Dorcely Brenda, Katz Karin, Jagannathan Ram, Chiang Stephanie S, Oluwadare Babajide, Goldberg Ira J, Bergman Michael
New York University School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes and Metabolism, NYU Langone Medical Center, New York, NY.
Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Diabetes Metab Syndr Obes. 2017 Aug 14;10:345-361. doi: 10.2147/DMSO.S100074. eCollection 2017.
The number of individuals with prediabetes is expected to grow substantially and estimated to globally affect 482 million people by 2040. Therefore, effective methods for diagnosing prediabetes will be required to reduce the risk of progressing to diabetes and its complications. The current biomarkers, glycated hemoglobin (HbA1c), fructosamine, and glycated albumin have limitations including moderate sensitivity and specificity and are inaccurate in certain clinical conditions. Therefore, identification of additional biomarkers is being explored recognizing that any single biomarker will also likely have inherent limitations. Therefore, combining several biomarkers may more precisely identify those at high risk for developing prediabetes and subsequent progression to diabetes. This review describes recently identified biomarkers and their potential utility for addressing the burgeoning epidemic of dysglycemic disorders.
预计糖尿病前期个体数量将大幅增长,据估计到2040年全球将有4.82亿人受其影响。因此,需要有效的糖尿病前期诊断方法以降低进展为糖尿病及其并发症的风险。目前的生物标志物,糖化血红蛋白(HbA1c)、果糖胺和糖化白蛋白存在局限性,包括敏感性和特异性中等,且在某些临床情况下不准确。因此,鉴于任何单一生物标志物可能也存在固有局限性,人们正在探索识别其他生物标志物。因此,联合使用几种生物标志物可能更精确地识别出有发展为糖尿病前期及随后进展为糖尿病高风险的人群。本综述描述了最近发现的生物标志物及其在应对血糖异常疾病迅速流行方面的潜在用途。