Social cognition in adults with neurofibromatosis type 1.

IF 2.6 4区 心理学 Q2 CLINICAL NEUROLOGY
Julie Remaud, Jérémy Besnard, Sébastien Barbarot, Arnaud Roy
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引用次数: 0

Abstract

Objective: Adult patients with the genetic disease neurofibromatosis type 1 (NF1) frequently report social difficulties. To date, however, only two studies have explored whether these difficulties are caused by social cognition deficits, and these yielded contradictory data. The aim of the present study was to exhaustively assess social cognition abilities (emotion, theory of mind, moral reasoning, and social information processing) in adults with NF1, compared with a control group, and to explore links between social cognition and disease characteristics (mode of inheritance, severity, and visibility).

Method: We administered a social cognition battery to 20 adults with NF1 (mean age = 26.5 years, SD = 7.4) and 20 healthy adults matched for sociodemographic variables.

Results: Patients scored significantly lower than controls on emotion, theory of mind, moral reasoning, and social information processing tasks. No effects of disease characteristics were found.

Conclusions: These results appear to confirm that adults with NF1 have a social cognition weaknesses that could explain, at least in part, their social difficulties, although social abilities are not all impaired to the same extent. Regarding the impact of the disease characteristics, the patient sample seemed slightly insufficient for the power analyses performed. Thus, this exploratory study should form the basis of further research, with the objective of replicating these results with larger and more appropriately matched samples.

1 型神经纤维瘤病成人的社会认知能力。
目的:患有遗传病 1 型神经纤维瘤病 (NF1) 的成年患者经常报告社交困难。然而,迄今为止,只有两项研究探讨了这些困难是否是由社会认知障碍造成的,而且这些研究得出的数据相互矛盾。本研究旨在与对照组相比,全面评估 NF1 成人的社会认知能力(情感、心智理论、道德推理和社会信息处理),并探讨社会认知与疾病特征(遗传方式、严重程度和可见性)之间的联系:我们对20名NF1成人患者(平均年龄=26.5岁,SD=7.4)和20名社会人口学变量匹配的健康成人进行了社会认知测试:结果:患者在情绪、心智理论、道德推理和社会信息处理任务上的得分明显低于对照组。没有发现疾病特征的影响:这些结果似乎证实,成年 NF1 患者存在社会认知缺陷,这至少可以部分解释他们的社交困难,尽管社交能力受损的程度不尽相同。关于疾病特征的影响,患者样本似乎略微不足以进行功率分析。因此,这项探索性研究应该成为进一步研究的基础,目的是用更大和更匹配的样本来重复这些结果。
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来源期刊
CiteScore
5.40
自引率
3.80%
发文量
185
审稿时长
4-8 weeks
期刊介绍: The Journal of the International Neuropsychological Society is the official journal of the International Neuropsychological Society, an organization of over 4,500 international members from a variety of disciplines. The Journal of the International Neuropsychological Society welcomes original, creative, high quality research papers covering all areas of neuropsychology. The focus of articles may be primarily experimental, applied, or clinical. Contributions will broadly reflect the interest of all areas of neuropsychology, including but not limited to: development of cognitive processes, brain-behavior relationships, adult and pediatric neuropsychology, neurobehavioral syndromes (such as aphasia or apraxia), and the interfaces of neuropsychology with related areas such as behavioral neurology, neuropsychiatry, genetics, and cognitive neuroscience. Papers that utilize behavioral, neuroimaging, and electrophysiological measures are appropriate. To assure maximum flexibility and to promote diverse mechanisms of scholarly communication, the following formats are available in addition to a Regular Research Article: Brief Communication is a shorter research article; Rapid Communication is intended for "fast breaking" new work that does not yet justify a full length article and is placed on a fast review track; Case Report is a theoretically important and unique case study; Critical Review and Short Review are thoughtful considerations of topics of importance to neuropsychology and include meta-analyses; Dialogue provides a forum for publishing two distinct positions on controversial issues in a point-counterpoint format; Special Issue and Special Section consist of several articles linked thematically; Letter to the Editor responds to recent articles published in the Journal of the International Neuropsychological Society; and Book Review, which is considered but is no longer solicited.
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