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      Incidence and Progression of Alcohol-Associated Liver Disease After Medical Therapy for Alcohol Use Disorder

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          Key Points

          Question

          Are patients with alcohol use disorder (AUD) who receive medical addiction therapy less likely to develop alcohol-associated liver disease (ALD)?

          Findings

          In this cohort study of 9635 patients with AUD, those who received medical addiction therapy had a significantly lower risk of developing ALD, whereas patients with cirrhosis who received medical addiction therapy had a significantly lower incidence of hepatic decompensation.

          Meaning

          Findings from this study suggest an association between use of medical addiction therapy for AUD and decreased incidence and progression of ALD.

          Abstract

          Importance

          Alcohol-associated liver disease (ALD) is one of the most devastating complications of alcohol use disorder (AUD), an increasingly prevalent condition. Medical addiction therapy for AUD may play a role in protecting against the development and progression of ALD.

          Objective

          To ascertain whether medical addiction therapy was associated with an altered risk of developing ALD in patients with AUD.

          Design, Setting, and Participants

          This retrospective cohort study used the Mass General Brigham Biobank, an ongoing research initiative that had recruited 127 480 patients between its start in 2010 and August 17, 2021, when data for the present study were retrieved. The mean follow-up duration from AUD diagnosis was 9.2 years. International Statistical Classification of Diseases and Related Health Problems, Tenth Revision diagnosis codes were used to identify ALD and AUD diagnoses.

          Exposures

          Medical addiction therapy was defined as the documented use of disulfiram, acamprosate, naltrexone, gabapentin, topiramate, or baclofen. Patients were considered to be treated if they initiated medical addiction therapy before the relevant outcome.

          Main Outcomes and Measures

          Adjusted odds ratios (aORs) for the development of ALD and hepatic decompensation were calculated and adjusted for multiple risk factors.

          Results

          The cohort comprised 9635 patients with AUD, of whom 5821 were male individuals (60.4%), and the mean (SD) age was 54.8 (16.5) years. A total of 1135 patients (11.8%) had ALD and 3906 patients (40.5%) were treated with medical addiction therapy. In multivariable analyses, medical addiction therapy for AUD was associated with decreased incidence of ALD (aOR, 0.37; 95% CI, 0.31-0.43; P < .001). This association was evident for naltrexone (aOR, 0.67; 95% CI, 0.46-0.95; P = .03), gabapentin (aOR, 0.36; 95% CI, 0.30-0.43; P < .001), topiramate (aOR, 0.47; 95% CI, 0.32-0.66; P < .001), and baclofen (aOR, 0.57; 95% CI, 0.36-0.88; P = .01). In addition, pharmacotherapy for AUD was associated with lower incidence of hepatic decompensation in patients with cirrhosis (aOR, 0.35; 95% CI, 0.23-0.53, P < .001), including naltrexone (aOR, 0.27; 95% CI, 0.10-0.64; P = .005) and gabapentin (aOR, 0.36; 95% CI, 0.23-0.56; P < .001). This association persisted even when medical addiction therapy was initiated only after the diagnosis of cirrhosis (aOR, 0.41; 95% CI, 0.23-0.71; P = .002).

          Conclusions and Relevance

          Results of this study showed that receipt of medical addiction therapy for AUD was associated with reduced incidence and progression of ALD. The associations of individual pharmacotherapy with the outcomes of ALD and hepatic decompensation varied widely.

          Abstract

          This cohort study assesses the association between pharmacotherapy and the development of alcohol-associated liver disease in patients with alcohol use disorder.

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          Most cited references43

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          Global burden of alcoholic liver diseases.

          Liver diseases contribute markedly to the global burden of mortality and disease. This paper provides an overview from a global perspective of the contribution of alcohol to liver diseases. The Global Burden of Disease study methodology was used to estimate the burden of alcohol-attributable liver cirrhosis and alcohol-attributable liver cancer in 2010 as measured by deaths and disability adjusted life years (DALYs). This methodology estimates attributable fractions based on alcohol exposure distribution and relative risks associated with different levels of drinking. Globally, in 2010, alcohol-attributable liver cirrhosis was responsible for 493,300 deaths (156,900 female deaths and 336,400 male deaths) and 14,544,000 DALYs (4,112,000 DALYs for women and 10,432,000 DALYs for men), representing 0.9% (0.7% for women and 1.2% for men) of all global deaths and 0.6% (0.4% for women and 0.8% for men) of all global DALYs, and 47.9% of all liver cirrhosis deaths (46.5% for women and 48.5% for men) and 46.9% of all liver cirrhosis DALYs (44.5% for women and 47.9% for men). Alcohol-attributable liver cancer was responsible for 80,600 deaths (14,800 female deaths and 65,900 male deaths) and 2,142,000 DALYs (335,000 DALYs for women and 1,807,000 DALYs for men). The burden of alcohol-attributable liver cirrhosis and liver cancer is high and entirely preventable. Interventions to reduce alcohol consumption are recommended as a population health priority and may range from taxation increases for alcoholic beverages to increases in screening and treatment rates for alcohol use disorders. Copyright © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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            Diagnosis and Treatment of Alcohol‐Related Liver Diseases: 2019 Practice Guidance from the American Association for the Study of Liver Diseases

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

              Diagnosis and Pharmacotherapy of Alcohol Use Disorder

              Alcohol consumption is associated with 88 000 US deaths annually. Although routine screening for heavy alcohol use can identify patients with alcohol use disorder (AUD) and has been recommended, only 1 in 6 US adults report ever having been asked by a health professional about their drinking behavior. Alcohol use disorder, a problematic pattern of alcohol use accompanied by clinically significant impairment or distress, is present in up to 14% of US adults during a 1-year period, although only about 8% of affected individuals are treated in an alcohol treatment facility.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                20 May 2022
                May 2022
                20 May 2022
                : 5
                : 5
                : e2213014
                Affiliations
                [1 ]Alcohol Liver Center, Massachusetts General Hospital, Harvard Medical School, Boston
                [2 ]Gastrointestinal Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston
                [3 ]Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston
                [4 ]Department of Medicine, University of Texas at Southwestern, Dallas
                Author notes
                Article Information
                Accepted for Publication: March 6, 2022.
                Published: May 20, 2022. doi:10.1001/jamanetworkopen.2022.13014
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2022 Vannier AGL et al. JAMA Network Open.
                Corresponding Author: Jay Luther, MD, MGH Alcohol Liver Center, Division of Gastroenterology, Massachusetts General Hospital, 55 Fruit St, Boston, MA 01224 ( jluther1@ 123456mgh.harvard.edu ).
                Author Contributions: Dr Luther had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Drs Schaefer, Goodman, and Luther shared coauthorship.
                Concept and design: All authors.
                Acquisition, analysis, or interpretation of data: Vannier, Shay, Fomin, Patel, Schaefer, Luther.
                Drafting of the manuscript: Vannier, Fomin, Luther.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Vannier, Schaefer, Luther.
                Obtained funding: Schaefer, Luther.
                Administrative, technical, or material support: Vannier, Patel, Luther.
                Supervision: Patel, Schaefer, Goodman, Luther.
                Conflict of Interest Disclosures: None reported.
                Funding/Support: The study was funded by a grant from the National Institutes of Health.
                Role of the Funder/Sponsor: The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
                Additional Contributions: Ryan Adler-Levine, BS, and Fabiola Puello, MFin, assisted with development of the statistical approach. These individuals received no additional compensation, outside of their usual salary, for their contributions.
                Article
                zoi220386
                10.1001/jamanetworkopen.2022.13014
                9123494
                35594048
                ed84f4f2-b4ee-4416-8936-bf761e1b67fa
                Copyright 2022 Vannier AGL et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 13 December 2021
                : 6 March 2022
                Categories
                Research
                Original Investigation
                Online Only
                Gastroenterology and Hepatology

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