Laughlin Gail A, Barrett-Connor Elizabeth, Criqui Michael H, Kritz-Silverstein Donna
Department of Family and Preventive Medicine, University of California-San Diego School of Medicine, La Jolla, California 92093-0607.
J Clin Endocrinol Metab. 2004 Jan;89(1):114-20. doi: 10.1210/jc.2003-030967.
The IGF system has been implicated in cardiovascular disease (CVD) development. The prospective association of serum IGF-I and IGF-binding protein-1 (IGFBP-1) with all cause, ischemic heart disease (IHD), and non-IHD CVD mortality was examined in 633 men and 552 nonestrogen-using postmenopausal women, aged 51-98 yr (mean, 74 yr) in 1988-1992, who were followed through July 2001 (96% follow-up). During the 9- to 13-yr follow-up, there were 522 deaths; 224 were attributed to CVD, and 105 were caused by IHD. IGF-I and IGFBP-1 were independently and jointly related to risk of IHD mortality. In a proportional hazards model including both IGF-I and IGFBP-1 and adjusting for CVD risk factors, the relative risk of IHD mortality was 38% higher for every 40 ng/ml (1 SD) decrease in IGF-I (95% confidence interval, 1.09-1.76; P = 0.005) and 3.11 times greater for those in the lowest quintile of IGFBP-1 (95% confidence interval, 1.74-5.56; P < 0.001) compared with those with higher IGFBP-1 levels. IGF-I and IGFBP-1 (alone or in combination) were not related to risk of all cause or non-IHD CVD mortality. We conclude that low baseline levels of IGF-I and IGFBP-1 increase the risk of fatal IHD among elderly men and women independent of prevalent IHD and CVD risk factors.
胰岛素样生长因子(IGF)系统与心血管疾病(CVD)的发生发展有关。1988年至1992年,对633名男性和552名未使用雌激素的绝经后女性(年龄51 - 98岁,平均74岁)进行了研究,检测血清IGF - I和胰岛素样生长因子结合蛋白 - 1(IGFBP - 1)与全因死亡、缺血性心脏病(IHD)及非IHD CVD死亡的前瞻性关联,并随访至2001年7月(随访率96%)。在9至13年的随访期间,共发生522例死亡;其中224例归因于CVD,105例由IHD导致。IGF - I和IGFBP - 1与IHD死亡风险独立相关且共同起作用。在一个包含IGF - I和IGFBP - 1并对CVD危险因素进行校正的比例风险模型中,IGF - I每降低40 ng/ml(1个标准差),IHD死亡的相对风险升高38%(95%置信区间为1.09 - 1.76;P = 0.005),与IGFBP - 1水平较高者相比,IGFBP - 1处于最低五分位数的人群IHD死亡风险高3.11倍(95%置信区间为1.74 - 5.56;P < 0.001)。IGF - I和IGFBP - 1(单独或联合)与全因或非IHD CVD死亡风险无关。我们得出结论,IGF - I和IGFBP - 1的低基线水平会增加老年男性和女性致命性IHD的风险,且独立于现患IHD和CVD危险因素。