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T细胞参与血压控制中的性别差异。

T-cell involvement in sex differences in blood pressure control.

作者信息

Crislip G Ryan, Sullivan Jennifer C

机构信息

Department of Physiology, Georgia Regents University, 1459 Laney Walker Blvd, Augusta, GA 30912, U.S.A.

出版信息

Clin Sci (Lond). 2016 May 1;130(10):773-83. doi: 10.1042/CS20150620.

Abstract

Hypertension affects one-third of adults in the Western world and is the most common independent risk factor for cardiovascular disease, and the leading cause of premature death globally. Despite available therapeutic options, approximately half of the hypertensive population taking medication does not achieve adequate blood pressure (BP) control leaving them at increased risk of chronic kidney disease, renal failure, stroke, congestive heart failure, myocardial infarction, aneurysm and peripheral artery disease. New therapeutic options need to be identified for the treatment of hypertension in order to increase the percentage of individuals with controlled BP. There is a growing basic science literature regarding the role of T-cells in the pathogenesis of hypertension and BP control; however, the majority of this literature has been performed exclusively in males despite the fact that both men and women develop hypertension. This is especially problematic since hypertension is well recognized as having distinct sex differences in the prevalence, absolute BP values and molecular mechanisms contributing to the pathophysiology of the disease. The purpose of this article is to review the available literature regarding sex differences in T-cells in hypertension followed by highlighting the potential pathways that may result in sex-specific effects on T-cell activation and differentiation.

摘要

高血压影响着西方世界三分之一的成年人,是心血管疾病最常见的独立危险因素,也是全球过早死亡的主要原因。尽管有可用的治疗选择,但大约一半服用药物的高血压人群血压控制不佳,使他们患慢性肾病、肾衰竭、中风、充血性心力衰竭、心肌梗死、动脉瘤和外周动脉疾病的风险增加。需要确定新的治疗方法来治疗高血压,以提高血压得到控制的个体比例。关于T细胞在高血压发病机制和血压控制中的作用,基础科学文献越来越多;然而,尽管男性和女性都会患高血压,但这些文献大多仅在男性中进行。这尤其成问题,因为高血压在患病率、绝对血压值以及导致该疾病病理生理的分子机制方面存在明显的性别差异。本文的目的是回顾关于高血压中T细胞性别差异的现有文献,然后强调可能导致对T细胞激活和分化产生性别特异性影响的潜在途径。

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