影响。然而,基因变异可能会影响血清中某种脂肪因子的浓度,从而导致新陈代谢紊乱,或者在 "保护性 "等位基因的作用下,产生有益的影响。这篇综述主要探讨了以下脂肪因子血清水平的遗传学决定因素:脂肪连通素、螯合素、瘦素、前谷蛋白、抵抗素、视黄醇结合蛋白 4、vaspin、adipsin、apelin 和网织蛋白。文章报告了全基因组关联研究(GWAS)和候选基因研究的最新发现,显示了脂肪因子基因和其他(非受体)基因中/附近的变异。另有一章重点介绍脂肪因子受体变异。此外,还讨论了有关脂肪因子的表观遗传学研究。
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Genetic Determination of Serum Levels of Diabetes-Associated Adipokines.

Adipose tissue secretes an abundance of proteins. Some of these proteins are known as adipokines and adipose-derived hormones which have been linked with metabolic disorders, including type 2 diabetes, and even with cancer. Variance in serum adipokine concentration is often closely associated with an increase (obesity) or decrease (lipodystrophy) in fat tissue mass, and it is affected by age, gender, and localization of the adipose tissue. However, there may be genetic variants which, in consequence, influence the serum concentration of a certain adipokine, and thereby promote metabolic disturbances or, with regard to the "protective" allele, exert beneficial effects. This review focuses on the genetic determination of serum levels of the following adipokines: adiponectin, chemerin, leptin, progranulin, resistin, retinol binding protein 4, vaspin, adipsin, apelin, and omentin. The article reports on the latest findings from genome-wide association studies (GWAS) and candidate gene studies, showing variants located in/nearby the adipokine genes and other (non-receptor) genes. An extra chapter highlights adipokine-receptor variants. Epigenetic studies on adipokines are also addressed.

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来源期刊
Review of Diabetic Studies
Review of Diabetic Studies Medicine-Internal Medicine
CiteScore
1.80
自引率
0.00%
发文量
28
期刊介绍: The Review of Diabetic Studies (RDS) is the society"s peer-reviewed journal published quarterly. The purpose of The RDS is to support and encourage research in biomedical diabetes-related science including areas such as endocrinology, immunology, epidemiology, genetics, cell-based research, developmental research, bioengineering and disease management.
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