Cognitive Genetics & Cognitive Therapy Group, The Center for Neuroimaging, Cognition and Genomics (NICOG), School of Psychology and Discipline of Biochemistry, National University of Ireland Galway, Galway, Ireland.
Neuropsychiatric Genetics Research Group, Department of Psychiatry, Institute of Molecular Medicine, Trinity College Dublin, Dublin, Ireland.
Genes Brain Behav. 2019 Nov;18(8):e12602. doi: 10.1111/gbb.12602. Epub 2019 Aug 30.
Variation in cognitive performance, which strongly predicts functional outcome in schizophrenia (SZ), has been associated with multiple immune-relevant genetic loci. These loci include complement component 4 (C4A), structural variation at which was recently associated with SZ risk and synaptic pruning during neurodevelopment and cognitive function. Here, we test whether this genetic association with cognition and SZ risk is specific to C4A, or extends more broadly to genes related to the complement system. Using a gene-set with an identified role in "complement" function (excluding C4A), we used MAGMA to test if this gene-set was enriched for genes associated with human intelligence and SZ risk, using genome-wide association summary statistics (IQ; N = 269 867, SZ; N = 105 318). We followed up this gene-set analysis with a complement gene-set polygenic score (PGS) regression analysis in an independent data set of patients with psychotic disorders and healthy participants with cognitive and genomic data (N = 1000). Enrichment analysis suggested that genes within the complement pathway were significantly enriched for genes associated with IQ, but not SZ. In a gene-based analysis of 90 genes, SERPING1 was the most enriched gene for the phenotype of IQ. In a PGS regression analysis, we found that a complement pathway PGS associated with IQ genome-wide association studies statistics also predicted variation in IQ in our independent sample. This association (observed across both patients and controls) remained significant after controlling for the relationship between C4A and cognition. These results suggest a robust association between the complement system and cognitive function, extending beyond structural variation at C4A.
认知表现的变异性强烈预测精神分裂症(SZ)的功能结果,与多个免疫相关的遗传位点有关。这些位点包括补体成分 4(C4A),其结构变异最近与 SZ 风险和神经发育及认知功能期间的突触修剪有关。在这里,我们测试这种与认知和 SZ 风险的遗传关联是否特定于 C4A,或者更广泛地扩展到与补体系统相关的基因。使用具有“补体”功能(不包括 C4A)鉴定作用的基因集,我们使用 MAGMA 来测试该基因集是否富集与人类智力和 SZ 风险相关的基因,使用全基因组关联汇总统计数据(IQ;N = 269867,SZ;N = 105318)。我们在具有认知和基因组数据的精神病患者和健康参与者的独立数据集中,对补体基因集多基因评分(PGS)回归分析进行了基因集分析的后续研究(N = 1000)。富集分析表明,补体途径中的基因在与 IQ 相关的基因中显著富集,但与 SZ 无关。在 90 个基因的基于基因的分析中,SERPING1 是与 IQ 表型最富集的基因。在 PGS 回归分析中,我们发现与 IQ 全基因组关联研究统计数据相关的补体途径 PGS 也预测了我们独立样本中 IQ 的变化。在控制 C4A 与认知之间的关系后,这种关联(在患者和对照者中均观察到)仍然显著。这些结果表明补体系统与认知功能之间存在稳健的关联,超出了 C4A 结构变异的范围。