Suppr超能文献

银-鲁综合征青少年和成人的生活质量和心理健康。

Quality of life and mental health of adolescents and adults with Silver-Russell syndrome.

机构信息

Univ Rennes, LP3C (Laboratoire de Psychologie, Cognition, Comportement et Communication), F-35000, Rennes, France.

Univ Rennes, LP3C (Laboratoire de Psychologie, Cognition, Comportement et Communication), F-35000, Rennes, France.

出版信息

Eur J Med Genet. 2022 May;65(5):104482. doi: 10.1016/j.ejmg.2022.104482. Epub 2022 Mar 16.

Abstract

Silver-Russell syndrome (SRS) is a rare imprinting disorder characterized by prenatal and postnatal growth retardation. Despite normal intellectual functioning, psychosocial and behavioral difficulties have been observed in this syndrome. However, few studies have dealt with these aspects, even though this could enhance the current understanding of the SRS and, more importantly, improve the management of potential psychosocial problems. Given the sparse literature, this cross-sectional study aimed to establish the psychosocial and behavioral profile of individuals with SRS. To this end, we assessed the quality of life (World Health Organization Quality of Life Questionnaire-Short Form), self-esteem (Coopersmith's Self-Esteem Inventory), anxiety (Spielberger's State-Trait Anxiety Inventory), and behavioral and emotional problems (Child Behavior Checklist and Adult Behavior Checklist) in a sample of 19 adolescents and adults with SRS and 18 without SRS (controls). We also analyzed clinical features, molecular genetic diagnosis, and past or current treatments of participants with SRS. Based on prior studies, we expected to observe psychological and behavioral difficulties in our clinical population. We also expected these difficulties, shared by both adolescents and adults with SRS, to be associated with factors such as height, genetics, or treatment. Overall, our results showed that participants with SRS had similar performances to those of controls, despite high interindividual variability among the adults with SRS. For example, while adults with SRS had a similar mean total self-esteem score to control participants, 45% of the adults with SRS still had very low self-esteem. In addition, adolescents and adults with SRS did not necessarily have the same difficulties. Social and behavioral problems appeared to be more common in adolescents with upd(7)mat while in adults, difficulties were not associated with either height, weight, NH-CSS score, or GH treatment but did appear to be associated with GnRHa treatment. Indeed, low self-esteem was associated with GnRHa treatment. Overall, this study shows that early intervention and multidisciplinary care right up to adulthood, including psychological support, are needed for this population, regardless of the molecular abnormality responsible for SRS, to cope with potential psychosocial problems.

摘要

银-罗素综合征(SRS)是一种罕见的印迹障碍,其特征为产前和产后生长迟缓。尽管智力正常,但在该综合征中观察到心理社会和行为困难。然而,很少有研究涉及这些方面,尽管这可以增强对 SRS 的现有认识,更重要的是,可以改善潜在心理社会问题的管理。鉴于文献稀少,这项横断面研究旨在确定 SRS 个体的心理社会和行为特征。为此,我们评估了 19 名 SRS 青少年和成年人以及 18 名无 SRS 对照组(对照)的生活质量(世界卫生组织生活质量问卷-简短形式)、自尊(库珀史密斯自尊量表)、焦虑(斯皮尔伯格状态-特质焦虑量表)以及行为和情绪问题(儿童行为检查表和成人行为检查表)。我们还分析了 SRS 参与者的临床特征、分子遗传诊断以及过去或当前的治疗情况。根据先前的研究,我们预计在我们的临床人群中会观察到心理和行为困难。我们还预计,这些困难,无论是青少年还是成年人 SRS 患者都会遇到,与身高、遗传或治疗等因素有关。总的来说,我们的结果表明,尽管 SRS 成人个体间存在高度的个体差异,但 SRS 参与者的表现与对照组相似。例如,虽然 SRS 成人的总自尊得分与对照组相似,但 45%的 SRS 成人仍存在极低的自尊。此外,青少年和成年人 SRS 患者不一定有相同的困难。社会和行为问题在 upd(7)mat 的青少年中更为常见,而在成年人中,这些问题与身高、体重、NH-CSS 评分或 GH 治疗无关,但与 GnRHa 治疗有关。事实上,低自尊与 GnRHa 治疗有关。总的来说,这项研究表明,无论导致 SRS 的分子异常如何,对于该人群,需要进行早期干预和多学科治疗,包括心理支持,以应对潜在的心理社会问题。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验