Internalizing Psychiatric Symptoms in People With Mosaicism for Trisomy 21.

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Ruth C Brown, Allison D'Aguilar, Quinn Hurshman, Rebekah NailorZee, Timothy P York, George Capone, Ananda B Amstadter, Colleen Jackson-Cook
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Abstract

People with mosaicism for trisomy 21 have been shown to exhibit many of the same phenotypic traits present in people with non-mosaic Down syndrome, but with varying symptom severity. However, the behavioral phenotype of people with mosaic Down syndrome (mDS) has not been well characterized. This study aimed to examine the prevalence of self-report and caregiver-report symptoms of depression and anxiety among a sample of 62 participants with mDS aged 12-46 and assess their association with the percentage of trisomy 21 in blood and/or buccal mucosa cells. The overall MANCOVA revealed a significant effect of trisomy on the set of internalizing scales, controlling for age and gender (p = 0.038, partial eta2 = 0.22). However, follow-up univariate analyses showed that the initial significant effect of trisomy on fear (p = 0.049, partial eta2 = 0.08) did not survive correction for multiple comparisons (adjusted p = 0.300). No other effects were significant. This study highlights the high occurrence of depression and anxiety symptoms in individuals with mDS and the need for routine assessment to optimize their care. It also demonstrates the ability of people with mDS to complete these evaluations, thereby supporting their inclusion in research studies/clinical trials.

21三体嵌合体患者的内化精神症状
21三体嵌合体患者表现出许多与非嵌合体唐氏综合征患者相同的表型特征,但症状严重程度不同。然而,马赛克唐氏综合征(mDS)患者的行为表型尚未得到很好的表征。本研究旨在检查62名年龄在12-46岁的mDS患者中自我报告和护理者报告的抑郁和焦虑症状的患病率,并评估其与血液和/或颊粘膜细胞中21三体百分比的关系。总体MANCOVA显示三体对内化量表集有显著影响,控制了年龄和性别(p = 0.038,部分eta2 = 0.22)。然而,随访的单变量分析显示,三体对恐惧的初始显著影响(p = 0.049,部分eta2 = 0.08)在多重比较校正后没有存在(调整后p = 0.300)。没有其他显著的影响。本研究强调了mDS患者抑郁和焦虑症状的高发生率,以及对其进行常规评估以优化护理的必要性。它还证明了医学博士有能力完成这些评估,从而支持将他们纳入研究/临床试验。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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