Instituto de Investigación Sanitaria (IDIS) de Santiago de Compostela, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Galicia, Spain.
Servizo de Psiquiatría, Complexo Hospitalario Universitario de Santiago de Compostela, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Galicia, Spain.
Acta Psychiatr Scand. 2022 Aug;146(2):139-150. doi: 10.1111/acps.13444. Epub 2022 Jun 3.
To test whether a schizophrenia polygenic risk score (PRS) based on the subset of polymorphisms that affect brain expression of genes with altered expression by antipsychotics (exprAP PRS) is associated with psychiatric readmission of patients with schizophrenia.
The study involved 427 patients with schizophrenia. Genes with altered expression by antipsychotics were extracted from the Comparative Toxigenomics Database. ExprAP PRS was estimated using the clumping and thresholding (p < 0.05) method. Two additional PRS were tested based on subsets of exprAP polymorphisms whose schizophrenia risk allele has the same (unrestored PRS) or opposite (restored PRS) direction of effect on gene expression than antipsychotics. A general SCZ PRS was tested for comparison. Logistic and ordinal regression were used to test for association of each PRS with ever readmission and admission history, an outcome based on length and number of admissions, respectively. Webgestalt was used for Gene Ontology enrichment analysis.
ExprAP PRS was associated with ever readmission (OR = 1.48, 95%CI:1.10-1.97) and admission history (OR = 1.30, 95%CI 1.07-1.57). SCZ PRS (OR = 1.22, 95%CI: 1.01-1.48) and unrestored PRS (OR = 1.26, 95%CI 1.04-1.53) were only associated with admission history. Genes at exprAP PRS were enriched in regulation of cytokine production.
Our findings suggest that PRS based on genes with altered expression by antipsychotics may be better predictors of readmission than SCZ PRS, warranting further investigation in larger cohorts of patients. The action of antipsychotics may be related to brain gene expression, mainly in genes involved in immunity.
检验基于抗精神病药改变基因表达的多态性子集的精神分裂症多基因风险评分(PRS)是否与精神分裂症患者的精神科再入院有关。
本研究纳入了 427 名精神分裂症患者。从比较毒效基因组学数据库中提取抗精神病药改变表达的基因。采用聚类和阈值(p < 0.05)方法估计 exprAP PRS。另外还测试了基于 exprAP 多态性子集的两个 PRS,这些多态性的精神分裂症风险等位基因对基因表达的作用方向与抗精神病药相同(未恢复 PRS)或相反(恢复 PRS)。还测试了一般的 SCZ PRS 作为比较。采用逻辑回归和有序回归分别检验每个 PRS 与再入院和入院史的关联,这是基于入院次数和入院时间的两个结果。采用 Webgestalt 进行基因本体论富集分析。
ExprAP PRS 与再入院(OR=1.48,95%CI:1.10-1.97)和入院史(OR=1.30,95%CI 1.07-1.57)相关。SCZ PRS(OR=1.22,95%CI:1.01-1.48)和未恢复 PRS(OR=1.26,95%CI 1.04-1.53)仅与入院史相关。在 exprAP PRS 中,基因富集于细胞因子产生的调控。
我们的研究结果表明,基于抗精神病药改变表达的基因的 PRS 可能比 SCZ PRS 更好地预测再入院,值得在更大的患者队列中进一步研究。抗精神病药的作用可能与大脑基因表达有关,主要涉及参与免疫的基因。