在英国开展唐氏综合症退行性障碍临床筛查的横断面研究调查

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Abinaya Seenivasan, Ella Rachamim, Jonathan D Santoro
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引用次数: 0

摘要

唐氏综合征退行性障碍(DSRD)的特征是唐氏综合征(DS)患者在没有明确原因的情况下突然丧失先前获得的技能或行为。最近,人们对这种疾病的认识有所提高,新的治疗方案正在试验中。由于混杂因素和在更广泛的社区内捕捉症状方面的差距,确切的发病率尚不清楚。在更广泛的DS社区中,应用较窄的指南对准确报告症状提出了挑战。根据2022年dsd共识指南,我们在英国各地对患有DS的儿童和年轻人的父母和照顾者进行了一项调查,收集了158份关于人口统计学、症状和触发因素的详细回复。这项调查揭示了父母和照顾者所面临挑战的关键见解。结果表明,在症状评分范围为20.2-25.6的范围内,dsd的诊断阈值显著,约占80%的病例。从统计学角度来看,评分高于20.2分的患者发生dsd的风险较高。这一阈值对于早期发现和干预至关重要,可能会改善患者的预后。虽然它可能高估了诊断结果,但问卷调查是一种筛查工具,可以识别出那些有风险的人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Cross-Sectional Study Survey to Develop a Clinical Screen for Down Syndrome Regression Disorder in the United Kingdom.

Down syndrome regression disorder (DSRD) is marked by a sudden loss of previously acquired skills or behavior without a clear cause in individuals with Down syndrome (DS). Awareness of this condition has increased recently, with new therapeutic options under trial. The precise incidence is unknown due to confounding factors and gaps in capturing symptoms within the broader community. The application of narrower guidelines presents challenges in accurately reporting symptoms across the wider DS community. We conducted a survey across the UK based on 2022 DSRD consensus guidelines among parents and carers of children and young adults with DS, with 158 detailed responses about demographics, symptoms, and triggers. The survey revealed critical insights into the challenges faced by parents and carers. Results indicate a significant diagnostic threshold for DSRD within a symptom score range of 20.2-25.6, capturing about 80% of cases. Patients scoring above 20.2 are at high risk for DSRD from a statistical perspective. This threshold is vital for early detection and intervention, potentially improving patient outcomes. While it may overestimate diagnoses, the questionnaire serves as a screening tool for identifying those at risk.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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