Cerebra Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Birmingham, B15 2TT, UK.
Institute of Cognitive Neuroscience, University College London, Alexandra House, 17-19 Queen Square, London, WC1N 3AR, UK.
J Neurodev Disord. 2018 Jan 10;10(1):2. doi: 10.1186/s11689-017-9221-x.
Potocki-Lupski syndrome (PTLS) and Smith-Magenis syndrome (SMS) are related genomic disorders, as duplication 17p11.2 (associated with PTLS) is the reciprocal recombination product of the SMS microdeletion. While SMS has a relatively well-delineated behavioural phenotype, the behavioural profile in PTLS is less well defined, despite purported associations with autism spectrum disorder (ASD) and the suggestion that some behaviours may be diametric to those seen in SMS.
Caregivers of individuals with PTLS (N = 34; M age = 12.43, SD = 6.78) completed online behavioural questionnaires, including the Challenging Behaviour Questionnaire (CBQ), the Activity Questionnaire (TAQ), the Repetitive Behaviour Questionnaire (RBQ), the Mood, Interest and Pleasure Questionnaire-Short Form (MIPQ-S) and the Social Communication Questionnaire (SCQ), which assesses behaviours associated with ASD. Individuals with PTLS were matched on age and adaptive functioning to individuals with SMS (N = 31; M age = 13.61, SD = 6.85) and individuals with idiopathic ASD (N = 33; M age = 12.04, SD = 5.85) from an existing dataset.
Individuals with PTLS and SMS were less impaired than those with idiopathic ASD on the communication and reciprocal social interaction subscales of the SCQ, but neither syndrome group differed from idiopathic ASD on the restricted, repetitive and stereotyped behaviours subscale. On the repetitive behaviour measure, individuals with PTLS and idiopathic ASD scored higher than individuals with SMS on the compulsive behaviour subscale. Rates of self-injury and property destruction were significantly lower in PTLS and idiopathic ASD than in SMS. No between-syndrome differences were found in relation to overactivity or mood; however, impulsivity was greater in SMS than in PTLS.
Findings suggest some overlap in the behavioural phenotype of PTLS and features of ASD symptomatology; however, the overall profile of behaviours in PTLS appears to be divergent from both idiopathic ASD and SMS. Relative to idiopathic ASD, PTLS is not characterised by communication or social interaction deficits. However, restricted and repetitive behaviours were evident in PTLS, and these may be characterised specifically by compulsive behaviours. While several behavioural differences were identified between PTLS and SMS, there was little evidence of diametric behavioural phenotypes, particularly in relation to social behaviour.
波托奇斯基-卢普斯基综合征(PTLS)和史密斯-马根尼斯综合征(SMS)是相关的基因组疾病,因为 17p11.2 号染色体重复(与 PTLS 相关)是 SMS 微缺失的反向重组产物。虽然 SMS 具有相对明确的行为表型,但 PTLS 的行为特征定义不明确,尽管据称与自闭症谱系障碍(ASD)有关,并表明某些行为可能与 SMS 相反。
PTLS 患者的照顾者(N=34;M 年龄=12.43,SD=6.78)完成了在线行为问卷,包括挑战性行为问卷(CBQ)、活动问卷(TAQ)、重复行为问卷(RBQ)、情绪、兴趣和愉悦问卷-短表(MIPQ-S)和社会沟通问卷(SCQ),评估与 ASD 相关的行为。PTLS 患者根据年龄和适应功能与 SMS(N=31;M 年龄=13.61,SD=6.85)和特发性 ASD(N=33;M 年龄=12.04,SD=5.85)患者进行匹配,这些患者来自一个现有的数据集。
与特发性 ASD 患者相比,PTLS 和 SMS 患者在 SCQ 的沟通和互惠社会互动分量表上的损伤程度较低,但这两个综合征组在限制、重复和刻板行为分量表上与特发性 ASD 没有差异。在重复行为测量中,PTLS 和特发性 ASD 患者在强迫行为分量表上的得分高于 SMS 患者。PTLS 和特发性 ASD 患者的自伤和财产破坏率明显低于 SMS 患者。在多动和情绪方面,PTLS 和 SMS 之间没有差异;然而,冲动性在 SMS 中比在 PTLS 中更大。
研究结果表明,PTLS 的行为表型与 ASD 症状学的某些方面存在重叠;然而,PTLS 的整体行为表现似乎与特发性 ASD 和 SMS 都不同。与特发性 ASD 相比,PTLS 没有沟通或社会互动缺陷。然而,PTLS 中存在受限和重复行为,这些行为可能以强迫行为为特征。尽管在 PTLS 和 SMS 之间发现了一些行为差异,但几乎没有证据表明存在相反的行为表型,尤其是在社交行为方面。