Diabetes Research Centre, Leicester General Hospital, Gwendolen Road, Leicester, LE5 4PW, UK.
NIHR Leicester Biomedical Research Centre, Leicester, UK.
Rev Endocr Metab Disord. 2020 Dec;21(4):569-575. doi: 10.1007/s11154-020-09553-w.
To systematically review the current literature investigating associations between zinc-alpha2-glycoprotein (ZAG) and dysglycaemia (including type 2 diabetes (T2DM), poly-cystic-ovary syndrome (PCOS), pre-diabetes or insulin resistance). This included relationships between ZAG and continuous measures of insulin and glucose. Additionally, we performed a meta-analysis to estimate the extent that ZAG differs between individuals with or without dysglycaemia; whilst examining the potential influence of adiposity. A systematic search was performed on four databases for studies on circulating ZAG concentrations in adult human populations, comparing healthy controls to individuals with dysglycaemia. Key characteristics, including the mean ZAG concentrations (mg∙L), and any correlational statistics between ZAG and continuous measures of glucose, glycated haemoglobin (HbA1c) or insulin were extracted. Meta-analyses were performed to compare metabolically healthy controls to cases, and on studies that compared controls and cases considered overweight or obese (body mass index (BMI) ≥25 kgm). 1575 papers were identified and 14 studies (16 cohorts) were considered eligible for inclusion. Circulating ZAG was lower in individuals with dysglycaemia compared to metabolically healthy controls (-4.14 [-8.17, -0.11] mgL; I = 98.5%; p < 0.001). When using data from only studies with overweight or obese groups with or without dysglycaemia (three studies (four cohorts); pooled n = 332), the difference in circulating ZAG was no longer significant (-0.30 [-3.67, 3.07] mg L; I = 28.0%; p = 0.225). These data suggest that ZAG may be implicated in dysglycaemia, although there was significant heterogeneity across different studies and the mediating effect of adiposity cannot be excluded. Therefore, more research is needed before robust conclusions can be drawn.
系统综述目前关于锌-α2-糖蛋白(ZAG)与糖代谢紊乱(包括 2 型糖尿病(T2DM)、多囊卵巢综合征(PCOS)、前驱糖尿病或胰岛素抵抗)之间关系的文献。这包括 ZAG 与胰岛素和葡萄糖连续测量值之间的关系。此外,我们进行了荟萃分析,以评估 ZAG 在糖代谢紊乱个体与非糖代谢紊乱个体之间的差异程度;同时研究了肥胖的潜在影响。在四个数据库中进行了系统检索,以研究成人人群中循环 ZAG 浓度与糖代谢紊乱的关系,比较健康对照组与糖代谢紊乱组。提取了关键特征,包括 ZAG 的平均浓度(mg·L),以及 ZAG 与葡萄糖、糖化血红蛋白(HbA1c)或胰岛素的连续测量值之间的任何相关统计学指标。对代谢健康对照组与病例组进行了荟萃分析,对比较超重或肥胖(体重指数(BMI)≥25 kg·m)的对照组和病例组的研究也进行了荟萃分析。共确定了 1575 篇论文,其中 14 项研究(16 个队列)被认为符合纳入标准。与代谢健康对照组相比,糖代谢紊乱个体的循环 ZAG 水平较低(-4.14 [-8.17,-0.11] mg·L;I = 98.5%;p < 0.001)。当仅使用超重或肥胖且伴有或不伴有糖代谢紊乱的组别的研究数据(三项研究(四个队列);汇总 n = 332)时,循环 ZAG 的差异不再显著(-0.30 [-3.67,3.07] mg·L;I = 28.0%;p = 0.225)。这些数据表明,ZAG 可能与糖代谢紊乱有关,尽管不同研究之间存在显著的异质性,且不能排除肥胖的中介作用。因此,在得出可靠结论之前,还需要进行更多的研究。