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Maternal and Infant Renal Safety Following Tenofovir Disoproxil Fumarate Exposure During Pregnancy in a Randomized Control Trial

BMC infectious diseases(2022)

Harvard T.H. Chan School of Public Health | University of Malawi | Johns Hopkins University | University of KwaZulu Natal | Stellenbosch University | University of Zimbabwe Clinical Trials Research Centre | University of the Witwatersrand | FHI 360 | Frontier Science Foundation | National Institute of Allergy and Infectious Diseases | United States Agency for International Development | Johns Hopkins Bloomberg School of Public Health

Cited 3|Views17
Abstract
Abstract Background Tenofovir disoproxil fumarate (TDF) in combination with other antiretroviral (ARV) drugs has been in clinical use for HIV treatment since its approval in 2001. Although the effectiveness of TDF in preventing perinatal HIV infection is well established, information about renal safety during pregnancy is still limited. Trial design The IMPAACT PROMISE study was an open-label, strategy trial that randomized pregnant women to one of three arms: TDF based antiretroviral therapy (ART), zidovudine (ZDV) based ART, and ZDV alone (standard of care at start of enrollment). The P1084s substudy was a nested, comparative study of renal outcomes in women and their infants. Methods PROMISE participants (n = 3543) were assessed for renal dysfunction using calculated creatinine clearance (CrCl) at study entry (> 14 weeks gestation), delivery, and postpartum weeks 6, 26, and 74. Of these women, 479 were enrolled in the P1084s substudy that also assessed maternal calcium and phosphate as well as infant calculated CrCl, calcium, and phosphate at birth. Results Among the 1338 women who could be randomized to TDF, less than 1% had a baseline calculated CrCl below 80 mL/min. The mean (standard deviation) maternal calculated CrCl at delivery in the TDF-ART arm [147.0 mL/min (51.4)] was lower than the ZDV-ART [155.0 mL/min (43.3); primary comparison] and the ZDV Alone [158.5 mL/min (45.0)] arms; the mean differences (95% confidence interval) were − 8.0 mL/min (− 14.5, − 1.5) and − 11.5 mL/min (− 18.0, − 4.9), respectively. The TDF-ART arm had lower mean maternal phosphate at delivery compared with the ZDV-ART [− 0.14 mg/dL (− 0.28, − 0.01)] and the ZDV Alone [− 0.17 mg/dL (− 0.31, − 0.02)] arms, and a greater percentage of maternal hypophosphatemia at delivery (4.23%) compared with the ZDV-ART (1.38%) and the ZDV Alone (1.46%) arms. Maternal calcium was similar between arms. In infants, mean calculated CrCl, calcium, and phosphate at birth were similar between arms (all CIs included 0). Conclusions Although mean maternal calculated CrCl at Delivery was lower in the TDF-ART arm, the difference between arms is unlikely to be clinically significant. During pregnancy, the TDF-ART regimen had no observed safety concerns for maternal or infant renal function. Trial Registration: NCT01061151 on 10/02/2010 for PROMISE (1077BF). NCT01066858 on 10/02/2010 for P1084s.
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HIV/AIDS,Antiretroviral therapy,Renal function,Pregnancy,Prevention of perinatal HIV transmission
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要点】:研究探讨了孕期使用替诺福韦酯(Tenofovir Disoproxil Fumarate, TDF)对母亲和婴儿肾功能的安全性,发现TDF方案对母亲和婴儿肾功能无显著影响。

方法】:采用随机对照试验设计,将孕妇分为三组:TDF为基础的抗逆转录病毒治疗(ART)组、齐多夫定(ZDV)为基础的ART组以及单独使用ZDV组(入组时的标准治疗)。

实验】:在IMPAACT PROMISE研究中,对3543名参与者的肾功能进行评估,包括计算肌酐清除率(CrCl)以及在分娩和产后6、26、74周的数据。其中479名妇女参与了P1084s子研究,评估了母体钙和磷水平以及婴儿出生时的CrCl、钙和磷水平。结果发现,TDF-ART组的母亲分娩时CrCl均值低于其他两组,但差异不太可能具有临床意义,且TDF方案对母体和婴儿肾功能未观察到安全问题。数据集名称为IMPAACT PROMISE和P1084s子研究数据。