Frambu Resource Centre for Rare Disorders, Siggerud, Norway.
University of Stavanger, Stavanger, Norway.
Mol Autism. 2018 Jan 8;9:1. doi: 10.1186/s13229-017-0184-2. eCollection 2018.
A substantial amount of research shows a higher rate of autistic type of problems in males compared to females. The 4:1 male to female ratio is one of the most consistent findings in autism spectrum disorder (ASD).Lately, the interest in studying ASD in genetic disorders has increased, and research has shown a higher prevalence of ASD in some genetic disorders than in the general population.Smith-Magenis syndrome (SMS) is a rare and complex genetic syndrome caused by an interstitial deletion of chromosome 17p11.2 or a mutation on the retinoic acid induced 1 gene. The disorder is characterised by intellectual disability, multiple congenital anomalies, obesity, neurobehavioural abnormalities and a disrupted circadian sleep-wake pattern.
Parents of 28 persons with SMS between 5 and 50 years old participated in this study. A total of 12 of the persons with SMS were above the age of 18 at the time of the study. A total of 11 came from Sweden and 17 were from Norway.We collected information regarding the number of autism spectrum symptoms using the Social Communication Questionnaire (SCQ) and the Social Responsiveness Scale (SRS). Adaptive behaviour was also measured using the Vineland Adaptive Behavior Scale II. The level of intellectual disability was derived from a review of the medical chart.
We found significant gender differences in ASD symptomatology using the SCQ and SRS questionnaires. We found approximately three females per male above the SCQ cutoff. The same differences were not found in the intellectual level and adaptive behaviour or for behavioural and emotional problems.Gender had an independent contribution in a regression model predicting the total SCQ score, and neither the Vineland Adaptive Behavior Scale II nor the Developmental Behaviour Checklist had an independent contribution to the SCQ scores.
We found a clear reversed gender difference in ASD symptomatology in persons with SMS. This may be relevant in the search for female protective factors assumed to explain the male bias in ASD.
大量研究表明,男性自闭症类型问题的发生率高于女性。4:1 的男女比例是自闭症谱系障碍(ASD)中最一致的发现之一。最近,人们对研究遗传障碍中的 ASD 兴趣增加,研究表明,一些遗传障碍中的 ASD 患病率高于普通人群。Smith-Magenis 综合征(SMS)是一种由 17p11.2 染色体的片段缺失或视黄酸诱导 1 基因的突变引起的罕见而复杂的遗传综合征。该疾病的特征为智力障碍、多种先天畸形、肥胖、神经行为异常和昼夜节律睡眠-觉醒模式紊乱。
28 名年龄在 5 至 50 岁之间的 SMS 患者的父母参与了这项研究。在研究时,共有 12 名 SMS 患者年龄超过 18 岁。其中 11 人来自瑞典,17 人来自挪威。我们使用社会沟通问卷(SCQ)和社会反应量表(SRS)收集了自闭症谱系症状的数量信息。适应性行为也使用 Vineland 适应性行为量表 II 进行测量。智力障碍的程度来自对病历的审查。
我们使用 SCQ 和 SRS 问卷发现了 ASD 症状学中的显著性别差异。我们发现,SCQ 截止值以上大约每 3 名女性就有 1 名男性。在智力水平和适应性行为或行为和情绪问题方面没有发现同样的差异。在预测 SCQ 总分的回归模型中,性别有独立的贡献,而 Vineland 适应性行为量表 II 和发育行为检查表对 SCQ 评分没有独立的贡献。
我们发现 SMS 患者的 ASD 症状学中存在明显的性别反转差异。这可能与寻找假设可以解释 ASD 中男性偏倚的女性保护因素有关。