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DUF1220拷贝数与精神分裂症风险及严重程度相关:对理解自闭症和精神分裂症作为相关疾病的启示

DUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseases.

作者信息

Searles Quick V B, Davis J M, Olincy A, Sikela J M

机构信息

Department of Biochemistry and Molecular Genetics, Human Medical Genetics and Genomics and Medical Scientist Training Programs, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

出版信息

Transl Psychiatry. 2015 Dec 15;5(12):e697. doi: 10.1038/tp.2015.192.

Abstract

The copy number of DUF1220, a protein domain implicated in human brain evolution, has been linearly associated with autism severity. Given the possibility that autism and schizophrenia are related disorders, the present study examined DUF1220 copy number variation in schizophrenia severity. There are notable similarities between autism symptoms and schizophrenia negative symptoms, and divergence between autism symptoms and schizophrenia positive symptoms. We therefore also examined DUF1220 copy number in schizophrenia subgroups defined by negative and positive symptom features, versus autistic individuals and controls. In the schizophrenic population (N=609), decreased DUF1220 copy number was linearly associated with increasing positive symptom severity (CON1 P=0.013, HLS1 P=0.0227), an association greatest in adult-onset schizophrenia (CON1 P=0.00155, HLS1 P=0.00361). In schizophrenic males, DUF1220 CON1 subtype copy number increase was associated with increased negative symptom severity (P=0.0327), a finding similar to that seen in autistic populations. Subgroup analyses demonstrated that schizophrenic individuals with predominantly positive symptoms exhibited reduced CON1 copy number compared with both controls (P=0.0237) and schizophrenic individuals with predominantly negative symptoms (P=0.0068). These findings support the view that (1) autism and schizophrenia exhibit both opposing and partially overlapping phenotypes and may represent a disease continuum, (2) variation in DUF1220 copy number contributes to schizophrenia disease risk and to the severity of both disorders, and (3) schizophrenia and autism may be, in part, a harmful by-product of the rapid and extreme evolutionary increase in DUF1220 copy number in the human species.

摘要

DUF1220是一种与人类大脑进化相关的蛋白质结构域,其拷贝数与自闭症严重程度呈线性相关。鉴于自闭症和精神分裂症可能是相关疾病,本研究检测了精神分裂症严重程度中的DUF1220拷贝数变异。自闭症症状与精神分裂症阴性症状之间存在显著相似性,而自闭症症状与精神分裂症阳性症状之间存在差异。因此,我们还检测了根据阴性和阳性症状特征定义的精神分裂症亚组与自闭症个体及对照组相比的DUF1220拷贝数。在精神分裂症患者群体(N = 609)中,DUF1220拷贝数减少与阳性症状严重程度增加呈线性相关(CON1 P = 0.013,HLS1 P = 0.0227),这种关联在成年期起病的精神分裂症中最为明显(CON1 P = 0.00155,HLS1 P = 0.00361)。在男性精神分裂症患者中,DUF1220 CON1亚型拷贝数增加与阴性症状严重程度增加相关(P = 0.0327),这一发现与自闭症群体中的情况相似。亚组分析表明,主要表现为阳性症状的精神分裂症患者与对照组(P = 0.0237)和主要表现为阴性症状的精神分裂症患者(P = 0.0068)相比,CON1拷贝数减少。这些发现支持以下观点:(1)自闭症和精神分裂症表现出既对立又部分重叠的表型,可能代表一种疾病连续体;(2)DUF1220拷贝数变异导致精神分裂症患病风险以及两种疾病的严重程度;(3)精神分裂症和自闭症可能部分是人类物种中DUF1220拷贝数快速且极端进化增加的有害副产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6d/5068589/ee9d7f859ec5/tp2015192f1.jpg

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