Academic Journal
Social skills and autism spectrum disorder symptoms in children with neurofibromatosis type 1: evidence for clinical trial outcomes
| العنوان: | Social skills and autism spectrum disorder symptoms in children with neurofibromatosis type 1: evidence for clinical trial outcomes |
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| المؤلفون: | Payne, Jonathan M, Walsh, Karin S, Pride, Natalie A, Haebich, Kristina M, Maier, Alice, Chisholm, Anita, Glad, Danielle M, Casnar, Christina L, Rouel, Melissa, Lorenzo, Jennifer, Del Castillo, Allison, North, Kathryn N, Klein‐Tasman, Bonita |
| المساهمون: | US Department of Defence Investigator Initiated Research Award as part of the Neurofibromatosis Research Program |
| المصدر: | Developmental Medicine & Child Neurology ; volume 62, issue 7, page 813-819 ; ISSN 0012-1622 1469-8749 |
| بيانات النشر: | Wiley |
| سنة النشر: | 2020 |
| المجموعة: | Wiley Online Library (Open Access Articles via Crossref) |
| الوصف: | Aim We examined key features of two outcome measures for social dysfunction and autism spectrum disorder traits, the Social Responsiveness Scale, Second Edition (SRS‐2) and the Social Skills Improvement System – Rating Scales (SSIS‐RS), in children with neurofibromatosis type 1 (NF1). The aim of the study was to provide objective evidence as to which behavioural endpoint should be used in clinical trials. Method Cross‐sectional behavioural and demographic data were pooled from four paediatric NF1 tertiary referral centres in Australia and the United States ( N =122; 65 males, 57 females; mean age [SD] 9y 2mo [3y], range 3–15y). Results Distributions of SRS‐2 and SSIS‐RS scores were unimodal and both yielded deficits, with a higher proportion of severely impaired scores on the SRS‐2 (16.4%) compared to the SSIS‐RS (8.2%). Pearson’s product‐moment correlations revealed that both questionnaires were highly related to each other ( r =−0.72, p <0.001) and to measures of adaptive social functioning (both p <0.001). Both questionnaires were significantly related to attention‐deficit/hyperactivity disorder symptoms, but only very weakly associated with intelligence. Interpretation The SRS‐2 and SSIS‐RS capture social dysfunction associated with NF1, suggesting both may be suitable choices for assessing social outcomes in this population in a clinical trial. However, careful thought needs to be given to the nature of the intervention when selecting either as a primary endpoint. What this paper adds The Social Responsiveness Scale, Second Edition yielded a large deficit relative to population norms. The Social Skills Improvement System – Rating Scales yielded a moderate deficit relative to population norms. Both scales were highly correlated, suggesting that they are measuring a unitary construct. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1111/dmcn.14517 |
| الاتاحة: | http://dx.doi.org/10.1111/dmcn.14517 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fdmcn.14517 https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.14517 https://onlinelibrary.wiley.com/doi/full-xml/10.1111/dmcn.14517 |
| Rights: | http://onlinelibrary.wiley.com/termsAndConditions#vor |
| رقم الانضمام: | edsbas.A9778D5 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1111/dmcn.14517 |
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