Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics (Riglin, A.K. Thapar, Langley, Collishaw, Tagg, A. Thapar), and School of Psychology (Livingston, Langley), Cardiff University, Cardiff, U.K.; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, U.K. (Wootton, Davey Smith, Stergiakouli, Tilling).
Am J Psychiatry. 2021 Aug 1;178(8):752-760. doi: 10.1176/appi.ajp.2020.20071119. Epub 2021 Apr 26.
Autism spectrum disorder (ASD) is currently considered an early-onset neurodevelopmental condition. Follow-up studies of clinic-ascertained autism suggest that autistic symptoms typically decline with age, although symptom improvement is limited for some. To date there have been no population-based prospective studies investigating the natural history of autistic symptoms from childhood to adulthood. The aim of this study was to characterize the development and heterogeneity of autistic symptoms in a population-based cohort from childhood to age 25.
Data were analyzed in a prospective U.K. population-based cohort (ALSPAC). Trajectories were derived using five assessments of the parent-rated Social and Communication Disorders Checklist (SCDC) spanning ages 7-25. Additional measures were used to validate symptom trajectories.
Three distinct SCDC symptom trajectory classes were identified: low (88.5%), declining (5.0%), and late-emerging (6.5%). Both the declining and late-emerging trajectory classes were associated with child and adult ASD measures, low IQ, communication problems, peer problems, and worse adult functioning compared with the low trajectory class. Male sex was associated with a higher likelihood of being in the declining trajectory class (odds ratio=2.84, 95% CI=2.19, 3.69). This sex difference was not observed in the late-emerging class (odds ratio=1.00, 95% CI=0.80, 1.24) compared with the low trajectory class.
ASD symptom levels that emerged early tended to decline across development, although impairment was still present in adulthood for some. For others, autistic symptoms emerged across adolescence and adulthood. This challenges our current understanding that ASD symptoms inevitably first manifest early in development.
自闭症谱系障碍(ASD)目前被认为是一种早期发病的神经发育障碍。对门诊确诊自闭症的随访研究表明,自闭症症状通常会随着年龄的增长而减轻,尽管有些症状的改善是有限的。迄今为止,还没有基于人群的前瞻性研究调查自闭症症状从儿童期到成年期的自然史。本研究旨在从儿童期到 25 岁的人群中,描述自闭症症状的发展和异质性。
对英国基于人群的前瞻性队列研究(ALSPAC)的数据进行了分析。使用父母评定的社会和交流障碍检查表(SCDC)的五次评估来确定轨迹,涵盖了 7 至 25 岁的年龄。使用额外的措施来验证症状轨迹。
确定了三种不同的 SCDC 症状轨迹类别:低(88.5%)、下降(5.0%)和晚发(6.5%)。下降和晚发轨迹类别的儿童和成年自闭症评估、低智商、沟通问题、同伴问题和较差的成年功能都与低轨迹类别的儿童和成年自闭症评估、低智商、沟通问题、同伴问题和较差的成年功能相关。与低轨迹类相比,男性(比值比=2.84,95%可信区间=2.19,3.69)更有可能处于下降轨迹类。这种性别差异在晚发轨迹类中没有观察到(比值比=1.00,95%可信区间=0.80,1.24)。
早期出现的 ASD 症状水平在整个发育过程中趋于下降,尽管一些人在成年后仍存在障碍。对于其他人,自闭症症状在青春期和成年期出现。这挑战了我们目前的认识,即 ASD 症状不可避免地首先在发育早期出现。