> 1,000 cases (or > 20,000 participants for continuous outcomes); statistical significance at P < 10−6 (random effects); no evidence of small study effects and excess significance bias; 95% prediction interval excluded null value; no large heterogeneity (I2 < 50%)
Class II: highly suggestive evidence
> 1,000 cases (or > 20,000 participants for continuous outcomes), statistical significance at P < 10−6 (random effects), and the largest study with a 95% confidence interval excluding null value
Class III: suggestive evidence
> 1,000 cases (or > 20,000 participants for continuous outcomes) and statistical significance at P < 0.001
HH: Writing—original draft, Writing—review & editing, Conceptualization, Methodology, Formal analysis, Investigation, Resources, Supervision. SS: Formal analysis, Investigation, Conceptualization. DL: Formal analysis, Investigation, Conceptualization. All authors read and approved the final manuscript.
Conflicts of interest
The authors declare that they have no conflicts of interest.
Ethical approval
Not applicable.
Consent to participate
Not applicable.
Consent to publication
Not applicable.
Availability of data and materials
The original contributions presented in the study are included in the article/supplementary materials. Further inquiries can be directed to the corresponding author.
Funding
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References
Reichman TW, Markmann JF, Odorico J, Witkowski P, Fung JJ, Wijkstrom M, et al.; VX-880-101 FORWARD Study Group. Stem Cell-Derived, Fully Differentiated Islets for Type 1 Diabetes.N Engl J Med. 2025;393:858–68. [DOI] [PubMed]
Zhao Y, Zhao W, Bu H, Toshiyoshi M, Zhao Y. Liraglutide on type 2 diabetes mellitus with nonalcoholic fatty liver disease: A systematic review and meta-analysis of 16 RCTs.Medicine (Baltimore). 2023;102:e32892. [DOI] [PubMed] [PMC]
Xu YY, Wang X, She YQ, Liu J, Zhang Q. Meta-analysis of the clinical efficacy of liraglutide in treating type 2 diabetes mellitus complicated with non-alcoholic fatty liver disease.Endocr J. 2024;71:881–94. [DOI] [PubMed]
Younossi ZM, Koenig AB, Abdelatif D, Fazel Y, Henry L, Wymer M. Global epidemiology of nonalcoholic fatty liver disease: Meta-analytic assessment of prevalence, incidence, and outcomes.Hepatology. 2016;64:73–84. [DOI] [PubMed]
Ge X, Zheng L, Wang M, Du Y, Jiang J. Prevalence trends in non-alcoholic fatty liver disease at the global, regional and national levels, 1990-2017: a population-based observational study.BMJ Open. 2020;10:e036663. [DOI] [PubMed] [PMC]
Riazi K, Azhari H, Charette JH, Underwood FE, King JA, Afshar EE, et al. The prevalence and incidence of NAFLD worldwide: a systematic review and meta-analysis.Lancet Gastroenterol Hepatol. 2022;7:851–61. [DOI] [PubMed]
Hashimoto E, Tokushige K, Ludwig J. Diagnosis and classification of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis: Current concepts and remaining challenges.Hepatol Res. 2015;45:20–8. [DOI] [PubMed]
Younossi Z, Tacke F, Arrese M, Chander Sharma B, Mostafa I, Bugianesi E, et al. Global Perspectives on Nonalcoholic Fatty Liver Disease and Nonalcoholic Steatohepatitis.Hepatology. 2019;69:2672–82. [DOI] [PubMed]
Lee BW, Lee YH, Park CY, Rhee EJ, Lee WY, Kim NH, et al.; Korean Diabetes Association (KDA) Fatty Liver Research Group. Non-Alcoholic Fatty Liver Disease in Patients with Type 2 Diabetes Mellitus: A Position Statement of the Fatty Liver Research Group of the Korean Diabetes Association.Diabetes Metab J. 2020;44:382–401. [DOI] [PubMed] [PMC]
Younossi Z, Anstee QM, Marietti M, Hardy T, Henry L, Eslam M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention.Nat Rev Gastroenterol Hepatol. 2018;15:11–20. [DOI] [PubMed]
Lu H, Zeng L, Liang B, Shu X, Xie D. High prevalence of coronary heart disease in type 2 diabetic patients with non-alcoholic fatty liver disease.Arch Med Res. 2009;40:571–5. [DOI] [PubMed]
Schuppan D, Schattenberg JM. Non-alcoholic steatohepatitis: pathogenesis and novel therapeutic approaches.J Gastroenterol Hepatol. 2013;28:68–76. [DOI] [PubMed]
Gusdon AM, Song KX, Qu S. Nonalcoholic Fatty liver disease: pathogenesis and therapeutics from a mitochondria-centric perspective.Oxid Med Cell Longev. 2014;2014:637027. [DOI] [PubMed] [PMC]
Nguyen V, George J. Nonalcoholic Fatty Liver Disease Management: Dietary and Lifestyle Modifications.Semin Liver Dis. 2015;35:318–37. [DOI] [PubMed]
Chalasani N, Younossi Z, Lavine JE, Charlton M, Cusi K, Rinella M, et al. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases.Hepatology. 2018;67:328–57. [DOI] [PubMed]
Glass LM, Dickson RC, Anderson JC, Suriawinata AA, Putra J, Berk BS, et al. Total body weight loss of ≥ 10 % is associated with improved hepatic fibrosis in patients with nonalcoholic steatohepatitis.Dig Dis Sci. 2015;60:1024–30. [DOI] [PubMed]
European Association for the Study of the Liver (EASL); European Association for the Study of Diabetes (EASD); European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines for the management of non-alcoholic fatty liver disease.Diabetologia. 2016;59:1121–40. [DOI] [PubMed]
Ghosal S, Datta D, Sinha B. A meta-analysis of the effects of glucagon-like-peptide 1 receptor agonist (GLP1-RA) in nonalcoholic fatty liver disease (NAFLD) with type 2 diabetes (T2D).Sci Rep. 2021;11:22063. [DOI] [PubMed] [PMC]
Papatheodorou SI, Evangelou E. Umbrella Reviews: What They Are and Why We Need Them.Methods Mol Biol. 2022;2345:135–46. [DOI] [PubMed]
Aromataris E, Fernandez R, Godfrey CM, Holly C, Khalil H, Tungpunkom P. Summarizing systematic reviews: methodological development, conduct and reporting of an umbrella review approach.Int J Evid Based Healthc. 2015;13:132–40. [DOI] [PubMed]
Huang Y, Chen Z, Chen B, Li J, Yuan X, Li J, et al. Dietary sugar consumption and health: umbrella review.BMJ. 2023;381:e071609. [DOI] [PubMed] [PMC]
Poole R, Kennedy OJ, Roderick P, Fallowfield JA, Hayes PC, Parkes J. Coffee consumption and health: umbrella review of meta-analyses of multiple health outcomes.BMJ. 2017;359:j5024. [DOI] [PubMed] [PMC]
Shea BJ, Grimshaw JM, Wells GA, Boers M, Andersson N, Hamel C, et al. Development of AMSTAR: a measurement tool to assess the methodological quality of systematic reviews.BMC Med Res Methodol. 2007;7:10. [DOI] [PubMed] [PMC]
Guyatt G, Oxman AD, Akl EA, Kunz R, Vist G, Brozek J, et al. GRADE guidelines: 1. Introduction-GRADE evidence profiles and summary of findings tables.J Clin Epidemiol. 2011;64:383–94. [DOI] [PubMed]
Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test.BMJ. 1997;315:629–34. [DOI] [PubMed] [PMC]
Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.BMJ. 2021;372:n71. [DOI] [PubMed] [PMC]
Peng S, Liu L, Xie Z, Zhang X, Xie C, Ye S, et al. Chinese Herbal Medicine for Type 2 Diabetes Mellitus With Nonalcoholic Fatty Liver Disease: A Systematic Review and Meta-Analysis.Front Pharmacol. 2022;13:863839. [DOI] [PubMed] [PMC]
Zeng Y, Zhang X, Luo W, Sheng Y. Effect of exercise intervention on clinical parameters in patients with non-alcoholic fatty liver disease and type 2 diabetes mellitus: a meta-analysis of randomized controlled trials.Eur J Gastroenterol Hepatol. 2024;36:1–12. [DOI] [PubMed]
Wei Q, Xu X, Guo L, Li J, Li L. Effect of SGLT2 Inhibitors on Type 2 Diabetes Mellitus With Non-Alcoholic Fatty Liver Disease: A Meta-Analysis of Randomized Controlled Trials.Front Endocrinol (Lausanne). 2021;12:635556. [DOI] [PubMed] [PMC]
Song T, Jia Y, Li Z, Wang F, Ren L, Chen S. Effects of Liraglutide on Nonalcoholic Fatty Liver Disease in Patients with Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis.Diabetes Ther. 2021;12:1735–49. [DOI] [PubMed] [PMC]
Wang X, Wu N, Sun C, Jin D, Lu H. Effects of SGLT-2 inhibitors on adipose tissue distribution in patients with type 2 diabetes mellitus: a systematic review and meta-analysis of randomized controlled trials.Diabetol Metab Syndr. 2023;15:113. [DOI] [PubMed] [PMC]
Jin Z, Yuan Y, Zheng C, Liu S, Weng H. Effects of sodium-glucose co-transporter 2 inhibitors on liver fibrosis in non-alcoholic fatty liver disease patients with type 2 diabetes mellitus: An updated meta-analysis of randomized controlled trials.J Diabetes Complications. 2023;37:108558. [DOI] [PubMed]
Xing B, Zhao Y, Dong B, Zhou Y, Lv W, Zhao W. Effects of sodium-glucose cotransporter 2 inhibitors on non-alcoholic fatty liver disease in patients with type 2 diabetes: A meta-analysis of randomized controlled trials.J Diabetes Investig. 2020;11:1238–47. [DOI] [PubMed] [PMC]
Zhu Y, Xu J, Zhang D, Mu X, Shi Y, Chen S, et al. Efficacy and Safety of GLP-1 Receptor Agonists in Patients With Type 2 Diabetes Mellitus and Non-Alcoholic Fatty Liver Disease: A Systematic Review and Meta-Analysis.Front Endocrinol (Lausanne). 2021;12:769069. [DOI] [PubMed] [PMC]
Duan H, Chen F. Efficacy of dapagliflozin to treat nonalcoholic fatty liver disease in patients with type 2 diabetes: A meta-analysis.Medicine (Baltimore). 2025;104:e40836. [DOI] [PubMed] [PMC]
Ong Lopez AMC, Pajimna JAT. Efficacy of sodium glucose cotransporter 2 inhibitors on hepatic fibrosis and steatosis in non-alcoholic fatty liver disease: an updated systematic review and meta-analysis.Sci Rep. 2024;14:2122. [DOI] [PubMed] [PMC]
Wong C, Lee MH, Yaow CYL, Chin YH, Goh XL, Ng CH, et al. Glucagon-Like Peptide-1 Receptor Agonists for Non-Alcoholic Fatty Liver Disease in Type 2 Diabetes: A Meta-Analysis.Front Endocrinol (Lausanne). 2021;12:609110. [DOI] [PubMed] [PMC]
Ma G, Zhang S, Yu B. Impact of Dipeptidyl Peptidase-4 Inhibitors on Aminotransferases Levels in Patients with Type 2 Diabetes Mellitus With Nonalcoholic Fatty Liver Disease: A Meta-Analysis of Randomized Controlled Trial.Curr Ther Res Clin Exp. 2024;102:100768. [DOI] [PubMed] [PMC]
Song T, Chen S, Zhao H, Wang F, Song H, Tian D, et al. Meta-analysis of the effect of sodium-glucose cotransporter 2 inhibitors on hepatic fibrosis in patients with type 2 diabetes mellitus complicated with non-alcoholic fatty liver disease.Hepatol Res. 2021;51:641–51. [DOI] [PubMed]
Sinha B, Datta D, Ghosal S. Meta-analysis of the effects of sodium glucose cotransporter 2 inhibitors in non-alcoholic fatty liver disease patients with type 2 diabetes.JGH Open. 2020;5:219–27. [DOI] [PubMed] [PMC]
Nowrouzi-Sohrabi P, Rezaei S, Jalali M, Ashourpour M, Ahmadipour A, Keshavarz P, et al. The effects of glucagon-like peptide-1 receptor agonists on glycemic control and anthropometric profiles among diabetic patients with non-alcoholic fatty liver disease: A systematic review and meta-analysis of randomized controlled trials.Eur J Pharmacol. 2021;893:173823. [DOI] [PubMed]
Hu C, Qu T, Li L, Huang Y, Liu H, Rao C. Therapeutic outcome of dapagliflozin in patients with type 2 diabetes and non-alcoholic fatty liver disease: a meta-analysis of randomized controlled trials.Afr Health Sci. 2023;23:416–21. [DOI] [PubMed] [PMC]
Arab JP, Arrese M, Trauner M. Recent Insights into the Pathogenesis of Nonalcoholic Fatty Liver Disease.Annu Rev Pathol. 2018;13:321–50. [DOI] [PubMed]
Parthasarathy G, Revelo X, Malhi H. Pathogenesis of Nonalcoholic Steatohepatitis: An Overview.Hepatol Commun. 2020;4:478–92. [DOI] [PubMed] [PMC]
Gupta NA, Mells J, Dunham RM, Grakoui A, Handy J, Saxena NK, et al. Glucagon-like peptide-1 receptor is present on human hepatocytes and has a direct role in decreasing hepatic steatosis in vitro by modulating elements of the insulin signaling pathway.Hepatology. 2010;51:1584–92. [DOI] [PubMed] [PMC]
Cuthbertson DJ, Irwin A, Gardner CJ, Daousi C, Purewal T, Furlong N, et al. Improved glycaemia correlates with liver fat reduction in obese, type 2 diabetes, patients given glucagon-like peptide-1 (GLP-1) receptor agonists.PLoS One. 2012;7:e50117. [DOI] [PubMed] [PMC]
Ben-Shlomo S, Zvibel I, Shnell M, Shlomai A, Chepurko E, Halpern Z, et al. Glucagon-like peptide-1 reduces hepatic lipogenesis via activation of AMP-activated protein kinase.J Hepatol. 2011;54:1214–23. [DOI] [PubMed]
Ding X, Saxena NK, Lin S, Gupta NA, Anania FA. Exendin-4, a glucagon-like protein-1 (GLP-1) receptor agonist, reverses hepatic steatosis in ob/ob mice.Hepatology. 2006;43:173–81. [DOI] [PubMed] [PMC]
Gastaldelli A, Gaggini M, Daniele G, Ciociaro D, Cersosimo E, Tripathy D, et al. Exenatide improves both hepatic and adipose tissue insulin resistance: A dynamic positron emission tomography study.Hepatology. 2016;64:2028–37. [DOI] [PubMed]
Bradley DP, Kulstad R, Schoeller DA. Exenatide and weight loss.Nutrition. 2010;26:243–9. [DOI] [PubMed]
Clamp LD, Hume DJ, Lambert EV, Kroff J. Enhanced insulin sensitivity in successful, long-term weight loss maintainers compared with matched controls with no weight loss history.Nutr Diabetes. 2017;7:e282. [DOI] [PubMed] [PMC]
Gupta NA, Kolachala VL, Jiang R, Abramowsky C, Romero R, Fifadara N, et al. The glucagon-like peptide-1 receptor agonist Exendin 4 has a protective role in ischemic injury of lean and steatotic liver by inhibiting cell death and stimulating lipolysis.Am J Pathol. 2012;181:1693–701. [DOI] [PubMed] [PMC]
Sharma S, Mells JE, Fu PP, Saxena NK, Anania FA. GLP-1 analogs reduce hepatocyte steatosis and improve survival by enhancing the unfolded protein response and promoting macroautophagy.PLoS One. 2011;6:e25269. [DOI] [PubMed] [PMC]
Trevaskis JL, Griffin PS, Wittmer C, Neuschwander-Tetri BA, Brunt EM, Dolman CS, et al. Glucagon-like peptide-1 receptor agonism improves metabolic, biochemical, and histopathological indices of nonalcoholic steatohepatitis in mice.Am J Physiol Gastrointest Liver Physiol. 2012;302:G762–72. [DOI] [PubMed]
Lee J, Hong SW, Chae SW, Kim DH, Choi JH, Bae JC, et al. Exendin-4 improves steatohepatitis by increasing Sirt1 expression in high-fat diet-induced obese C57BL/6J mice.PLoS One. 2012;7:e31394. [DOI] [PubMed] [PMC]
Ji J, Feng M, Huang Y, Niu X. Liraglutide inhibits receptor for advanced glycation end products (RAGE)/reduced form of nicotinamide-adenine dinucleotide phosphate (NAPDH) signaling to ameliorate non-alcoholic fatty liver disease (NAFLD) in vivo and vitro.Bioengineered. 2022;13:5091–102. [DOI] [PubMed] [PMC]
Tsiampali C, Vachliotis ID, Goulas A, Polyzos SA. Animal studies on glucagon-like peptide-1 receptor agonists and related polyagonists in nonalcoholic fatty liver disease.Hormones (Athens). 2024;23:611–9. [DOI] [PubMed] [PMC]
Daniele G, Xiong J, Solis-Herrera C, Merovci A, Eldor R, Tripathy D, et al. Dapagliflozin Enhances Fat Oxidation and Ketone Production in Patients With Type 2 Diabetes.Diabetes Care. 2016;39:2036–41. [DOI] [PubMed] [PMC]
Shiba K, Tsuchiya K, Komiya C, Miyachi Y, Mori K, Shimazu N, et al. Canagliflozin, an SGLT2 inhibitor, attenuates the development of hepatocellular carcinoma in a mouse model of human NASH.Sci Rep. 2018;8:2362. [DOI] [PubMed] [PMC]
Ferré P, Foufelle F. Hepatic steatosis: a role for de novo lipogenesis and the transcription factor SREBP-1c.Diabetes Obes Metab. 2010;12:83–92. [DOI] [PubMed]
Jojima T, Tomotsune T, Iijima T, Akimoto K, Suzuki K, Aso Y. Empagliflozin (an SGLT2 inhibitor), alone or in combination with linagliptin (a DPP-4 inhibitor), prevents steatohepatitis in a novel mouse model of non-alcoholic steatohepatitis and diabetes.Diabetol Metab Syndr. 2016;8:45. [DOI] [PubMed] [PMC]
Ideta T, Shirakami Y, Miyazaki T, Kochi T, Sakai H, Moriwaki H, et al. The Dipeptidyl Peptidase-4 Inhibitor Teneligliptin Attenuates Hepatic Lipogenesis via AMPK Activation in Non-Alcoholic Fatty Liver Disease Model Mice.Int J Mol Sci. 2015;16:29207–18. [DOI] [PubMed] [PMC]
Sharma A, Virmani T, Sharma A, Chhabra V, Kumar G, Pathak K, et al. Potential Effect of DPP-4 Inhibitors Towards Hepatic Diseases and Associated Glucose Intolerance.Diabetes Metab Syndr Obes. 2022;15:1845–64. [DOI] [PubMed] [PMC]
Vavrinec P, Henning RH, Landheer SW, Wang Y, Deelman LE, Dokkum RP, et al. Vildagliptin restores renal myogenic function and attenuates renal sclerosis independently of effects on blood glucose or proteinuria in zucker diabetic fatty rat.Curr Vasc Pharmacol. 2014;12:836–44. [DOI] [PubMed]
Ozutsumi T, Namisaki T, Shimozato N, Kaji K, Tsuji Y, Kaya D, et al. Combined Treatment with Sodium-Glucose Cotransporter-2 Inhibitor (Canagliflozin) and Dipeptidyl Peptidase-4 Inhibitor (Teneligliptin) Alleviates NASH Progression in A Non-Diabetic Rat Model of Steatohepatitis.Int J Mol Sci. 2020;21:2164. [DOI] [PubMed] [PMC]
Maiztegui B, Borelli MI, Madrid VG, Del Zotto H, Raschia MA, Francini F, et al. Sitagliptin prevents the development of metabolic and hormonal disturbances, increased β-cell apoptosis and liver steatosis induced by a fructose-rich diet in normal rats.Clin Sci (Lond). 2011;120:73–80. [DOI] [PubMed]
Karlas T, Petroff D, Sasso M, Fan JG, Mi YQ, de Lédinghen V, et al. Individual patient data meta-analysis of controlled attenuation parameter (CAP) technology for assessing steatosis.J Hepatol. 2017;66:1022–30. [DOI] [PubMed]
Firneisz G, Lakatos PL, Szalay F; Hungarian Viral Hepatitis Study Group. Serum dipeptidyl peptidase IV (DPP IV, CD26) activity in chronic hepatitis C.Scand J Gastroenterol. 2001;36:877–80. [DOI] [PubMed]
Aso Y, Terasawa T, Kato K, Jojima T, Suzuki K, Iijima T, et al. The serum level of soluble CD26/dipeptidyl peptidase 4 increases in response to acute hyperglycemia after an oral glucose load in healthy subjects: association with high-molecular weight adiponectin and hepatic enzymes.Transl Res. 2013;162:309–16. [DOI] [PubMed]
Sagara M, Iijima T, Kase M, Kato K, Sakurai S, Tomaru T, et al. Serum levels of soluble dipeptidyl peptidase-4 in type 2 diabetes are associated with severity of liver fibrosis evaluated by transient elastography (FibroScan) and the FAST (FibroScan-AST) score, a novel index of non-alcoholic steatohepatitis with significant fibrosis.J Diabetes Complications. 2021;35:107885. [DOI] [PubMed]
Banerji MA, Lebowitz J, Chaiken RL, Gordon D, Kral JG, Lebovitz HE. Relationship of visceral adipose tissue and glucose disposal is independent of sex in black NIDDM subjects.Am J Physiol. 1997;273:E425–32. [DOI] [PubMed]
Park HK, Kwak MK, Kim HJ, Ahima RS. Linking resistin, inflammation, and cardiometabolic diseases.Korean J Intern Med. 2017;32:239–47. [DOI] [PubMed] [PMC]
Yavari A, Hajiyev AM, Naghizadeh F. The effect of aerobic exercise on glycosylated hemoglobin values in type 2 diabetes patients.J Sports Med Phys Fitness. 2010;50:501–5. [PubMed]
American Diabetes Association. 7. Obesity Management for the Treatment of Type 2 Diabetes: Standards of Medical Care in Diabetes—2018.Diabetes Care. 2018;41:S65–72. [DOI] [PubMed]
Oh S, Tsujimoto T, Kim B, Uchida F, Suzuki H, Iizumi S, et al. Weight-loss-independent benefits of exercise on liver steatosis and stiffness in Japanese men with NAFLD.JHEP Rep. 2021;3:100253. [DOI] [PubMed] [PMC]
Schult A, Eriksson H, Wallerstedt S, Kaczynski J. Overweight and hypertriglyceridemia are risk factors for liver cirrhosis in middle-aged Swedish men.Scand J Gastroenterol. 2011;46:738–44. [DOI] [PubMed]
Chen M, Zhu JY, Mu WJ, Guo L. Cysteine dioxygenase type 1 (CDO1): Its functional role in physiological and pathophysiological processes.Genes Dis. 2022;10:877–90. [DOI] [PubMed] [PMC]
Chen M, Zhu JY, Mu WJ, Luo HY, Li Y, Li S, et al. Cdo1-Camkk2-AMPK axis confers the protective effects of exercise against NAFLD in mice.Nat Commun. 2023;14:8391. [DOI] [PubMed] [PMC]
Gao Y, Zhang W, Zeng LQ, Bai H, Li J, Zhou J, et al. Exercise and dietary intervention ameliorate high-fat diet-induced NAFLD and liver aging by inducing lipophagy.Redox Biol. 2020;36:101635. [DOI] [PubMed] [PMC]
Zhu W, Sahar NE, Javaid HMA, Pak ES, Liang G, Wang Y, et al. Exercise-Induced Irisin Decreases Inflammation and Improves NAFLD by Competitive Binding with MD2.Cells. 2021;10:3306. [DOI] [PubMed] [PMC]
Yin R, Xu Y, Wang X, Yang L, Zhao D. Role of Dipeptidyl Peptidase 4 Inhibitors in Antidiabetic Treatment.Molecules. 2022;27:3055. [DOI] [PubMed] [PMC]
Lin T, Li L, Liang C, Peng L. Network Pharmacology-Based Investigation of the Therapeutic Mechanisms of Action of Danning Tablets in Nonalcoholic Fatty Liver Disease.Evid Based Complement Alternat Med. 2021;2021:3495360. [DOI] [PubMed] [PMC]
Shi R, Chai K, Wang H, Guo S, Zhai Y, Huang J, et al. Comparative effectiveness of five Chinese patent medicines for non-alcoholic fatty liver disease: A systematic review and Bayesian network meta-analysis.Phytomedicine. 2024;135:156124. [DOI] [PubMed]
Lijuan D, Shuanglan C, Tianyuan W, Xiaojie Y, Xiuyan L, Hongfei S, et al. Progress of Chinese Medicine in Regulating AMPK Signaling Pathway Against Non-alcoholic Fatty Liver Disease.Chin J Exp Tradit Med Form. 2025:1–26.