Abou Kamar Sabrina, Bracun Valentina, El-Qendouci Maissa, Bomer Nils, Bakker Stephan J L, Gansevoort Ron T, Boersma Eric, Kardys Isabella, de Boer Rudolf A, Suthahar Navin
Department of Cardiology, Thorax Center, Cardiovascular Institute, Erasmus MC, Rotterdam, The Netherlands.
Department of Cardiology, Franciscus Gasthuis & Vlietland, Rotterdam, The Netherlands.
Eur J Heart Fail. 2024 Jul 17. doi: 10.1002/ejhf.3328.
Senescence is a major risk factor for heart failure (HF), and insulin-like growth factor-binding protein-7 (IGFBP7) has been identified as an important senescence-inducing factor. The aim of this study was to examine the value of baseline and repeat IGFBP7 measurements in predicting future HF among community-dwelling Dutch adults from the Prevention of Renal and Vascular End-stage Disease (PREVEND) study.
Individuals without prevalent HF who attended PREVEND visits 2 and 4 median of 5.1 years apart (25th-75th percentile, 4.9-5.2) with measurements of IGFBP7 were included. We used Cox proportional hazards models to investigate the association between IGFBP7 and HF incidence. A total of 6125 participants attending visit 2 (mean ± standard deviation [SD] age 53.1 ± 12.2 years; 3151 [51.4%] men) were followed for a median of 8.4 (7.8-8.9) years, and 194 participants (3.2%) developed incident HF. Median baseline IGFBP7 concentration was 87.0 (75.1-97.3) ng/ml, and baseline IGFBP7 levels were significantly associated with risk for incident HF (HF risk factors adjusted hazard ratio [HR] per 1 SD change in log-transformed IGFBP7: 1.22, 95% confidence interval [CI] 1.03-1.46). Baseline IGFBP7 was also significantly associated with incident HF in individuals with N-terminal pro-B-type natriuretic peptide <125 ng/L. Among 3879 participants attending both visits 2 and 4 (mean ± SD age 57.5 ± 11.3 years; 1952 [50.3%] men), 93 individuals developed HF (after visit 4) during a median follow-up of 3.2 (2.8-3.9) years. Median increase in IGFBP7 concentration between visits was 0.68 (-7.09 to 8.36) ng/ml, and changes in IGFBP7 levels were significantly associated with risk for incident HF (HF risk factors adjusted HR per 1 SD change in log-transformed IGFBP7: 1.68, 95% CI 1.19-2.36).
Both baseline as well as repeat IGFBP7 measurements provide information about the risk of developing HF.
衰老为心力衰竭(HF)的主要危险因素,胰岛素样生长因子结合蛋白7(IGFBP7)已被确定为一种重要的衰老诱导因子。本研究旨在通过预防肾脏和血管终末期疾病(PREVEND)研究,探讨荷兰社区成年居民中,基线及重复检测IGFBP7水平在预测未来发生HF中的价值。
纳入PREVEND研究中无HF病史、分别于第2次和第4次随访(间隔时间中位数为5.1年,四分位数间距为4.9 - 5.2年)时检测过IGFBP7的个体。我们使用Cox比例风险模型研究IGFBP7与HF发病率之间的关联。共有6125名参与者接受了第2次随访(平均年龄±标准差[SD]为53.1±12.2岁;3151名[51.4%]为男性),随访中位数为8.4(7.8 - 8.9)年,其中194名参与者(3.2%)发生了HF。基线IGFBP7浓度中位数为87.0(75.1 - 97.3)ng/ml,基线IGFBP7水平与HF发病风险显著相关(校正HF风险因素后,log转换后的IGFBP7每变化1个标准差的风险比[HR]:1.22,95%置信区间[CI]为1.03 - 1.46)。在N末端B型利钠肽原<125 ng/L的个体中,基线IGFBP7也与HF发病显著相关。在3879名同时接受第2次和第4次随访的参与者中(平均年龄±SD为57.5±11.3岁;1952名[50.3%]为男性),93名个体在随访中位数3.2(2.8 - 3.9)年期间(第4次随访后)发生了HF。两次随访间IGFBP7浓度增加的中位数为0.68(-7.09至8.36)ng/ml,IGFBP7水平变化与HF发病风险显著相关(校正HF风险因素后,log转换后的IGFBP7每变化1个标准差的HR:1.68,95%CI为1.19 - 2.36)。
基线及重复检测IGFBP7水平均能提供发生HF风险的相关信息。