Department of Endocrinology, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Front Endocrinol (Lausanne). 2023 Mar 1;14:1144838. doi: 10.3389/fendo.2023.1144838. eCollection 2023.
Clinical trials have shown that sodium-glucose cotransporter 2 inhibitors (SGLT2i) are closely associated with hepatic fibrosis and steatosis by FibroScan. This paper aimed at evaluating the effects of SGLT2i on hepatic fibrosis and steatosis, which are presented as liver stiffness measurement (LSM) and controlled attenuation parameter (CAP).
PubMed, Embase, Cochrane Library, Web of Science, China National Knowledge Infrastructure Database, China Science and Technology Journal Database, and Wanfang Database were searched for randomized clinical trials from database establishment to 30 November 2022 with no language restrictions. The risk of bias was evaluated by Collaboration Handbook. Software Stata 17 and Review Manager (version 5.3) were used for meta-analysis.
A total of eight articles including 686 patients were included. Compared with the control group, our results showed that SGLT2i could lower levels of LSM [MD = -0.82, 95%CI (-1.38, -0.25), p = 0.005] and CAP [MD = -12.80, 95%CI (-20.57, -5.03), p = 0.001]. Further subgroup analyses indicated that SGLT2i presented more advantages on longer treatment duration and more serious steatosis in decreasing LSM. For CAP, SGLT2i exhibited a clear advantage in subgroup analyses of longer treatment duration, younger people, dapagliflozin, worse fibrosis, and steatosis.
SGLT2i could reduce LSM and CAP in contrast to other antihyperglycemic drugs. However, the included studies are not definitive, and well-designed, more multi-centered, blinded randomized clinical trials are warranted to definitively establish reliable evidence.
临床试验表明,通过 FibroScan,钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)与肝纤维化和脂肪变性密切相关。本文旨在评估 SGLT2i 对肝纤维化和脂肪变性的影响,这些影响表现为肝硬度测量(LSM)和受控衰减参数(CAP)。
检索建库至 2022 年 11 月 30 日的 PubMed、Embase、Cochrane 图书馆、Web of Science、中国知网、中国科技期刊数据库和万方数据库中关于 SGLT2i 对肝纤维化和脂肪变性影响的随机对照临床试验,语种不限。采用协作手册评价偏倚风险。采用 Stata 17 软件和 Review Manager(版本 5.3)进行 Meta 分析。
共纳入 8 篇文献,包括 686 例患者。与对照组相比,SGLT2i 可降低 LSM [MD=-0.82,95%CI(-1.38,-0.25),p=0.005]和 CAP [MD=-12.80,95%CI(-20.57,-5.03),p=0.001]。进一步的亚组分析表明,SGLT2i 在延长治疗时间和更严重脂肪变性方面对降低 LSM 具有更大优势。对于 CAP,SGLT2i 在延长治疗时间、更年轻、达格列净、更严重纤维化和脂肪变性的亚组分析中具有明显优势。
与其他降糖药物相比,SGLT2i 可降低 LSM 和 CAP。但纳入的研究并不确定,需要设计更好、更多中心、盲法随机临床试验来明确可靠的证据。