Convergencias y divergencias genéticas, neurobiológicas y ambientales entre el autismo y el espectro de la esquizofrenia

IF 0.6 Q4 PSYCHOLOGY
Isabel Paula-Pérez
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引用次数: 1

Abstract

Introduction

The autistic spectrum and the schizophrenia spectrum and other psychotic disorders concur more frequently than would be expected by chance alone. This article analyzes the evidence related to convergent and divergent risk factors at a genetic, neuroanatomical and environmental level that could explain this greater co-occurrence between both conditions.

Development

The high number of deletions and shared CNV duplications, including the genes NRXN1, CNTNAP2, 22q11.2, 1q21.1 and 15q13.3, mutations Shank3 and 7q11.23, among others, definitively calls into question the assumption that the spectrum of the schizophrenia and autism are 2 etiologically totally differentiated conditions. The epigenetic effects contribute to brain cytoarchitecture anomalies in both spectra related to the volume of gray matter, reduced values of fractional anisotropy, hypoactivation patterns of certain cerebral structures, alterations in brain connectivity and neurochemicals among others. Autism and the spectrum of schizophrenia and other psychotic disorders also share environmental risk factors, many of them related above all with obstetric complications and paternal age.

Conclusion

There is a genotypic overlap between the spectrum of autism and the spectrum of schizophrenia and other psychotic disorders that supports the hypothesis that both conditions may emerge from common shared pathogenic mechanisms. These mechanisms, together with environmental risk factors, would explain some of the neurobiological similarities. It is important to clarify that phenotypically remain 2 clearly differentiated conditions and that the possible appearance of psychotic symptoms in a subgroup of people with autism does not necessarily imply the development of schizophrenia.

自闭症和精神分裂症谱系之间的遗传、神经生物学和环境趋同和分化
自闭症谱系、精神分裂症谱系和其他精神障碍的合并比预期的单独的偶然性更频繁。本文分析了遗传、神经解剖学和环境水平上与趋同和发散风险因素相关的证据,这些证据可以解释这两种情况之间更大的共同发生。大量的缺失和共享的CNV重复,包括NRXN1、CNTNAP2、22q11.2、1q21.1和15q13.3基因,突变Shank3和7q11.23等,明确地质疑了精神分裂症和自闭症谱系是两种病因上完全不同的疾病的假设。表观遗传效应导致大脑细胞结构在与灰质体积相关的两个光谱中的异常,分数各向异性值的降低,某些大脑结构的低激活模式,大脑连接和神经化学物质的改变等。自闭症和精神分裂症谱系及其他精神障碍也有共同的环境风险因素,其中许多因素首先与产科并发症和父亲年龄有关。结论自闭症谱系与精神分裂症及其他精神障碍谱系存在基因型重叠,这支持了这两种疾病可能来自共同致病机制的假设。这些机制,加上环境风险因素,可以解释一些神经生物学上的相似性。重要的是要澄清,表型上仍然是两种明显不同的情况,在自闭症患者亚群中可能出现的精神病症状并不一定意味着精神分裂症的发展。
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来源期刊
CiteScore
0.80
自引率
40.00%
发文量
21
期刊介绍: The Anuario de Psicología, one of Spain"s most important general psychology journals, is published by the Faculty of Psychology of the University of Barcelona. It appears three times a year. The Anuario combines continuity with the past with a strong commitment to the present and the future. The journal is broad-ranging, interdisciplinary, and innovative. The Anuario publishes research reports and applied studies in all fields of psychology. We also accept theorical, epistemological studies, organize dossiers on topical themes, and hold debates on controversial subjects deriving from a central article.
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