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Efficacy of orlistat in non‑alcoholic fatty liver disease: A systematic review and meta‑analysis
Open accessAbstract
In the present meta-analysis, the efficacy and safety of orlistat in the treatment of non-alcoholic fatty liver (NAFLD) and non-alcoholic steatohepatitis (NASH) were evaluated. PubMed, Embase, the Cochrane Library, Web of Science, and Wan Fang data were searched for controlled trials of orlistat in patients with NAFLD or NASH, published before August 2017. Three randomized controlled trials and four single-arm trials were included. The involved participants with NAFLD or NASH (330 patients) were analyzed for clinical outcomes including alteration in hepatic histological variables and biomarkers of liver function. Improvements were observed in levels of alanine aminotransferase [standard mean difference (SMD)=-1.41; P=0.01], aspartate aminotransferase (SMD=-2.06; P=0.0005), γ-glutamyl transpeptidase (SMD=-1.91; P=0.05), glucose [mean difference (MD)=-0.51; P=0.01], triglycerides (MD=-0.93; P=0.01), homeostasis model assessment of insulin resistance index (MD=-1.05; P=0.04) and body mass index (MD=-1.97; P=0.02), but not in liver fibrosis score (SMD=-0.14; P=0.71). On sub-analyses of the different patient groups, no significant differences were observed in patients with NASH. Taken together, these findings demonstrate that orlistat could serve as a therapeutic drug to improve biochemical indicators of liver damage, but not as first-choice drug for the management of NAFLD or NASH; thus suggesting a novel palliative drug only for the treatment of NAFLD.
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A meta-analysis confirmed modest reductions in liver fat and enzymes with orlistat but did not affect liver fibrosis.
“A meta-analysis confirmed modest reductions in liver fat and enzymes but did not affect liver fibrosis.”
From Precision obesity medicine: A phenotype-guided framework for pharmacologic therapy across the lifespan (2025) · cites this paper as [58]
Although biopsy-controlled data are lacking, orlistat improves steatosis, ALT, and insulin sensitivity in MASLD when paired with lifestyle changes.
“Although biopsy-controlled data are lacking, orlistat improves steatosis, ALT, and insulin sensitivity in MASLD when paired with lifestyle changes.”
From Precision obesity medicine: A phenotype-guided framework for pharmacologic therapy across the lifespan (2025) · cites this paper as [58]
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Metadata
- Authors
- Wang, H., Wang, L., Cheng, Y., Xia, Z., Liao, Y., & Cao, J.
- Affiliations
- Xuzhou Medical College (CN)
- Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221002, P.R. China
- Venue
- Biomedical Reports
- Publisher
- Spandidos Publications
- Published
- 2018-05-22
- Volume
- 9
- Issue
- 1
- Pages
- 90-96
- ISSN
- 2049-9434 (ISSN-L)
- 2049-9442
- PMC
- PMC6007047
- OpenAlex
- W2804448616
- Cited by
- 70
- References
- 37
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 11 · 2023: 10 · 2022: 12 · 2021: 9 · 2020: 11 · 2019: 5 · 2018: 2
- FWCI
- 0.96
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Biomedical Reports (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Pharmacology (medical) › Pharmacology and Obesity Treatment
- Health Sciences › Medicine › Surgery › Bariatric Surgery and Outcomes
- Keywords
- orlistat, non-alcoholic fatty liver disease, nonalcoholic steatohepatitis, lipase inhibitors, alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transferase, insulin resistance, triglycerides, body mass index, liver fibrosis, drug safety and efficacy
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