| Literature DB >> 27168803 |
Motoyuki Kohjima1, Miho Kurokawa1, Munechika Enjoji2, Tsuyoshi Yoshimoto1, Tsukasa Nakamura1, Tomoko Ohashi1, Kunitaka Fukuizumi1, Naohiko Harada1, Yusuke Murata2, Kazuhisa Matsunaga2, Masaki Kato3, Kazuhiro Kotoh3, Makoto Nakamuta1.
Abstract
Telaprevir (TVR) is used for the treatment of chronic hepatitis C in a combination therapy with pegylated-interferon and ribavirin. Although renal dysfunction is one of the critical adverse outcomes of this treatment, little is known regarding the mechanism of its onset. The present study assessed the association of renal function with TVR dose and viral response. Hematological, biochemical, urinary and virological parameters of renal function were examined during the TVR-based triple therapy of patients infected with hepatitis C virus (HCV) genotype 1b. Serum creatinine levels were increased and the estimated glomerular filtration rate (eGFR) was decreased in every patient during TVR administration, but these values recovered to normal levels following cessation of TVR. Fractional excretion of sodium was <1% at days 3 and 7, appearing similar regardless of baseline renal function. Urinary β2-microglobulin levels were elevated and were significantly higher in patients with renal dysfunction, as compared with those not exhibiting renal dysfunction (P<0.05). The reduction in renal function was milder in patients treated with a reduced TVR dose, and these patients had a significantly lower risk of developing renal dysfunction (P<0.05). Using a multivariate analysis, TVR dose and eGFR at the initiation of treatment were identified as significant contributory factors in the development of renal dysfunction. Reduction in TVR dose did not lead to a significant increase in the viral kinetics of HCV or detrimental effects on the sustained viral response (SVR) rate. It is hypothesized that renal dysfunction during TVR treatment is caused by damage of the renal tubule, in addition to pre-renal dysfunction, and that reduction in TVR dose reduces the rate of renal dysfunction without causing a significant decrease in the SVR rate.Entities:
Keywords: HCV; interferon; renal dysfunction; ribavirin; telaprevir
Year: 2016 PMID: 27168803 PMCID: PMC4840744 DOI: 10.3892/etm.2016.3133
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447