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作为强迫症内表型的皮质下和皮质形态异常

Subcortical and cortical morphological anomalies as an endophenotype in obsessive-compulsive disorder.

作者信息

Shaw P, Sharp W, Sudre G, Wharton A, Greenstein D, Raznahan A, Evans A, Chakravarty M M, Lerch J P, Rapoport J

机构信息

1] Section on Neurobehavioral Clinical Research, Social and Behavioral Research Branch, National Human Genome Research Institute,Bethesda, MD, USA [2] Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.

Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.

出版信息

Mol Psychiatry. 2015 Feb;20(2):224-31. doi: 10.1038/mp.2014.3. Epub 2014 Feb 11.

DOI:10.1038/mp.2014.3
PMID:24514568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5912882/
Abstract

Endophentoypes, quantifiable traits lying on the causal chain between a clinical phenotype and etiology, can be used to accelerate genomic discovery in obsessive-compulsive disorder (OCD). Here we identify the neuroanatomic changes that are shared by 22 OCD adult and adolescent patients and 25 of their unaffected siblings who are at genetic risk for the disorder. Comparisons were made against 47 age and sex matched healthy controls. We defined the surface morphology of the striatum, globus pallidus and thalamus, and thickness of the cerebral cortex. Patients with OCD show significant surface expansion compared with healthy controls, following adjustment for multiple comparisons, in interconnected regions of the caudate, thalamus and right orbitofrontal cortex. Their unaffected siblings show similar, significant expansion, most marked in the ventromedial caudate bilaterally, the right pulvinar thalamic nucleus and the right orbitofrontal cortex. These regions define a network that has been consistently implicated in OCD. In addition, both patients with OCD and unaffected siblings showed similar increased thickness of the right precuneus, which receives rich input from the thalamic pulvinar nuclei and the left medial temporal cortex. Anatomic change within the orbitofrontostriatal and posterior brain circuitry thus emerges as a promising endophenotype for OCD.

摘要

内表型是位于临床表型和病因之间因果链上的可量化特征,可用于加速强迫症(OCD)的基因组发现。在这里,我们确定了22名成年和青少年强迫症患者及其25名有该疾病遗传风险的未受影响的兄弟姐妹所共有的神经解剖学变化。并与47名年龄和性别匹配的健康对照进行了比较。我们定义了纹状体、苍白球和丘脑的表面形态以及大脑皮层的厚度。在对多个比较进行校正后,与健康对照相比,强迫症患者在尾状核、丘脑和右侧眶额皮质的相互连接区域显示出明显的表面扩张。他们未受影响的兄弟姐妹也表现出类似的、明显的扩张,最明显的是双侧腹内侧尾状核、右侧丘脑枕核和右侧眶额皮质。这些区域定义了一个一直与强迫症有关的网络。此外,强迫症患者和未受影响的兄弟姐妹均显示右侧楔前叶厚度有类似增加,该区域从丘脑枕核和左侧内侧颞叶皮质接收丰富的输入。因此,眶额纹状体和后脑回路内的解剖学变化成为强迫症一个有前景的内表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/bf0a186a99a1/nihms547864f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/90be81dc7f44/nihms547864f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/e8441a33f9bc/nihms547864f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/3795a0f0d3cd/nihms547864f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/bf0a186a99a1/nihms547864f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/90be81dc7f44/nihms547864f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/e8441a33f9bc/nihms547864f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/3795a0f0d3cd/nihms547864f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da7/5912882/bf0a186a99a1/nihms547864f4.jpg

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