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Coffee intake is associated with lower rates of liver disease progression in chronic hepatitis C

dc.contributor.authorFreedman, Neal D.en_US
dc.contributor.authorEverhart, James E.en_US
dc.contributor.authorLindsay, Karen L.en_US
dc.contributor.authorGhany, Marc G.en_US
dc.contributor.authorCurto, Teresa M.en_US
dc.contributor.authorShiffman, Mitchell L.en_US
dc.contributor.authorLee, William M.en_US
dc.contributor.authorLok, Anna Suk-Fongen_US
dc.contributor.authorDi Bisceglie, Adrian M.en_US
dc.contributor.authorBonkovsky, Herbert L.en_US
dc.contributor.authorHoefs, John C.en_US
dc.contributor.authorDienstag, Jules L.en_US
dc.contributor.authorMorishima, Chihiroen_US
dc.contributor.authorAbnet, Christian C.en_US
dc.contributor.authorSinha, Rashmien_US
dc.date.accessioned2009-11-06T16:49:04Z
dc.date.available2010-03-01T21:10:29Zen_US
dc.date.issued2009-11en_US
dc.identifier.citationFreedman, Neal D.; Everhart, James E.; Lindsay, Karen L.; Ghany, Marc G.; Curto, Teresa M.; Shiffman, Mitchell L.; Lee, William M.; Lok, Anna S.; Di Bisceglie, Adrian M.; Bonkovsky, Herbert L.; Hoefs, John C.; Dienstag, Jules L.; Morishima, Chihiro; Abnet, Christian C.; Sinha, Rashmi (2009). "Coffee intake is associated with lower rates of liver disease progression in chronic hepatitis C This is publication #38 from the HALT-C Trial Group. Financial relationships of the authors with Hoffmann-La Roche, Inc., are as follows: K.L.L. is a consultant and receives research support; M.L.S. is a consultant, on the speaker's bureau, and receives research support; W.M.L. receives research support; A.S.L. is a consultant; A.M.D. is a consultant, on the speaker's bureau, and receives research support; H.L.B. receives research support; J.C.H. is on the speaker's bureau. Authors with no financial relationships related to this project are: N.D.F., J.E.E., M.G.G., T.M.C., C.C.A., R.S., J.L.D., and C.M. The funding organizations had no role in the design and conduct of the study; the collection, analysis, and interpretation of the data; or the preparation, review, or approval of the manuscript. ." Hepatology 50(5): 1360-1369. <http://hdl.handle.net/2027.42/64314>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/64314
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19676128&dopt=citationen_US
dc.description.abstractHigher coffee consumption has been associated inversely with the incidence of chronic liver disease in population studies. We examined the relationship of coffee consumption with liver disease progression in individuals with advanced hepatitis C–related liver disease. Baseline coffee and tea intake were assessed in 766 participants of the Hepatitis C Antiviral Long-Term Treatment against Cirrhosis (HALT-C) trial who had hepatitis C–related bridging fibrosis or cirrhosis on liver biopsy and failed to achieve a sustained virological response to peginterferon plus ribavirin treatment. Participants were followed for 3.8 years for clinical outcomes and, for those without cirrhosis, a 2-point increase in Ishak fibrosis score on protocol biopsies. At baseline, higher coffee consumption was associated with less severe steatosis on biopsy, lower serum aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ratio, alpha-fetoprotein, insulin, and homeostatic model assessment (HOMA2) score, and higher albumin ( P < 0.05 for all). Two hundred thirty patients had outcomes. Outcome rates declined with increasing coffee intake: 11.1/100 person-years for none, 12.1 for less than 1 cup/day, 8.2 for 1 to fewer than 3 cups/day, and 6.3 for 3 or more cups/day ( P -trend = 0.0011). Relative risks (95% confidence intervals) were 1.11 (0.76-1.61) for less than 1 cup/day; 0.70 (0.48-1.02) for 1 to fewer than 3 cups/day; and 0.47 (0.27-0.85) for 3 or more cups/day ( P -trend = 0.0003) versus not drinking. Risk estimates did not vary by treatment assignment or cirrhosis status at baseline. Tea intake was not associated with outcomes. Conclusion: In a large prospective study of participants with advanced hepatitis C–related liver disease, regular coffee consumption was associated with lower rates of disease progression. (H EPATOLOGY 2009.)en_US
dc.format.extent238793 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleCoffee intake is associated with lower rates of liver disease progression in chronic hepatitis Cen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Gastroenterology, University of Michigan Medical Center, Ann Arbor, MIen_US
dc.contributor.affiliationotherNutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Rockville, MD ; fax: 301-496-6829 ; Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Boulevard, EPS/320, MSC 7232, Rockville, MD 20852en_US
dc.contributor.affiliationotherDivision of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.contributor.affiliationotherDivision of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, Los Angeles, CAen_US
dc.contributor.affiliationotherLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.contributor.affiliationotherNew England Research Institutes, Watertown, MAen_US
dc.contributor.affiliationotherHepatology Section, Virginia Commonwealth University Medical Center, Richmond, VAen_US
dc.contributor.affiliationotherDivision of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, TXen_US
dc.contributor.affiliationotherDivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MOen_US
dc.contributor.affiliationotherDepartments of Medicine and Molecular & Structural Biology and The Liver-Biliary-Pancreatic Center, University of Connecticut Health Center, Farmington, CTen_US
dc.contributor.affiliationotherDivision of Gastroenterology, University of California—Irvine, Irvine, CAen_US
dc.contributor.affiliationotherGastrointestinal Unit (Medical Services), Massachusetts General Hospital and the Department of Medicine, Harvard Medical School, Boston, MAen_US
dc.contributor.affiliationotherVirology Division, Department of Laboratory Medicine, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherNutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Rockville, MDen_US
dc.contributor.affiliationotherNutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Rockville, MDen_US
dc.identifier.pmid19676128en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/64314/1/23162_ftp.pdf
dc.identifier.doi10.1002/hep.23162en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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