2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Fibrosis‐4 Index as an Independent Predictor of Mortality and Liver‐Related Outcomes in NAFLD

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease worldwide, and its prevalence continues to rise. Fibrosis‐4 index (FIB‐4) has been shown to be a prognostic marker of liver‐related outcomes in patients with NAFLD. We analyzed data from TriNetX global federated research network, combining data on 30 million patients. Patients were categorized into three diagnostic groups: NAFLD, nonalcoholic steatohepatitis (NASH), and at risk of NASH. Primary outcome was all‐cause mortality, and secondary outcomes included progression to NASH, development of cirrhosis, end‐stage liver disease, hepatocellular carcinoma (HCC), and liver transplantation. A total of 442,277 subjects (1.5% of the cohort) were assessed, and 81,108 were retained for analysis. Median follow‐up was 34.8 months (interquartile range 12.2). FIB‐4 was < 1.3 in 52.3% patients and ≥ 2.67 in 11.4% patients. In multivariate analysis, FIB‐4 ≥ 2.67 was significantly and independently associated with all‐cause mortality (hazard ratio [HR] 2.49, 95% confidence interval [CI] 2.20‐2.82, P < 0.001) as well as with progression to NASH (HR 5.78, 95% CI 4.72‐7.07, P < 0.001), cirrhosis (HR 2.04, 95% CI 1.86‐2.24, P < 0.001), end‐stage liver disease (HR 1.86, 95% CI 1.68‐2.05, P < 0.001), HCC (HR 3.66, 95% CI 2.71‐4.94, P < 0.001), and liver transplantation (HR 7.98, 95% CI 4.62‐13.79, P < 0.001). Conclusion: In a real‐world nationwide database, FIB‐4 ≥ 2.67 was a strong predictor of both all‐cause mortality and liver‐related adverse outcomes independently of the baseline diagnostic group and common risk factors. Our findings indicate that FIB‐4 could play a role as a risk‐stratification tool for a population health approach. Significant underdiagnosis of both NAFLD/NASH and NASH cirrhosis in electronic medical records was observed.

          Abstract

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: not found

          Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes.

          Nonalcoholic fatty liver disease (NAFLD) is a major cause of liver disease worldwide. We estimated the global prevalence, incidence, progression, and outcomes of NAFLD and nonalcoholic steatohepatitis (NASH). PubMed/MEDLINE were searched from 1989 to 2015 for terms involving epidemiology and progression of NAFLD. Exclusions included selected groups (studies that exclusively enrolled morbidly obese or diabetics or pediatric) and no data on alcohol consumption or other liver diseases. Incidence of hepatocellular carcinoma (HCC), cirrhosis, overall mortality, and liver-related mortality were determined. NASH required histological diagnosis. All studies were reviewed by three independent investigators. Analysis was stratified by region, diagnostic technique, biopsy indication, and study population. We used random-effects models to provide point estimates (95% confidence interval [CI]) of prevalence, incidence, mortality and incidence rate ratios, and metaregression with subgroup analysis to account for heterogeneity. Of 729 studies, 86 were included with a sample size of 8,515,431 from 22 countries. Global prevalence of NAFLD is 25.24% (95% CI: 22.10-28.65) with highest prevalence in the Middle East and South America and lowest in Africa. Metabolic comorbidities associated with NAFLD included obesity (51.34%; 95% CI: 41.38-61.20), type 2 diabetes (22.51%; 95% CI: 17.92-27.89), hyperlipidemia (69.16%; 95% CI: 49.91-83.46%), hypertension (39.34%; 95% CI: 33.15-45.88), and metabolic syndrome (42.54%; 95% CI: 30.06-56.05). Fibrosis progression proportion, and mean annual rate of progression in NASH were 40.76% (95% CI: 34.69-47.13) and 0.09 (95% CI: 0.06-0.12). HCC incidence among NAFLD patients was 0.44 per 1,000 person-years (range, 0.29-0.66). Liver-specific mortality and overall mortality among NAFLD and NASH were 0.77 per 1,000 (range, 0.33-1.77) and 11.77 per 1,000 person-years (range, 7.10-19.53) and 15.44 per 1,000 (range, 11.72-20.34) and 25.56 per 1,000 person-years (range, 6.29-103.80). Incidence risk ratios for liver-specific and overall mortality for NAFLD were 1.94 (range, 1.28-2.92) and 1.05 (range, 0.70-1.56).
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention

              NAFLD is one of the most important causes of liver disease worldwide and will probably emerge as the leading cause of end-stage liver disease in the coming decades, with the disease affecting both adults and children. The epidemiology and demographic characteristics of NAFLD vary worldwide, usually parallel to the prevalence of obesity, but a substantial proportion of patients are lean. The large number of patients with NAFLD with potential for progressive liver disease creates challenges for screening, as the diagnosis of NASH necessitates invasive liver biopsy. Furthermore, individuals with NAFLD have a high frequency of metabolic comorbidities and could place a growing strain on health-care systems from their need for management. While awaiting the development effective therapies, this disease warrants the attention of primary care physicians, specialists and health policy makers.
                Bookmark

                Author and article information

                Contributors
                mlai@bidmc.harvard.edu
                Journal
                Hepatol Commun
                Hepatol Commun
                10.1002/(ISSN)2471-254X
                HEP4
                Hepatology Communications
                John Wiley and Sons Inc. (Hoboken )
                2471-254X
                30 December 2021
                April 2022
                : 6
                : 4 ( doiID: 10.1002/hep4.v6.4 )
                : 765-779
                Affiliations
                [ 1 ] Division of Gastroenterology and Hepatology Beth Israel Deaconess Medical Center Harvard Medical School Boston MA USA
                [ 2 ] Division of Gastroenterology and Hepatology Lausanne University Hospital and University of Lausanne Switzerland
                [ 3 ] Trio Health Analytics Cypress TX USA
                [ 4 ] Center for Liver Diseases Department of Medicine Inova Fairfax Hospital Falls Church VA USA
                [ 5 ] Betty and Guy Beatty Center for Integrated Research Inova Health System Falls Church VA USA
                Author notes
                [*] [* ] ADDRESS CORRESPONDENCE AND REPRINT REQUESTS TO:

                Michelle Lai

                Division of Gastroenterology and Hepatology

                Beth Israel Deaconess Medical Center

                Harvard Medical School, Liver Center

                110 Francis St. Suite 8E

                Boston, MA 02115, USA

                E‐mail: mlai@ 123456bidmc.harvard.edu

                Tel.:+1‐617‐632‐1070

                Author information
                https://orcid.org/0000-0001-9313-577X
                Article
                HEP41841
                10.1002/hep4.1841
                8948572
                34970870
                55b90058-c54e-4da8-a0b0-dc2c473a1783
                © 2021 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 30 July 2021
                : 08 February 2021
                : 21 September 2021
                Page count
                Figures: 3, Tables: 4, Pages: 15, Words: 8658
                Funding
                Funded by: University Hospital of Lausanne (Centre Hospitalier Universitaire Vaudois)
                Funded by: Gottfried und Julia Bangerter‐Rhyner‐Stiftung
                Funded by: Novartis Foundation for Medical‐Biological Research
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                April 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.2 mode:remove_FC converted:25.03.2022

                Comments

                Comment on this article