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Elevated serum uric acid level was a notable adverse event during combination therapy with sofosbuvir and ribavirin
Author(s) -
Sato Ken,
Naganuma Atsushi,
Nagashima Tamon,
Hoshino Takashi,
Uehara Daisuke,
Arai Yousuke,
Horiuchi Katsuhiko,
Yuasa Kazuhisa,
Takayama Hisashi,
Arai Hirotaka,
Hatanaka Takeshi,
Ohyama Tatsuya,
Tahara Hiroki,
Sohara Naondo,
Kobayashi Takeshi,
Horiguchi Norio,
Yamazaki Yuichi,
Kakizaki Satoru,
Kusano Motoyasu,
Yamada Masanobu,
Murase Takayo,
Nakamura Takashi
Publication year - 2018
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/hepr.12971
Subject(s) - medicine , sofosbuvir , hyperuricemia , ribavirin , creatinine , gastroenterology , adverse effect , uric acid , body mass index , chronic hepatitis , immunology , virus
Aim Combination therapy with sofosbuvir and ribavirin (SOF/RBV) has been recently available for chronic hepatitis C patients with genotype 2 (CHG2) in Japan. The domestic phase III clinical trial showed a high antiviral effect with a relatively safe adverse event (AE) profile. Our aim was to report an important AE detected during treatment. Methods A prospective multi‐institutional study of 12‐week combination therapy with SOF/RBV for CHG2 was carried out to evaluate efficacy and safety. Results The eligible subjects included 142 patients. Out of 50 assessable patients, 16% of the patients were diagnosed with hyperuricemia. The proportions of subjects with grade 1, grade 3, and grade 4 hyperuricemia were 12, 2, and 2%, respectively. Serum uric acid (UA) levels at week 1 of the therapy (W1) were numerically the highest during therapy in patients with hyperuricemia, and the ratio of W1/baseline serum UA levels was significantly higher than that of post‐treatment week 4 or 8/baseline serum UA levels in assessable patients. Serum UA levels at W1 were significantly correlated with body mass index. The difference between serum UA levels at W1 and baseline serum UA levels was significantly correlated with the difference between serum creatinine levels at W1 and baseline serum creatinine levels. Conclusions Elevated serum UA level was a notable AE associated with SOF/RBV therapy for CHG2. However, because of the small number of subjects, the exact frequency of AEs should be re‐evaluated with larger cohorts. We need to remember that elevated serum UA level might develop during the therapy, especially at W1.