低血清胰岛素样生长因子I与缺血性心脏病风险增加相关:一项基于人群的病例对照研究

A. Juul, T. Scheike, M. Davidsen, J. Gyllenborg, T. Jørgensen
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引用次数: 616

摘要

背景:胰岛素样生长因子I (IGF-I)已被认为参与动脉粥样硬化的发病机制。我们假设低igf - 1和高IGFBP-3水平可能与缺血性心脏病(IHD)风险增加有关。方法与结果:我们在一项大型心血管流行病学前瞻性研究(DAN-MONICA)中进行了巢式病例对照研究。我们测量了231名血液采样后诊断为IHD的个体的血清IGF-I和IGFBP-3,以及374名年龄、性别和日历时间相匹配的对照受试者。在基线时,当所有个体均无疾病时,在15年随访期间,低IGF-I四分位数的受试者患IHD的风险显著高于高IGF-I四分位数组,在控制IGFBP-3、体重指数、吸烟、更年期、糖尿病和使用抗高血压药物的情况下,IHD的相对风险(RR)为1.94 (95% CI, 1.03至3.66)。相反,高IGFBP-3四分位数组的个体患IHD的调整RR为2.16 (95% CI, 1.18至3.95)。igf - 1水平低和IGFBP-3水平高的高危人群的识别导致IHD的风险显著增加(RR 4.07;95% CI, 1.48 ~ 11.22)与指数组比较。结论:在15年的随访期间,没有IHD但循环igf - 1水平低和IGFBP-3水平高的个体发生IHD的风险显著增加。我们的发现提示igf - 1可能参与了IHD的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low Serum Insulin-Like Growth Factor I Is Associated With Increased Risk of Ischemic Heart Disease: A Population-Based Case-Control Study
Background—Insulin-like growth factor I (IGF-I) has been suggested to be involved in the pathogenesis of atherosclerosis. We hypothesize that low IGF-I and high IGFBP-3 levels might be associated with increased risk of ischemic heart disease (IHD). Methods and Results—We conducted a nested case-control study within a large prospective study on cardiovascular epidemiology (DAN-MONICA). We measured IGF-I and IGFBP-3 in serum from 231 individuals who had a diagnosis of IHD 7.63 years after blood sampling and among 374 control subjects matched for age, sex, and calendar time. At baseline when all individuals were free of disease, subjects in the low IGF-I quartile had significantly higher risk of IHD during the 15-year follow-up period, with a relative risk (RR) of 1.94 (95% CI, 1.03 to 3.66) of IHD compared with the high IGF-I quartile group, when IGFBP-3, body mass index, smoking, menopause, diabetes, and use of antihypertensives were controlled for. Conversely, individuals in the high IGFBP-3 quartile group had an adjusted RR of 2.16 (95% CI, 1.18 to 3.95) of having IHD. Identification of a high-risk population with low IGF-I and high IGFBP-3 levels resulted in markedly higher risk of IHD (RR 4.07; 95% CI, 1.48 to 11.22) compared with the index group. Conclusions—Individuals without IHD but with low circulating IGF-I levels and high IGFBP-3 levels have significantly increased risk of developing IHD during a 15-year follow-up period. Our findings suggest that IGF-I may be involved in the pathogenesis of IHD.
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