Decreased Gross Motor, Working Memory, and Adaptive Behavior in Children with Congenital Adrenal Hyperplasia

先天性肾上腺增生症患儿的大运动能力、工作记忆和适应性行为下降

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Abstract

INTRODUCTION: Youth and adults with classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) are at risk for cognitive deficits and brain structural changes. Although factors inherent to CAH have been implicated in cognitive dysfunction, little is known about early developmental skills in these patients. Thus, we aimed to investigate development in younger children with CAH. METHODS: Cross-sectional study of 13 infants and toddlers (0.4-3.5 yrs) and 21 children (3.5-11 yrs) with classical CAH due to 21OHD. Infants and toddlers completed cognitive and motor skills screening (Bayley-4). Children also completed age-appropriate assessment of cognition (WISC-V Digit Span and Spatial Span subtests, NIH Toolbox-Version 2, WRAML-2 Design Memory subtest, CVLT-C) and motor skills (NIH Toolbox-Version 2). Their parents completed standardized reports of adaptive behavior and motor skills (Vineland-3). T tests compared the CAH group (mean percentile, mean ± SD) with normative means. RESULTS: Infants and toddlers with CAH exhibited lower gross motor skills (27th percentile, 8.2 ± 2.4, p = 0.03) compared to the normative mean. Children with CAH exhibited decreased auditory working memory skills (WISC-V, 27th percentile, 8.2 ± 1.8, p = 0.01), and lower nonverbal learning skills (WRAML-2, 21st percentile, 7.6 ± 3.4, p = 0.02). Their parents reported lower adaptive behavior (Vineland-3, 30th percentile, 92.2 ± 9.1, p = 0.004) and overall motor skills (26th percentile, 90.3 ± 11.4, p = 0.006) than the normative mean. CONCLUSIONS: Pediatric patients with CAH due to 21OHD exhibit distinct, age-dependent developmental deficits, with infants and toddlers displaying lower gross motor performance, and children exhibiting decreased auditory working memory and adaptive behavior skills. These findings suggest that early signs of developmental deficits in CAH may emerge at a younger age than previously recognized, emphasizing the role of clinical factors inherent to the disease.

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