Long term effects of left frontal rTMS on EEG and ERPs in patients with depression

被引:46
作者
Spronk, Desiree [1 ]
Arns, Martijn [2 ]
Bootsma, Aukje [2 ]
van Ruth, Rosalinde [2 ]
Fitzgerald, Paul B. [3 ]
机构
[1] Brainclin Diagnost BV, NL-6525 EC Nijmegen, Netherlands
[2] Brainclin Treatment BV, Nijmegen, Netherlands
[3] Alfred & Monash Univ, Sch Psychol Psychiat & Psychol Med, Alfred Psychiat Res Ctr, Melbourne, Vic, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
depression; dorsolateral prefrontal cortex; event-related potenital; QEEG; repetitive transcranial magnetic stimulation; treatment;
D O I
10.1177/155005940803900305
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Repetitive transcranial magnetic stimulation (rTMS) treatment for depression has been under investigation in many controlled studies over the last 20 years. Little is known about the neurobiological action of rTMS in patients. We therefore investigated pre- and post-treatment effects on QEEG, ERP's and behavior (BDI and NEO-FFI). rTMS treatment was applied in 8 subjects for an average of 21 sessions to the left Dorsolateral Prefrontal Cortex (left DLPFC). Clients were assessed on a QEEG and Oddball ERP evaluation pre-and post-treatment. Clients were stimulated over the left DLPFC with 10 Hz rTMS (100% MT). Furthermore, rTMS treatment was complimented by psychotherapy. All subjects showed full remission within 20 sessions and there was a significant reduction in depressive symptomatology (BDI score) after 10 and 15 sessions and a clear decrease in the Neuroticism and an increase on the extraversion scale of the NEO-FFI personality questionnaire. Pre- and post-l measurements did not reveal treatment specific effects, but only an indirect right frontal increase in delta power. On the other hand. ERP measures did reveal treatment specific effects by showing an increased positivity in the post-treatment ERP's specifically left frontal. The P2 amplitude demonstrated a significant left frontal increase in amplitude, whereas for the negative N1 and N2 a significant decrease in amplitude was observed. The results of this pilot study demonstrate that rTMS can be a safe and efficacious treatment modality for depression. Furthermore, a specific left frontal increase in positivity for the ERP's was found (increased P2 and decreased N1 and N2 components) most likely related to the rTMS over the left DLPFC. Furthermore, there was no change in the alpha asymmetry lending support to the fact that frontal alpha asymmetry can be considered a trait marker for depression. The findings from this pilot study require future replication with larger sample sizes.
引用
收藏
页码:118 / 124
页数:7
相关论文
共 39 条
[1]
BAEHR E, 1997, J NEUROTHERAPY, P2
[2]
Boutros NN, 2000, DEPRESS ANXIETY, V12, P166, DOI 10.1002/1520-6394(2000)12:3<166::AID-DA8>3.0.CO
[3]
2-M
[4]
SLOW CORTICAL POTENTIAL BIOFEEDBACK AND THE STARTLE REFLEX [J].
BRODY, S ;
RAU, H ;
KOHLER, F ;
SCHUPP, H ;
LUTZENBERGER, W ;
BIRBAUMER, N .
BIOFEEDBACK AND SELF-REGULATION, 1994, 19 (01) :1-11
[5]
CHARLES G, 1992, Encephale, V18, P225
[6]
Costa P., 1992, REVISED PERSONALITY
[7]
Anterior electrophysiological asymmetries, emotion, and depression: Conceptual and methodological conundrums [J].
Davidson, RJ .
PSYCHOPHYSIOLOGY, 1998, 35 (05) :607-614
[8]
Psychotherapy alone and combined with pharmacotherapy in the treatment of depression [J].
de Jonghe, F ;
Hendriksen, M ;
van Aalst, G ;
Kool, S ;
Peen, J ;
Van, R ;
van den Eijnden, E ;
Dekker, J .
BRITISH JOURNAL OF PSYCHIATRY, 2004, 185 :37-45
[9]
A functional magnetic resonance imaging study of the effects of low frequency right prefrontal transcranial magnetic stimulation in depression [J].
Fitzgerald, Paul B. ;
Sritharan, Anusha ;
Daskalakis, Zafiris J. ;
de Castella, Anthony R. ;
Kulkarni, Jayashri ;
Egan, Gary .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2007, 27 (05) :488-492
[10]
An analysis of functional neuroimaging studies of dorsolateral prefrontal cortical activity in depression [J].
Fitzgerald, Paul B. ;
Oxley, Tom J. ;
Laird, Angela R. ;
Kulkarni, Jayashri ;
Egan, Gary F. ;
Daskalakis, Zafiris J. .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2006, 148 (01) :33-45