Cited by 470Liver Disease Diagnosis and TreatmentPharmacology and Obesity TreatmentBariatric Surgery and Outcomes

Orlistat for overweight subjects with nonalcoholic steatohepatitis: A randomized, prospective trial†‡§

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Harrison, Stephen A., Fecht, Will, Brunt, Elizabeth M., Neuschwander‐Tetri, Brent A.·2009·Hepatology

Abstract

The aim of this study was to determine if orlistat, an inhibitor of fat absorption, combined with caloric restriction in overweight subjects with nonalcoholic steatohepatitis results in weight loss and improved liver histology. Fifty overweight subjects (body mass index = >or=27) with biopsy proven nonalcoholic steatohepatitis were randomized to receive a 1,400 Kcal/day diet plus vitamin E (800 IU) daily with or without orlistat (120 mg three times a day) for 36 weeks. Liver biopsies were repeated at week 36. Twenty-three subjects in the orlistat/diet/vitamin E group and 18 in the diet/vitamin E group completed the study. The mean age was 47 +/- 9.0 (standard deviation) years and mean body mass index was 36.4 +/- 6.3 kg/m(2). Four subjects were diabetic. The orlistat group lost a mean of 8.3% body weight compared to 6.0% in the diet plus vitamin E group (not significant). Both groups also had similarly improved serum aminotransferases, hepatic steatosis, necroinflammation, ballooning, and nonalcoholic fatty liver disease activity scores. Stratified according to weight loss instead of treatment group, a loss of >or=5% body weight (n = 24) compared to <5% body weight (n = 17) correlated with improvement in insulin sensitivity (P = 0.001) and steatosis (P = 0.015). Comparing subjects who lost >or=9% of body weight (n = 16), to those that did not (n = 25), improved insulin sensitivity (P < 0.001), adiponectin (P = 0.03), steatosis (P = 0.005), ballooning (P = 0.04), inflammation (P = 0.045), and nonalcoholic fatty liver disease activity score (P = 0.009) were seen. Increases in adiponectin strongly correlated with improved ballooning and nonalcoholic fatty liver disease activity score (P = 0.03). Orlistat did not enhance weight loss or improve liver enzymes, measures of insulin resistance, and histopathology. However, subjects who lost >or=5% of body weight over 9 months improved insulin resistance and steatosis, and those subjects who lost >or=9% also achieved improved hepatic histologic changes.

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Crossref · 10.1002/hep.22575

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  • Controlled trials (with histological endpoints or liver-related outcomes) of weight-loss agents other than incretin hormone analogues have either not been performed or have been inconclusive.

    “Controlled trials (with histological endpoints or liver-related outcomes) of weight-loss agents other than incretin hormone analogues 433 ( e.g. orlistat, phentermine-topiramate, naltrexone-bupropion) have either not been performed or have been inconclusive.”

    From EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). (2024) · cites this paper as [434]

    The Results (page not provided) describe a randomized orlistat trial with follow-up liver biopsies and no significant between-group differences in biopsy findings. This supports the claim for orlistat, but the paper does not establish whether controlled trials of other named weight-loss agents were absent or inconclusive. (LLM, conf=0.86)

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References 27 · Cited by 470

Research works printed but not linked: 1

  1. Harrison SA, Oliver DA, Gogia S, Neuschwander-Tetri BA. NASH: Clin- ical assessment of 827 patients from two separate academic medical centers with validation of a clinical scoring system for advanced hepatic fibrosis. Gut 2008;57:1441-1447.

Authors
Harrison, S. A., Fecht, W., Brunt, E. M., & Neuschwander‐Tetri, B. A.
Affiliations
  • Brooke Army Medical Center (US)
  • Indianapolis Public Library (US)
  • Washington University in St. Louis (US)
  • Saint Louis University (US)
Corresponding author
Harrison, Stephen A.
Venue
Hepatology
Published
2009-01
Volume
49
Issue
1
Pages
80-86
ISSN
0270-9139 (ISSN-L)
OpenAlex
W1990168800
Cited by
470
References
27
Citations by year
2026: 9 · 2025: 7 · 2024: 17 · 2023: 17 · 2022: 22 · 2021: 25 · 2020: 22 · 2019: 23 · 2018: 29 · 2017: 31 · 2016: 46 · 2015: 40 · 2014: 38 · 2013: 32 · 2012: 35
FWCI
19.11
Type
journal article
Language
en
Open access
Locations
  • Hepatology (publishedVersion)
  • PubMed (publishedVersion)
Funders
U.S. Department of Defense
Topics
  • Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
  • Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
  • Health Sciences › Medicine › Surgery › Bariatric Surgery and Outcomes
Keywords
orlistat, nonalcoholic steatohepatitis, overweight, weight loss, caloric restriction, vitamin E, insulin resistance, adiponectin, hepatic steatosis, liver histopathology, non-alcoholic fatty liver disease, hepatic necroinflammation, transaminases, fat absorption inhibition, obesity treatment
MeSH terms
Orlistat, Adult, Diet, Reducing, Fatty Liver, Female, Humans, Lactones, Male, Middle Aged, Obesity, Weight Loss, Anti-Obesity Agents

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