Division of Infectious Disease, Department of Internal Medicine, Pusan National University Hospital, Busan, Korea.
Division of Nephrology, Department of Internal Medicine, Pusan National University Hospital, Busan, Korea.
Korean J Intern Med. 2019 Mar;34(2):409-417. doi: 10.3904/kjim.2016.418. Epub 2017 Oct 12.
BACKGROUND/AIMS: Little is known about tenofovir disoproxil fumarate (TDF)-induced nephrotoxicity in human immunodeficiency virus (HIV)-infected patients in Korea. The objective of this study was to evaluate the incidence and risk factors of TDF-associated nephrotoxicity among HIV-infected patients in Korea.
A single-center retrospective cohort study was conducted on HIVinfected patients in Korea. We included patients who had started TDF or abacavir (ABC)-based antiretroviral therapy (ART) between October 2006 and December 2014. Estimated glomerular filtration rate (eGFR) was estimated using the Chronic Kidney Disease-Epidemiology Collaboration equation. Renal dysfunction was defined as > 25% decrease of baseline eGFR. A propensity matched case-control study was conducted to compare renal dysfunction rates between the two groups. The risk factors of nephrotoxicity were analyzed by Cox regression analysis.
A total of 210 HIV-infected patients were included in the study, of which, 108 were TDF-based ART group and 102 were ABC-based ART group. Renal dysfunction occurred in 16 patients (14.8%) in the TDF group and 11 (10.8%) in the ABC group. Incidence of renal dysfunction of TDF and ABC group was 9.66 per 100 person-years (PYs) and 5.14 per 100 PYs, respectively (p = 0.176). In propensityscore-matched analysis, renal dysfunction rates were TDF 13.3% versus ABC 13.3% (p > 0.999). In multivariable analysis, Centers for Disease Control and Prevention clinical category C was a significant risk factor for renal dysfunction.
Approximately, 13% of HIV-infected patients treated with TDF had renal dysfunction. Advanced stage of HIV infection was a significant risk factor for renal dysfunction.
背景/目的:在韩国,关于替诺福韦二吡呋酯(TDF)引起的人类免疫缺陷病毒(HIV)感染患者的肾毒性知之甚少。本研究的目的是评估韩国 HIV 感染患者中 TDF 相关肾毒性的发生率和危险因素。
对韩国的 HIV 感染患者进行了一项单中心回顾性队列研究。我们纳入了 2006 年 10 月至 2014 年 12 月期间开始使用 TDF 或阿巴卡韦(ABC)为基础的抗逆转录病毒疗法(ART)的患者。采用慢性肾脏病-流行病学合作(CKD-EPI)方程估算肾小球滤过率(eGFR)。肾功能障碍定义为基线 eGFR 下降> 25%。进行倾向评分匹配病例对照研究,比较两组的肾功能障碍发生率。采用 Cox 回归分析肾毒性的危险因素。
本研究共纳入 210 例 HIV 感染患者,其中 108 例为 TDF 为基础的 ART 组,102 例为 ABC 为基础的 ART 组。TDF 组中有 16 例(14.8%)和 ABC 组中有 11 例(10.8%)患者出现肾功能障碍。TDF 和 ABC 组肾功能障碍的发生率分别为 9.66/100 人年(PYs)和 5.14/100 PYs(p=0.176)。在倾向评分匹配分析中,TDF 组和 ABC 组的肾功能障碍发生率分别为 13.3%和 13.3%(p>0.999)。多变量分析中,疾病控制与预防中心(CDC)临床分类 C 是肾功能障碍的显著危险因素。
约 13%接受 TDF 治疗的 HIV 感染患者出现肾功能障碍。HIV 感染的晚期是肾功能障碍的一个显著危险因素。