Genetic Basis for Sex Differences in Obesity and Lipid Metabolism

被引:188
|
作者
Link, Jenny C. [1 ]
Reue, Karen [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
来源
基金
美国国家卫生研究院;
关键词
gonadal hormones; sex chromosome complement; metabolic syndrome; adipose tissue; glucose metabolism; microbiome; FATTY LIVER-DISEASE; SUBCUTANEOUS ADIPOSE-TISSUE; DENSITY-LIPOPROTEIN CHOLESTEROL; AMERICAN-DIABETES-ASSOCIATION; GUT MICROBIOTA COMPOSITION; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; ESTROGEN-RECEPTOR; BODY-COMPOSITION; KLINEFELTERS-SYNDROME;
D O I
10.1146/annurev-nutr-071816-064827
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Men and women exhibit significant differences in obesity, cardiovascular disease, and diabetes. To provide better diagnosis and treatment for both sexes, it is important to identify factors that underlie the observed sex differences. Traditionally, sex differences have been attributed to the differential effects of male and female gonadal secretions (commonly referred to as sex hormones), which substantially influence many aspects of metabolism and related diseases. Less appreciated as a contributor to sex differences are the fundamental genetic differences between males and females, which are ultimately determined by the presence of an XX or XY sex chromosome complement. Here, we review the mechanisms by which gonadal hormones and sex chromosome complement each contribute to lipid metabolism and associated diseases, and the current approaches that are used to study them. We focus particularly on genetic approaches including genome-wide association studies in humans and mice, -omics and systems genetics approaches, and unique experimental mouse models that allow distinction between gonadal and sex chromosome effects.
引用
收藏
页码:225 / 245
页数:21
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