Lundström Sebastian, Taylor Mark, Larsson Henrik, Lichtenstein Paul, Kuja-Halkola Ralf, Gillberg Christopher
Gillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Center for Ethics, Law and Mental health (CELAM), Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
J Child Psychol Psychiatry. 2022 May;63(5):591-598. doi: 10.1111/jcpp.13497. Epub 2021 Aug 7.
The prevalence of diagnosed Autism Spectrum Disorder (ASD) has increased substantially across the world. Much - or even most - prevalence increase seems to reflect changes in diagnostic practice and ascertainment. A key part of ASD assessment is to document that the relevant symptoms are associated with clinical impairment. The aim of the present study is to capitalize on a nationwide longitudinal study spanning 15 consecutive birth year cohorts in order to investigate whether there has been a secular change in how parents perceive the impairment and suffering conferred by autism symptomatology in their children.
Data came from the Child and Adolescent Twin Study in Sweden (27,240 individuals), where parents had reported on their child's ASD symptoms and impairment. Impairment due to ASD symptoms was regressed on an ASD symptom score across time. This was done for five 3-year birth cohorts (1995-1997, 1998-2000, 2001-2003, 2004-2006, and 2007-2009).
Reported impairment increased with consecutively later birth cohorts. This was evident across all levels of autism symptomatology. At clinically relevant levels of symptomatology, parents of those born 2007-2009 reported a 23% higher degree of impairment as compared with parents of those born in 1995-1997. The relative difference, however, was even greater at levels that previously would have been considered below the diagnostic threshold.
The results presented here contribute to the notion of a growing diffuseness in the conceptualization of the ASD diagnosis by adding the element of secular changes in the parental perception of the consequences of ASD symptom expression.
在全球范围内,已确诊的自闭症谱系障碍(ASD)患病率大幅上升。大部分——甚至是绝大部分——患病率的增加似乎反映了诊断实践和确诊率的变化。ASD评估的一个关键部分是记录相关症状与临床损害相关。本研究的目的是利用一项覆盖连续15个出生队列的全国性纵向研究,以调查父母对其子女自闭症症状所带来的损害和痛苦的认知是否存在长期变化。
数据来自瑞典儿童和青少年双胞胎研究(27240名个体),其中父母报告了孩子的ASD症状和损害情况。将ASD症状导致的损害随时间推移与ASD症状评分进行回归分析。对五个3年出生队列(1995 - 1997年、1998 - 2000年、2001 - 2003年、2004 - 2006年和2007 - 2009年)进行了此项分析。
报告的损害随着出生队列时间的推移而增加。这在所有自闭症症状水平上都很明显。在具有临床相关性的症状水平上,2007 - 2009年出生孩子的父母报告的损害程度比1995 - 1997年出生孩子的父母高23%。然而,在之前被认为低于诊断阈值的水平上,相对差异甚至更大。
此处呈现的结果通过增加父母对ASD症状表达后果认知的长期变化这一要素,有助于ASD诊断概念日益模糊这一观点的形成。