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转化精神病学的 RDoC 方法:具有精神症状的遗传疾病能否帮助填补矩阵?以普拉德-威利综合征为例。

The RDoC approach for translational psychiatry: Could a genetic disorder with psychiatric symptoms help fill the matrix? the example of Prader-Willi syndrome.

机构信息

Université de Toulouse III, Toulouse, F-31000, France.

CHU Toulouse, Service de psychiatrie et psychologie, psychiatrie, Toulouse, F-31000, France.

出版信息

Transl Psychiatry. 2020 Aug 8;10(1):274. doi: 10.1038/s41398-020-00964-6.

DOI:10.1038/s41398-020-00964-6
PMID:32772048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7415132/
Abstract

The Research Domain Criteria project (RDoc) proposes a new classification system based on information from several fields in order to encourage translational perspectives. Nevertheless, integrating genetic markers into this classification has remained difficult because of the lack of powerful associations between targeted genes and RDoC domains. We hypothesized that genetic diseases with psychiatric manifestations would be good models for RDoC gene investigations and would thereby extend the translational approach to involve targeted gene pathways. To explore this possibility, we reviewed the current knowledge on Prader-Willi syndrome, a genetic disorder caused by the absence of expression of some of the genes of the chromosome 15q11-13 region inherited from the father. Indeed, we found that the associations between genes of the PW locus and the modification identified in the relevant behavioral, physiological, and brain imaging studies followed the structure of the RDoC matrix and its six domains (positive valence, negative valence, social processing, cognitive systems, arousal/regulatory systems, and sensorimotor systems).

摘要

研究领域标准项目(RDoc)提出了一种新的分类系统,该系统基于来自多个领域的信息,以鼓励转化视角。然而,由于目标基因与 RDoc 领域之间缺乏有力的关联,因此将遗传标记纳入这一分类仍然具有挑战性。我们假设具有精神表现的遗传疾病将是 RDoc 基因研究的良好模型,从而将转化方法扩展到靶向基因途径。为了探索这种可能性,我们回顾了关于普拉德-威利综合征的现有知识,这是一种由从父亲那里遗传的染色体 15q11-13 区域的一些基因表达缺失引起的遗传疾病。事实上,我们发现 PW 基因座的基因与相关行为、生理和脑成像研究中发现的修饰之间的关联遵循 RDoc 矩阵及其六个领域(正价、负价、社会处理、认知系统、觉醒/调节系统和感觉运动系统)的结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efcf/7415132/4a94532253d0/41398_2020_964_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efcf/7415132/4a94532253d0/41398_2020_964_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efcf/7415132/4a94532253d0/41398_2020_964_Fig1_HTML.jpg

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Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature.Prader-Willi 综合征的面部加工和社会信号探索:遗传特征。
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Impact of Deprivation on Obesity in Children with PWS.贫困对普拉德-威利综合征患儿肥胖的影响。
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