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Clinical Outcomes in Persons Coinfected With Human Immunodeficiency Virus and Hepatitis C Virus: Impact of Hepatitis C Virus Treatment.
Mocroft, Amanda; Lundgren, Jens; Gerstoft, Jan; Rasmussen, Line D; Bhagani, Sanjay; Aho, Inka; Pradier, Christian; Bogner, Johannes R; Mussini, Christina; Uberti Foppa, Caterina; Maltez, Fernando; Laguno, Montse; Wandeler, Gilles; Falconer, Karolin; Trofimova, Tatyana; Borodulina, Elena; Jevtovic, Djordje; Bakowska, Elzbieta; Kase, Kerstin; Kyselyova, Galina; Haubrich, Richard; Rockstroh, Jürgen K; Peters, Lars.
  • Mocroft A; Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, United Kingdom.
  • Lundgren J; Centre of Excellence for Health, Immunity and Infections, Rigshospitalet, Copenhagen, and Department of Infectious Diseases, Copenhagen.
  • Gerstoft J; Department of Infectious Diseases, Rigshospitalet, Copenhagen.
  • Rasmussen LD; Department of Infectious Diseases, Odense University Hospital, Denmark.
  • Bhagani S; Department of Infectious Diseases, Royal Free Hospital, London, United Kingdom.
  • Aho I; Division of Infectious Diseases, Helsinki University Hospital, Finland.
  • Pradier C; Department of Public Health, Centre Hospitalier Universitaire de Nice, France.
  • Bogner JR; Division of Infectious Diseases, Medizinische Klinik und Poliklinik IV, Ludwig Maximilians University of Munich, Germany.
  • Mussini C; Clinic of Infectious Diseases, University of Modena and Reggio Emilia, Milan, Italy.
  • Uberti Foppa C; Vita-Salute San Raffaele University, San Raffaele Scientific Institue, Clinic of Infectious Diseases, Milan, Italy.
  • Maltez F; Hospital de Curry Cabral, Serviço de Doenças Infecciosas, Lisbon, Portugal.
  • Laguno M; Infectious Diseases Service, Hospital Clinic-L'Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Spain.
  • Wandeler G; Department of Infectious Diseases, Bern University Hospital, University of Bern, Switzerland.
  • Falconer K; Infectious Diseases Department, Karolinska University Hospital, Stockholm, Sweden.
  • Trofimova T; Novgorod Centre for Acquired Immunodeficiency Syndrome Prevention and Control, Novgorod the Great, Russia.
  • Borodulina E; Samara State Medical University, Russia.
  • Jevtovic D; Belgrade University School of Medicine, Infectious & Tropical Diseases Hospital, Serbia.
  • Bakowska E; Wojewodzki Szpital Zakazny, Warsaw, Poland.
  • Kase K; Centre of Infectious Diseases, West-Tallin Central Hospital, Tallin, Estonia.
  • Kyselyova G; Crimean Republican Acquired Immunodeficiency Syndrome Centre, Simferopol.
  • Haubrich R; Gilead Sciences Inc., Foster City, California.
  • Rockstroh JK; Department of Medicine, University Hospital Bonn, Germany.
  • Peters L; Centre of Excellence for Health, Immunity and Infections, Rigshospitalet, Copenhagen, and Department of Infectious Diseases, Copenhagen.
Clin Infect Dis ; 70(10): 2131-2140, 2020 05 06.
Article en En | MEDLINE | ID: mdl-31504296
ABSTRACT

BACKGROUND:

A hepatitis C (HCV) cure is associated with changes in lipids and inflammatory biomarkers, but its impact on clinical endpoints among treated human immunodeficiency virus (HIV)/HCV coinfected persons is unclear.

METHODS:

People living with HIV from EuroSIDA with a known HCV status after January 2001 were classified into strata based on time-updated HCV RNA measurements and HCV treatment, as either HCV antibody-negative; spontaneously resolved HCV; chronic, untreated HCV; cured HCV (HCV RNA-negative); or HCV treatment failures (HCV RNA-positive). Poisson regression was used to compare incidence rates between HCV groups for end-stage liver disease (ESLD; including hepatocellular carcinoma [HCC]), non-acquired immunodeficiency virus defining malignancy (NADM; excluding HCC), and cardiovascular disease (CVD).

RESULTS:

There were 16 618 persons included (median follow-up 8.3 years, interquartile range 3.1-13.7). There were 887 CVD, 902 NADM, and 436 ESLD events; crude incidence rates/1000 person-years follow-up were 6.4 (95% confidence interval [CI] 6.0-6.9) for CVD, 6.5 (95% CI 6.1-6.9) for NADM, and 3.1 (95% CI 2.8-3.4) for ESLD. After adjustment, there were no differences in incidence rates of NADM or CVD across the 5 groups. HCV-negative individuals (adjusted incidence rate ratio [aIRR] 0.22, 95% CI 0.14-0.34) and those with spontaneous clearance (aIRR 0.61, 95% CI 0.36-1.02) had reduced rates of ESLD compared to cured individuals. Persons with chronic, untreated HCV infections (aIRR 1.47, 95% CI 1.02-2.13) or treatment failure (aIRR 1.80, 95% CI 1.22-2.66) had significantly raised rates of ESLD, compared to those who were cured.

CONCLUSIONS:

Incidences of NADM or CVD were independent of HCV group, whereas those cured had substantially lower incidences of ESLD, underlining the importance of successful HCV treatment for reducing ESLD.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Hepatitis C / Carcinoma Hepatocelular / Hepatitis C Crónica / Coinfección / Neoplasias Hepáticas Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Hepatitis C / Carcinoma Hepatocelular / Hepatitis C Crónica / Coinfección / Neoplasias Hepáticas Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article