National Centre for Register-based Research, Aarhus BSS, Aarhus University, Aarhus, Denmark.
iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark.
Schizophr Bull. 2017 Sep 1;43(5):1064-1069. doi: 10.1093/schbul/sbx007.
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.
治疗抵抗性精神分裂症(TRS)影响约三分之一的精神分裂症患者。尽管已经确定了一些与 TRS 相关的社会人口学和临床预测因素,但有关 TRS 的遗传风险数据却很少。我们旨在研究精神分裂症多基因风险评分与精神分裂症患者治疗抵抗之间的关系。我们在丹麦开展了一项全国性的基于人群的随访研究,纳入了所有在 1981 年以后出生的、在 1999 年至 2007 年间确诊患有精神分裂症的个体。根据全基因组数据,我们计算了 862 名精神分裂症患者的精神分裂症多基因风险评分。TRS 的定义为氯氮平起始治疗或至少 2 次不同的抗精神病药物单药治疗且仍住院治疗。我们在调整了人群分层、年龄、性别、出生地的地理位置、临床治疗环境、精神共病和日历年后,估计了与多基因风险评分相关的 TRS 风险比(HR)。在 862 名精神分裂症患者中,有 181 名(21.0%)在 4674 人年的随访期间符合 TRS 的标准。我们没有发现多基因风险评分与 TRS 之间存在显著关联,调整后的 HR = 1.13(95%CI:0.95-1.35)。根据这些结果,目前使用精神分裂症多基因风险评分来识别 TRS 患者在个体患者层面上还不能充分发挥临床实用性。未来的研究应包括更大的遗传样本,并结合非遗传标志物。此外,开发一种针对 TRS 的特定多基因风险评分将对 TRS 的早期预测非常有意义。