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Liver-related deaths in persons infected with the human immunodeficiency virus -: The D:A:D study

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ARCHIVES OF INTERNAL MEDICINE
卷 166, 期 15, 页码 1632-1641

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AMER MEDICAL ASSOC
DOI: 10.1001/archinte.166.15.1632

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  1. NIAID NIH HHS [5U01 AI 046362-03, 5U01 AI 042170-10] Funding Source: Medline

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Background: An increasing proportion of deaths among human immunodeficiency virus (HIV)-infected persons with access to combination antiretroviral therapy (cART) are due to complications of liver diseases. Methods: We investigated the frequency of and risk factors associated with liver-related deaths in the Data Collection on Adverse Events of Anti-HIV Drugs study, which prospectively evaluated 76893 person-years of follow-up in 23441 HIV-infected persons. Multivariable Poisson regression analyses identified factors associated with liver-related, AIDS- related, and other causes of death. Results: There were 1246 deaths ( 5.3%; 1.6 per 100 person-years); 14.5% were from liver-related causes. Of these, 16.9% had active hepatitis B virus ( HBV), 66.1% had hepatitis C virus ( HCV), and 7.1% had dual viral hepatitis coinfections. Predictors of liver-related deaths were latest CD4 cell count ( adjusted relative rate [RR], 16.1; 95% confidence interval [CI], 8.1-31.7 for < 50 vs >= 500/mu L), age ( RR, 1.3; 95% CI, 1.2-1.4 per 5 years older), intravenous drug use ( RR, 2.0; 95% CI, 1.2- 3.4), HCV infection ( RR, 6.7; 95% CI, 4.0-11.2), and active HBV infection ( RR, 3.7; 95% CI, 2.4-5.9). Univariable analyses showed no relationship between cumulative years patients were receiving cART and liver-related death ( RR, 1.00; 95% CI, 0.93-1.07). Adjustment for the most recent CD4 cell count and patient characteristics resulted in an increased risk of liver-related mortality per year of mono or dual antiretroviral therapy before cART ( RR, 1.09; 95% CI, 1.02-1.16; P=.008) and per year of cART ( RR, 1.11; 95% CI, 1.02-1.21; P=.02). Conclusions: Liver-related death was the most frequent cause of non-AIDS-related death. We found a strong association between immunodeficiency and risk of liver related death. Longer follow-up is required to investigate whether clinically significant treatment-associated liver-related mortality will develop.

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