Effects of Angiotensin Converting Enzyme Inhibitors on Liver Fibrosis in HIV and Hepatitis C Coinfection
Author(s) -
Lindsey Reese,
Diane Tider,
Alicia Stivala,
Dawn Fishbein
Publication year - 2012
Publication title -
aids research and treatment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.749
H-Index - 27
eISSN - 2090-1259
pISSN - 2090-1240
DOI - 10.1155/2012/978790
Subject(s) - coinfection , medicine , fibrosis , gastroenterology , hepatitis c , liver fibrosis , angiotensin converting enzyme , hepatitis b , chronic hepatitis , immunology , human immunodeficiency virus (hiv) , blood pressure , virus
Background . Liver fibrosis is accelerated in HIV and hepatitis C coinfection, mediated by profibrotic effects of angiotensin. The objective of this study was to determine if angiotensin converting enzyme inhibitors (ACE-Is) attenuate liver fibrosis in coinfection. Methods . A retrospective review of 156 coinfected subjects was conducted to analyze the association between exposure to ACE-Is and liver fibrosis. Noninvasive indices of liver fibrosis (APRI, FIB-4, Forns indices) were compared between subjects who had taken ACE-Is and controls who had not taken them. Linear regression was used to evaluate ACE-I use as an independent predictor of fibrosis. Results . Subjects taking ACE-Is for three years were no different than controls on the APRI and the FIB-4 but had significantly higher scores than controls on the Forns index, indicating more advanced fibrosis. The use of ACE-Is for three years remained independently associated with an elevated Forns score when adjusted for age, race, and HIV viral load ( P < 0.001). There were significant associations between all of the indices and significant fibrosis, as determined clinically and radiologically. Conclusions . There was not a protective association between angiotensin inhibition and liver fibrosis in coinfection. These noninvasive indices may be useful for ruling out significant fibrosis in coinfection.
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