Bakhireva Ludmila N, Lowe Jean R, Gutierrez Hilda L, Stephen Julia M
Department of Pharmacy Practice and Administrative Sciences, University of New Mexico College of Pharmacy, Albuquerque, NM, USA ; Department of Family and Community Medicine, University of New Mexico, Albuquerque, NM, USA.
Department of Pediatrics, University of New Mexico, Albuquerque, NM, USA.
Adv Pediatr Res. 2015 Apr 28;2(2015). doi: 10.12715/apr.2015.2.10.
While intervention is the leading factor in reducing long-term disabilities in children with fetal alcohol spectrum disorder (FASD), early identification of children affected by prenatal alcohol exposure (PAE) remains challenging. Deficits in higher-order cognitive domains (e.g. executive function) might be more specific to FASD than global neurodevelopmental tests, yet these functions are not developed in very young children. Measures of early sensorimotor development may provide early indications of atypical brain development during the first two years of life.
This paper describes the novel methodology of the Ethanol, Neurodevelopment, Infant and Child Health (ENRICH) prospective cohort study of 120 maternal-infant pairs with a goal to identify early indices of functional brain impairment associated with PAE. The cohort is established by recruiting women early in pregnancy and classifying them into one of three study groups: patients on opioid-maintenance therapy who consume alcohol during pregnancy (Group 1), patients on opioid-maintenance therapy who abstain from alcohol during pregnancy (Group 2), and healthy controls (Group 3). After the initial prenatal assessment (Visit 1), patients are followed to Visit 2 occurring at delivery, and two comprehensive assessments of children at six (Visit 3) and 20 months (Visit 4) of age. ENRICH recruitment started in November 2013 and 87 women were recruited during the first year. During Year 1, the biospecimen (maternal whole blood, serum, urine, dry blood spots of a newborn) collection rate was 100% at Visit 1, and 97.6% for those who completed Visit 2.
The tiered screening approach, evaluation of confounders, neurocognitive and magneto-/electro-encephalography (MEG/EEG) outcomes, and ethical considerations are discussed.
虽然干预是降低胎儿酒精谱系障碍(FASD)儿童长期残疾的主要因素,但早期识别受产前酒精暴露(PAE)影响的儿童仍然具有挑战性。与全球神经发育测试相比,高阶认知领域(如执行功能)的缺陷可能更具FASD特异性,但这些功能在幼儿中尚未发育。早期感觉运动发育的测量可能为生命最初两年非典型脑发育提供早期迹象。
本文描述了乙醇、神经发育、婴儿和儿童健康(ENRICH)前瞻性队列研究的新方法,该研究涉及120对母婴,目的是确定与PAE相关的功能性脑损伤的早期指标。该队列通过在孕期早期招募女性并将她们分为三个研究组之一来建立:孕期饮酒的阿片类药物维持治疗患者(第1组)、孕期戒酒的阿片类药物维持治疗患者(第2组)和健康对照组(第3组)。在最初的产前评估(第1次访视)后,对患者进行随访直至分娩时的第2次访视,并在儿童6个月(第3次访视)和20个月(第4次访视)时进行两次全面评估。ENRICH招募工作于2013年11月开始,第一年招募了87名女性。在第1年,生物样本(母亲全血、血清、尿液、新生儿干血斑)在第1次访视时的采集率为100%,完成第2次访视的患者采集率为97.6%。
讨论了分层筛查方法、混杂因素评估以及神经认知和脑磁图/脑电图(MEG/EEG)结果及伦理考量。