• 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

钠-葡萄糖协同转运蛋白2抑制剂对2型糖尿病日本患者代谢功能障碍相关脂肪性肝病发生发展的长期影响的回顾性纵向观察研究

Retrospective Longitudinal Observational Study on the Long-Term Effects of Sodium-Glucose Cotransporter-2 Inhibitors on the Development of Metabolic Dysfunction-Associated Steatotic Liver Disease in Type 2 Diabetic Japanese Patients.

作者信息

Katsuyama Hisayuki, Horinaka Seiichi, Hakoshima Mariko, Adachi Hiroki, Yanai Hidekatsu

机构信息

Department of Diabetes, Endocrinology and Metabolism, National Center for Global Health and Medicine Kohnodai Hospital, 1-7-1 Kohnodai, Ichikawa 272-8516, Chiba, Japan.

出版信息

J Clin Med. 2024 Aug 21;13(16):4929. doi: 10.3390/jcm13164929.

DOI:10.3390/jcm13164929
PMID:39201071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11355713/
Abstract

: The health burden of metabolic dysfunction-associated fatty liver disease (MASLD) has been increasing lately. Cardiovascular disease (CVD) is the main cause of death in MASLD patients; therefore, the treatments for MASLD should improve both CV risk factors such as obesity, diabetes, and dyslipidemia, in addition to an improvement in liver function. The evidence on the long-term effects of sodium-glucose cotransporter 2 inhibitors (SGLT2is) on the progression of MASLD in Asian populations is very limited. : The retrospective longitudinal study was performed by using the medical records at our institute. We picked up patients with type 2 diabetes who had taken SGLT2is for at least 3 years or longer between 1 April 2014 and 31 March 2018. We collected the data on metabolic parameters, including laboratory data and anthropometric parameters, and compared the data before and after the initiation of SGLT2is treatment. : During the observation period, 324 patients had taken SGLT2is for 3 years. Three-year SGLT2is treatment significantly reduced body weight, hemoglobin A1c, low-density lipoprotein cholesterol, triglyceride, and non-high-density lipoprotein cholesterol (non-HDL-C). Such favorable changes in serum lipids were remarkable in patients with statins. Furthermore, this treatment significantly improved liver function and the markers for hepatic steatosis and hepatic fibrosis. : Considering that the development of CVD determines the prognosis of MASLD patients, long-term SGLT2is treatment may be an ideal therapy for MASLD patients.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)的健康负担近来一直在增加。心血管疾病(CVD)是MASLD患者的主要死因;因此,MASLD的治疗除了改善肝功能外,还应改善肥胖、糖尿病和血脂异常等心血管危险因素。关于钠-葡萄糖协同转运蛋白2抑制剂(SGLT2is)对亚洲人群MASLD进展的长期影响的证据非常有限。:本回顾性纵向研究使用了我们研究所的病历。我们选取了在2014年4月1日至2018年3月31日期间服用SGLT2is至少3年或更长时间的2型糖尿病患者。我们收集了代谢参数数据,包括实验室数据和人体测量参数,并比较了开始SGLT2is治疗前后的数据。:在观察期内,324例患者服用SGLT2is达3年。三年的SGLT2is治疗显著降低了体重、糖化血红蛋白、低密度脂蛋白胆固醇、甘油三酯和非高密度脂蛋白胆固醇(非HDL-C)。他汀类药物治疗的患者血脂的这种有利变化很显著。此外,这种治疗显著改善了肝功能以及肝脂肪变性和肝纤维化的标志物。:考虑到CVD的发生决定了MASLD患者的预后,长期SGLT2is治疗可能是MASLD患者的理想治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/621c/11355713/02fa8ef03d61/jcm-13-04929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/621c/11355713/501a489f9f73/jcm-13-04929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/621c/11355713/02fa8ef03d61/jcm-13-04929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/621c/11355713/501a489f9f73/jcm-13-04929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/621c/11355713/02fa8ef03d61/jcm-13-04929-g002.jpg

相似文献

1
Retrospective Longitudinal Observational Study on the Long-Term Effects of Sodium-Glucose Cotransporter-2 Inhibitors on the Development of Metabolic Dysfunction-Associated Steatotic Liver Disease in Type 2 Diabetic Japanese Patients.钠-葡萄糖协同转运蛋白2抑制剂对2型糖尿病日本患者代谢功能障碍相关脂肪性肝病发生发展的长期影响的回顾性纵向观察研究
J Clin Med. 2024 Aug 21;13(16):4929. doi: 10.3390/jcm13164929.
2
Metabolic-Dysfunction-Associated Steatotic Liver Disease-Its Pathophysiology, Association with Atherosclerosis and Cardiovascular Disease, and Treatments.代谢功能障碍相关性脂肪性肝病及其病理生理学、与动脉粥样硬化和心血管疾病的关联,以及治疗方法。
Int J Mol Sci. 2023 Oct 23;24(20):15473. doi: 10.3390/ijms242015473.
3
Comparative effectiveness of sodium-glucose cotransporter-2 inhibitors and dipeptidyl peptidase-4 inhibitors in improvement of fatty liver index in patients with type 2 diabetes mellitus and metabolic dysfunction-associated steatotic liver disease: A retrospective nationwide claims database study in Japan.钠-葡萄糖共转运蛋白 2 抑制剂和二肽基肽酶-4 抑制剂在改善 2 型糖尿病伴代谢功能障碍相关脂肪性肝病患者的脂肪肝指数方面的疗效比较:日本一项回顾性全国性索赔数据库研究。
Diabetes Obes Metab. 2024 Aug;26(8):3099-3109. doi: 10.1111/dom.15632. Epub 2024 May 6.
4
Prolonged impacts of sodium glucose cotransporter-2 inhibitors on metabolic dysfunction-associated steatotic liver disease in type 2 diabetes: a retrospective analysis through magnetic resonance imaging.钠-葡萄糖协同转运蛋白2抑制剂对2型糖尿病中代谢功能障碍相关脂肪性肝病的长期影响:一项通过磁共振成像的回顾性分析
Endocr J. 2024 Aug 8;71(8):767-775. doi: 10.1507/endocrj.EJ24-0005. Epub 2024 May 30.
5
2024 UPDATE: the Brazilian Diabetes Society position on the management of metabolic dysfunction-associated steatotic liver disease (MASLD) in people with prediabetes or type 2 diabetes.2024年更新:巴西糖尿病学会关于糖尿病前期或2型糖尿病患者代谢功能障碍相关脂肪性肝病(MASLD)管理的立场
Diabetol Metab Syndr. 2024 Jan 19;16(1):23. doi: 10.1186/s13098-024-01259-2.
6
Association of Metabolic Dysfunction-Associated Steatotic Liver Disease/Non-alcoholic Fatty Liver Disease With Type 2 Diabetes Mellitus: A Case-Control Study in a Tertiary Care Hospital in Pakistan.代谢功能障碍相关脂肪性肝病/非酒精性脂肪性肝病与2型糖尿病的关联:巴基斯坦一家三级医疗医院的病例对照研究
Cureus. 2023 Oct 17;15(10):e47240. doi: 10.7759/cureus.47240. eCollection 2023 Oct.
7
Triglyceride to HDL Cholesterol Ratio for the Identification of MASLD in Obesity: A Liver Biopsy-Based Case-Control Study.甘油三酯与高密度脂蛋白胆固醇比值在肥胖症合并代谢相关性脂肪性肝病诊断中的应用:一项基于肝活检的病例对照研究。
Nutrients. 2024 Apr 27;16(9):1310. doi: 10.3390/nu16091310.
8
Glycaemic control metrics and metabolic dysfunction-associated steatotic liver disease in children and adolescents with type 1 diabetes.儿童和青少年 1 型糖尿病患者的血糖控制指标与代谢功能障碍相关脂肪性肝病。
Diabetes Obes Metab. 2024 Dec;26(12):5896-5905. doi: 10.1111/dom.15961. Epub 2024 Sep 30.
9
Management of cardiovascular risk in patients with metabolic dysfunction-associated steatotic liver disease.代谢功能障碍相关脂肪性肝病患者的心血管风险管理。
Eur J Intern Med. 2024 Apr;122:28-34. doi: 10.1016/j.ejim.2023.11.012. Epub 2023 Nov 25.
10
Effects of carnosine supplementation on markers for the pathophysiological development of metabolic dysfunction-associated steatotic liver disease in a diet-induced model.肌肽补充对饮食诱导模型中代谢功能障碍相关脂肪性肝病病理生理发展标志物的影响。
Mol Cell Endocrinol. 2024 Mar 1;582:112138. doi: 10.1016/j.mce.2023.112138. Epub 2023 Dec 24.

引用本文的文献

1
Inflammatory and metabolic markers mediate the association of hepatic steatosis and fibrosis with 10-year ASCVD risk.炎症和代谢标志物介导肝脂肪变性和肝纤维化与10年动脉粥样硬化性心血管疾病(ASCVD)风险之间的关联。
Ann Med. 2025 Dec;57(1):2486594. doi: 10.1080/07853890.2025.2486594. Epub 2025 Apr 6.
2
The Effects of SGLT2 Inhibitors on Blood Pressure and Other Cardiometabolic Risk Factors.钠-葡萄糖协同转运蛋白 2 抑制剂对血压和其他心血管代谢风险因素的影响。
Int J Mol Sci. 2024 Nov 18;25(22):12384. doi: 10.3390/ijms252212384.

本文引用的文献

1
Non-alcoholic fatty liver disease in type 2 diabetes: Emerging evidence of benefit of peroxisome proliferator-activated receptors agonists and incretin-based therapies.2型糖尿病中的非酒精性脂肪性肝病:过氧化物酶体增殖物激活受体激动剂和基于肠促胰岛素疗法益处的新证据。
World J Methodol. 2024 Jun 20;14(2):91319. doi: 10.5662/wjm.v14.i2.91319.
2
Long-term effects of ipragliflozin and pioglitazone on metabolic dysfunction-associated steatotic liver disease in patients with type 2 diabetes: 5 year observational follow-up of a randomized, 24 week, active-controlled trial: Effect of ipragliflozin in MASLD.吡格列酮和伊格列净对 2 型糖尿病代谢功能障碍相关脂肪性肝病的长期影响:一项为期 24 周、随机、活性对照试验的 5 年观察随访:伊格列净在 MASLD 中的作用。
J Diabetes Investig. 2024 Sep;15(9):1220-1230. doi: 10.1111/jdi.14246. Epub 2024 May 22.
3
Influence of glucagon-like peptide-1 receptor agonists on fat accumulation in patients with diabetes mellitus and non-alcoholic fatty liver disease or obesity: A systematic review and meta-analysis of randomized control trials.胰高血糖素样肽-1 受体激动剂对糖尿病伴非酒精性脂肪性肝病或肥胖患者脂肪堆积的影响:系统评价和随机对照试验的荟萃分析。
J Diabetes Complications. 2024 Jun;38(6):108743. doi: 10.1016/j.jdiacomp.2024.108743. Epub 2024 Apr 4.
4
Effects of GLP-1 receptor agonists on the degree of liver fibrosis and CRP in non-alcoholic fatty liver disease and non-alcoholic steatohepatitis: A systematic review and meta-analysis.GLP-1 受体激动剂对非酒精性脂肪性肝病和非酒精性脂肪性肝炎肝纤维化程度和 CRP 的影响:系统评价和荟萃分析。
Prim Care Diabetes. 2024 Jun;18(3):268-276. doi: 10.1016/j.pcd.2024.03.005. Epub 2024 Mar 30.
5
Dapagliflozin ameliorates hepatic steatosis via suppressing LXRα-mediated synthesis of lipids and bile acids.达格列净通过抑制 LXRα 介导的脂质和胆汁酸合成改善肝脂肪变性。
Biochem Pharmacol. 2024 May;223:116167. doi: 10.1016/j.bcp.2024.116167. Epub 2024 Mar 26.
6
Effect of sodium-glucose cotransporter 2 inhibitors on serum low-density lipoprotein cholesterol in Japanese patients with type 2 diabetes mellitus.钠-葡萄糖共转运蛋白 2 抑制剂对日本 2 型糖尿病患者血清低密度脂蛋白胆固醇的影响。
J Diabetes Investig. 2024 Jul;15(7):843-850. doi: 10.1111/jdi.14179. Epub 2024 Mar 8.
7
Advance of Metformin in Liver Disease.二甲双胍在肝病治疗中的进展
Curr Med Chem. 2024 Jan 30. doi: 10.2174/0109298673274268231215110330.
8
Metabolic-Dysfunction-Associated Steatotic Liver Disease-Its Pathophysiology, Association with Atherosclerosis and Cardiovascular Disease, and Treatments.代谢功能障碍相关性脂肪性肝病及其病理生理学、与动脉粥样硬化和心血管疾病的关联,以及治疗方法。
Int J Mol Sci. 2023 Oct 23;24(20):15473. doi: 10.3390/ijms242015473.
9
The impact of sodium-glucose Cotransporter-2 inhibitors on lipid profile: A meta-analysis of 28 randomized controlled trials.钠-葡萄糖共转运蛋白 2 抑制剂对血脂谱的影响:28 项随机对照试验的荟萃分析。
Eur J Pharmacol. 2023 Nov 15;959:176087. doi: 10.1016/j.ejphar.2023.176087. Epub 2023 Sep 28.
10
SGLT2-inhibition increases total, LDL, and HDL cholesterol and lowers triglycerides: Meta-analyses of 60 randomized trials, overall and by dose, ethnicity, and drug type.SGLT2 抑制剂增加总胆固醇、LDL 胆固醇、HDL 胆固醇并降低甘油三酯:60 项随机试验的荟萃分析,按剂量、种族和药物类型进行总体和分析。
Atherosclerosis. 2024 Jul;394:117236. doi: 10.1016/j.atherosclerosis.2023.117236. Epub 2023 Aug 9.