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1
Considering sex as a biological variable in preclinical research.将性别视为临床前研究中的生物学变量。
FASEB J. 2017 Jan;31(1):29-34. doi: 10.1096/fj.201600781R. Epub 2016 Sep 28.
2
Microbiome, trimethylamine N-oxide, and cardiometabolic disease.微生物群、氧化三甲胺与心脏代谢疾病
Transl Res. 2017 Jan;179:108-115. doi: 10.1016/j.trsl.2016.07.007. Epub 2016 Jul 18.
3
Female rats are not more variable than male rats: a meta-analysis of neuroscience studies.雌性大鼠并不比雄性大鼠更具变异性:神经科学研究的荟萃分析。
Biol Sex Differ. 2016 Jul 26;7:34. doi: 10.1186/s13293-016-0087-5. eCollection 2016.
4
Sex differences and hormonal effects on gut microbiota composition in mice.小鼠肠道微生物群组成中的性别差异及激素影响
Gut Microbes. 2016 Jul 3;7(4):313-322. doi: 10.1080/19490976.2016.1203502. Epub 2016 Jun 29.
5
The Adipose Tissue Microenvironment Regulates Depot-Specific Adipogenesis in Obesity.脂肪组织微环境调节肥胖症中的特定部位脂肪生成。
Cell Metab. 2016 Jul 12;24(1):142-50. doi: 10.1016/j.cmet.2016.05.012. Epub 2016 Jun 16.
6
Intestinal Microbiota-Generated Metabolite Trimethylamine-N-Oxide and 5-Year Mortality Risk in Stable Coronary Artery Disease: The Contributory Role of Intestinal Microbiota in a COURAGE-Like Patient Cohort.肠道微生物群产生的代谢物氧化三甲胺与稳定型冠状动脉疾病的5年死亡风险:肠道微生物群在类似COURAGE研究患者队列中的作用
J Am Heart Assoc. 2016 Jun 10;5(6):e002816. doi: 10.1161/JAHA.115.002816.
7
Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study.孤立性低高密度脂蛋白胆固醇是心血管疾病的危险因素吗?弗雷明汉后代研究的新见解。
Circ Cardiovasc Qual Outcomes. 2016 May;9(3):206-212. doi: 10.1161/CIRCOUTCOMES.115.002436. Epub 2016 May 10.
8
Gut Microbial Metabolite TMAO Enhances Platelet Hyperreactivity and Thrombosis Risk.肠道微生物代谢产物氧化三甲胺增强血小板高反应性和血栓形成风险。
Cell. 2016 Mar 24;165(1):111-124. doi: 10.1016/j.cell.2016.02.011. Epub 2016 Mar 10.
9
The importance of having two X chromosomes.拥有两条X染色体的重要性。
Philos Trans R Soc Lond B Biol Sci. 2016 Feb 19;371(1688):20150113. doi: 10.1098/rstb.2015.0113. Epub 2016 Feb 1.
10
Are females more variable than males in gene expression? Meta-analysis of microarray datasets.在基因表达方面,女性比男性更具变异性吗?微阵列数据集的荟萃分析。
Biol Sex Differ. 2015 Oct 29;6:18. doi: 10.1186/s13293-015-0036-8. eCollection 2015.

肥胖与脂质代谢性别差异的遗传基础

Genetic Basis for Sex Differences in Obesity and Lipid Metabolism.

作者信息

Link Jenny C, Reue Karen

机构信息

Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, California 90095; email:

Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California 90095.

出版信息

Annu Rev Nutr. 2017 Aug 21;37:225-245. doi: 10.1146/annurev-nutr-071816-064827. Epub 2017 Jun 19.

DOI:10.1146/annurev-nutr-071816-064827
PMID:28628359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5759759/
Abstract

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.

摘要

男性和女性在肥胖、心血管疾病及糖尿病方面存在显著差异。为了为两性提供更好的诊断和治疗,识别导致观察到的性别差异的因素很重要。传统上,性别差异被归因于男性和女性性腺分泌物(通常称为性激素)的不同作用,这些分泌物对新陈代谢及相关疾病的许多方面有重大影响。作为性别差异的一个促成因素,男性和女性之间的基本基因差异较少受到重视,而这种差异最终由XX或XY性染色体组成决定。在此,我们综述性腺激素和性染色体组成各自对脂质代谢及相关疾病产生影响的机制,以及目前用于研究它们的方法。我们特别关注遗传方法,包括人类和小鼠的全基因组关联研究、组学和系统遗传学方法,以及能够区分性腺和性染色体效应的独特实验小鼠模型。