智力残疾的严重程度和/或神经发育障碍的存在是否影响唐氏综合征患者痴呆的发生?

IF 1.6 4区 医学 Q2 EDUCATION, SPECIAL
M. Anderson, Katy Oak, R. Goodey, Karen Dodd, R. Shankar
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引用次数: 0

摘要

唐氏综合征(DS)诊断与智力残疾(ID)、广泛性发育障碍和阿尔茨海默氏痴呆(AD)相关。这些情况之间的联系还没有得到很好的评价。本文旨在研究目前有关退行性痴呆与ID严重程度和广泛性发育障碍之间关系的证据。方法采用PRISMA指南进行范围综述。2018年12月检索了Medline、Cochrane数据库、NHS证据、试验登记册和Open Grey,并于2020年7月完成了更新的检索。使用三种搜索策略检索与退行性障碍、痴呆、广泛性发育障碍(包括自闭症、自闭症谱系障碍(ASD)和注意力缺陷多动障碍(ADHD))和ID严重程度相关的文章。如果研究符合预定义的纳入标准,即调查自闭症/ASD、ADHD或ID严重程度与DS患者痴呆发展之间的关系,则纳入研究。如果研究不包括原始数据,如果人群中包括非唐氏原因的ID,或者没有报道与诊断为DS的患者的共病自闭症/ASD, ADHD或ID和痴呆严重程度相关的特定结果测量,则排除研究。没有与研究设计相关的排除。使用混合方法评估工具(MMAT)评估论文的质量。结果:搜索确定了15篇论文,发表了12项研究的结果,涉及ID, DS和痴呆的严重程度。未发现与广泛性发育障碍、退行性痴呆相关的论文。关于ID严重程度如何影响DS患者痴呆的表现、诊断、管理或预后的证据有限。然而,没有证据表明共病的广泛性发育障碍,退行性痴呆。结论:本文确定了未来研究的多个领域。迫切需要对退行性痴呆患者痴呆的表现、发展和进展进行纵向研究,确保定期捕获ID的严重程度和共病的普遍发育状况,以了解它们对痴呆病因和结果的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do the severity of Intellectual Disability and /or the presence of neurodevelopmental disorders influence the onset of dementia in people with Down syndrome?
ABSTRACT Introduction Having a diagnosis of Down syndrome (DS) is associated with intellectual disability (ID), pervasive developmental disorders and Alzheimer’s dementia (AD). The association between these conditions has not been well evaluated. This paper looks to examine the current evidence pertaining to the relationship between dementia in people with DS and severity of ID and the presence of pervasive developmental disorders. Methods A scoping review using PRISMA guidance was undertaken. Medline, Cochrane database, NHS evidence, Trial registers and Open Grey were searched in December 2018 and an updated search was completed in July 2020. Three search strategies were used to retrieve articles relating to DS, dementia, pervasive developmental disorders (including autism, autism spectrum disorder (ASD) and attention-deficit hyperactivity disorder (ADHD)) and severity of ID. Studies were included if they met the pre-defined inclusion criteria of investigating an association between autism/ASD, ADHD, or severity of ID and the development of dementia in people with DS. Studies were excluded if they did not include primary data, if the population included non-Down causes of ID, or if no specific outcome measure related to comorbid autism/ASD, ADHD, or severity of ID and dementia in people with a diagnosis of DS were reported. There were no exclusions related to study design. Papers were assessed for quality using the Mixed Methods Appraisal Tool (MMAT). Results: The search identified 15 papers, publishing results from 12 studies, relating to severity of ID, DS and dementia. No papers were identified relating to pervasive developmental disorders, DS and dementia. There is limited evidence on how severity of ID impacts on the presentation, diagnosis, management or prognosis of dementia in people with DS. However, no evidence was found on comorbid pervasive developmental disorders, DS and dementia. Conclusion: This paper has identified multiple areas for future research. There is an urgent need for longitudinal studies into the presentation, development and progression of dementia in people with DS ensuring the severity of ID and comorbid pervasive developmental conditions are captured regularly to understand their influence on the dementia etiology and outcome.
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来源期刊
CiteScore
3.30
自引率
8.00%
发文量
23
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