Kaplan Robert C, McGinn Aileen P, Pollak Michael N, Kuller Lewis H, Strickler Howard D, Rohan Tom E, Cappola Anne R, Xue XiaoNan, Psaty Bruce M
Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York 10461, USA, and Department of Medicine, Lady Davis Research Institute of Jewish General Hospital, Montreal, Quebec, Canada.
J Clin Endocrinol Metab. 2007 Apr;92(4):1319-25. doi: 10.1210/jc.2006-1631. Epub 2007 Jan 30.
Prior observational studies have demonstrated that the GH/IGF axis is associated with cardiovascular disease. However, this association has not been extensively studied among older adults.
The objective of this study was to assess the association between levels of total IGF-I and IGF binding proteins (IGFBP-1, IGFBP-3) and risk of incident coronary events and ischemic stroke.
A case-cohort analysis was conducted among adults 65 yr and older in the Cardiovascular Health Study.
A total of 534 coronary events [316 nonfatal myocardial infarctions (MIs), 48 fatal MIs, and 170 fatal coronary heart disease events] and 370 ischemic strokes were identified on follow-up. Comparison subjects were 1122 randomly selected participants from the Cardiovascular Health Study.
Mean follow-up time was 6.7 yr for coronary events, 5.6 yr for strokes, and 9.3 yr for comparison subjects. Hazard ratios (95% confidence intervals) associated with baseline levels of total IGF-I and IGFBPs were estimated using multivariate adjusted Cox proportional hazards models. Neither IGF-I nor IGFBP-1 levels predicted risk of incident coronary events or stroke. IGFBP-3 had an inverse association with risk of coronary events [adjusted hazard ratio per sd=0.88 (0.78-1.00), P=0.05] but was not associated with stroke. Exploratory analyses suggested that low IGF-I and low IGFBP-3 levels were significantly associated with higher risk of nonfatal MI (P<0.05) but not with risk of fatal MI or fatal coronary heart disease.
Circulating levels of total IGF-I or IGFBP-1 were not associated with risk of total coronary events or ischemic stroke among older adults, whereas low IGFBP-3 level was associated with increased risk of incident coronary events.
先前的观察性研究表明,生长激素/胰岛素样生长因子轴与心血管疾病有关。然而,这种关联在老年人中尚未得到广泛研究。
本研究的目的是评估总胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子结合蛋白(IGFBP-1、IGFBP-3)水平与冠心病事件和缺血性中风风险之间的关联。
在心血管健康研究中对65岁及以上的成年人进行了病例队列分析。
随访期间共确定了534例冠心病事件[316例非致命性心肌梗死(MI)、48例致命性MI和170例致命性冠心病事件]和370例缺血性中风。对照对象是从心血管健康研究中随机选取的1122名参与者。
冠心病事件的平均随访时间为6.7年,中风为5.6年,对照对象为9.3年。使用多变量调整的Cox比例风险模型估计与总IGF-I和IGFBPs基线水平相关的风险比(95%置信区间)。IGF-I和IGFBP-1水平均不能预测冠心病事件或中风的风险。IGFBP-3与冠心病事件风险呈负相关[每标准差调整风险比=0.88(0.78 - 1.00),P = 0.05],但与中风无关。探索性分析表明,低IGF-I和低IGFBP-3水平与非致命性MI风险显著相关(P < 0.05),但与致命性MI或致命性冠心病风险无关。
在老年人中,总IGF-I或IGFBP-1的循环水平与总冠心病事件或缺血性中风风险无关,而低IGFBP-3水平与冠心病事件风险增加有关。