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Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene–environment interaction approach

机译:多基因风险和应激性生活事件是否可以预测强迫症的药理治疗反应?基因-环境相互作用方法

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The rate of response to pharmacological treatment in Obsessive-compulsive disorder (OCD) oscillates between 40 and 70%. Genetic and environmental factors have been associated with treatment response in OCD. This study analyzes the predictive ability of a polygenic risk score (PRS) built from OCD-risk variants, for treatment response in OCD, and the modulation role of stressful life events (SLEs) at the onset of the disorder. PRSs were calculated for a sample of 103 patients. Yale–Brown Obsessive Compulsive Scale (YBOCS) scores were obtained before and after a 12-week treatment. Regression analyses were performed to analyze the influence of the PRS and SLEs at onset on treatment response. PRS did not predict treatment response. The best predictive model for post-treatment YBOCS (post YBOCS) included basal YBOCS and age. PRS appeared as a predictor for basal and post YBOCS. SLEs at onset were not a predictor for treatment response when included in the regression model. No evidence for PRS predictive ability for treatment response was found. The best predictor for treatment response was age, agreeing with previous literature specific for SRI treatment. Suggestions are made on the possible role of neuroplasticity as a mediator on this association. PRS significantly predicted OCD severity independent on pharmacological treatment. SLE at onset modulation role was not evidenced. Further research is needed to elucidate the genetic and environmental bases of treatment response in OCD.
机译:强迫症(OCD)对药物治疗的反应率在40%至70%之间波动。遗传和环境因素已与强迫症中的治疗反应相关。这项研究分析了由OCD风险变异体建立的多基因风险评分(PRS)对OCD的治疗反应的预测能力,以及该疾病发作时应激性生活事件(SLE)的调节作用。计算了103名患者的样本的PRS。在接受12周治疗之前和之后获得了耶鲁-布朗强迫症量表(YBOCS)评分。进行回归分析以分析PRS和SLE发作时对治疗反应的影响。 PRS不能预测治疗反应。治疗后YBOCS(后YBOCS)的最佳预测模型包括基础YBOCS和年龄。 PRS似乎是YBOCS基底和基底后的预测因子。回归模型中包括SLE发作时,不是治疗反应的预测指标。没有发现PRS预测治疗反应能力的证据。治疗反应的最佳预测指标是年龄,这与以前针对SRI治疗的文献一致。提出了关于神经可塑性作为这种关联的中介者的可能作用的建议。 PRS显着预测了强迫症的严重程度,而与药物治疗无关。没有证据表明SLE具有起效调节作用。需要进一步的研究来阐明强迫症中治疗反应的遗传和环境基础。

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