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Polygenic Risk Score for Schizophrenia and Treatment-Resistant Schizophrenia

机译:精神分裂症和治疗抗性精神分裂症的多基因风险分数

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Treatment-resistant schizophrenia (TRS) affects around one-third of individuals with schizophrenia. Although a number of sociodemographic and clinical predictors of TRS have been identified, data on the genetic risk of TRS are sparse. We aimed to investigate the association between a polygenic risk score for schizophrenia and treatment resistance in patients with schizophrenia. We conducted a nationwide, population-based follow-up study among all Danish individuals born after 1981 and with an incident diagnosis of schizophrenia between 1999 and 2007. Based on genome-wide data polygenic risk scores for schizophrenia were calculated in 862 individuals with schizophrenia. TRS was defined as either clozapine initiation or at least 2 periods of different antipsychotic monotherapies and still being hospitalized. We estimated hazard rate ratios (HRs) for TRS in relation to the polygenic risk score while adjusting for population stratification, age, sex, geographical area at birth, clinical treatment setting, psychiatric comorbidity, and calendar year. Among the 862 individuals with schizophrenia, 181 (21.0%) met criteria for TRS during 4674 person-years of follow-up. We found no significant association between the polygenic risk score and TRS, adjusted HR = 1.13 (95% CI: 0.95–1.35). Based on these results, the use of the polygenic risk score for schizophrenia to identify individuals with TRS is at present inadequate to be of clinical utility at the individual patient level. Future research should include larger genetic samples in combination with non-genetic markers. Moreover, a TRS-specific developed polygenic risk score would be of great interest towards early prediction of TRS.
机译:治疗抗性精神分裂症(TRS)影响有精神分裂症的含量约三分之一。虽然已经识别了许多人的社会阶段和TRS的临床预测因子,但对TRS的遗传风险的数据是稀疏的。我们的旨在调查精神分裂症患者精神分裂症和治疗抗性的多基因风险分数之间的关联。我们在1981年后出生的所有丹麦人进行了一项基于人口的后续研究,并在1999年至2007年间出生的精神分裂症诊断。基于基于基因组的数据,精神分裂症的多种子则风险评分在862名与精神分裂症中计算。 TRS被定义为氯氮平发起或至少2个不同的抗精神病药物单治疗,仍在住院。我们估计与多种基因风险分数相关的TRS的危险率比率(HRS),同时调整出生,年龄,性别,地理区域,临床治疗环境,精神病合作和日历年。在862个具有精神分裂症的个体中,181名(21.0%)在4674人的随访期间符合TRS标准。我们发现多基因风险评分和TRS之间没有显着关联,调整后的HR = 1.13(95%CI:0.95-1.35)。基于这些结果,目前使用用于鉴定具有TRS的个体的精神分裂症的多基因风险分数是在个体患者水平的临床用途。未来的研究应包括较大的遗传样品与非遗传标志物组合。此外,TRS特异性发达的多基因风险评分对于早期预测TRS是巨大的兴趣。

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