• 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

达格列净对 2 型糖尿病合并非酒精性脂肪性肝病患者肝及胰腺脂肪的影响。

Effect of dapagliflozin on liver and pancreatic fat in patients with type 2 diabetes and non-alcoholic fatty liver disease.

机构信息

Department of Nutrition of Xinqiao Hospital, Army Medical University, Chongqing, China.

Department of Endocrinology of Xinqiao Hospital, Army Medical University, Chongqing, China.

出版信息

J Diabetes Complications. 2023 Oct;37(10):108610. doi: 10.1016/j.jdiacomp.2023.108610. Epub 2023 Sep 1.

DOI:10.1016/j.jdiacomp.2023.108610
PMID:37722211
Abstract

AIMS

To evaluate the effect of dapagliflozin on liver fat content (LFC) and pancreatic fat content (PFC).

MATERIALS AND METHODS

84 patients with type 2 diabetes (T2D) and non-alcoholic fatty liver disease (NAFLD) were randomly assigned to receive either dapagliflozin (n = 42) or serve as controls (n = 42). The primary endpoint is changes in LFC and PFC using magnetic resonance imaging estimated proton density fat fraction. Secondary outcomes include liver fibrosis index, inflammatory cytokine levels, and liver enzyme levels.

RESULTS

At week 24, the dapagliflozin group significantly reduced LFC (P < 0.001) and PFC (P = 0.033) compared to the control group. Differences were also observed in serum levels of tumor necrosis factor-α (TNF-α) (P = 0.004), interleukin-6 (IL-6) (P = 0.001), and alanine aminotransferase (ALT) (P < 0.001) between the two groups.

CONCLUSIONS

Dapagliflozin can significantly decrease LFC and PFC in patients with T2D and NAFLD. It also improves serum ALT, TNF-α, and IL-6 levels, making it a promising treatment option for NAFLD. The trial is registered on Chinese Clinical Trial Registry (Registration No. ChiCTR2100054612).

摘要

目的

评估达格列净对肝脂肪含量(LFC)和胰腺脂肪含量(PFC)的影响。

材料和方法

84 例 2 型糖尿病(T2D)合并非酒精性脂肪性肝病(NAFLD)患者被随机分为达格列净组(n=42)或对照组(n=42)。主要终点是使用磁共振成像估计质子密度脂肪分数评估 LFC 和 PFC 的变化。次要结局包括肝纤维化指数、炎症细胞因子水平和肝酶水平。

结果

在 24 周时,与对照组相比,达格列净组显著降低了 LFC(P<0.001)和 PFC(P=0.033)。两组间肿瘤坏死因子-α(TNF-α)(P=0.004)、白细胞介素-6(IL-6)(P=0.001)和丙氨酸氨基转移酶(ALT)(P<0.001)的血清水平也存在差异。

结论

达格列净可显著降低 T2D 和 NAFLD 患者的 LFC 和 PFC。它还改善了血清 ALT、TNF-α 和 IL-6 水平,是治疗 NAFLD 的一种有前途的方法。该试验在中国临床试验注册中心(注册号 ChiCTR2100054612)注册。

相似文献

1
Effect of dapagliflozin on liver and pancreatic fat in patients with type 2 diabetes and non-alcoholic fatty liver disease.达格列净对 2 型糖尿病合并非酒精性脂肪性肝病患者肝及胰腺脂肪的影响。
J Diabetes Complications. 2023 Oct;37(10):108610. doi: 10.1016/j.jdiacomp.2023.108610. Epub 2023 Sep 1.
2
Evaluation of the effects of dapagliflozin, a sodium-glucose co-transporter-2 inhibitor, on hepatic steatosis and fibrosis using transient elastography in patients with type 2 diabetes and non-alcoholic fatty liver disease.评估钠-葡萄糖共转运蛋白 2 抑制剂达格列净对 2 型糖尿病合并非酒精性脂肪性肝病患者肝脂肪变性和纤维化的影响:应用瞬时弹性成像技术。
Diabetes Obes Metab. 2019 Feb;21(2):285-292. doi: 10.1111/dom.13520. Epub 2018 Oct 2.
3
Effects of dapagliflozin and n-3 carboxylic acids on non-alcoholic fatty liver disease in people with type 2 diabetes: a double-blind randomised placebo-controlled study.达格列净和 n-3 羧酸对 2 型糖尿病患者非酒精性脂肪性肝病的影响:一项双盲随机安慰剂对照研究。
Diabetologia. 2018 Sep;61(9):1923-1934. doi: 10.1007/s00125-018-4675-2. Epub 2018 Jul 3.
4
Comparison of the effects of three kinds of glucose-lowering drugs on non-alcoholic fatty liver disease in patients with type 2 diabetes: A randomized, open-label, three-arm, active control study.三种降糖药物对 2 型糖尿病患者非酒精性脂肪肝影响的比较:一项随机、开放标签、三臂、阳性对照研究。
J Diabetes Investig. 2020 Nov;11(6):1612-1622. doi: 10.1111/jdi.13279. Epub 2020 May 26.
5
Impact of dapagliflozin, an SGLT2 inhibitor, on serum levels of soluble dipeptidyl peptidase-4 in patients with type 2 diabetes and non-alcoholic fatty liver disease.钠-葡萄糖协同转运蛋白2抑制剂达格列净对2型糖尿病合并非酒精性脂肪性肝病患者血清可溶性二肽基肽酶-4水平的影响。
Int J Clin Pract. 2019 May;73(5):e13335. doi: 10.1111/ijcp.13335. Epub 2019 Apr 1.
6
The effects of dapagliflozin on hepatic and visceral fat in type 2 diabetes patients with non-alcoholic fatty liver disease.达格列净对非酒精性脂肪性肝病 2 型糖尿病患者肝性和内脏性脂肪的影响。
J Gastroenterol Hepatol. 2021 Oct;36(10):2952-2959. doi: 10.1111/jgh.15580. Epub 2021 Jun 23.
7
Effect of dulaglutide on liver fat in patients with type 2 diabetes and NAFLD: randomised controlled trial (D-LIFT trial).度拉糖肽对 2 型糖尿病合并非酒精性脂肪性肝病患者肝脂肪的影响:随机对照试验(D-LIFT 试验)。
Diabetologia. 2020 Nov;63(11):2434-2445. doi: 10.1007/s00125-020-05265-7. Epub 2020 Aug 31.
8
Effect of Empagliflozin on Liver Fat in Patients With Type 2 Diabetes and Nonalcoholic Fatty Liver Disease: A Randomized Controlled Trial (E-LIFT Trial).恩格列净对 2 型糖尿病合并非酒精性脂肪性肝病患者肝脏脂肪的影响:一项随机对照试验(E-LIFT 试验)。
Diabetes Care. 2018 Aug;41(8):1801-1808. doi: 10.2337/dc18-0165. Epub 2018 Jun 12.
9
Impact of sodium glucose cotransporter-2 inhibitors on liver steatosis/fibrosis/inflammation and redox balance in non-alcoholic fatty liver disease.钠-葡萄糖共转运蛋白 2 抑制剂对非酒精性脂肪性肝病肝脂肪变性/纤维化/炎症及氧化还原平衡的影响。
World J Gastroenterol. 2022 Jul 14;28(26):3243-3257. doi: 10.3748/wjg.v28.i26.3243.
10
Serum high-molecular-weight adiponectin and response to dapagliflozin in patients with type 2 diabetes and non-alcoholic fatty liver disease.血清高分子量脂联素与达格列净治疗 2 型糖尿病合并非酒精性脂肪性肝病患者的疗效反应。
J Investig Med. 2021 Oct;69(7):1324-1329. doi: 10.1136/jim-2020-001621. Epub 2021 May 20.

引用本文的文献

1
Comparative efficacy of sodium-glucose transporter 2 inhibitors on lipid profiles in nonalcoholic fatty liver disease (NAFLD): a comprehensive Bayesian network meta-analysis.钠-葡萄糖协同转运蛋白2抑制剂对非酒精性脂肪性肝病(NAFLD)脂质谱的比较疗效:一项全面的贝叶斯网络荟萃分析。
Ann Med Surg (Lond). 2025 Jul 25;87(9):6008-6022. doi: 10.1097/MS9.0000000000003658. eCollection 2025 Sep.
2
SGLT2 Inhibitors: Multifaceted Therapeutic Agents in Cardiometabolic and Renal Diseases.钠-葡萄糖协同转运蛋白2抑制剂:心血管代谢疾病和肾脏疾病中的多面治疗药物
Metabolites. 2025 Aug 7;15(8):536. doi: 10.3390/metabo15080536.
3
Pathological Evolution and Internal Medicine Management of Nonalcoholic Fatty Liver Disease (NAFLD) in the Era of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).
代谢功能障碍相关脂肪性肝病(MASLD)时代非酒精性脂肪性肝病(NAFLD)的病理演变与内科管理
Cureus. 2025 Jun 29;17(6):e86963. doi: 10.7759/cureus.86963. eCollection 2025 Jun.
4
Efficacy of Sodium-Glucose Cotransporter 2 Inhibitors in Patients With Type 2 Diabetes Mellitus and Nonalcoholic Fatty Liver Disease: A Systematic Review of Randomized Controlled Trials.钠-葡萄糖协同转运蛋白2抑制剂在2型糖尿病合并非酒精性脂肪性肝病患者中的疗效:一项随机对照试验的系统评价
Cureus. 2025 Jun 17;17(6):e86232. doi: 10.7759/cureus.86232. eCollection 2025 Jun.
5
Evaluating the Safety and Efficacy of SGLT-2 Inhibitors on Reducing Cardiovascular and Renal Mortality, Morbidity and Inflammatory Outcomes in Various Patient Populations: A Systematic Review and Meta-Analysis of 92 920 Patients.评估钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂在降低各类患者群体心血管和肾脏死亡率、发病率及炎症结局方面的安全性和有效性:一项对92920例患者的系统评价和荟萃分析
Clin Med Insights Cardiol. 2025 Jun 30;19:11795468251347777. doi: 10.1177/11795468251347777. eCollection 2025.
6
Increased depth of pancreas incisure on computed tomography as an independent predictor for T2DM.计算机断层扫描中胰腺切迹深度增加作为2型糖尿病的独立预测指标。
Sci Rep. 2025 Jul 2;15(1):23389. doi: 10.1038/s41598-025-08193-x.
7
Fatty Pancreas: Its Potential as a Risk Factor for Pancreatic Cancer and Clinical Implications.脂肪胰腺:其作为胰腺癌风险因素的可能性及临床意义
Cancers (Basel). 2025 May 24;17(11):1765. doi: 10.3390/cancers17111765.
8
Targeting Metabolism: Innovative Therapies for MASLD Unveiled.靶向代谢:非酒精性脂肪性肝炎的创新疗法揭秘。
Int J Mol Sci. 2025 Apr 25;26(9):4077. doi: 10.3390/ijms26094077.
9
Metabolic-Dysfunction-Associated Steatotic Liver Disease: Molecular Mechanisms, Clinical Implications, and Emerging Therapeutic Strategies.代谢功能障碍相关脂肪性肝病:分子机制、临床意义及新兴治疗策略
Int J Mol Sci. 2025 Mar 25;26(7):2959. doi: 10.3390/ijms26072959.
10
Efficacy of dapagliflozin to treat nonalcoholic fatty liver disease in patients with type 2 diabetes: A meta-analysis.达格列净治疗2型糖尿病患者非酒精性脂肪性肝病的疗效:一项荟萃分析。
Medicine (Baltimore). 2025 Jan 3;104(1):e40836. doi: 10.1097/MD.0000000000040836.