rasopathy的神经心理学特征:一项涉及努南综合症儿童家庭的家长培训计划的试点研究

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY American Journal of Medical Genetics Part C: Seminars in Medical Genetics Pub Date : 2022-12-09 DOI:10.1002/ajmg.c.32025
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Francesca Cumbo, Simone Piga, Marco Tartaglia, Serena Licchelli, Maria Cristina Digilio, Stefano Vicari
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引用次数: 0

摘要

努南综合征(Noonan syndrome, NS)是一种临床可变多系统疾病,由参与RAS/丝裂原活化蛋白激酶信号通路的编码蛋白基因突变引起。NS的特点是相异、身材矮小和先天性心脏缺陷。精神运动迟缓、学习困难和社会缺陷也很常见。此外,行为和注意力问题可以被认为是NS的关键症状,其功能类似于注意缺陷多动障碍(ADHD)的模式。复杂的行为表型对患者的生活质量有很大的影响,也给患者家属提出了苛刻的管理问题。家长管理培训(PMT)被推荐作为ADHD的一线治疗方法;然而,到目前为止,还没有研究测试PMT对NS的疗效。这项试点研究的目的是实施和评估一种专门针对精神病家庭的PMT。研究人员招募了7名NS患儿的父母,并对他们进行了10期的PMT治疗。对父母双方进行了三种不同的问卷调查:康纳斯父母评定量表、父母压力指数简表(PSI-SF)和阿拉巴马父母问卷(APQ)。我们对第一个小队列家庭的研究结果表明,干预后母亲对孩子及其互动的积极感知和满意度增加,分别由PSI-SF困难儿童(DC)和PSI-SF亲子功能障碍互动(PCDI)测量,而母亲的压力水平在PMT后下降,由PSI-SF总分显示。此外,衡量与孩子积极关系行为的APQ积极育儿在干预后的母亲中有所增加。经PMT治疗后,对父亲问卷的统计分析没有显示出显著差异。这项初步研究表明,PMT对有行为和ADHD症状的NS儿童的父母来说是一种很有希望的干预措施。在母亲的态度和痛苦的变化表明,行为导向的方案可能有助于父母管理与NS表型。
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Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome

Noonan syndrome (NS) is a clinical variable multisystem disorder caused by mutations in genes encoding proteins involved in the RAS/mitogen-activated protein kinase signaling pathway. NS is characterized by a distinctive facies, short stature, and congenital heart defects. Psychomotor delay, learning difficulties, and social deficits are also common. Furthermore, behavioral and attention problems can be reckoned as a key symptom in NS, with functioning resembling the patterns observed in attention deficit hyperactivity disorder (ADHD). The complex behavioral phenotype has great impact on the quality of life and raises demanding management issues also for patients' families. Parent management training (PMT) is recommended as first-line treatment for ADHD; however, no study has been performed to test the efficacy of PMT in NS, thus far. The aim of this pilot study is the implementation and evaluation of a PMT dedicated to NS families. Parents of seven children with NS were recruited and underwent to a 10-session PMT. Three different questionnaires were administered to both parents: Conners Parent Rating Scales, Parenting Stress Index Short Form (PSI-SF), and Alabama Parenting Questionnaire (APQ). Our findings on this first small cohort of families indicate that positive perception and satisfaction about the child and the interaction with him increased in mothers after the intervention, as measured respectively by PSI-SF difficult child (DC) and PSI-SF parent–child dysfunctional interaction (PCDI), while mothers' level of stress decreased after the PMT, as indicated by PSI-SF total scores. Furthermore, APQ positive parenting, which measures behaviors of positive relationship with the child, increased in mothers after the intervention. Statistical analysis on fathers' questionnaires did not show significant differences after the PMT sessions. This pilot study suggests that PMT is a promising intervention for parents of NS children with behavioral and ADHD symptoms. Changes in mothers' attitudes and distress indicate that behaviorally oriented programs may help parents to manage with NS phenotype.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
期刊最新文献
My Journey With Arthrogryposis and Some of the People Who Made a Difference. Everyone Is a Tomato: Metagnostic Narratives of Genetic Revelation. Correction to "Experiences With Offering Pro Bono Medical Genetics Services in the West Indies: Benefits to Patients, Physicians, and the Community". Family Lore, a Variant of Uncertain Significance, and CADASIL. Pink, White, and Probability.
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