Safety and efficacy of resmetirom in the treatment of patients with non-alcoholic steatohepatitis and liver fibrosis: a systematic review and meta-analysis

Author:

Raja Adarsh1,Subhash Sagar Raja2,Saeed Sadia3,Zia ul haq Amna4,Khan Owais4,Dileep Bhimani Parshant1,Raja Sandesh4,Deepak Fnu1,Ahmed Muhammad1,Ashir Shafique Muhammad5,Saqlain Mustafa Muhammad5,Sohaib Asghar Muhammad6,Sharma Varsha7

Affiliation:

1. Department of Internal Medicine, Shaheed Mohtarma Benazir Bhutto Medical College Lyari

2. Department of Internal Medicine, Liaquat University of Medical & Health Science, Jamshoro

3. Department of Internal Medicine, Women Medical College Abbotabad, Abbottabad, Pakistan

4. Department of Internal Medicine, Dow University of Health Sciences

5. Department of Internal Medicine, Jinnah Sindh Medical University, Karachi

6. Department of Internal Medicine, Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA

7. Department of Internal Medicine, Nepal Medical College, Gokarneshwar, Nepal

Abstract

Introduction: Non-alcoholic fatty liver disease (NAFLD), spanning from non-alcoholic steatohepatitis (NASH) to liver fibrosis, poses a global health challenge amid rising obesity and metabolic syndrome rates. Effective pharmacological treatments for NASH and liver fibrosis are limited. Objective: This study systematically reviews and meta-analyzes the safety and efficacy of resmetirom, a selective thyroid hormone receptor-β agonist, in NASH and liver fibrosis treatment. By analyzing data from clinical trials, we aim to offer evidence-based recommendations for resmetirom’s use in managing these conditions and identify avenues for future research. Methods: Electronic databases (PubMed, Scopus, Science Direct, Google Scholar, ClinicalTrials.gov, and Cochrane CENTRAL) were systematically searched, supplemented by manual screening of relevant sources. Only English-language randomized controlled trials were included. Data extraction, risk of bias assessment, pooled analyses, and meta-regression were performed. Results: Three randomized controlled trials involving 2231 participants were analyzed. Resmetirom demonstrated significant reductions in hepatic fat fraction [standardized mean difference (SMD) −4.61, 95% CI −6.77 to −2.44, P < 0.0001], NASH resolution without worsening fibrosis [risk ratio (RR) 2.51, 95% CI 1.74–3.64, P = 0.00001), and liver fibrosis improvement (RR 2.31, 95% CI 1.20–4.44, P = 0.01). Secondary outcomes showed significant improvements in lipid profiles, liver enzymes, and NASH biomarkers with resmetirom treatment. Meta-regression revealed associations between covariates and primary outcomes. Conclusion: Resmetirom exhibits promising efficacy in reducing hepatic fat, improving NASH resolution, and ameliorating liver fibrosis with a favorable safety profile. Further research is warranted to validate findings and optimize therapeutic strategies for NASH and liver fibrosis management.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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