Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, USA.
Am J Gastroenterol. 2013 Jun;108(6):881-91; quiz 892. doi: 10.1038/ajg.2013.5. Epub 2013 Feb 5.
Several preclinical and observational studies have shown that anti-diabetic medications (ADMs) can modify the risk of hepatocellular cancer (HCC) in patients with diabetes mellitus (DM). We performed a systematic review and meta-analyses of studies evaluating the effect of metformin, thiazolidinediones (TZDs), sulfonylureas, and/or insulin on the risk of HCC. We conducted a systematic search of Medline, EMBASE, and Web of Science up to August 2012. Studies were included if they (1) evaluated and clearly defined exposure to metformin, TZDs, sulfonylureas, and/or insulin, (2) reported HCC outcomes in patients with DM, and (3) reported relative risks or odds ratio (OR) or provided data for their estimation. Summary OR estimates with 95% confidence intervals (CIs) were estimated using the random-effects model. Ten studies reporting 22,650 cases of HCC in 334,307 patients with type 2 DM were included in the analysis. Meta-analysis of observational studies showed a 50% reduction in HCC incidence with metformin use (n=8 studies; OR 0.50, 95% CI 0.34-0.73), 62% and 161% increase in HCC incidence with sulfonylurea (n=8 studies; OR 1.62, 95% CI 1.16-2.24) or insulin use (n=7; OR 2.61, 95% CI 1.46-4.65), respectively. TZDs did not modify the risk of HCC (n=4; OR 0.54, 95% CI 0.28-1.02). There was considerable heterogeneity across studies, which was partly explained by study setting, location, and whether the studies adjusted for the concomitant use of other ADMs. Post-hoc analysis of randomized controlled trials did not reveal any significant association between ADM use and risk of HCC. ADMs may modify the risk of HCC in patients with DM, especially in the Western population. However, the effect of each individual agent should be interpreted with caution owing to inherent cancer-modifying effect of the comparator group.
几项临床前和观察性研究表明,抗糖尿病药物(ADM)可改变糖尿病患者发生肝细胞癌(HCC)的风险。我们对评估二甲双胍、噻唑烷二酮类(TZDs)、磺酰脲类和/或胰岛素对 HCC 风险影响的研究进行了系统综述和荟萃分析。我们对 Medline、EMBASE 和 Web of Science 进行了系统检索,检索截止日期为 2012 年 8 月。如果研究(1)评估并明确界定二甲双胍、TZDs、磺酰脲类和/或胰岛素的暴露情况,(2)报告了糖尿病患者的 HCC 结局,且(3)报告了相对风险比(RR)或提供了其估计值的数据,则将其纳入分析。使用随机效应模型估算汇总 RR 估计值及其 95%置信区间(CI)。纳入分析的 10 项研究共报告了 334307 例 2 型糖尿病患者中的 22650 例 HCC 病例。对观察性研究的荟萃分析显示,使用二甲双胍可使 HCC 发病率降低 50%(n=8 项研究;RR 0.50,95%CI 0.34-0.73),使用磺酰脲类(n=8 项研究;RR 1.62,95%CI 1.16-2.24)或胰岛素(n=7 项研究;RR 2.61,95%CI 1.46-4.65)可分别使 HCC 发病率增加 62%和 161%。TZDs 并未改变 HCC 的风险(n=4 项研究;RR 0.54,95%CI 0.28-1.02)。研究之间存在很大的异质性,这种异质性部分可由研究设置、地点以及研究是否调整了同时使用其他 ADM 来解释。事后分析未发现 ADM 使用与 HCC 风险之间存在任何显著关联。ADM 可能改变糖尿病患者 HCC 的风险,尤其是在西方人群中。然而,由于对照药物组具有潜在的癌症改变作用,应谨慎解释每种药物的效果。