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本文引用的文献

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Coronary Microvascular Function and Cardiovascular Risk Factors in Women With Angina Pectoris and No Obstructive Coronary Artery Disease: The iPOWER Study.无阻塞性冠状动脉疾病的心绞痛女性患者的冠状动脉微血管功能与心血管危险因素:iPOWER研究
J Am Heart Assoc. 2016 Mar 15;5(3):e003064. doi: 10.1161/JAHA.115.003064.
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Sex differences in inflammation during atherosclerosis.动脉粥样硬化过程中炎症的性别差异。
Clin Med Insights Cardiol. 2015 Apr 19;8(Suppl 3):49-59. doi: 10.4137/CMC.S17068. eCollection 2014.
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Multiplex serum cytokine immunoassay using nanoplasmonic biosensor microarrays.使用纳米等离子体生物传感器微阵列的多重血清细胞因子免疫测定。
ACS Nano. 2015;9(4):4173-81. doi: 10.1021/acsnano.5b00396. Epub 2015 Mar 23.
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Inflammatory cytokines and risk of coronary heart disease: new prospective study and updated meta-analysis.炎症细胞因子与冠心病风险:一项新的前瞻性研究和更新的荟萃分析。
Eur Heart J. 2014 Mar;35(9):578-89. doi: 10.1093/eurheartj/eht367. Epub 2013 Sep 10.
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Autoimmune heart disease: role of sex hormones and autoantibodies in disease pathogenesis.自身免疫性心脏病:性激素和自身抗体在疾病发病机制中的作用。
Expert Rev Clin Immunol. 2012 Mar;8(3):269-84. doi: 10.1586/eci.12.10.
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Inflammatory cell recruitment in cardiovascular disease: murine models and potential clinical applications.心血管疾病中的炎症细胞募集:鼠模型与潜在临床应用。
Clin Sci (Lond). 2010 Mar 9;118(11):641-55. doi: 10.1042/CS20090488.
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The vicious circle between oxidative stress and inflammation in atherosclerosis.动脉粥样硬化中氧化应激与炎症的恶性循环。
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Women and ischemic heart disease: evolving knowledge.女性与缺血性心脏病:不断发展的认知
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9
Immune and inflammatory mechanisms of atherosclerosis (*).动脉粥样硬化的免疫和炎症机制(*)
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10
Atherosclerosis as a disease of failed endogenous repair.动脉粥样硬化是一种内源性修复失败的疾病。
Front Biosci. 2008 May 1;13:3621-36. doi: 10.2741/2954.

绝经前女性的早发性动脉粥样硬化:细胞因子平衡是否起作用?

Premature atherosclerosis in premenopausal women: Does cytokine balance play a role?

机构信息

University of California Los Angeles, United States.

Texas Heart Institute, Houston, United States.

出版信息

Med Hypotheses. 2017 Nov;109:38-41. doi: 10.1016/j.mehy.2017.09.010. Epub 2017 Sep 21.

DOI:10.1016/j.mehy.2017.09.010
PMID:29150290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5728183/
Abstract

Contributory risk factors to premature coronary artery disease (CAD) in premenopausal women are poorly understood and data on this subset of women is lacking. There is growing evidence that the process of inflammation is a part of the atherosclerotic process. Mechanistic insights from animal work suggest that the profile of circulating cytokines reflects both endothelial integrity and the presence of immune and progenitor cells. Significant differences in pro- and anti-inflammatory cytokine concentrations between patients with and without CAD exist. Young women with obstructive CAD may experience differences in pro-inflammatory cytokines and the recruitment of reparative cells that secrete T-Helper (Th2 cytokines compared to women without CAD. Thus, cytokine balance may play a role in obstructive CAD in young women. In this pilot study we set out to identify an array of circulating inflammatory marker profiles which could be useful for the development of risk assessment and preventive strategies. We tested the hypothesis that an increase in serologic Th1 cytokines relative to Th2)/hematopoietic regulatory (HR) cytokines is related to premature coronary atherosclerosis in premenopausal women.

摘要

绝经前妇女发生早发冠心病(CAD)的促发风险因素了解甚少,而且针对这部分女性的数据也很缺乏。越来越多的证据表明,炎症过程是动脉粥样硬化过程的一部分。动物研究的机制研究表明,循环细胞因子的特征既反映了内皮完整性,也反映了免疫和祖细胞的存在。存在 CAD 的患者和不存在 CAD 的患者之间的促炎细胞因子和抗炎细胞因子浓度存在显著差异。有阻塞性 CAD 的年轻女性可能在促炎细胞因子和分泌 T 辅助细胞(Th2 细胞因子的修复细胞的募集方面存在差异,与没有 CAD 的女性相比。因此,细胞因子平衡可能在年轻女性的阻塞性 CAD 中起作用。在这项初步研究中,我们旨在确定一系列可能有助于开发风险评估和预防策略的循环炎症标志物谱。我们检验了这样一个假设,即相对于 Th2)/造血调节(HR)细胞因子,血清 Th1 细胞因子的增加与绝经前妇女的早发冠状动脉粥样硬化有关。