Impact of Lifetime Alcohol Use on Liver Fibrosis in a Population of HIV-Infected Patients With and Without Hepatitis C Coinfection

Background The effect of alcohol on liver disease in HIV infection has not been well characterized. Methods We performed a cross‐sectional multivariable analysis of the association between lifetime alcohol use and liver fibrosis in a longitudinal cohort of HIV‐infected patients with alcohol problems...

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Veröffentlicht in:Alcoholism, clinical and experimental research clinical and experimental research, 2013-09, Vol.37 (9), p.1527-1535
Hauptverfasser: Fuster, Daniel, Tsui, Judith I., Cheng, Debbie M., Quinn, Emily K., Bridden, Carly, Nunes, David, Libman, Howard, Saitz, Richard, Samet, Jeffrey H.
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container_issue 9
container_start_page 1527
container_title Alcoholism, clinical and experimental research
container_volume 37
creator Fuster, Daniel
Tsui, Judith I.
Cheng, Debbie M.
Quinn, Emily K.
Bridden, Carly
Nunes, David
Libman, Howard
Saitz, Richard
Samet, Jeffrey H.
description Background The effect of alcohol on liver disease in HIV infection has not been well characterized. Methods We performed a cross‐sectional multivariable analysis of the association between lifetime alcohol use and liver fibrosis in a longitudinal cohort of HIV‐infected patients with alcohol problems. Liver fibrosis was estimated with 2 noninvasive indices, “FIB‐4,” which includes platelets, liver enzymes, and age; and aspartate aminotransferase/platelet ratio index (“APRI”), which includes platelets and liver enzymes. FIB‐4 1.5 defined advanced liver fibrosis. The main independent variable was lifetime alcohol consumption (600 kg). Results Subjects (n = 308) were 73% men, mean age 43 years, 49% with hepatitis C virus (HCV) infection, 60% on antiretroviral therapy, 49% with an HIV RNA load
doi_str_mv 10.1111/acer.12129
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Methods We performed a cross‐sectional multivariable analysis of the association between lifetime alcohol use and liver fibrosis in a longitudinal cohort of HIV‐infected patients with alcohol problems. Liver fibrosis was estimated with 2 noninvasive indices, “FIB‐4,” which includes platelets, liver enzymes, and age; and aspartate aminotransferase/platelet ratio index (“APRI”), which includes platelets and liver enzymes. FIB‐4 <1.45 and APRI <0.5 defined the absence of liver fibrosis. FIB‐4 >3.25 and APRI >1.5 defined advanced liver fibrosis. The main independent variable was lifetime alcohol consumption (<150 kg, 150 to 600 kg, >600 kg). Results Subjects (n = 308) were 73% men, mean age 43 years, 49% with hepatitis C virus (HCV) infection, 60% on antiretroviral therapy, 49% with an HIV RNA load <1,000 copies/ml, and 18.7% with a CD4 count <200 cells/mm3. Forty‐five percent had lifetime alcohol consumption >600 kg, 32.7% 150 to 600 kg, and 22.3% <150 kg; 33% had current heavy alcohol use, and 69% had >9 years of heavy episodic drinking. Sixty‐one percent had absence of liver fibrosis and 10% had advanced liver fibrosis based on FIB‐4. In logistic regression analyses, controlling for age, gender, HCV infection, and CD4 count, no association was detected between lifetime alcohol consumption and the absence of liver fibrosis (FIB‐4 <1.45) (adjusted odds ratio [AOR] = 1.12 [95% CI: 0.25 to 2.52] for 150 to 600 kg vs. <150 kg; AOR = 1.11 [95% CI: 0.52 to 2.36] for >600 kg vs. <150 kg; global p = 0.95). Additionally, no association was detected between lifetime alcohol use and advanced liver fibrosis (FIB‐4 >3.25). Results were similar using APRI, and among those with and without HCV infection. Conclusions In this cohort of HIV‐infected patients with alcohol problems, we found no significant association between lifetime alcohol consumption and the absence of liver fibrosis or the presence of advanced liver fibrosis, suggesting that alcohol may be less important than other known factors that promote liver fibrosis in this population.]]></description><identifier>ISSN: 0145-6008</identifier><identifier>EISSN: 1530-0277</identifier><identifier>DOI: 10.1111/acer.12129</identifier><identifier>PMID: 23647488</identifier><identifier>CODEN: ACRSDM</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Age ; Alcohol ; Alcohol Drinking - epidemiology ; Alcohol Drinking - pathology ; Alcoholism - diagnosis ; Alcoholism - epidemiology ; Cohort Studies ; Coinfection - diagnosis ; Coinfection - epidemiology ; Cross-Sectional Studies ; Female ; Hepatitis C - diagnosis ; Hepatitis C - epidemiology ; Hepatitis C Virus ; HIV ; HIV Infections - diagnosis ; HIV Infections - epidemiology ; Humans ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - epidemiology ; Liver Fibrosis ; Longitudinal Studies ; Male ; Middle Aged ; Population Surveillance - methods ; Prospective Studies</subject><ispartof>Alcoholism, clinical and experimental research, 2013-09, Vol.37 (9), p.1527-1535</ispartof><rights>Copyright © 2013 by the Research Society on Alcoholism</rights><rights>Copyright © 2013 by the Research Society on Alcoholism.</rights><rights>2013 Research Society on Alcoholism</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5199-58cbfae27385ba7de10474abdf14aeeebba96cffeabbbcb31a8e51df8836212e3</citedby><cites>FETCH-LOGICAL-c5199-58cbfae27385ba7de10474abdf14aeeebba96cffeabbbcb31a8e51df8836212e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Facer.12129$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Facer.12129$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23647488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fuster, Daniel</creatorcontrib><creatorcontrib>Tsui, Judith I.</creatorcontrib><creatorcontrib>Cheng, Debbie M.</creatorcontrib><creatorcontrib>Quinn, Emily K.</creatorcontrib><creatorcontrib>Bridden, Carly</creatorcontrib><creatorcontrib>Nunes, David</creatorcontrib><creatorcontrib>Libman, Howard</creatorcontrib><creatorcontrib>Saitz, Richard</creatorcontrib><creatorcontrib>Samet, Jeffrey H.</creatorcontrib><title>Impact of Lifetime Alcohol Use on Liver Fibrosis in a Population of HIV-Infected Patients With and Without Hepatitis C Coinfection</title><title>Alcoholism, clinical and experimental research</title><addtitle>Alcohol Clin Exp Res</addtitle><description><![CDATA[Background The effect of alcohol on liver disease in HIV infection has not been well characterized. Methods We performed a cross‐sectional multivariable analysis of the association between lifetime alcohol use and liver fibrosis in a longitudinal cohort of HIV‐infected patients with alcohol problems. Liver fibrosis was estimated with 2 noninvasive indices, “FIB‐4,” which includes platelets, liver enzymes, and age; and aspartate aminotransferase/platelet ratio index (“APRI”), which includes platelets and liver enzymes. FIB‐4 <1.45 and APRI <0.5 defined the absence of liver fibrosis. FIB‐4 >3.25 and APRI >1.5 defined advanced liver fibrosis. The main independent variable was lifetime alcohol consumption (<150 kg, 150 to 600 kg, >600 kg). Results Subjects (n = 308) were 73% men, mean age 43 years, 49% with hepatitis C virus (HCV) infection, 60% on antiretroviral therapy, 49% with an HIV RNA load <1,000 copies/ml, and 18.7% with a CD4 count <200 cells/mm3. Forty‐five percent had lifetime alcohol consumption >600 kg, 32.7% 150 to 600 kg, and 22.3% <150 kg; 33% had current heavy alcohol use, and 69% had >9 years of heavy episodic drinking. Sixty‐one percent had absence of liver fibrosis and 10% had advanced liver fibrosis based on FIB‐4. In logistic regression analyses, controlling for age, gender, HCV infection, and CD4 count, no association was detected between lifetime alcohol consumption and the absence of liver fibrosis (FIB‐4 <1.45) (adjusted odds ratio [AOR] = 1.12 [95% CI: 0.25 to 2.52] for 150 to 600 kg vs. <150 kg; AOR = 1.11 [95% CI: 0.52 to 2.36] for >600 kg vs. <150 kg; global p = 0.95). Additionally, no association was detected between lifetime alcohol use and advanced liver fibrosis (FIB‐4 >3.25). Results were similar using APRI, and among those with and without HCV infection. Conclusions In this cohort of HIV‐infected patients with alcohol problems, we found no significant association between lifetime alcohol consumption and the absence of liver fibrosis or the presence of advanced liver fibrosis, suggesting that alcohol may be less important than other known factors that promote liver fibrosis in this population.]]></description><subject>Adult</subject><subject>Age</subject><subject>Alcohol</subject><subject>Alcohol Drinking - epidemiology</subject><subject>Alcohol Drinking - pathology</subject><subject>Alcoholism - diagnosis</subject><subject>Alcoholism - epidemiology</subject><subject>Cohort Studies</subject><subject>Coinfection - diagnosis</subject><subject>Coinfection - epidemiology</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Hepatitis C - diagnosis</subject><subject>Hepatitis C - epidemiology</subject><subject>Hepatitis C Virus</subject><subject>HIV</subject><subject>HIV Infections - diagnosis</subject><subject>HIV Infections - epidemiology</subject><subject>Humans</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - epidemiology</subject><subject>Liver Fibrosis</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Population Surveillance - methods</subject><subject>Prospective Studies</subject><issn>0145-6008</issn><issn>1530-0277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9vEzEQxVcIRNPChQ-ALHFBlbbY6_3jvSCFpU0ihRAhSo-W7R0Tl911sL2FXvnkuEkbAQd8sTXze08zfknyguAzEs8bocCdkYxk9aNkQgqKU5xV1eNkgklepCXG7Cg59v4aY5yzsnyaHGW0zKucsUnya9FvhQrIarQ0GoLpAU07ZTe2Q5cekB1i_QYcujDSWW88MgMSaG23YyeCie2onC--pItBgwrQonUswxA8ujJhg8TQ7h52DGgO29gL0aNBjTU7QXR4ljzRovPw_P4-SS4vzj8383T5cbZopstUFaSu04IpqQVkFWWFFFULBMcdhGw1yQUASCnqUmkNQkqpJCWCQUFazRgt498APUne7n23o-yhVXFIJzq-daYX7pZbYfjfncFs-Fd7w2lVsLyoosHrewNnv4_gA--NV9B1YgA7ek5yWmdZkbM6oq_-Qa_t6Ia4XqQyVpKaVTRSp3tKxa_1DvRhGIL5XbT8Llq-izbCL_8c_4A-ZBkBsgd-mA5u_2PFp835pwfTdK8xPsDPg0a4b7ys4t78ajXjH1az9-_Wq5xT-hu7iMA3</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Fuster, Daniel</creator><creator>Tsui, Judith I.</creator><creator>Cheng, Debbie M.</creator><creator>Quinn, Emily K.</creator><creator>Bridden, Carly</creator><creator>Nunes, David</creator><creator>Libman, Howard</creator><creator>Saitz, Richard</creator><creator>Samet, Jeffrey H.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K7.</scope><scope>K9.</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>201309</creationdate><title>Impact of Lifetime Alcohol Use on Liver Fibrosis in a Population of HIV-Infected Patients With and Without Hepatitis C Coinfection</title><author>Fuster, Daniel ; 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Medical Complete (Alumni)</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Alcoholism, clinical and experimental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuster, Daniel</au><au>Tsui, Judith I.</au><au>Cheng, Debbie M.</au><au>Quinn, Emily K.</au><au>Bridden, Carly</au><au>Nunes, David</au><au>Libman, Howard</au><au>Saitz, Richard</au><au>Samet, Jeffrey H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Lifetime Alcohol Use on Liver Fibrosis in a Population of HIV-Infected Patients With and Without Hepatitis C Coinfection</atitle><jtitle>Alcoholism, clinical and experimental research</jtitle><addtitle>Alcohol Clin Exp Res</addtitle><date>2013-09</date><risdate>2013</risdate><volume>37</volume><issue>9</issue><spage>1527</spage><epage>1535</epage><pages>1527-1535</pages><issn>0145-6008</issn><eissn>1530-0277</eissn><coden>ACRSDM</coden><abstract><![CDATA[Background The effect of alcohol on liver disease in HIV infection has not been well characterized. Methods We performed a cross‐sectional multivariable analysis of the association between lifetime alcohol use and liver fibrosis in a longitudinal cohort of HIV‐infected patients with alcohol problems. Liver fibrosis was estimated with 2 noninvasive indices, “FIB‐4,” which includes platelets, liver enzymes, and age; and aspartate aminotransferase/platelet ratio index (“APRI”), which includes platelets and liver enzymes. FIB‐4 <1.45 and APRI <0.5 defined the absence of liver fibrosis. FIB‐4 >3.25 and APRI >1.5 defined advanced liver fibrosis. The main independent variable was lifetime alcohol consumption (<150 kg, 150 to 600 kg, >600 kg). Results Subjects (n = 308) were 73% men, mean age 43 years, 49% with hepatitis C virus (HCV) infection, 60% on antiretroviral therapy, 49% with an HIV RNA load <1,000 copies/ml, and 18.7% with a CD4 count <200 cells/mm3. Forty‐five percent had lifetime alcohol consumption >600 kg, 32.7% 150 to 600 kg, and 22.3% <150 kg; 33% had current heavy alcohol use, and 69% had >9 years of heavy episodic drinking. Sixty‐one percent had absence of liver fibrosis and 10% had advanced liver fibrosis based on FIB‐4. In logistic regression analyses, controlling for age, gender, HCV infection, and CD4 count, no association was detected between lifetime alcohol consumption and the absence of liver fibrosis (FIB‐4 <1.45) (adjusted odds ratio [AOR] = 1.12 [95% CI: 0.25 to 2.52] for 150 to 600 kg vs. <150 kg; AOR = 1.11 [95% CI: 0.52 to 2.36] for >600 kg vs. <150 kg; global p = 0.95). Additionally, no association was detected between lifetime alcohol use and advanced liver fibrosis (FIB‐4 >3.25). Results were similar using APRI, and among those with and without HCV infection. Conclusions In this cohort of HIV‐infected patients with alcohol problems, we found no significant association between lifetime alcohol consumption and the absence of liver fibrosis or the presence of advanced liver fibrosis, suggesting that alcohol may be less important than other known factors that promote liver fibrosis in this population.]]></abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23647488</pmid><doi>10.1111/acer.12129</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Age
Alcohol
Alcohol Drinking - epidemiology
Alcohol Drinking - pathology
Alcoholism - diagnosis
Alcoholism - epidemiology
Cohort Studies
Coinfection - diagnosis
Coinfection - epidemiology
Cross-Sectional Studies
Female
Hepatitis C - diagnosis
Hepatitis C - epidemiology
Hepatitis C Virus
HIV
HIV Infections - diagnosis
HIV Infections - epidemiology
Humans
Liver Cirrhosis - diagnosis
Liver Cirrhosis - epidemiology
Liver Fibrosis
Longitudinal Studies
Male
Middle Aged
Population Surveillance - methods
Prospective Studies
title Impact of Lifetime Alcohol Use on Liver Fibrosis in a Population of HIV-Infected Patients With and Without Hepatitis C Coinfection
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