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.
引用
收藏
页数:28
相关论文
共 50 条
  • [31] The impact of resistance training in patients diagnosed with metabolic dysfunction-associated steatotic liver disease: a systematic review
    Medeiros, Daniele Gorski
    Ferreira, Luis Fernando
    Lamp, Jessica da Silva
    da Rosa, Luis Henrique Telles
    EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2025, 37 (02) : 129 - 136
  • [32] Efficacy and safety of incretin-based therapies in patients with metabolic dysfunction-associated steatotic liver disease complicated by type 2 diabetes mellitus
    Kawano, Tadamichi
    Arai, Taeang
    Atsukawa, Masanori
    Tada, Toshifumi
    Oikawa, Tsunekazu
    Tsubota, Akihito
    Matsuura, Kentaro
    Ishikawa, Toru
    Abe, Hiroshi
    Kato, Keizo
    Morishita, Asahiro
    Tani, Joji
    Okubo, Tomomi
    Iwakiri, Katsuhiko
    JOURNAL OF HEPATOLOGY, 2024, 80 : S616 - S616
  • [33] Diabetes and metabolic dysfunction-associated steatotic liver disease, CVD: a continuum
    Chawla, Rajeev
    Kumar, Anshul
    INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES, 2024, 44 (03) : 417 - 418
  • [34] Identifying metabolic dysfunction-associated steatotic liver disease in patients with type 2 diabetes mellitus using clinic-based prediction tools
    Alkaabi, Juma
    Afandi, Bachar
    Alhaj, Omar
    Kanwal, Darakhshan
    Agha, Adnan
    FRONTIERS IN MEDICINE, 2024, 11
  • [35] Sarcopenia and Metabolic Dysfunction-Associated Steatotic Liver Disease: A Narrative Review
    Abenavoli, Ludovico
    Statsenko, Michael
    Scarlata, Giuseppe Guido Maria
    Morano, Domenico
    Myazin, Roman
    Emelyanov, Dmitriy
    LIVERS, 2024, 4 (04): : 495 - 506
  • [36] Prevalence and predictive features of metabolic dysfunction-associated steatotic liver disease in type 1 diabetes
    Snethlage, Coco M. Fuhri
    Meijnikman, Abraham S.
    Mak, Anne Linde
    Rampanelli, Elena
    Voermans, Bas
    Callender, Cengiz A. K.
    de Groen, Pleun
    Roep, Bart O.
    van Raalte, Daniel H.
    Knop, Filip K.
    Holleboom, Adriaan G.
    Nieuwdorp, Max
    Hanssen, Nordin M. J.
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2024, 190 (05) : 391 - 400
  • [37] Editorial: Noninvasive tests for metabolic dysfunction-associated steatotic liver disease: A refinement of the Nash-FibroTest for type 2 diabetes mellitus
    Liu, Chen-Hua
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2023, 58 (10) : 1111 - 1112
  • [38] Metabolic dysfunction-associated steatotic liver disease is associated with worse time in ranges in type 1 diabetes
    Aernouts, Chloe
    Belde, Sarah P. W.
    Lambrechts, Julie
    Mertens, Jonathan
    Ledeganck, Kristien J.
    Francque, Sven M.
    De Block, Christophe E. M.
    DIABETES OBESITY & METABOLISM, 2024, 26 (09): : 3781 - 3790
  • [39] Metabolic dysfunction-associated steatotic liver disease and the heart
    Driessen, Stan
    Francque, Sven M.
    Anker, Stefan D.
    Cabezas, Manuel Castro
    Grobbee, Diederick E.
    Tushuizen, Maarten E.
    Holleboom, Adriaan G.
    HEPATOLOGY, 2023,
  • [40] Beneficial effect of oral semaglutide for type 2 diabetes mellitus in patients with metabolic dysfunction-associated steatotic liver disease: A prospective, multicentre, observational study
    Arai, Taeang
    Atsukawa, Masanori
    Tsubota, Akihito
    Oikawa, Tsunekazu
    Tada, Toshifumi
    Matsuura, Kentaro
    Ishikawa, Toru
    Abe, Hiroshi
    Kato, Keizo
    Morishita, Asahiro
    Tani, Joji
    Okubo, Tomomi
    Nagao, Mototsugu
    Iwabu, Masato
    Iwakiri, Katsuhiko
    DIABETES OBESITY & METABOLISM, 2024, 26 (11): : 4958 - 4965