Disease State Transition Probabilities Across the Spectrum of NAFLD: A Systematic Review and Meta-Analysis of Paired Biopsy or Imaging Studies

Phuc Le*, Julia Yang Payne, Lu Zhang, Abhishek Deshpande, Michael B. Rothberg, Naim Alkhouri, William Herman, Adrian V. Hernandez, Mary Schleicher, Wen Ye, Srinivasan Dasarathy

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

26 Scopus citations

Abstract

Background & Aims: We conducted a meta-analysis to summarize the rates of progression to and regression of nonalcoholic fatty liver (NAFL), nonalcoholic steatohepatitis (NASH), and fibrosis in adults with nonalcoholic fatty liver disease (NAFLD). Methods: We searched PubMed/Medline and 4 other databases from 1985 through 2020. We included observational studies and randomized controlled trials in any language that used liver biopsy or imaging to diagnose NAFLD in adults with a follow-up period ≥48 weeks. Rates were calculated as incident cases per 100 person-years and pooled using the random-effects Poisson distribution model. Heterogeneity was assessed using the I2 statistic. Results: We screened 9744 articles and included 54 studies involving 26,738 patients. Among observational studies, 20% of healthy adults developed NAFL (incidence rate, 4.8/100 person-years) while 21% of people with fatty liver had resolution of NAFL (incidence rate, 2.4/100 person-years) after a median of approximately 4.5 years. In addition, 31% of patients developed NASH after 4.7 years (incidence rate, 7.4/100 person-years), whereas in 29% of those with NASH, resolution occurred after a median of 3.5 years (incidence rate, 5.1/100 person-years). Time to progress by 1 fibrosis stage was 9.9, 10.3, 13.3, and 22.2 years for F0, F1, F2, and F3, respectively. Time to regress by 1 stage was 21.3, 12.5, 20.4, and 40.0 years for F4, F3, F2, and F1, respectively. Rates estimated from randomized controlled trials were higher than those from observational studies. Conclusions: In our meta-analysis, progression to NASH was more common than regression from NASH. Rates of fibrosis progression were similar across baseline stage, but patients with advanced fibrosis were more likely to regress than those with mild fibrosis.

Original languageEnglish (US)
Pages (from-to)1154-1168
Number of pages15
JournalClinical Gastroenterology and Hepatology
Volume21
Issue number5
DOIs
StatePublished - May 2023

Funding

Funding The study was funded by the Agency for Healthcare Research and Quality grant R01HS026937. Also supported by National Institutes of Health grants R01 GM119174, R01 DK113196, P50 AA024333, R01 AA021890, 3U01AA026976, U01 AA 026976, R56HL141744, U01 DK061732, 5U01 DK062470-17S2, and R21 AR 071046, which are independent of the submitted work (S.D.). Conflicts of interest These authors disclose the following: Naim Alkhouri is a speaker for Echosens (makers of Fibroscan), and has received research funding from Gilead, Intercept, Allergan, Cirius, Madrigal, and Genfit, which was not related to this study; Abhishek Deshpande is a consultant for Merck; and William Herman serves on a Data Safety Monitoring Board for Merck. The remaining authors disclose no conflicts. Funding The study was funded by the Agency for Healthcare Research and Quality grant R01HS026937 . Also supported by National Institutes of Health grants R01 GM119174, R01 DK113196, P50 AA024333, R01 AA021890, 3U01AA026976, U01 AA 026976, R56HL141744, U01 DK061732, 5U01 DK062470-17S2, and R21 AR 071046, which are independent of the submitted work (S.D.).

Keywords

  • Fibrosis
  • Meta-Analysis
  • Nonalcoholic Steatohepatitis
  • Simple Steatosis

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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