Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany.
Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany.
Schizophr Res. 2018 Jul;197:315-320. doi: 10.1016/j.schres.2018.01.013. Epub 2018 Mar 1.
Schizophrenia is a disorder with a high heritability. Patients as well as their first degree relatives display lower levels of performance in a number of cognitive domains compared to subjects without genetic risk. Several studies could link these aberrations to single genetic variants, however, only recently, polygenic risk scores as proxies for genetic risk have been associated with cognitive domains and their neural correlates. In the present study, a sample of healthy subjects (n=137) performed a letter version of the n-back task while scanned with 3-T fMRI. All subjects were genotyped with the PsychChip and polygenic risk scores were calculated based on the PGC2 schizophrenia GWAS results. Polygenic risk for schizophrenia was associated with a lower degree of brain activation in prefrontal areas during the 3-back compared to the 0-back baseline condition. Furthermore, polygenic risk was associated with lower levels of brain activation in the right inferior frontal gyrus during the 3-back compared to a 2-back condition. Polygenic risk leads to a shift in the underlying activation pattern to the left side, thus resembling results reported in patients with schizophrenia. The data may point to polygenic risk for schizophrenia being associated with brain function in a cognitive task known to be impaired in patients and their relatives.
精神分裂症是一种遗传性很高的疾病。与无遗传风险的受试者相比,患者及其一级亲属在许多认知领域的表现水平较低。有几项研究可以将这些异常与单一的遗传变异联系起来,但直到最近,多基因风险评分作为遗传风险的替代物才与认知领域及其神经相关性相关联。在本研究中,一组健康受试者(n=137)在 3-T fMRI 扫描下完成了字母 n-back 任务。所有受试者均采用 PsychChip 进行基因分型,并基于 PGC2 精神分裂症 GWAS 结果计算多基因风险评分。与精神分裂症的多基因风险与在 3 次回溯与 0 次回溯基线条件相比,前额叶区域的大脑激活程度较低相关。此外,与在 2 次回溯相比,在 3 次回溯时右侧额下回的大脑激活水平较低。多基因风险导致潜在激活模式向左侧转移,从而类似于在精神分裂症患者中报告的结果。这些数据可能表明,精神分裂症的多基因风险与认知任务中的大脑功能有关,而该认知任务在患者及其亲属中已被证明存在障碍。