Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
PLoS One. 2021 Feb 5;16(2):e0246272. doi: 10.1371/journal.pone.0246272. eCollection 2021.
We set out to evaluate the effect of postnatal exposure to tenofovir-containing antiretroviral therapy on bone mineral density among breastfeeding women living with HIV.
IMPAACT P1084s is a sub-study of the PROMISE randomized trial conducted in four African countries (ClinicalTrials.gov number NCT01066858).
IMPAACT P1084s enrolled eligible mother-infant pairs previously randomised in the PROMISE trial at one week after delivery to receive either maternal antiretroviral therapy (Tenofovir disoproxil fumarate / Emtricitabine + Lopinavir/ritonavir-maternal TDF-ART) or administer infant nevirapine, with no maternal antiretroviral therapy, to prevent breastmilk HIV transmission. Maternal lumbar spine and hip bone mineral density were measured using dual-energy x-ray absorptiometry (DXA) at postpartum weeks 1 and 74. We studied the effect of the postpartum randomization on percent change in maternal bone mineral density in an intention-to-treat analysis with a t-test; mean and 95% confidence interval (95%CI) are presented.
Among 398/400 women included in this analysis, baseline age, body-mass index, CD4 count, mean bone mineral density and alcohol use were comparable between study arms. On average, maternal lumbar spine bone mineral density declined significantly through week 74 in the maternal TDF-ART compared to the infant nevirapine arm; mean difference (95%CI) -2.86 (-4.03, -1.70) percentage points (p-value <0.001). Similarly, maternal hip bone mineral density declined significantly more through week 74 in the maternal TDF-ART compared to the infant nevirapine arm; mean difference -2.29% (-3.20, -1.39) (p-value <0.001). Adjusting for covariates did not change the treatment effect.
Bone mineral density decline through week 74 postpartum was greater among breastfeeding HIV-infected women randomized to receive maternal TDF-ART during breastfeeding compared to those mothers whose infants received nevirapine prophylaxis.
我们旨在评估在接受含替诺福韦的抗逆转录病毒疗法的 HIV 感染产妇中,产后暴露对骨密度的影响。
IMPACT P1084s 是在四个非洲国家(ClinicalTrials.gov 编号:NCT01066858)进行的 PROMISE 随机试验的子研究。
IMPACT P1084s 在产后一周时,招募了先前在 PROMISE 试验中随机分组的合格母婴对,他们要么接受替诺福韦二吡呋酯/恩曲他滨/洛匹那韦/利托那韦(富马酸替诺福韦二吡呋酯)+洛匹那韦/利托那韦(替诺福韦-ART)的母亲抗逆转录病毒治疗,要么给婴儿服用奈韦拉平,而不给予母亲抗逆转录病毒治疗,以预防母乳 HIV 传播。在产后 1 周和 74 周时,使用双能 X 射线吸收仪(DXA)测量产妇腰椎和髋骨的骨矿物质密度。我们通过 t 检验对意向治疗分析中的产后随机分组对产妇骨矿物质密度变化的影响进行了研究;呈现均值和 95%置信区间(95%CI)。
在这项分析中的 398/400 名女性中,研究臂之间的基线年龄、体重指数、CD4 计数、平均骨矿物质密度和酒精使用情况相当。平均而言,与婴儿服用奈韦拉平组相比,接受替诺福韦-ART 的母亲的腰椎骨矿物质密度在 74 周时明显下降;平均差值(95%CI)-2.86(-4.03,-1.70)个百分点(p 值<0.001)。同样,与婴儿服用奈韦拉平组相比,接受替诺福韦-ART 的母亲的髋骨矿物质密度在 74 周时明显下降更多;平均差值-2.29%(-3.20,-1.39)(p 值<0.001)。调整协变量后,治疗效果没有改变。
与接受婴儿奈韦拉平预防的母亲相比,接受母乳喂养期间替诺福韦-ART 的 HIV 感染母乳喂养妇女在产后 74 周时骨矿物质密度下降幅度更大。