Pharmacological treatment options for metabolic dysfunction-associated steatotic liver disease in patients with type 2 diabetes mellitus: A systematic review

被引:0
|
作者
Konings, Laura A. M. [1 ,2 ]
Miguelanez-Matute, Lorena [1 ]
Boeren, Anna M. P. [1 ]
van de Luitgaarden, Inge A. T. [3 ]
Dirksmeier, Femme [4 ]
de Knegt, Rob J. [5 ]
Tushuizen, Maarten E. [6 ]
Grobbee, Diederick E. [3 ]
Holleboom, Adriaan G. [7 ]
Cabezas, Manuel Castro [1 ,2 ,3 ]
机构
[1] Franciscus Gasthuis & Vlietland, Dept Internal Med, Rotterdam, Netherlands
[2] Erasmus MC, Dept Internal Med & Endocrinol, Rotterdam, Netherlands
[3] Julius Clin, Zeist, Netherlands
[4] Franciscus Gasthuis & Vlietland, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[5] Erasmus MC, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[6] LUMC, Dept Gastroenterol & Hepatol, Leiden, Netherlands
[7] Amsterdam UMC, Dept Internal Med, Amsterdam, Netherlands
关键词
MASH; MASLD; NAFLD; NASH; pharmacotherapy; T2DM; NONALCOHOLIC STEATOHEPATITIS; INSULIN SENSITIVITY; PIOGLITAZONE; LIRAGLUTIDE; SITAGLIPTIN; PREVALENCE; EXENATIDE; PLACEBO; TRIAL;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundMetabolic dysfunction-associated steatotic liver disease (MASLD) is closely related to type 2 diabetes mellitus (T2DM) through a common root in insulin resistance. The more severe stage, metabolic dysfunction-associated steatohepatitis (MASH), increases the risk for cardiovascular complications, liver cirrhosis and hepatocellular carcinoma. Several trials investigating established antidiabetic-drugs in patients with T2DM and MASLD have yielded promising results. Therefore, we aimed to systematically review the effect of T2DM-drug treatment on MALSD parameters.MethodsMedical databases were searched until January 2025 for controlled trials in patients with T2DM and MASLD/MASH. Studies that evaluated the effect of T2DM-medication on the severity of MASLD/MASH in T2DM patients were included. The quality of the studies was assessed by three independent reviewers using a set of Cochrane risk-of-bias tools.ResultsOf 1748 references, 117 studies fulfilled the inclusion-criteria and were assessed for eligibility in full-text. Fifty-two articles were included. Data included a total of 64.708 patients and study populations ranged from 9 to 50.742. Heterogeneity in study-design and analysis hampered the comparability of the results. Most evidence was present for GLP-1 receptor agonists, SGLT2-inhibitors and PPAR-gamma-agonists for regression of liver fibrosis and MASH.ConclusionStudies on the value of T2DM-drug treatment in the improvement of MASLD vary significantly in study design, size and quality. GLP-1 receptor agonists, PPAR-gamma-agonists, SGLT2-inhibitors may all be preferred pharmacological interventions for patients with MASLD/MASH and T2DM. Newer agents like dual GLP-1/GIP or triple GLP-1/GIP/Glucagon agonists will likely play an important role in the treatment of MASLD/MASH in the near future.
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页数:28
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