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Atherosclerosis. 2013 Jul;229(1):149-54. doi: 10.1016/j.atherosclerosis.2013.03.037. Epub 2013 Apr 22.
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Involvement of DDAH/ADMA pathway in the pathogenesis of rheumatoid arthritis in rats.DDAH/ADMA 通路在大鼠类风湿关节炎发病机制中的作用。
Int Immunopharmacol. 2013 Jun;16(2):322-31. doi: 10.1016/j.intimp.2013.04.009. Epub 2013 Apr 22.
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Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study.四项美国人群研究(人口基因组学和流行病学研究 [PAGE])中,十种候选冠心病风险遗传变异与亚临床动脉粥样硬化之间缺乏关联。
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Mechanisms involved in the aging-induced vascular dysfunction.衰老诱导的血管功能障碍所涉及的机制。
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Age-related differences in the effects of α and γ peroxisome proliferator-activated receptor subtype agonists on endothelial vasodilation in human microvessels.年龄相关的α和γ过氧化物酶体增殖物激活受体亚型激动剂对人微血管内皮血管舒张作用的差异。
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Connection between telomerase activity in PBMC and markers of inflammation and endothelial dysfunction in patients with metabolic syndrome.外周血单核细胞中端粒酶活性与代谢综合征患者炎症和内皮功能障碍标志物的关系。
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Searching for an operational definition of frailty: a Delphi method based consensus statement: the frailty operative definition-consensus conference project.寻找虚弱的操作性定义:基于德尔菲法的共识声明:虚弱操作性定义共识会议项目。
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10
Sex differences in the association between serum levels of testosterone and frailty in an elderly population: the Toledo Study for Healthy Aging.老年人群中睾酮血清水平与虚弱之间的关联存在性别差异:托莱多健康老龄化研究。
PLoS One. 2012;7(3):e32401. doi: 10.1371/journal.pone.0032401. Epub 2012 Mar 5.

内皮功能障碍与衰弱之间的关联:托莱多健康老龄化研究

Association between endothelial dysfunction and frailty: the Toledo Study for Healthy Aging.

作者信息

Alonso-Bouzón Cristina, Carcaillon Laure, García-García Francisco J, Amor-Andrés María S, El Assar Mariam, Rodríguez-Mañas Leocadio

出版信息

Age (Dordr). 2014 Feb;36(1):495-505. doi: 10.1007/s11357-013-9576-1.

DOI:10.1007/s11357-013-9576-1
PMID:23959520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3889911/
Abstract

Cardiovascular disease (CVD), both clinical and subclinical, has been proposed as one of the mechanisms underlying frailty. However, there is no evidence addressing the relationship between the earliest stage of CVD (endothelial dysfunction) and frailty. The goal of the study was to analyze the association between endothelial dysfunction, evaluated by asymmetric dimethylarginine (ADMA) levels, and frailty. We used data from the Toledo Study for Healthy Aging, a prospective Spanish cohort study. Biological samples were obtained and ADMA levels were determined using an enzyme immunoassay method. Logistic regression was used to estimate the odds ratio (OR) and 95 % confidence intervals of frailty associated with ADMA. Adjustments were made for age, gender, cardiovascular risk factors, and presence of atherosclerotic disease (assessed by ankle–brachial index; ABI). One thousand two hundred eighty-seven community-dwelling elderly were included. One hundred seven (8.3 %) were identified as frail, 542 (42.1 %) as pre-frail, and 638 (49.6 %) as non-frail. ADMAvalues were higher in frail subjects than in non-frail ones. In addition, an interaction between the presence of atherosclerotic disease and ADMA on the odds of frailty (p=0.045) was detected. After adjustments for age, classical cardiovascular risk factors, and ABI, the risk of frailty was associated with increasing levels of ADMA in subjects without atherosclerotic disease [OR for 1 standard deviation increase in ADMA=1.14 (1.01–1.28), p=0.032] but not in those with atherosclerotic disease. In our study, endothelial dysfunction, assessed by ADMA levels, is associated with frailty. These findings provide additional support for a relevant role of vascular system since its earliest stage in frailty.

摘要

心血管疾病(CVD),包括临床和亚临床疾病,已被认为是虚弱背后的机制之一。然而,尚无证据表明CVD的最早阶段(内皮功能障碍)与虚弱之间的关系。本研究的目的是分析通过不对称二甲基精氨酸(ADMA)水平评估的内皮功能障碍与虚弱之间的关联。我们使用了来自西班牙一项前瞻性队列研究——托莱多健康老龄化研究的数据。采集了生物样本,并采用酶免疫测定法测定ADMA水平。使用逻辑回归来估计与ADMA相关的虚弱的比值比(OR)和95%置信区间。对年龄、性别、心血管危险因素和动脉粥样硬化疾病的存在情况(通过踝臂指数;ABI评估)进行了校正。纳入了1287名居住在社区的老年人。其中107人(8.3%)被确定为虚弱,542人(42.1%)为虚弱前期,638人(49.6%)为非虚弱。虚弱受试者的ADMA值高于非虚弱受试者。此外,还检测到动脉粥样硬化疾病的存在与ADMA之间在虚弱几率方面的相互作用(p = 0.045)。在对年龄、经典心血管危险因素和ABI进行校正后,在无动脉粥样硬化疾病的受试者中,虚弱风险与ADMA水平升高相关[ADMA每增加1个标准差的OR = 1.14(1.01 - 1.28),p = 0.032],而在有动脉粥样硬化疾病的受试者中则不然。在我们的研究中,通过ADMA水平评估的内皮功能障碍与虚弱相关。这些发现为血管系统在虚弱的最早阶段所起的相关作用提供了额外支持。