Frontal Theta Cordance Predicts 6-Month Antidepressant Response to Subcallosal Cingulate Deep Brain Stimulation for Treatment-Resistant Depression: A Pilot Study

被引:86
作者
Broadway, James M. [1 ]
Holtzheimer, Paul E. [2 ,3 ]
Hilimire, Matthew R. [1 ]
Parks, Nathan A. [4 ]
DeVylder, Jordan E. [5 ]
Mayberg, Helen S. [6 ]
Corballis, Paul M. [7 ]
机构
[1] Georgia Inst Technol, Sch Psychol, Atlanta, GA 30332 USA
[2] Dartmouth Coll, Dartmouth Med Sch, Hanover, NH USA
[3] Emory Univ, Dept Psychiat & Behav Sci, Atlanta, GA 30322 USA
[4] Univ Illinois, Beckman Inst, Urbana, IL USA
[5] Columbia Univ, Sch Social Work, New York, NY USA
[6] Emory Univ, Sch Med, Atlanta, GA USA
[7] Univ Auckland, Dept Psychol, Auckland 1, New Zealand
基金
美国国家卫生研究院;
关键词
deep brain stimulation; depression; EEG; theta cordance; biomarker; MAJOR DEPRESSION; NEURAL CIRCUITS; METABOLISM; CORTEX;
D O I
10.1038/npp.2012.23
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Deep brain stimulation (DBS) of subcallosal cingulate white matter (SCC) may be an effective approach for treatment-resistant depression (TRD) that otherwise fails to respond to more conventional therapies, but DBS is invasive, costly, and has potential for adverse effects. Therefore, it is important to identify potential biomarkers for predicting antidepressant response before intervention. Resting-state EEG was recorded from 12 TRD patients at pre-treatment baseline, after 4 weeks SCC DBS, and after 24 weeks SCC DBS. Lower frontal theta cordance (FTC) at baseline (and higher FTC after 4 weeks) predicted lower depression severity scores after 24 weeks. Greater FTC increases (baseline-4 weeks) predicted greater decreases in depression severity scores subsequently (4-24 weeks) and over the course of the study (baseline-24 weeks). Predictive relationships were topographically specific to theta cordance for frontal electrodes. Thus, results from this pilot study suggest that baseline FTC and changes early in treatment each have utility as biomarkers for predicting 6-month clinical response to SCC DBS for TRD. Neuropsychopharmacology (2012) 37, 1764-1772; doi:10.1038/npp.2012.23; published online 14 March 2012
引用
收藏
页码:1764 / 1772
页数:9
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