Kunutsor Setor K, Apekey Tanefa A, Cheung Bernard M Y
aMusculoskeletal Research Unit, School of Clinical Sciences, University of Bristol, Southmead Hospital, Southmead bFaculty of Health and Social Sciences, School of Health and Wellbeing, Leeds Beckett University, Leeds, UK cDepartment of Medicine dState Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong, Hong Kong.
J Hypertens. 2015 Dec;33(12):2373-81. doi: 10.1097/HJH.0000000000000763.
The objective of this review was to obtain a reliable estimate of the magnitude of the prospective association between gamma-glutamyltransferase (GGT) and risk of hypertension, and to characterize the nature of the dose-response relationship. We conducted a systematic review and dose-response meta-analysis of published prospective studies. Relevant studies were identified in a literature search of MEDLINE, EMBASE, and Web of Science databases up to May 2015. Study-specific relative risks (RRs) were meta-analyzed using random effects models. We examined a potential nonlinear relationship using restricted cubic splines. Of the 612 titles reviewed, we included 14 cohort studies with data on 44 582 participants and 5 270 hypertension cases. In a comparison of extreme thirds of baseline levels of GGT, RR for hypertension in pooled analysis of all 14 studies was 1.32 (95% confidence interval: 1.23-1.43). There was heterogeneity among the studies (P < 0.001), which was to a large part explained by average age of participants at baseline, average duration of follow-up, and the degree of confounder adjustment. In a pooled dose-response analysis of 10 studies with relevant data, there was evidence of a linear association between GGT and hypertension risk (P for nonlinearity = 0.37). The pooled RR of hypertension per 5 U/l increment in GGT levels was 1.08 (95% confidence interval: 1.04-1.13). Baseline circulating GGT level is associated with an increased risk of hypertension in the general population, consistent with a linear dose-response relationship. Further investigation of any potential relevance of GGT in hypertension prevention is warranted.
本综述的目的是获得γ-谷氨酰转移酶(GGT)与高血压风险之间前瞻性关联强度的可靠估计,并描述剂量反应关系的性质。我们对已发表的前瞻性研究进行了系统综述和剂量反应荟萃分析。通过检索MEDLINE、EMBASE和Web of Science数据库直至2015年5月来识别相关研究。使用随机效应模型对各研究的特异性相对风险(RRs)进行荟萃分析。我们使用受限立方样条来检验潜在的非线性关系。在审查的612篇标题中,我们纳入了14项队列研究,这些研究包含44582名参与者的数据以及5270例高血压病例。在比较GGT基线水平的极端三分位数时,所有14项研究的汇总分析中高血压的RR为1.32(95%置信区间:1.23 - 1.43)。研究之间存在异质性(P<0.001),这在很大程度上可由基线时参与者的平均年龄、平均随访时间以及混杂因素调整程度来解释。在对10项有相关数据的研究进行的汇总剂量反应分析中,有证据表明GGT与高血压风险之间存在线性关联(非线性P值 = 0.37)。GGT水平每升高5 U/l,高血压的汇总RR为1.08(95%置信区间:1.04 - 1.13)。基线循环GGT水平与普通人群中高血压风险增加相关,这与线性剂量反应关系一致。有必要进一步研究GGT在高血压预防中的任何潜在相关性。