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초록
Clevudine is a potent antiviral agent against HBV. However, long-term clevudine therapy may cause myopathy. This study was carried out to identify the efficacy of entecavir switching therapy in chronic hepatitis B patients experiencing clevudine-induced myopathy. One hundred forty six patients with chronic hepatitis B treated with 30 mg of clevudine per day for 73 weeks (range, 36-132 weeks) were enrolled. Among them, clevudine-induced myopathy occurred in 21 patients (14.4%) which was diagnosed if the patients had symptoms related to myopathy with concurrent CK and AST elevation. All the patients who were diagnosed as clevudine-induced myopathy stopped the therapy, and 17 patients (81%) were switched to entecavir 0.5 mg. The patients with clevudine-induced myopathy were switched to entecavir 0.5 mg for median 68 weeks, and all of them showed disappearance of clinical myopathic symptoms and normalization of CK and AST level within median 2.2 months. Eight patients (47%) were HBeAg positive before entecavir treatment, and HBeAg seroconversion was achieved in 2 patients (25%). HBV DNA level was elevated in 3 patients (17.6%) at the time when the patients were diagnosed as myopathy, all of them achieved virological response with entecavir switching therapy. ALT level was elevated in 3 patients (17.6%) before entecavir treatment, all of them showed normalization of ALT level. During entecavir therapy, genotypic resistance to entecavir or virological breakthrough was not noted. In chronic hepatitis B patients experiencing clevudine-induced myopathy, switching to entecavir 0.5 mg per day showed a resolution of myopathy and adequate viral suppression.
키워드
- 제목
- Efficacy of entecavir switching therapy in chronic hepatitis B patients with clevudine-induced myopathy
- 제목 (타언어)
- 클레부딘 근육병증이 발생한 만성 B형간염 환자들에서 엔테카비어 전환 치료의 효과
- 저자
- 이지원; 이영준; 이종준; 김정호; 정영걸; 권오상; 최덕주; 김연수; 김주현
- 발행일
- 2013-01
- 유형
- Article
- 저널명
- 대한소화기학회지
- 권
- 61
- 호
- 1
- 페이지
- 30 ~ 36
- 언어
- KOR
- 출판사
- 대한소화기학회
- 발행국가
- 대한민국
- 분량
- 7 페이지
- ISSN
- E 2233-6869
P 1598-9992