Department of Surveillance, Prevention, and Control of STIs, AIDS, and Viral Hepatitis, Ministry of Health, Brasília, Brazil.
Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Lancet HIV. 2021 Jan;8(1):e33-e41. doi: 10.1016/S2352-3018(20)30268-X.
Dolutegravir has been widely available in Brazil since 2017. Following the signal that infants born to women with dolutegravir exposure at conception in Botswana had a higher risk of neural tube defects (NTDs), public health leaders initiated a national investigation to evaluate periconception dolutegravir exposure among all pregnant Brazilian women with HIV and its potential association with risk of NTDs, stillbirth, or miscarriage before 22 weeks (also called spontaneous abortion).
In this retrospective, observational, national, cohort study, we identified all women with pregnancies and possible dolutegravir exposure within 8 weeks of estimated date of conception between Jan 1, 2017, and May 31, 2018, and approximately 3:1 matched pregnant women exposed to efavirenz between Jan 1, 2015, and May 31, 2018, using the Brazilian antiretroviral therapy database. We did detailed chart reviews for identified women. The primary outcomes were NTD and a composite measure of NTD, stillbirth, or miscarriage. NTD incidences were calculated with 95% CI. The composite outcome was examined with logistic regression using propensity score matching weights to balance confounders.
Of 1427 included women, 382 were exposed to dolutegravir within 8 weeks of estimated date of conception. During pregnancy, 183 (48%) of 382 dolutegravir-exposed and 465 (44%) of 1045 efavirenz-exposed women received folic acid supplementation. There were 1452 birth outcomes. There were no NTDs in either dolutegravir-exposed (0, 95% CI 0-0·0010) or efavirenz-exposed groups (0, 95% CI 0-0·0036). There were 23 (6%) stillbirths or miscarriages in 384 dolutegravir-exposed fetuses and 28 (3%) in the 1068 efavirenz-exposed fetuses (p=0·0037). Logistic regression models did not consistently indicate an association between dolutegravir exposure and risk of stillbirths or miscarriages. After study closure, two confirmed NTD outcomes in fetuses with periconception dolutegravir exposure were reported to public health officials. An updated estimate of NTD incidence incorporating these cases and the estimated number of additional dolutegravir-exposed pregnancies between Jan 1, 2015 and Feb 28, 2019, is 0·0018 (95% CI 0·0005-0·0067).
Neither dolutegravir nor efavirenz exposure was associated with NTDs in our national cohort; incidence of NTDs is probably well under 1% in dolutegravir-exposed HIV-positive women but still slightly above HIV-uninfected women (0·06%) in Brazil.
The Brazilian Ministry of Health and the United States' National Institutes of Health.
自 2017 年以来,多替拉韦在巴西已广泛使用。博茨瓦纳的一项信号提示,在受孕时母亲接触多替拉韦的婴儿出现神经管缺陷(NTD)的风险较高,此后公共卫生领导人启动了一项全国性调查,评估所有感染艾滋病毒的巴西孕妇在受孕前 8 周内接触多替拉韦的情况及其与 NTD、死胎或 22 周前(亦称自然流产)流产的潜在关联。
在这项回顾性、观察性、全国性队列研究中,我们通过巴西抗逆转录病毒治疗数据库,确定了在 2017 年 1 月 1 日至 2018 年 5 月 31 日期间受孕前 8 周内可能接触过多替拉韦的所有孕妇,以及 2015 年 1 月 1 日至 2018 年 5 月 31 日期间接触依非韦伦的孕妇(约为 3:1)。我们对确定的女性进行了详细的病历回顾。主要结局是 NTD 和 NTD、死胎或流产的复合指标。用 95%CI 计算 NTD 发生率。用 logistic 回归模型分析复合结局,并使用倾向评分匹配权重来平衡混杂因素。
在 1427 名纳入的女性中,有 382 名在受孕前 8 周内接触过多替拉韦。在怀孕期间,183 名(48%)多替拉韦暴露组和 465 名(44%)依非韦伦暴露组接受了叶酸补充。共有 1452 例分娩结局。多替拉韦暴露组(0,95%CI 0-0.0010)和依非韦伦暴露组(0,95%CI 0-0.0036)均未发生 NTD。384 例多替拉韦暴露胎儿中有 23 例(6%)发生死胎或流产,1068 例依非韦伦暴露胎儿中有 28 例(3%)(p=0.0037)。logistic 回归模型并未一致表明多替拉韦暴露与死胎或流产风险之间存在关联。在研究结束后,向公共卫生官员报告了两例在受孕前接触多替拉韦的胎儿确诊 NTD 病例。纳入这些病例和 2015 年 1 月 1 日至 2019 年 2 月 28 日期间估计的额外多替拉韦暴露妊娠数量后,更新的 NTD 发生率估计值为 0.0018(95%CI 0.0005-0.0067)。
在我们的全国性队列中,多替拉韦和依非韦伦暴露均与 NTD 无关;在多替拉韦暴露的 HIV 阳性女性中,NTD 发生率可能远低于 1%,但仍略高于巴西的 HIV 未感染女性(0.06%)。
巴西卫生部和美国国立卫生研究院。