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DOI 10.1001/jama.2012.7844

Медицинская библиотека · JAMA · 2012

Relationship of liver disease stage and antiviral therapy with liver-related events and death in adults coinfected with HIV/HCV.

Limketkai Berkeley N, Mehta Shruti H, Sutcliffe Catherine G, Higgins Yvonne M, Torbenson Michael S, Brinkley Sherilyn C, Moore Richard D, Thomas David L, Sulkowski Mark S

СтатьяПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

CONTEXT: Human immunodeficiency virus (HIV) accelerates hepatitis C virus (HCV) disease progression; however, the effect of liver disease stage and antiviral therapy on the risk of clinical outcomes is incompletely understood.

OBJECTIVE

To determine the incidence of end-stage liver disease (ESLD), hepatocellular carcinoma (HCC), or death according to baseline hepatic fibrosis and antiviral treatment for HIV/HCV coinfected individuals.

DESIGN, SETTING, AND

PARTICIPANTS

Prospective cohort of 638 coinfected adults (80% black, 66% men) receiving care at the Johns Hopkins HIV clinic and receiving a liver biopsy and who were prospectively monitored for clinical events between July 1993 and August 2011 (median follow-up, 5.82 years; interquartile range, 3.42-8.85 years). Histological specimens were scored for hepatic fibrosis stage according to the METAVIR scoring system.

MAIN OUTCOME MEASURE: Incidence of composite outcome of ESLD, HCC, or death.

RESULTS

Patients experienced a graded increased risk in incidence of clinical outcomes based on baseline hepatic fibrosis stage (classification range, F0-F4): F0, 23.63 (95% CI, 16.80-33.24); F1, 36.33 (95% CI, 28.03-47.10); F2, 53.40 (95% CI, 33.65-84.76); F3, 56.14 (95% CI, 31.09-101.38); and F4, 79.43 (95% CI, 55.86-112.95) per 1000 person-years (P < .001). In multivariable negative binomial regression, fibrosis stages F2 through F4 and antiretroviral therapy were independently associated with composite ESLD, HCC, or all-cause mortality after adjustment for demographic characteristics, injection drug use, and CD4 cell count. Compared with F0, the incidence rate ratio (RR) for F2 was 2.31 (95% CI, 1.23-4.34; P = .009); F3, 3.18 (95% CI, 1.47-6.88; P = .003); and F4, 3.57 (95% CI, 2.06-6.19; P < .001). Human immunodeficiency virus treatment was associated with fewer clinical events (incidence RR, 0.27; 95% CI, 0.19-0.38; P < .001). For the 226 patients who underwent HCV treatment, the incidence of clinical events did not significantly differ between treatment nonresponders and untreated patients (incidence RR, 1.27; 95% CI, 0.86-1.86; P = .23). In contrast, no events were observed in the 51 patients with sustained virologic response (n = 36) and relapse (n = 15), including 19 with significant fibrosis.

CONCLUSION

In this cohort of patients with HIV/HCV coinfection, hepatic fibrosis stage was independently associated with a composite outcome of ESLD, HCC, or death.

Для цитирования: Limketkai Berkeley N, Mehta Shruti H, Sutcliffe Catherine G, Higgins Yvonne M, Torbenson Michael S, Brinkley Sherilyn C, Moore Richard D, Thomas David L, Sulkowski Mark S. Relationship of liver disease stage and antiviral therapy with liver-related events and death in adults coinfected with HIV/HCV.. JAMA. 2012. DOI: 10.1001/jama.2012.7844.

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