用分类和回归树评价定量脑电图对抗抑郁药和安慰剂治疗的反应。

The open medical informatics journal Pub Date : 2011-01-01 Epub Date: 2011-02-11 DOI:10.2174/1874431101105010001
M Rabinoff, C M R Kitchen, I A Cook, A F Leuchter
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引用次数: 20

摘要

研究目的是评估分类和回归树(CART)的有效性,利用症状严重程度和定量脑电图(QEEG)数据对抗抑郁药和安慰剂治疗的临床反应者进行分类。患者包括51名患有单相抑郁症的成年人,他们完成了使用氟西汀、文拉法辛或安慰剂的治疗试验。分别于基线、2、7、14、28和56 d记录汉密尔顿抑郁评定量表(HAM-D)和单电极数据。患者被分为药物和安慰剂反应者和无反应者。HAM-D评分的CART分析显示,与无反应者相比,第7天HAM-D评分低于13的患者更有可能对氟西汀或文拉法辛治疗有反应(p=0.001)。约登指数γ显示,使用QEEG测量的CART模型比基于ham - d的模型更准确。在给予氟西汀治疗的患者中,第2天AF2 θ关联度下降的患者被CART分类为治疗应答者(p=0.02)。对于那些接受文拉法辛治疗的患者,CART发现第7天PO2区的δ绝对功率下降是治疗应答的特征(p=0.01)。在所有接受药物治疗的患者中,CART发现第2天FP1区域δ绝对功率的下降是对药物治疗无反应的特征(p=0.003)。从QEEG CART分析中得到的最优树主要利用了关联度值,但也包含了一些δ绝对功率值。我们的研究结果表明,CART可能是一种有效的方法,用于识别治疗重度抑郁症的潜在结果预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of quantitative EEG by classification and regression trees to characterize responders to antidepressant and placebo treatment.

Evaluation of quantitative EEG by classification and regression trees to characterize responders to antidepressant and placebo treatment.

Evaluation of quantitative EEG by classification and regression trees to characterize responders to antidepressant and placebo treatment.

Evaluation of quantitative EEG by classification and regression trees to characterize responders to antidepressant and placebo treatment.

The study objective was to evaluate the usefulness of Classification and Regression Trees (CART), to classify clinical responders to antidepressant and placebo treatment, utilizing symptom severity and quantitative EEG (QEEG) data. Patients included 51 adults with unipolar depression who completed treatment trials using either fluoxetine, venlafaxine or placebo. Hamilton Depression Rating Scale (HAM-D) and single electrodes data were recorded at baseline, 2, 7, 14, 28 and 56 days. Patients were classified as medication and placebo responders or non-responders. CART analysis of HAM-D scores showed that patients with HAM-D scores lower than 13 by day 7 were more likely to be treatment responders to fluoxetine or venlafaxine compared to non-responders (p=0.001). Youden's index γ revealed that CART models using QEEG measures were more accurate than HAM-D-based models. For patients given fluoxetine, patients with a decrease at day 2 in θ cordance at AF2 were classified by CART as treatment responders (p=0.02). For those receiving venlafaxine, CART identified a decrease in δ absolute power at day 7 at the PO2 region as characterizing treatment responders (p=0.01). Using all patients receiving medication, CART identified a decrease in δ absolute power at day 2 in the FP1 region as characteristic of nonresponse to medication (p=0.003). Optimal trees from the QEEG CART analysis primarily utilized cordance values, but also incorporated some δ absolute power values. The results of our study suggest that CART may be a useful method for identifying potential outcome predictors in the treatment of major depression.

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