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      The Role of Current and Historical Alcohol Use in Hepatic Fibrosis Among HIV-infected Individuals

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          Abstract

          We examined risk factors for advanced hepatic fibrosis (FIB-4 >3.25) including both current alcohol use and a diagnosis of alcohol use disorder among HIV-infected patients. Of the 12,849 patients in our study, 2,133 (17%) reported current hazardous drinking by AUDIT-C, 2,321 (18%) had a diagnosis of alcohol use disorder, 2,376 (18%) were co-infected with chronic hepatitis C (HCV); 596 (5%) had high FIB-4 scores >3.25 as did 364 (15%) of HIV/HCV coinfected patients. In multivariable analysis, HCV (aOR 6.3, 95% CI 5.2–7.5), chronic hepatitis B (aOR 2.0, 95% CI 1.5–2.8), diabetes (aOR 2.3, 95% CI 1.8–2.9), current CD4 <200 cells/mm 3 (aOR 5.4, 95% CI 4.2–6.9) and HIV RNA >500 copies/mL (aOR 1.3, 95% CI 1.0–1.6) were significantly associated with advanced fibrosis. A diagnosis of an alcohol use disorder (aOR 1.9, 95% CI 1.6–2.3) rather than report of current hazardous alcohol use was associated with high FIB-4. However, among HIV/HCV coinfected patients, both current hazardous drinkers (aOR 1.6, 95% CI 1.1–2.4) and current non-drinkers (aOR 1.6, 95% CI 1.2–2.0) were more likely than non-hazardous drinkers to have high FIB-4, with the latter potentially reflecting the impact of sick abstainers. These findings highlight the importance of using a longitudinal measure of alcohol exposure when evaluating the impact of alcohol on liver disease and associated outcomes.

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          Author and article information

          Journal
          9712133
          21042
          AIDS Behav
          AIDS Behav
          AIDS and behavior
          1090-7165
          1573-3254
          23 June 2018
          July 2017
          03 July 2018
          : 21
          : 7
          : 1878-1884
          Affiliations
          [1 ]School of Medicine, Department of Medicine, University of Washington, Seattle, WA, United States
          [2 ]Fenway Institute, Fenway Health, Boston, Massachusetts, United States
          [3 ]School of Medicine, University of California San Francisco, San Francisco, CA, United States
          [4 ]Institute for Global Health and Infectious Diseases, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States
          [5 ]Department of Medicine, Johns Hopkins University, Baltimore, MD, United States
          [6 ]Department of Psychiatry & Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore MD, United States
          [7 ]Department of Medicine, University of California San Diego, San Diego, CA, United States
          [8 ]Department of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AB, United States
          Author notes
          Corresponding author: H. Nina Kim, MD MSc, Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, 325 Ninth Avenue Box 359930, Seattle, WA 98104; hyangkim@ 123456uw.edu
          Alternate corresponding author: Mari M. Kitahata, MD MPH, Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, 325 Ninth Avenue Box 359930, Seattle, WA 98104; kitahata@ 123456uw.edu
          Article
          PMC6029880 PMC6029880 6029880 nihpa976830
          10.1007/s10461-016-1665-6
          6029880
          28035496
          17c46ed2-6fe4-40c1-98fd-edd59cfd7b8a
          History
          Categories
          Article

          alcohol,HIV,liver fibrosis,CNICS
          alcohol, HIV, liver fibrosis, CNICS

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