• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

沙格列汀治疗非酒精性脂肪性肝病或非酒精性脂肪性肝炎的疗效:系统评价和荟萃分析。

Effects of saroglitazar in the treatment of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis: A systematic review and meta-analysis.

机构信息

Department of Gastroenterology, ILS Dumdum Hospital, Kolkata 700 080, India.

Department of Clinical and Experimental Pharmacology, Calcutta School of Tropical Medicine, Kolkata, India.

出版信息

Clin Res Hepatol Gastroenterol. 2023 Aug;47(7):102174. doi: 10.1016/j.clinre.2023.102174. Epub 2023 Jun 26.

DOI:10.1016/j.clinre.2023.102174
PMID:37380128
Abstract

AIM

This systematic review and meta-analysis was conducted to evaluate the efficacy and safety of 4 mg saroglitazar treatment in patients with non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH).

METHODS

PubMed, Embase, Scopus, Cochrane CENTRAL, medRxiv (pre-print), bioRxiv (pre-print), and ClinicalTrials.gov databases were searched for relevant studies. The primary outcome was the change in the serum alanine transaminase (ALT) level. The secondary outcomes were changes in liver stiffness, liver function test parameters, and metabolic parameters. Pooled mean differences were calculated using random-effects models.

RESULTS

Of 331 studies that were screened, ten were included. Treatment with adjunct saroglitazar showed a reduction in ALT [mean difference: 26.01 U/L (95% CI: 10.67 to 41.35); p = 0.009; i: 98%; moderate GRADE evidence] and aspartate transaminase [mean difference: 19.68 U/L (95% CI: 8.93 to 30.43); p<0.001; i: 97%; moderate GRADE evidence] levels. There was a significant improvement in liver stiffness [mean difference: 2.22 kPa (95% CI: 0.80 to 3.63); p = 0.002; i: 99%; moderate GRADE evidence]. There were significant improvements in glycated hemoglobin [mean difference: 0.59% (95% CI: 0.32 to 0.86); p<0.001; i: 78%; moderate GRADE evidence], total cholesterol [mean difference: 19.20 (95% CI: 1.54 to 36.87); p = 0.03; i: 95%; moderate GRADE evidence], and triglyceride [mean difference: 105.49 mg/dL (95% CI: 11.18 to 199.80); p = 0.03; i: 100%; moderate GRADE evidence] levels. Saroglitazar treatment was safe.

CONCLUSION

Treatment with adjunct 4 mg saroglitazar could significantly improve liver enzymes, reduce liver stiffness, and improve metabolic parameters (serum glucose and lipid profile) in patients with NAFLD or NASH.

摘要

目的

本系统评价和荟萃分析旨在评估 4mg 沙格列汀治疗非酒精性脂肪性肝病(NAFLD)或非酒精性脂肪性肝炎(NASH)患者的疗效和安全性。

方法

检索了 PubMed、Embase、Scopus、Cochrane 中心、medRxiv(预印本)、bioRxiv(预印本)和 ClinicalTrials.gov 数据库中相关研究。主要结局是血清丙氨酸氨基转移酶(ALT)水平的变化。次要结局是肝硬度、肝功能试验参数和代谢参数的变化。使用随机效应模型计算汇总均数差异。

结果

在筛选出的 331 项研究中,有 10 项研究被纳入。辅助沙格列汀治疗可降低 ALT[平均差异:26.01U/L(95%CI:10.67 至 41.35);p=0.009;I²:98%;中等级别证据]和天门冬氨酸氨基转移酶[平均差异:19.68U/L(95%CI:8.93 至 30.43);p<0.001;I²:97%;中等级别证据]水平。肝硬度显著改善[平均差异:2.22kPa(95%CI:0.80 至 3.63);p=0.002;I²:99%;中等级别证据]。糖化血红蛋白[平均差异:0.59%(95%CI:0.32 至 0.86);p<0.001;I²:78%;中等级别证据]、总胆固醇[平均差异:19.20(95%CI:1.54 至 36.87);p=0.03;I²:95%;中等级别证据]和甘油三酯[平均差异:105.49mg/dL(95%CI:11.18 至 199.80);p=0.03;I²:100%;中等级别证据]水平均有显著改善。沙格列汀治疗是安全的。

结论

辅助应用 4mg 沙格列汀治疗可显著改善 NAFLD 或 NASH 患者的肝功能,降低肝硬度,并改善代谢参数(血糖和血脂谱)。

相似文献

1
Effects of saroglitazar in the treatment of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis: A systematic review and meta-analysis.沙格列汀治疗非酒精性脂肪性肝病或非酒精性脂肪性肝炎的疗效:系统评价和荟萃分析。
Clin Res Hepatol Gastroenterol. 2023 Aug;47(7):102174. doi: 10.1016/j.clinre.2023.102174. Epub 2023 Jun 26.
2
Role of semaglutide in the treatment of nonalcoholic fatty liver disease or non-alcoholic steatohepatitis: A systematic review and meta-analysis.司美格鲁肽在治疗非酒精性脂肪性肝病或非酒精性脂肪性肝炎中的作用:系统评价和荟萃分析。
Diabetes Metab Syndr. 2023 Oct;17(10):102849. doi: 10.1016/j.dsx.2023.102849. Epub 2023 Sep 13.
3
Saroglitazar improved hepatic steatosis and fibrosis by modulating inflammatory cytokines and adiponectin in an animal model of non-alcoholic steatohepatitis.沙格列汀通过调节非酒精性脂肪性肝炎动物模型中的炎症细胞因子和脂联素改善肝脂肪变性和纤维化。
BMC Pharmacol Toxicol. 2021 Oct 1;22(1):53. doi: 10.1186/s40360-021-00524-8.
4
Saroglitazar, a PPAR-α/γ Agonist, for Treatment of NAFLD: A Randomized Controlled Double-Blind Phase 2 Trial.沙格列汀,一种 PPAR-α/γ 激动剂,用于治疗非酒精性脂肪性肝病:一项随机对照、双盲 2 期试验。
Hepatology. 2021 Oct;74(4):1809-1824. doi: 10.1002/hep.31843. Epub 2021 Jul 19.
5
Saroglitazar in patients with non-alcoholic fatty liver disease and diabetic dyslipidemia: a prospective, observational, real world study.非酒精性脂肪性肝病合并糖尿病血脂异常患者应用沙格列汀:一项前瞻性、观察性、真实世界研究。
Sci Rep. 2020 Dec 3;10(1):21117. doi: 10.1038/s41598-020-78342-x.
6
Safety and Efficacy of Saroglitazar in Nonalcoholic Fatty Liver Patients With Diabetic Dyslipidemia-A Prospective, Interventional, Pilot Study.沙罗格列扎用于合并糖尿病血脂异常的非酒精性脂肪肝患者的安全性和有效性——一项前瞻性、干预性、试点研究
J Clin Exp Hepatol. 2022 Jan-Feb;12(1):61-67. doi: 10.1016/j.jceh.2021.03.012. Epub 2021 Apr 9.
7
Dual PPARα/γ agonist saroglitazar improves liver histopathology and biochemistry in experimental NASH models.双重过氧化物酶体增殖物激活受体α/γ激动剂沙格列汀改善实验性 NASH 模型的肝脏组织病理学和生物化学。
Liver Int. 2018 Jun;38(6):1084-1094. doi: 10.1111/liv.13634. Epub 2017 Dec 14.
8
New dual peroxisome proliferator activated receptor agonist-Saroglitazar in diabetic dyslipidemia and non-alcoholic fatty liver disease: integrated analysis of the real world evidence.新型双重过氧化物酶体增殖物激活受体激动剂-沙格列汀在糖尿病血脂异常和非酒精性脂肪性肝病中的应用:真实世界证据的综合分析。
Cardiovasc Diabetol. 2019 Jun 17;18(1):80. doi: 10.1186/s12933-019-0884-3.
9
Efficacy of statins in treatment and development of non-alcoholic fatty liver disease and steatohepatitis: A systematic review and meta-analysis.他汀类药物在治疗和发展非酒精性脂肪性肝病和脂肪性肝炎中的疗效:系统评价和荟萃分析。
Clin Res Hepatol Gastroenterol. 2022 Apr;46(4):101816. doi: 10.1016/j.clinre.2021.101816. Epub 2021 Oct 2.
10
The PPAR α/γ Agonist Saroglitazar Improves Insulin Resistance and Steatohepatitis in a Diet Induced Animal Model of Nonalcoholic Fatty Liver Disease.PPARα/γ 激动剂罗格列酮改善非酒精性脂肪性肝病动物模型的胰岛素抵抗和脂肪性肝炎。
Sci Rep. 2020 Jun 9;10(1):9330. doi: 10.1038/s41598-020-66458-z.

引用本文的文献

1
Evaluation of Effectiveness and Tolerability of Saroglitazar in Metabolic Disease Patients of India: A Retrospective, Observational, Electronic Medical Record-Based Real-World Evidence Study.印度代谢疾病患者中沙罗格列扎有效性及耐受性评估:一项基于电子病历的回顾性观察性真实世界证据研究
Cureus. 2025 Jul 30;17(7):e89028. doi: 10.7759/cureus.89028. eCollection 2025 Jul.
2
Therapeutic Targeting of PPARγ in Nonalcoholic Fatty Liver Disease: Efficacy, Safety, and Drug Development.非酒精性脂肪性肝病中PPARγ的治疗靶点:疗效、安全性与药物研发
Drug Des Devel Ther. 2025 Aug 22;19:7293-7319. doi: 10.2147/DDDT.S524893. eCollection 2025.
3
Saroglitazar Ameliorates Pulmonary Fibrosis Progression in Mice by Suppressing NF-κB Activation and Attenuating Macrophage M1 Polarization.
司格列他扎通过抑制NF-κB激活和减轻巨噬细胞M1极化改善小鼠肺纤维化进展。
Medicina (Kaunas). 2025 Jun 26;61(7):1157. doi: 10.3390/medicina61071157.
4
Unlocking therapeutic potential: exploring cross-talk among emerging nuclear receptors to combat metabolic dysfunction in steatotic liver disease.释放治疗潜力:探索新兴核受体之间的相互作用以对抗脂肪性肝病中的代谢功能障碍。
NPJ Metab Health Dis. 2024 Jul 3;2(1):13. doi: 10.1038/s44324-024-00013-6.
5
Innovative Drugs First Implemented in Type 2 Diabetes Mellitus and Obesity and Their Effects on Metabolic Dysfunction-Associated Steatohepatitis (MASH)-Related Fibrosis and Cirrhosis.创新药物在2型糖尿病和肥胖症中的首次应用及其对代谢功能障碍相关脂肪性肝炎(MASH)相关纤维化和肝硬化的影响。
J Clin Med. 2025 Feb 7;14(4):1042. doi: 10.3390/jcm14041042.
6
Metformin: Beyond Type 2 Diabetes Mellitus.二甲双胍:超越2型糖尿病
Cureus. 2024 Oct 17;16(10):e71730. doi: 10.7759/cureus.71730. eCollection 2024 Oct.
7
Novel Therapeutics for Type 2 Diabetes Mellitus-A Look at the Past Decade and a Glimpse into the Future.2型糖尿病的新型疗法——回顾过去十年并展望未来
Biomedicines. 2024 Jun 21;12(7):1386. doi: 10.3390/biomedicines12071386.
8
Saroglitazar in Non-alcoholic Fatty Liver Disease From Bench to Bedside: A Comprehensive Review and Sub-group Meta-Analysis.非酒精性脂肪性肝病中从实验室到临床的司美格鲁他扎:一项全面综述与亚组荟萃分析
Cureus. 2023 Oct 22;15(10):e47493. doi: 10.7759/cureus.47493. eCollection 2023 Oct.
9
Current Clinical Trial Status and Future Prospects of PPAR-Targeted Drugs for Treating Nonalcoholic Fatty Liver Disease.PPAR 靶向药物治疗非酒精性脂肪性肝病的临床研究现状与展望。
Biomolecules. 2023 Aug 18;13(8):1264. doi: 10.3390/biom13081264.