Alonso Joan Francesc, Romero Sergio, Mañanas Miguel Ángel, Rojas Mónica, Riba Jordi, Barbanoj Manel José
Department of Automatic Control, Biomedical Engineering Research Center, Universitat Politècnica de Catalunya. BarcelonaTech (UPC), Barcelona, Spain.
Barcelona College of Industrial Engineering (EUETIB), UPC, Barcelona, Spain.
Med Biol Eng Comput. 2015 Oct;53(10):1011-23. doi: 10.1007/s11517-015-1315-6. Epub 2015 Jun 4.
The identification of the brain regions involved in the neuropharmacological action is a potential procedure for drug development. These regions are commonly determined by the voxels showing significant statistical differences after comparing placebo-induced effects with drug-elicited effects. LORETA is an electroencephalography (EEG) source imaging technique frequently used to identify brain structures affected by the drug. The aim of the present study was to evaluate different methods for the correction of multiple comparisons in the LORETA maps. These methods which have been commonly used in neuroimaging and also simulated studies have been applied on a real case of pharmaco-EEG study where the effects of increasing benzodiazepine doses on the central nervous system measured by LORETA were investigated. Data consisted of EEG recordings obtained from nine volunteers who received single oral doses of alprazolam 0.25, 0.5, and 1 mg, and placebo in a randomized crossover double-blind design. The identification of active regions was highly dependent on the selected multiple test correction procedure. The combined criteria approach known as cluster mass was useful to reveal that increasing drug doses led to higher intensity and spread of the pharmacologically induced changes in intracerebral current density.
确定参与神经药理学作用的脑区是药物研发的一种潜在方法。这些脑区通常通过比较安慰剂诱导效应和药物引发效应后显示出显著统计学差异的体素确定。低分辨率电磁断层成像(LORETA)是一种常用于识别受药物影响的脑结构的脑电图(EEG)源成像技术。本研究的目的是评估在LORETA图谱中进行多重比较校正的不同方法。这些在神经成像以及模拟研究中常用的方法已应用于一项药物脑电图研究的实际案例,该研究调查了通过LORETA测量的苯二氮䓬剂量增加对中枢神经系统的影响。数据由9名志愿者的脑电图记录组成,这些志愿者在随机交叉双盲设计中接受了单次口服0.25、0.5和1毫克阿普唑仑以及安慰剂。活跃区域的识别高度依赖于所选的多重检验校正程序。被称为簇质量的联合标准方法有助于揭示药物剂量增加会导致脑内电流密度药理诱导变化的强度和范围增加。