难治性精神病和罕见拷贝数变异患者的医学多病:24例回顾性病例系列

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Tyler E Dietterich, Rose Mary Xavier, Maya L Lichtenstein, Matthew K Harner, Lisa Bruno, Robert Stowe, Martilias Farrell, Rita A Shaughnessy, Jonathan S Berg, Patrick F Sullivan, Richard C Josiassen
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引用次数: 0

摘要

神经发育障碍风险拷贝数变异(NDD CNVs)与复杂的神经精神表型相关。这些CNVs还会给成人带来许多医疗结果的风险;然而,在共病精神疾病的背景下,长期的健康后果尚未得到很好的记录。作为宾夕法尼亚州立医院基因组学研究的一部分,24名难治性精神病住院患者被确定为NDD CNVs携带者。通过回顾医疗记录、专门的神经行为评估和使用人类表型本体的数据合成,进行了全面的生命历程表型分析。在整个队列中检查的表型显示了跨多个器官系统的共病医学表现。96%的患者存在心血管疾病,92%的患者存在运动障碍。所有患者都有多器官系统受累,大多数器官系统(12/17个系统)在50%或更多的患者中受到影响,最终导致高度的个体多重发病率。将我们的观察结果与先前已知的CNV相关表型进行比较,表明单个CNV位点可能出现一些新的健康结果。我们的描述性病例系列支持一个复杂的和多维的病程。全面报道这些变异的长期影响是推进这些携带NDD基因拷贝变异的复杂精神病患者临床护理的第一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medical Multimorbidity in Patients With Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 Patients.

Neurodevelopmental disorder-risk copy number variations (NDD CNVs) are associated with complex neuropsychiatric phenotypes. These CNVs also confer risk for a host of medical outcomes in adults; yet, the long-term health consequences in the context of comorbid psychiatric illness have not been well documented. Twenty-four psychiatric inpatients with treatment-resistant psychosis were identified as carriers of NDD CNVs as part of a larger Pennsylvania State Hospital genomics study. Comprehensive life course phenotyping was performed through review of medical records, specialized neurobehavioral evaluation, and synthesis of data using the Human Phenotype Ontology. Phenotypes examined across the cohort indicated comorbid medical manifestations across multiple organ systems. Cardiovascular disorders were present in 96% of patients and motor disorders in 92%. All patients had multiple organ system involvement, and most organ systems (12/17 systems) were affected in 50% or more of patients, culminating in a high degree of individual-level multimorbidity. Comparing our observations to previously known CNV-associated phenotypes indicated several potentially novel health outcomes for individual CNV loci. Our descriptive case series supports a complex and multidimensional course of illness. Thorough reporting on the long-term implications of these variants is the first step toward advancing clinical care for these complex psychiatric patients carrying NDD CNVs.

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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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