Liu Yi, Wu Minliang, Ling Jie, Cai Libing, Zhang Dandan, Gu Harvest F, Wang Hao, Zhu Yimin, Lai Maode
Department of Epidemiology &Biostatistics, Zhejiang University School of Public Health, Hangzhou 310058, China.
Department of Laboratory, the second Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou 310003, China.
Sci Rep. 2015 May 18;5:10227. doi: 10.1038/srep10227.
Metabolic syndrome (MetS), one of the major public health concerns, is regarded as the "common soil" of incidence of common chronic diseases and may increase the risk of type 2 diabetes. The predominant underlying mechanism of MetS is insulin resistance (IR). Additionally, previous studies have indicated that IGFBP7 has high affinity of binding with insulin and might induce IR. The objective of this study was to firstly evaluate the associations of serum IGFBP7 levels with IR and MetS with a relatively large sample and population based design. In a population based MetS case-control study, HOMA-IR was used to evaluate the insulin sensitivity and serum IGFBP7 levels were determined with chemiluminescence-linked immunoassay. As a result, the subjects of MetS and IR had higher serum levels of IGFBP7 than control healthy subjects. High serum IGFBP7 levels increased the risk of MetS and IR. Serum IGFBP7 levels were also found to be significantly correlated with metabolic-associated parameters of Waist-to-hip ratio (WHR), HDL and LDL. These findings suggest that serum IGFBP7 levels are associated with IR and MetS, providing new insight into the mechanism of IR and Mets. IGFBP7 may be a potential interventional target for IR and Mets.
代谢综合征(MetS)是主要的公共卫生问题之一,被视为常见慢性病发病的“共同土壤”,可能会增加2型糖尿病的风险。MetS的主要潜在机制是胰岛素抵抗(IR)。此外,先前的研究表明,胰岛素样生长因子结合蛋白7(IGFBP7)与胰岛素具有高亲和力,可能会诱导IR。本研究的目的是首先通过相对大样本和基于人群的设计,评估血清IGFBP7水平与IR和MetS之间的关联。在一项基于人群的MetS病例对照研究中,采用稳态模型评估法(HOMA-IR)来评估胰岛素敏感性,并通过化学发光免疫测定法测定血清IGFBP7水平。结果显示,MetS和IR患者的血清IGFBP7水平高于健康对照者。血清IGFBP7水平升高会增加患MetS和IR的风险。还发现血清IGFBP7水平与腰臀比(WHR)、高密度脂蛋白(HDL)和低密度脂蛋白(LDL)等代谢相关参数显著相关。这些发现表明,血清IGFBP7水平与IR和MetS相关,为IR和MetS的发病机制提供了新的见解。IGFBP7可能是IR和MetS的一个潜在干预靶点。