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  3. Influence of hepatitis C virus co-infection and hepatitis C virus treatment on risk of chronic kidney disease in HIV-positive persons.
 

Influence of hepatitis C virus co-infection and hepatitis C virus treatment on risk of chronic kidney disease in HIV-positive persons.

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BORIS DOI
10.7892/boris.148540
Publisher DOI
10.1097/QAD.0000000000002570
PubMed ID
32675562
Description
BACKGROUND

Hepatitis C virus (HCV) infection has been associated with increased risk of chronic kidney disease (CKD). We investigated the impact of HCV cure on CKD in HIV-positive persons in the EuroSIDA study.

METHODS

HIV-positive persons with known HCV status and at least three serum creatinine measurements after 1/1/2004 were compared based on time-updated HCV-RNA and HCV treatment: anti-HCV-negative, spontaneously cleared HCV, chronic untreated HCV, successfully treated HCV, and HCV-RNA positive after HCV treatment. Poisson regression compared incidence rates of CKD [confirmed (>3 months apart) eGFR <60 ml/min per 1.73 m] between HCV strata.

RESULTS

Fourteen thousand, seven hundred and fifty-four persons were included; at baseline 9273 (62.9%) were HCV-Ab negative, 696 (4.7%) spontaneous clearers, 3021 (20.5%) chronically infected, 922 (6.2%) successfully treated and 842 (5.7%) HCV-RNA positive after treatment. During 115 335 person-years of follow-up (PYFU), 1128 (7.6%) developed CKD; crude incidence 9.8/1000 PYFU (95% CI 9.2-10.4). After adjustment, persons anti-HCV negative [adjusted incidence rate ratio (aIRR) 0.59; 95% CI 0.46-0.75] and spontaneous clearers (aIRR 0.67; 95% CI 0.47-0.97) had significantly lower rates of CKD compared with those cured whereas persons chronically infected (aIRR 0.85; 95% CI 0.65-1.12) and HCV-RNA positive after treatment (aIRR 0.71; 95% CI 0.49-1.04) had similar rates. Analysis in those without F3/F4 liver fibrosis using a more rigorous definition of CKD showed similar results.

CONCLUSION

This large study found no evidence that successful HCV treatment reduced CKD incidence. Confounding by indication, where those with highest risk of CKD were prioritized for HCV treatment in the DAA era, may contribute to these findings.
Date of Publication
2020-08-01
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Contributor(s)
Mocroft, Amanda
Ryom, Lene
Oprea, Cristiana
Li, Qiuju
Rauch, Andriorcid-logo
Universitätsklinik für Infektiologie
Boesecke, Christoph
Uzdaviniene, Vilma
Sedlacek, Dalibor
Llibre, Josep M
Lacombe, Karine
Nielsen, Lars N
Florence, Eric
Aho, Inka
Chkhartishvili, Nikoloz
Szlavik, János
Dragovic, Gordana
Leen, Clifford
Sambatakou, Helen
Staub, Therese
Laguno, Montse
Elinav, Hila
Tomažič, Janez
Peters, Lars
Additional Credits
Universitätsklinik für Infektiologie
Series
AIDS
Publisher
Lippincott Williams & Wilkins
ISSN
0269-9370
Access(Rights)
restricted
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