Social cognition, psychosocial development and well-being in galactosemia.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Clémentine Bry, Klervi Propice, Jessica Bourgin, Morgane Métral
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Abstract

Background: Classic galactosemia is a rare inherited metabolic disease with long-term complications, particularly in the psychosocial domain. Patients report a lower quality of social life, difficulties in interactions and social relationships, and a lower mental health. We hypothesised that social cognition deficits could partially explain this psychological symptomatology. Eleven adults with galactosemia and 31 control adults participated in the study. We measured social cognition skills in cognitive and affective theory of Mind, and in basic and complex emotion recognition. We explored psychosocial development and mental well-being.

Results: We found significant deficits on all 4 social cognition measures. Compared to controls, participants with galactosemia were impaired in the 2nd-order cognitive theory of mind, in affective theory of mind, and in basic and complex emotion recognition. Participants with galactosemia had a significant delay in their psychosexual development, but we found no delay in social development and no significant decrease in mental health.

Conclusion: Social cognition processes seem impaired among our participants with galactosemia. We discuss the future path research may follow. More research is needed to replicate and strengthen these results and establish the links between psychosocial complications and deficits in social cognition.

半乳糖血症患者的社会认知、社会心理发展和幸福感。
背景:典型半乳糖血症是一种罕见的遗传性代谢疾病,具有长期并发症,尤其是在社会心理方面。患者的社会生活质量较低,在人际交往和社会关系方面存在困难,心理健康水平较低。我们假设社会认知障碍可以部分解释这种心理症状。11名半乳糖血症成人患者和31名对照组成人患者参加了研究。我们测量了认知和情感心智理论方面的社会认知能力,以及基本和复杂情绪识别能力。我们还探讨了社会心理发展和心理健康问题:结果:我们发现,在所有 4 项社会认知测量中,半乳糖罹患者都存在明显的缺陷。与对照组相比,半乳糖血症患者在二阶认知心智理论、情感心智理论以及基本和复杂情感识别方面均存在缺陷。半乳糖血症患者的性心理发育明显延迟,但我们发现他们的社会性发育没有延迟,心理健康水平也没有明显下降:结论:半乳糖血症患者的社会认知过程似乎受到了影响。我们讨论了未来的研究方向。我们需要进行更多的研究,以复制和加强这些结果,并确定社会心理并发症与社会认知缺陷之间的联系。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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