From the *Department of Medicine, Divisions of Infectious Diseases and General Medicine, Department of Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine, Mount Sinai; and †ICAP, Mailman School of Public Health and College of Physicians and Surgeons, Columbia University, New York, NY.
Pediatr Infect Dis J. 2014 Jul;33(7):734-40. doi: 10.1097/INF.0000000000000224.
Despite a wide body of literature supporting the use of antenatal antiretrovirals (ARV) for the prevention of mother-to-child transmission, there remains a need for continued monitoring as the intrauterine interval is a critical period during which fetal programming influences the future health and development of the child.
We conducted a systematic review of the current literature addressing potential metabolic complications of in utero HIV and ARV exposure. We describe studies evaluating metabolic outcomes such as intrauterine and early postnatal growth, bone health and mitochondrial toxicity.
Overall, infants exposed to HIV/ARV do not appear to exhibit vastly compromised intrauterine or early postnatal growth. However, some studies on the effect of combination antiretroviral therapy on small for gestational age and low birth weight outcomes in low-middle income countries show a risk for small for gestational age/low birth weight while those in the United States do not. Postnatal growth to 1 year does not appear to be affected by intrauterine tenofovir exposure in African studies, but a US study found statistically significant differences in length for age z scores (LAZ) at 1 year. Little data exists on long-term bone health. Mitochondrial toxicity including abnormal mitochondrial morphology and DNA content, as well as neurologic deficits and death, have been demonstrated in HIV/ARV-exposed infants.
Although gross measures of metabolic well-being appear to be reassuring, careful vigilance of even small risks for potential serious adverse effects to infants exposed to intrauterine HIV/ARVs is warranted as intrauterine fetal metabolic programming may substantially impact the future health of the child.
尽管有大量文献支持使用产前抗逆转录病毒药物 (ARV) 来预防母婴传播,但仍需要继续监测,因为子宫内间隔是胎儿发育过程中影响儿童未来健康和发育的关键时期。
我们对当前关于宫内 HIV 和 ARV 暴露潜在代谢并发症的文献进行了系统评价。我们描述了评估代谢结果的研究,如宫内和早期产后生长、骨骼健康和线粒体毒性。
总体而言,暴露于 HIV/ARV 的婴儿似乎并没有表现出严重的宫内或早期产后生长受损。然而,一些关于中低收入国家联合抗逆转录病毒疗法对小于胎龄儿和低出生体重结局影响的研究表明,存在小于胎龄/低出生体重的风险,而在美国则没有。在非洲的研究中,产前替诺福韦暴露似乎不会影响 1 岁时的产后生长,但美国的一项研究发现,1 岁时年龄身长 Z 评分 (LAZ) 的统计学差异有意义。关于长期骨骼健康的数据很少。已经证明,宫内 HIV/ARV 暴露的婴儿存在线粒体毒性,包括线粒体形态和 DNA 含量异常以及神经缺陷和死亡。
尽管代谢健康的总体衡量标准似乎令人放心,但对于宫内 HIV/ARV 暴露的婴儿,即使存在潜在严重不良影响的微小风险,也需要谨慎监测,因为宫内胎儿代谢编程可能会对儿童的未来健康产生重大影响。