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  3. Clinical Outcomes in Persons Coinfected With Human Immunodeficiency Virus and Hepatitis C Virus: Impact of Hepatitis C Virus Treatment.
 

Clinical Outcomes in Persons Coinfected With Human Immunodeficiency Virus and Hepatitis C Virus: Impact of Hepatitis C Virus Treatment.

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BORIS DOI
10.7892/boris.133233
Date of Publication
May 6, 2020
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
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
Universitätsklinik für Infektiologie
Falconer, Karolin
Trofimova, Tatyana
Borodulina, Elena
Jevtovic, Djordje
Bakowska, Elzbieta
Kase, Kerstin
Kyselyova, Galina
Haubrich, Richard
Rockstroh, Jürgen K
Peters, Lars
Subject(s)

600 - Technology::610...

Series
Clinical infectious diseases
ISSN or ISBN (if monograph)
1537-6591
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/cid/ciz601
PubMed ID
31504296
Uncontrolled Keywords

HIV cardiovascular di...

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/182123
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