Astley Susan J, Bledsoe Julia M, Davies Julian K
Professor of Epidemiology/Pediatrics, University of Washington, Seattle, WA 98195, USA.
Clinical Professor of Pediatrics, University of Washington, Seattle, WA 98195,USA.
Adv Pediatr Res. 2016;3(3). doi: 10.12715/apr.2016.3.9. Epub 2016 Dec 1.
Laboratory studies confirm prenatal alcohol exposure (PAE) causes growth deficiency (GD). GD has traditionally been a core diagnostic feature of fetal alcohol spectrum disorders (FASD), but was removed from the Canadian and Australian FASD diagnostic guidelines in 2016. This study aimed to empirically assess the clinical role and value of GD in FASD diagnosis.
Data from 1814 patients with FASD from the University of Washington Fetal Alcohol Syndrome Diagnostic & Prevention dataset were analyzed to answer the following questions: 1) Is there evidence of a causal association between PAE and GD in our clinical population? 2) Is GD sufficiently prevalent among individuals with PAE to warrant its inclusion as a diagnostic criterion? 3) Does GD aid the diagnostic team in identifying and/or predicting which individuals will be most impaired by their PAE?
GD significantly correlated with PAE. GD was as prevalent as the other core diagnostic features (facial and CNS abnormalities). GD occurred in all FASD diagnoses and increased in prevalence with increasing severity of diagnosis. The most prevalent form of GD was postnatal short stature. GD was as highly correlated with, and predictive of, severe brain dysfunction as the FAS facial phenotype. Individuals with GD had a two to three-fold increased risk for severe brain dysfunction. Sixty percent of patients with severe GD had severe brain dysfunction. GD accurately predicted which infants presented with severe brain dysfunction later in childhood.
GD is an essential diagnostic criterion for FASD and will remain in the FASD 4-Digit Code.
实验室研究证实,孕期酒精暴露(PAE)会导致生长发育迟缓(GD)。传统上,生长发育迟缓一直是胎儿酒精谱系障碍(FASD)的核心诊断特征,但在2016年被加拿大和澳大利亚的FASD诊断指南删除。本研究旨在实证评估生长发育迟缓在FASD诊断中的临床作用和价值。
分析了来自华盛顿大学胎儿酒精综合征诊断与预防数据集的1814例FASD患者的数据,以回答以下问题:1)在我们的临床人群中,是否有证据表明PAE与GD之间存在因果关系?2)生长发育迟缓在PAE个体中是否足够普遍,足以将其作为诊断标准纳入?3)生长发育迟缓是否有助于诊断团队识别和/或预测哪些个体将受到PAE的最大损害?
生长发育迟缓与孕期酒精暴露显著相关。生长发育迟缓与其他核心诊断特征(面部和中枢神经系统异常)一样普遍。生长发育迟缓出现在所有FASD诊断中,并且随着诊断严重程度的增加而患病率上升。生长发育迟缓最常见的形式是出生后身材矮小。生长发育迟缓与FAS面部表型一样,与严重脑功能障碍高度相关且具有预测性。患有生长发育迟缓的个体出现严重脑功能障碍的风险增加两到三倍。60%的严重生长发育迟缓患者患有严重脑功能障碍。生长发育迟缓准确地预测了哪些婴儿在儿童后期会出现严重脑功能障碍。
生长发育迟缓是FASD的一项重要诊断标准,并将保留在FASD四位数字编码中。