Developmental associations between cognition and adaptive behavior in intellectual and developmental disability.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Andrew Dakopolos, Emma Condy, Elizabeth Smith, Danielle Harvey, Aaron J Kaat, Jeanine Coleman, Karen Riley, Elizabeth Berry-Kravis, David Hessl
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引用次数: 0

Abstract

Background: Intellectual and developmental disabilities (IDDs) are associated with both cognitive challenges and difficulties in conceptual, social, and practical areas of living, commonly referred to as adaptive behavior (DSM-5). Although cross-sectional associations between intelligence or cognition and adaptive behavior have been reported in IDD populations, no study to date has examined whether developmental changes in cognition contribute to or track with changes in adaptive behavior. The present study sought to examine associations of longitudinal developmental change in domains of cognition (NIH Toolbox Cognition Battery, NIHTB-CB) and adaptive behavior domains (Vineland Adaptive Behavior Scales-3; VABS-3) including Socialization, Communication, and Daily Living Skills (DLS) over a two year period in a large sample of children, adolescents and young adults with IDD.

Methods: Three groups were recruited, including those with fragile X syndrome, Down syndrome, and other/idiopathic intellectual disability. Eligible participants (n = 263) included those who were between 6 and 26 years (mage = 15.52, sd = 5.17) at Visit 1, and who had a diagnosis of, or suspected intellectual disability (ID), including borderline ID, with a mental age of at least 3.0 years. Participants were given cognitive and adaptive behavior assessments at two time points over a two year period (m = 2.45 years, range = 1.27 to 5.56 years). In order to examine the association of developmental change between cognitive and adaptive behavior domains, bivariate latent change score (BLCS) models were fit to compare change in the three cognitive domains measured by the NIHTB-CB (Fluid Cognition, Crystallized Cognition, Total Cognition) and the three adaptive behavior domains measured by the VABS-3 (Communication, DLS, and Socialization).

Results: Over a two year period, change in cognition (both Crystallized and Total Composites) was significantly and positively associated with change in daily living skills. Also, baseline cognition level predicted growth in adaptive behavior, however baseline adaptive behavior did not predict growth in cognition in any model.

Conclusions: The present study demonstrated that developmental changes in cognition and adaptive behavior are associated in children and young adults with IDD, indicating the potential for cross-domain effects of intervention. Notably, improvements in DLS emerged as a primary area of adaptive behavior that positively related to improvements in cognition. This work provides evidence for the clinical, "real life" meaningfulness of changes in cognition detected by the NIHTB-CB in IDD, and provides empirical support for the NIHTB-CB as a fit-for-purpose performance-based outcome measure for this population.

智力和发育障碍患者认知与适应行为之间的发展关联。
背景:智力和发育障碍(IDDs)既与认知挑战有关,也与概念、社交和实际生活方面的困难有关,这些困难通常被称为适应行为(DSM-5)。虽然有报道称在 IDD 群体中智力或认知与适应行为之间存在横断面关联,但迄今为止还没有研究探讨认知的发展变化是否会导致适应行为的变化或与之相关。本研究试图通过对大量IDD儿童、青少年和年轻成人样本的研究,探讨认知领域(美国国立卫生研究院工具箱认知测验,NIHTB-CB)和适应行为领域(维尼兰适应行为量表-3,VABS-3)的纵向发展变化与两年内社交、沟通和日常生活技能(DLS)的关联:招募了三组患者,包括脆性 X 综合征患者、唐氏综合征患者和其他/特发性智障患者。符合条件的参与者(n = 263)包括访问 1 时年龄在 6 至 26 岁之间(mage = 15.52,sd = 5.17)、被诊断为或疑似智障(ID)(包括边缘型智障)且心智年龄至少为 3.0 岁的人。在两年的时间里(m = 2.45 岁,范围 = 1.27 至 5.56 岁),参与者在两个时间点接受了认知和适应行为评估。为了研究认知领域和适应行为领域之间发展变化的关联,我们拟合了双变量潜在变化得分(BLCS)模型,以比较 NIHTB-CB 测定的三个认知领域(流体认知、结晶认知、总体认知)和 VABS-3 测定的三个适应行为领域(沟通、DLS 和社交)的变化:在为期两年的时间里,认知能力(晶体化认知能力和总认知能力)的变化与日常生活技能的变化呈显著正相关。此外,基线认知水平也能预测适应行为的增长,但在任何模型中,基线适应行为都不能预测认知的增长:本研究表明,在患有 IDD 的儿童和青少年中,认知和适应行为的发展变化是相关联的,这表明干预措施有可能产生跨领域的效果。值得注意的是,DLS 的改善是适应行为的主要领域,与认知的改善呈正相关。这项研究为通过 NIHTB-CB 检测到的 IDD 认知变化的临床 "现实生活 "意义提供了证据,并为 NIHTB-CB 作为适用于该人群的基于表现的结果测量提供了经验支持。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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