Mayo Clinic Alix School of Medicine, Phoenix, Arizona.
Department of Genetic Medicine, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Curr Opin Pediatr. 2021 Dec 1;33(6):570-575. doi: 10.1097/MOP.0000000000001071.
The purpose of this review is to describe recent findings on the clinical presentation, pathogenesis, and management of fetal alcohol spectrum disorders (FASDs). Alcohol causes a range of physical, developmental, and cognitive impairments on the developing fetus. Individuals exposed to alcohol prenatally have a wide variability in dysmorphic and neurologic features. Hence, a greater understanding of the mechanisms through which alcohol induces defects in the developing fetus is imperative in developing therapies that prevent alcohol-induced effects.
Current research has focused on leveraging technology to developing tools that can aid in the diagnostic process, defining patterns of neurocognition and neuroimaging specific to FASD, developing neurobehavioral and pharmacologic interventions, and expanding access to care.
FASDs are a common cause of neurodevelopmental impairment in school-age children, and their recognition is essential to provide early interventions in order to optimize the outcome for these individuals when they reach adulthood. Although previously thought to be the result of irreversible neurologic injury from prenatal alcohol exposure, recent evidence points to the benefits of applying principles regarding neuroplasticity in improving the lives for patients and their families.
本文旨在描述胎儿酒精谱系障碍(FASD)的临床表现、发病机制和治疗的最新研究进展。酒精对发育中的胎儿会造成一系列的身体、发育和认知损伤。产前接触酒精的个体在畸形和神经特征方面存在广泛的差异。因此,深入了解酒精导致胎儿发育缺陷的机制对于开发预防酒精引起的效应的治疗方法至关重要。
目前的研究重点是利用技术开发工具,以帮助诊断,确定与 FASD 相关的特定神经认知和神经影像学模式,制定神经行为和药物干预措施,并扩大获得护理的途径。
FASD 是学龄儿童神经发育障碍的常见原因,为了优化这些人成年后的结果,早期干预对于识别 FASD 至关重要。尽管之前认为这是产前酒精暴露导致的不可逆神经损伤的结果,但最近的证据表明,应用神经可塑性原则改善患者及其家属生活的益处。