基于志愿者脑电功率谱变量的四种临床治疗性精神药物分类规则的建立。

W M Herrmann, K Fichte, T M Itil, S Kubicki
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引用次数: 28

摘要

制定了精神药物分类的客观规则。分类基于同时设计和实施的5项基础研究的数据,这些研究涉及75名健康志愿者,他们服用了20种不同的精神药物和5种单次口服安慰剂。每个志愿者服用一种精神兴奋剂,一种抗抑郁药,一种神经抑制剂,一种轻微镇静剂和一种安慰剂,采用双盲拉丁方形交叉设计。变量为6个频段,基于功率谱估计并由因子分析确定,加上1.5-30.0 Hz范围内的总功率。通过多组(5组)线性判别分析,建立了客观的分类规则。根据新规定重新分类的物质对20种精神药物中的17种和5种安慰剂中的4种产生了正确的结果。在未用于建立分类规则的各种研究中的安慰剂中,7/9被正确分类。该规则对其他类别物质的有效性必须在独立研究中加以验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a classification rule for four clinical therapeutic psychotropic drug classes with EEG power-spectrum variables of human volunteers.

An objective rule for the classification of psychotropic substances has been developed. Classification is based on data from five basic studies simultaneously designed and performed and involving 75 healthy volunteers who ingested 20 different psychotropic drugs and 5 placebos in single oral dosages. Each volunteer took one psychostimulant, one antidepressant, one neuroleptic, one minor tranquilizer and one placebo in a double-blind Latin square cross-over design. The variables were 6 frequency bands, based on power spectrum estimates and determined by factor analysis, plus total power in the 1.5-30.0 Hz range. An objective classification rule was established by multi-group (5 groups) linear discriminant analysis. Reclassification of the substances by the new rule yielded correct results for 17 out of 20 psychotropic drugs and 4 out of 5 placebos. Of placebos from various studies not used for the establishment of the classification rule, 7/9 were classified correctly. The validity of the rule for other classes of substances will have to be verified in independent studies.

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