Department of Hygiene, Fujita Health University School of Medicine, 1-98, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
Department of Preventive Medical Sciences, Fujita Health University School of Health Sciences, Toyoake, Aichi, Japan.
Sci Rep. 2021 Mar 5;11(1):5298. doi: 10.1038/s41598-021-84707-7.
Primary prevention of premature death is a public health concern worldwide. Circulating microRNAs (miRNAs) have been described as potential diagnostic biomarkers for diseases as cancer and cardiovascular disease (CVD). This case-cohort study aimed to investigate the potential relationship between circulating miRNAs and the risk of premature death. A total of 39,242 subjects provided baseline serum samples in 1988-1990. Of these, 345 subjects who died of intrinsic disease (< 65 years old) and for which measurable samples were available were included in this study. We randomly selected a sub-cohort of 879 subjects. Circulatring miR-21, miR-29a, and miR-126 were determined using qRT-PCR. Conditional logistic regression models were used to analyse the data with respect to stratified miRNA levels. Multivariable logistic regression revealed that subjects with high circulating miR-21 and miR-29a individual levels had a significantly higher risk of total death, cancer death, and CVD death than those with medium miR-21 and miR-29a individual levels. Conversely, subjects with low circulating miR-126 levels had a significantly higher risk of total death than those with medium levels. This suggests that circulating miRNAs are associated with the risk of premature death from cancer and CVD, identifying them as potential biomarkers for early detection of high-risk individuals.
原发性预防过早死亡是全世界公共卫生关注的问题。循环 microRNAs(miRNAs)已被描述为癌症和心血管疾病(CVD)等疾病的潜在诊断生物标志物。本病例-队列研究旨在探讨循环 miRNAs 与过早死亡风险之间的潜在关系。共有 39242 名受试者于 1988-1990 年提供了基线血清样本。其中,345 名因内在疾病(<65 岁)死亡且可测量样本可用的受试者纳入本研究。我们随机选择了 879 名受试者的亚队列。使用 qRT-PCR 测定循环 miR-21、miR-29a 和 miR-126。使用条件逻辑回归模型分析分层 miRNA 水平的数据。多变量逻辑回归显示,与中 miR-21 和 miR-29a 个体水平相比,高循环 miR-21 和 miR-29a 个体水平的受试者总死亡、癌症死亡和 CVD 死亡的风险显著更高。相反,低循环 miR-126 水平的受试者总死亡风险显著高于中水平。这表明循环 miRNAs 与癌症和 CVD 导致的过早死亡风险相关,将其鉴定为高危个体早期检测的潜在生物标志物。