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精神分裂症断裂基因1的变异调节首发精神病患者皮质厚度的长期纵向差异。

Variations in Disrupted-in-Schizophrenia 1 gene modulate long-term longitudinal differences in cortical thickness in patients with a first-episode of psychosis.

作者信息

Vázquez-Bourgon Javier, Roiz-Santiañez Roberto, Papiol Sergi, Ferro Adele, Varela-Gómez Noemí, Fañanás Lourdes, Crespo-Facorro Benedicto

机构信息

Department of Psychiatry, University Hospital Marqués de Valdecilla, School of Medicine, University of Cantabria, Avda.Valdecilla s/n, 39008, Santander, Spain.

Centro Investigación Biomédica en Red Salud Mental, CIBERSAM, Madrid, Spain.

出版信息

Brain Imaging Behav. 2016 Sep;10(3):629-35. doi: 10.1007/s11682-015-9433-1.

Abstract

Schizophrenia patients typically present a widespread bilateral cortical thinning from the early stages of the illness. However, there is controversy whether this reduction in cortical thickness (CT) is static or progressive over the evolution of the disorder. Disrupted-in-Schizophrenia 1 (DISC1) is one of the main candidates genes for schizophrenia, as it has been found associated to the illness, and to several endophenotypes of the disorder including structural brain differences. This gene is known to be involved in neurodevelopment and brain maturation processes. We therefore hypothesized that variations in this gene modulate different progressions of CT in psychosis. Seventy-nine Caucasian drug-naive patients experiencing a first episode of non-affective psychosis were genotyped for rs6675281 (Leu607Phe) and rs821616 (Ser704Cys) SNPs of the DISC1 gene. Brain MRIs were carried out at baseline and 3 years after initiating the treatment. Other clinical and socio-demographic variables were recorded to rule out possible confounding effects. Patients homozygous for the Leu allele of the rs6675281 SNP had a significant (p < 0.05) descend in CT over the 3-years period, while those carrying the Phe allele presented an increase in CT. When combining the two SNPs we found a synergic effect on CT progression, presenting those patients homozygous for Leu607 +Ser704 a more pronounced cortical thinning. In conclusion, DISC1 gene variations may modulate the longitudinal changes in cortical thickness in patients suffering from a first episode of non-affective psychosis.

摘要

精神分裂症患者通常从疾病早期就出现广泛的双侧皮质变薄。然而,关于这种皮质厚度(CT)的减少在疾病发展过程中是静态的还是渐进的,存在争议。精神分裂症破坏基因1(DISC1)是精神分裂症的主要候选基因之一,因为它已被发现与该疾病以及该疾病的几种内表型相关,包括脑结构差异。已知该基因参与神经发育和脑成熟过程。因此,我们假设该基因的变异会调节精神病患者CT的不同进展。对79名首次发作非情感性精神病的未服用过药物的白种人患者进行了DISC1基因rs6675281(Leu607Phe)和rs821616(Ser704Cys)单核苷酸多态性的基因分型。在基线时和开始治疗3年后进行脑部MRI检查。记录了其他临床和社会人口统计学变量,以排除可能的混杂效应。rs6675281单核苷酸多态性Leu等位基因纯合的患者在3年期间CT有显著下降(p<0.05),而携带Phe等位基因的患者CT增加。当将这两个单核苷酸多态性结合起来时,我们发现对CT进展有协同作用,Leu607 + Ser704纯合的患者皮质变薄更明显。总之,DISC1基因变异可能调节首次发作非情感性精神病患者皮质厚度的纵向变化。

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