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
  • [1] Type 2 diabetes mellitus and cardiometabolic outcomes in metabolic dysfunction-associated steatotic liver disease population
    Chew, Nicholas W. S.
    Pan, Xin Hui
    Chong, Bryan
    Chandramouli, Chanchal
    Muthiah, Mark
    Lam, Carolyn S. P.
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2024, 211
  • [2] The Influence of Coffee on Reducing Metabolic Dysfunction-Associated Steatotic Liver Disease in Patients With Type 2 Diabetes: A Review
    Kaur, Manpreet
    Murugesan, Shanmathi
    Singh, Sachpreet
    Uy, Katherine N.
    Kaur, Jasjeet
    Mann, Navina
    Sekhon, Rajneet K.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (12)
  • [3] Adipocytokines as Predictors of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) Development in Type 2 Diabetes Mellitus Patients
    Fajkic, Almir
    Jahic, Rijad
    Hadzovic-Dzuvo, Almira
    Lepara, Orhan
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (03)
  • [4] Implementing metabolic dysfunction-associated steatotic liver disease guidelines in patients with type 2 diabetes
    Ciardullo, Stefano
    Perseghin, Gianluca
    LANCET GASTROENTEROLOGY & HEPATOLOGY, 2025, 10 (02): : 97 - 98
  • [5] Diabetes and Metabolic Dysfunction-Associated Steatotic Liver Disease
    Stefan, Norbert
    Roden, Michael
    DIABETOLOGIE UND STOFFWECHSEL, 2024, 19 : S290 - S296
  • [6] Systematic review of exercise for the treatment of pediatric metabolic dysfunction-associated steatotic liver disease
    Smith, Martha R.
    Yu, Elizabeth L.
    Malki, Ghattas J.
    Newton, Kimberly P.
    Goyal, Nidhi P.
    Heskett, Karen M.
    Schwimmer, Jeffrey B.
    PLOS ONE, 2024, 19 (12):
  • [7] SYSTEMATIC REVIEW OF EXERCISE FOR THE TREATMENT OF PEDIATRIC METABOLIC DYSFUNCTION-ASSOCIATED STEATOTIC LIVER DISEASE
    Smith, Martha
    Yu, Elizabeth
    Malki, Ghattas
    Newton, Kimberly
    Goyal, Nidhi
    Heskett, Karen
    Schwimmer, Jeffrey
    HEPATOLOGY, 2024, 80 : S1949 - S1950
  • [8] Machine Learning Identifies Metabolic Dysfunction-Associated Steatotic Liver Disease in Patients With Diabetes Mellitus
    Nabrdalik, Katarzyna
    Kwiendacz, Hanna
    Irlik, Krzysztof
    Hendel, Mirela
    Drozdz, Karolina
    Wijata, Agata M.
    Nalepa, Jakub
    Janota, Oliwia
    Wojcik, Wiktoria
    Gumprecht, Janusz
    Lip, Gregory Y. H.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2024, 109 (08): : 2029 - 2038
  • [9] Metabolic dysfunction-associated steatotic liver disease-associated fibrosis and cardiac dysfunction in patients with type 2 diabetes
    Cernea, Simona
    Onisor, Danusia
    Roiban, Andrada Larisa
    Benedek, Theodora
    Rat, Nora
    WORLD JOURNAL OF CARDIOLOGY, 2024, 16 (10):
  • [10] Efficacy of imeglimin in patients with type 2 diabetes mellitus complicated by metabolic dysfunction-associated steatotic liver disease: A multicentre study
    Fukunaga, Kensaku
    Morishita, Asahiro
    Imachi, Hitomi
    Oura, Kyoko
    Sato, Seisuke
    Kobayashi, Toshihiro
    Saheki, Takanobu
    Yoshimura, Takafumi
    Komori, Kurumi
    Nakahara, Mai
    Tadokoro, Tomoko
    Fujita, Koji
    Tani, Joji
    Kobara, Hideki
    Murao, Koji
    DIABETES OBESITY & METABOLISM, 2025, 27 (03): : 1498 - 1506