Lundström Sebastian, Reichenberg Abraham, Anckarsäter Henrik, Lichtenstein Paul, Gillberg Christopher
Gillberg Neuropsychiatry Centre, University of Gothenburg, Kungsgatan 12, 411 19, Gothenburg, Sweden Centre for Ethics, Law and Mental Health, University of Gothenburg, Sweden
Departments of Psychiatry and Preventive Medicine, Mount Sinai School of Medicine, New York, NY, USA.
BMJ. 2015 Apr 28;350:h1961. doi: 10.1136/bmj.h1961.
To compare the annual prevalence of the autism symptom phenotype and of registered diagnoses for autism spectrum disorder during a 10 year period in children.
Population based study.
Child and Adolescent Twin Study and national patient register, Sweden.
19, 993 twins (190 with autism spectrum disorder) and all children (n=1,078,975; 4620 with autism spectrum disorder) born in Sweden over a 10 year period from 1993 to 2002.
Annual prevalence of the autism symptom phenotype (that is, symptoms on which the diagnostic criteria are based) assessed by a validated parental telephone interview (the Autism-Tics, ADHD and other Comorbidities inventory), and annual prevalence of reported diagnoses of autism spectrum disorder in the national patient register.
The annual prevalence of the autism symptom phenotype was stable during the 10 year period (P=0.87 for linear time trend). In contrast, there was a monotonic significant increase in prevalence of registered diagnoses of autism spectrum disorder in the national patient register (P<0.001 for linear trend).
The prevalence of the autism symptom phenotype has remained stable in children in Sweden while the official prevalence for registered, clinically diagnosed, autism spectrum disorder has increased substantially. This suggests that administrative changes, affecting the registered prevalence, rather than secular factors affecting the pathogenesis, are important for the increase in reported prevalence of autism spectrum disorder.
比较10年间儿童自闭症症状表型的年患病率以及自闭症谱系障碍的登记诊断率。
基于人群的研究。
瑞典儿童和青少年双胞胎研究及国家患者登记处。
19993对双胞胎(190例患有自闭症谱系障碍)以及1993年至2002年这10年间在瑞典出生的所有儿童(n = 1078975;4620例患有自闭症谱系障碍)。
通过经过验证的家长电话访谈(自闭症-抽动、注意缺陷多动障碍及其他共病量表)评估自闭症症状表型(即诊断标准所依据的症状)的年患病率,以及国家患者登记处报告的自闭症谱系障碍诊断的年患病率。
在这10年期间,自闭症症状表型的年患病率保持稳定(线性时间趋势的P = 0.87)。相比之下,国家患者登记处登记的自闭症谱系障碍诊断患病率呈单调显著增加(线性趋势的P < 0.001)。
瑞典儿童自闭症症状表型的患病率保持稳定,而官方登记的临床诊断自闭症谱系障碍的患病率大幅上升。这表明影响登记患病率的行政变化而非影响发病机制的长期因素,对于自闭症谱系障碍报告患病率的增加很重要。