4.7 Article

Factors associated with seronegative chronic hepatitis C virus infection in HIV infection

期刊

CLINICAL INFECTIOUS DISEASES
卷 44, 期 4, 页码 577-583

出版社

UNIV CHICAGO PRESS
DOI: 10.1086/511038

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资金

  1. NCRR NIH HHS [M01 RR000865, RR00083, RR0636, M01 RR000052, RR00051, M01-RR00036, M01 RR000036, M01 RR000051, RR00865, RR00052, M01 RR000083, M01 RR000054, RR00054] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL074814-07, HL74814, R01 HL074814-05, R01 HL074814-04, HL 53359, R01 HL074814-06, R01 HL074814] Funding Source: Medline
  3. NIAAA NIH HHS [AA015287, K24 AA015287] Funding Source: Medline
  4. NIAID NIH HHS [AI 027767, K23 AI095034, K23 AI 66943-01, P30 AI027767, K23 AI066943] Funding Source: Medline
  5. NIDDK NIH HHS [R01 DK057508-01S1, R01 DK057508-03, R01 DK057508-02, R01 DK057508, R01-DK57508, R01 DK057508-03S2, R01 DK057508-03S1, R01 DK057508-01] Funding Source: Medline
  6. NIMH NIH HHS [R01 MH054907, MH54907] Funding Source: Medline

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Background. Chronic seronegative hepatitis C virus (HCV) infection is defined as being HCV antibody (anti-HCV) negative, but HCV RNA positivity occurs in individuals infected with human immunodeficiency virus (HIV). However, associated factors are not well established because of the small number of reported cases. Methods. Multivariate logistic regression analysis of HIV-infected subjects from 4 cohorts ( Tien et al.,2006; Bonacini et al., 2001; George et al., 2002; and Hall et al., 2004) determined factors associated with HCV RNA positivity in anti-HCV-negative subjects. HCV enzyme immunoassay 2.0 was used to determine anti-HCV status. Results. Among 1174 anti-HCV-negative, HIV-infected subjects, the prevalence of seronegative HCV infection was 3.2% (95% confidence interval [CI], 2.2%-4.3%). History of injection drug use (IDU; OR, 5.8; 95% CI, 2.7-12.8), higher alanine aminotransferase (ALT) level ( OR, 2.0 per doubling; 95% CI, 1.3-3.2), and CD4 cell count < 200 cells/mu L (OR, 2.3; 95% CI, 1.1-4.8) were associated with HCV RNA positivity in anti-HCV-negative subjects. Among those with a history of IDU who had either a CD4 cell count < 200 cells/mu L or an ALT level greater than the upper limit of normal, the prevalence of seronegative HCV infection was 24% (95% CI, 13%-39%). Conclusions. Detectable HCV RNA in the context of a negative HCV enzyme immunoassay 2.0 result in HIV-infected patients is low, but higher than the reported prevalence in HIV-uninfected patients. Our findings suggest that HCVRNA testing should be performed in anti-HCV-negative, HIV-infected patients, especially those with a history of IDU and either a CD4 cell count < 200 cells/mu L or an abnormal ALT level.

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