Kara A V, Yıldırım Y, Ozcicek F, Aldemir M N, Arslan Y, Bayan K, Çelen M K
Department of Nephrology, Faculty of Medicine, Erzincan University, 24030, Erzincan, Turkey.
Department of Nephrology, Faculty of Medicine, Dicle University, 21200, Diyarbakır, Turkey.
Acta Gastroenterol Belg. 2019 Apr-Jun;82(2):273-277.
The aim of this study was to enlighten the controversy about the renal safety of entecavir, tenofovir, and telbivudine treatments in chronic hepatitis B (CHB) patients by comparing these treatments in real-world conditions.
We retrospectively enrolled 104 treatment-naive patients with CHB monoinfection into our study. Patients were treated with entecavir monotherapy (n=38), tenofovir monotherapy (n=35), or telbivudine monotherapy (n=31). We then compared and statistically analyzed the effects of these drugs on the estimated glomerular filtration rate (eGFR) over a 24-month follow-up period.
In the entecavir group, time-dependent change in eGFR was not statistically significant (p = 0.357). There was a statistically significant increase in eGFR in the telbivudine group at 12 months (p<0.001) and at 24 months (p<0.001) and, in contrast, a statistically significant decrease in the tenofovir group at 12 months (p<0.001) and at 24 months (p<0.001). There was no significant relationship between entecavir and eGFR change (p = 0.763). We found that tenofovir and telbivudine were independent predictors of eGFR change (decrease in eGFR, p<0.001 and increase in eGFR, p = 0.001, respectively).
We recommend close follow-up of renal functions, especially for patients treated with tenofovir. Telbivudine was superior to the other drugs in terms of renal function. We conclude that an individualized therapy program considering treatment efficacy and side effects is the best option for patients.
本研究旨在通过在实际临床环境中比较恩替卡韦、替诺福韦和替比夫定治疗慢性乙型肝炎(CHB)患者的疗效,以阐明关于这三种药物肾脏安全性的争议。
我们回顾性纳入了104例初治的单纯CHB感染患者。患者分别接受恩替卡韦单药治疗(n = 38)、替诺福韦单药治疗(n = 35)或替比夫定单药治疗(n = 31)。然后,我们比较并统计分析了这些药物在24个月随访期内对估算肾小球滤过率(eGFR)的影响。
在恩替卡韦组,eGFR的时间依赖性变化无统计学意义(p = 0.357)。替比夫定组在12个月(p<0.001)和24个月(p<0.001)时eGFR有统计学意义的升高,相反,替诺福韦组在12个月(p<0.001)和24个月(p<0.001)时eGFR有统计学意义的降低。恩替卡韦与eGFR变化之间无显著相关性(p = 0.763)。我们发现替诺福韦和替比夫定是eGFR变化的独立预测因素(替诺福韦使eGFR降低,p<0.001;替比夫定使eGFR升高,p = 0.001)。
我们建议密切随访肾功能,尤其是接受替诺福韦治疗的患者。就肾功能而言,替比夫定优于其他药物。我们得出结论,考虑治疗效果和副作用的个体化治疗方案对患者是最佳选择。