骨质疏松症
医学
小RNA
肌萎缩
内科学
骨关节炎
接收机工作特性
肿瘤科
曲线下面积
疾病
荟萃分析
生物信息学
生物标志物
病理
生物
遗传学
基因
替代医学
作者
Tania Jones,Mohammed S. Esa,K.H. Christien Li,Subha Krishnan,George M. Elgallab,Mark S. Pearce,David A. Young,Fraser Birrell
出处
期刊:Bone
[Elsevier]
日期:2021-06-22
卷期号:152: 116068-116068
被引量:39
标识
DOI:10.1016/j.bone.2021.116068
摘要
Circulating microRNAs (c-miRs) show promise as biomarkers. This systematic review explores their potential association with age-related fracture/osteoporosis (OP), osteoarthritis (OA) and sarcopenia (SP), as well as cross-disease association. Most overlap occurred between OA and OP, suggesting potentially shared microRNA activity. There was little agreement in results across studies. Few reported receiver operating characteristic analysis (ROC) and many identified significant dysregulation in disease, but direction of effect was commonly conflicting. c-miRs with most evidence for consistency in dysregulation included miR-146a, miR-155 and miR-98 for OA (upregulated). Area under the curve (AUC) for miR-146a biomarker performance was AUC 0.92, p = 0.028. miR-125b (AUC 0.76-0.89), miR-100, miR-148a and miR-24 were consistently upregulated in OP. Insufficient evidence exists for c-miRs in SP. Study quality was typically rated intermediate/high risk of bias. Wide study heterogeneity meant meta-analysis was not possible. We provide detailed critique and recommendations for future approaches in c-miR analyses based on this review.
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