Suppr超能文献

四体和五体的临床、认知及神经发育概况:一项系统评价

Clinical, Cognitive and Neurodevelopmental Profile in Tetrasomies and Pentasomies: A Systematic Review.

作者信息

Ricciardi Giacomina, Cammisa Luca, Bove Rossella, Picchiotti Giorgia, Spaziani Matteo, Isidori Andrea M, Aceti Franca, Giacchetti Nicoletta, Romani Maria, Sogos Carla

机构信息

Section of Child and Adolescents Neuropsychiatry, Department of Human Neuroscience, Sapienza University of Rome, 00185 Rome, Italy.

Advanced Endocrine Diagnostics Unit, Department of Experimental Medicine, Policlinico Umberto I Hospital, Sapienza University of Rome, 00161 Rome, Italy.

出版信息

Children (Basel). 2022 Nov 9;9(11):1719. doi: 10.3390/children9111719.

Abstract

: Sex chromosome aneuploidies (SCAs) are a group of disorders characterised by an abnormal number of sex chromosomes. Collective prevalence rate of SCAs is estimated to be around 1 in 400-500 live births; sex chromosome trisomies (e.g., XXX, XXY, XYY) are most frequent, while tetra- and pentasomies (e.g., XXXX, XXXXX, XXXY, XXXXY) are rarer, and the most common is 48, XXYY syndrome. The presence of additional X and/or Y chromosomes is believed to cause neurodevelopmental differences, with increased risk for developmental delays, language-based learning disabilities, cognitive impairments, executive dysfunction, and behavioural and psychological disorders. : Our review has the purpose of analysing the neurocognitive, linguistical and behavioural profile of patients affected by sex chromosomes supernumerary aneuploidies (tetrasomy and pentasomy) to better understand the specific areas of weakness, in order to provide specific rehabilitation therapy. : The literature search was performed by two authors independently. We used MEDLINE, PubMed, and PsycINFO search engines to identify sources of interest, without year or language restrictions. At the end of an accurate selection, 16 articles fulfilled the inclusion and exclusion criteria. : International literature has described single aspects of the neuropsychological profile of 48, XXYY and 49, XXXXY patients. In 48, XXYY patients, various degrees of psychosocial/executive functioning issues have been reported and there is an increased frequency of behavioural problems in childhood. Developmental delay and behavioural problems are the most common presenting problems, even if anxiety, depression and oppositional defiant disorder are also reported. They also show generalized difficulties with socialization and communication. Cognitive abilities are lower in measures of verbal IQ than in measures of performance IQ. Visuospatial skills are a relative strength compared to verbal skills. In patients with 49, XXXXY, both intellectual and adaptive functioning skills fall into the disability range, with better non-verbal cognitive performance. Speech and language testing reveals more deficits in expressive language than receptive language and comprehension. Anxiety, thought problems, internalizing and externalizing problems, and deficits in social cognition and communication are reported. Behavioural symptoms lessen from school age to adolescence, with the exception of thought problems and anxiety. Individuals affected by sex chromosome aneuploidies show testosterone deficiency, microorchidism, lack of pubertal progression and infertility. Hormone replacement therapy (HRT) is usually recommended for these patients: different studies have found that testosterone-based HRT benefit a wide range of areas initiated in these disorders, affecting not only neuromotor, cognitive and behavioural profile but also structural anomalies of the brain (i.e., increase of volume of grey temporal lobe matter). In conclusion, further studies are needed to better understand the neuropsychological profile with a complete evaluation, including neurocognitive and psychosocial aspects and to establish the real impact of HRT on improving the cognitive and behavioural profile of these patients.

摘要

性染色体非整倍体(SCA)是一组以性染色体数量异常为特征的疾病。据估计,SCA在活产婴儿中的总体患病率约为1/400 - 1/500;性染色体三体(如XXX、XXY、XYY)最为常见,而四体和五体(如XXXX、XXXXX、XXXY、XXXXY)则较为罕见,其中最常见的是48,XXYY综合征。额外的X和/或Y染色体的存在被认为会导致神经发育差异,增加发育迟缓、基于语言的学习障碍、认知障碍、执行功能障碍以及行为和心理障碍的风险。

我们的综述旨在分析受性染色体超数非整倍体(四体和五体)影响的患者的神经认知、语言和行为特征,以更好地了解其特定的薄弱领域,从而提供针对性的康复治疗。

文献检索由两位作者独立进行。我们使用MEDLINE、PubMed和PsycINFO搜索引擎来识别感兴趣的文献来源,不受年份或语言限制。经过精确筛选,最终有16篇文章符合纳入和排除标准。

国际文献已经描述了48,XXYY和49,XXXXY患者神经心理特征的各个方面。在48,XXYY患者中,已报道存在不同程度的心理社会/执行功能问题,且儿童期行为问题的发生率增加。发育迟缓与行为问题是最常见的临床表现,即便也有焦虑、抑郁和对立违抗障碍的报道。他们在社交和沟通方面也普遍存在困难。言语智商测试中的认知能力低于操作智商测试。与言语技能相比,视觉空间技能是相对优势。在49,XXXXY患者中,智力和适应性功能技能均处于残疾范围,非言语认知表现较好。言语和语言测试显示,表达性语言缺陷多于接受性语言和理解能力缺陷。有焦虑、思维问题、内化和外化问题以及社会认知和沟通缺陷的报道。除思维问题和焦虑外,行为症状从学龄期到青春期会有所减轻。受性染色体非整倍体影响的个体表现出睾酮缺乏、小睾丸、青春期发育停滞和不育。通常建议这些患者接受激素替代疗法(HRT):不同研究发现,基于睾酮的HRT对这些疾病引发的广泛领域有益,不仅影响神经运动、认知和行为特征,还影响大脑的结构异常(即颞叶灰质体积增加)。总之,需要进一步研究以通过全面评估更好地了解神经心理特征,包括神经认知和社会心理方面,并确定HRT对改善这些患者认知和行为特征的实际影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef66/9688827/8cc4c3e622b4/children-09-01719-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验