Frank Elmar, Landgrebe Michael, Poeppl Timm B, Schecklmann Martin, Kreuzer Peter M, Prasser Julia, Rupprecht Rainer, Eichhammer Peter, Hajak Göran, Langguth Berthold
Department of Psychiatry and Psychotherapy, University of Regensburg, Universitaetsstraße 84, D-93053 Regensburg, Germany.
Department of Psychiatry and Psychotherapy, University of Regensburg, Universitaetsstraße 84, D-93053 Regensburg, Germany; Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, Social Foundation, Bamberg, Bamberg, Germany; Department of Psychiatry, Psychosomatics and Psychotherapy, kbo-Lech-Mangfall-Klinik Agatharied, Germany.
Schizophr Res. 2014 Jun;156(1):128-32. doi: 10.1016/j.schres.2014.03.028. Epub 2014 Apr 29.
Measurement of motor cortex excitability with single and paired pulse transcranial magnetic stimulation has become an established method for in vivo characterization of the effects of central-acting drugs. The comparison of drug-free and medicated patients with schizophrenia suggests an association of neuroleptics intake and prolongation of the cortical silent period (CSP). However all available data come from cross-sectional non-randomized studies. Thus it is not clear whether the observed difference is an effect of medication or reflects differences in disease severity or both.
We aimed to investigate whether the CSP or other parameters of cortical excitability change, when cortical excitability is measured in drug-free patients with acute psychosis before and after 3week intake of the atypical neuroleptic quetiapine.
Different parameters of cortical excitability were studied in 24 drug-free patients with acute psychosis before and after 3weeks of treatment with a mean dose of 352±199mg quetiapine.
We observed a significant prolongation of the cortical silent period (CSP) after three week treatment with quetiapine. Other parameters of cortical excitability such as motor threshold (MT), short intracortical inhibition (SICI) and intracortical facilitation (ICF) remained unaffected. There was a significant improvement in clinical parameters (PANS, GAF) but no significant correlation between clinical improvement and changes in cortical excitability.
These longitudinal data are in line with previous reports from cross-sectional studies. The excitability changes induced by three-week intake of quetiapine in acute psychotic patients confirm the notion that neuroleptic treatment is associated with an increase in CSP.
采用单脉冲和双脉冲经颅磁刺激来测量运动皮质兴奋性,已成为一种用于体内表征中枢作用药物效果的既定方法。对未服药及服药的精神分裂症患者进行比较,结果提示抗精神病药物的摄入与皮质静息期(CSP)延长之间存在关联。然而,所有现有数据均来自横断面非随机研究。因此,尚不清楚所观察到的差异是药物治疗的效果,还是反映了疾病严重程度的差异,抑或是两者皆有。
我们旨在研究,在未服药的急性精神病患者中,于服用非典型抗精神病药物喹硫平3周前后测量皮质兴奋性时,CSP或其他皮质兴奋性参数是否会发生变化。
对24例未服药的急性精神病患者,在平均剂量为352±199mg喹硫平治疗3周前后,研究其不同的皮质兴奋性参数。
我们观察到,喹硫平治疗3周后,皮质静息期(CSP)显著延长。其他皮质兴奋性参数,如运动阈值(MT)、短皮质内抑制(SICI)和皮质内易化(ICF)均未受影响。临床参数(PANS、GAF)有显著改善,但临床改善与皮质兴奋性变化之间无显著相关性。
这些纵向数据与先前横断面研究的报告一致。急性精神病患者服用喹硫平3周所引起的兴奋性变化,证实了抗精神病药物治疗与CSP增加有关这一观点。