TY - JOUR
T1 - Efficacy of reduction therapy of natural human β-interferon and ribavirin in elderly patients with chronic hepatitis C, genotype 1b and high viral load
AU - Arase, Yasuji
AU - Kawamura, Yusuke
AU - Suzuki, Yoshiyuki
AU - Suzuki, Fumitaka
AU - Akuta, Norio
AU - Matsumoto, Naoki
AU - Seko, Yuya
AU - Sezaki, Hitomi
AU - Kobayashi, Masahiro
AU - Hosaka, Tetsuya
AU - Hirakawa, Miharu
AU - Saito, Satoshi
AU - Ikeda, Kenji
AU - Kobayashi, Mariko
AU - Kumada, Hiromitsu
PY - 2012/10
Y1 - 2012/10
N2 - Aim: To evaluate the efficacy of reduction therapy of natural human interferon (IFN)-β and ribavirin in elderly patients with hepatitis C virus (HCV) genotype 1b and high viral load who had complications of anemia, low bodyweight (<50kg), diabetes mellitus and/or hypertension. Methods: Inclusion criteria were age of 65years or older, HCV genotype 1b, and serum HCV RNA level of 5.0logIU/mL or higher. A total of 23 subjects with hemoglobin level of less than 13g/dL, low bodyweight, diabetes mellitus and/or hypertension were enrolled in this study (reduction-dose group). IFN-β was administrated i.v. at a dose of 6million units daily for 4weeks initially, followed by three times a week for 44weeks. Ribavirin was given daily for 48weeks at a decreased dose of one tablet per day compared to the ordinary dose described based on bodyweight. As a control, another 22 patients without anemia, low bodyweight and/or complications treated with the standard dose of ribavirin (standard-dose group) were enrolled. Results: Patients' rates with further dose reduction or discontinuation of treatment was 26.1% (6/23) in the reduction-dose group and 77.3% (17/22) in the standard-dose group. The sustained virological response (SVR) was 39.1% (9/23) in the reduction-dose group and 27.3% (6/22) in the standard-dose group (P=0.404). Based on genetic variations near the IL28B gene (rs8099917), SVR was 44.1% (15/34) in patients with TT and 0% (0/11) in patients with TG (P=0.008). Conclusion: The reduction therapy of IFN-β and ribavirin in elderly HCV patients with genotype 1b, high viral load, IL28B gene (rs8099917) of TT who had complications of anemia, low bodyweight, diabetes mellitus and/or hypertension is one possible selection of treatment.
AB - Aim: To evaluate the efficacy of reduction therapy of natural human interferon (IFN)-β and ribavirin in elderly patients with hepatitis C virus (HCV) genotype 1b and high viral load who had complications of anemia, low bodyweight (<50kg), diabetes mellitus and/or hypertension. Methods: Inclusion criteria were age of 65years or older, HCV genotype 1b, and serum HCV RNA level of 5.0logIU/mL or higher. A total of 23 subjects with hemoglobin level of less than 13g/dL, low bodyweight, diabetes mellitus and/or hypertension were enrolled in this study (reduction-dose group). IFN-β was administrated i.v. at a dose of 6million units daily for 4weeks initially, followed by three times a week for 44weeks. Ribavirin was given daily for 48weeks at a decreased dose of one tablet per day compared to the ordinary dose described based on bodyweight. As a control, another 22 patients without anemia, low bodyweight and/or complications treated with the standard dose of ribavirin (standard-dose group) were enrolled. Results: Patients' rates with further dose reduction or discontinuation of treatment was 26.1% (6/23) in the reduction-dose group and 77.3% (17/22) in the standard-dose group. The sustained virological response (SVR) was 39.1% (9/23) in the reduction-dose group and 27.3% (6/22) in the standard-dose group (P=0.404). Based on genetic variations near the IL28B gene (rs8099917), SVR was 44.1% (15/34) in patients with TT and 0% (0/11) in patients with TG (P=0.008). Conclusion: The reduction therapy of IFN-β and ribavirin in elderly HCV patients with genotype 1b, high viral load, IL28B gene (rs8099917) of TT who had complications of anemia, low bodyweight, diabetes mellitus and/or hypertension is one possible selection of treatment.
KW - Chronic hepatitis C
KW - Hepatitis C virus genotype 1b
KW - Natural ribavirin
KW - β-interferon
UR - http://www.scopus.com/inward/record.url?scp=84866771470&partnerID=8YFLogxK
U2 - 10.1111/j.1872-034X.2012.01008.x
DO - 10.1111/j.1872-034X.2012.01008.x
M3 - Article
AN - SCOPUS:84866771470
SN - 1386-6346
VL - 42
SP - 949
EP - 957
JO - Hepatology Research
JF - Hepatology Research
IS - 10
ER -