Abstract

Objective: To determine whether EEG occipital alpha and frontal alpha asymmetry (FAA) distinguishes outpatients with major depression (MDD) from controls, predicts antidepressant treatment outcome, and to explore the role of gender. Methods: In the international Study to Predict Optimized Treatment in Depression (iSPOT-D), a multi-center, randomized, prospective open-label trial, 1008 MDD participants were randomized to escitalopram, sertraline or venlafaxine-extended release. The study also recruited 336 healthy controls. Treatment response was established after eight weeks and resting EEG was measured at baseline (two minutes eyes open and eyes closed). Results: No differences in EEG alpha for occipital and frontal cortex, or for FAA, were found in MDD participants compared to controls. Alpha in the occipital and frontal cortex was not associated with treatment outcome. However, a gender and drug-class interaction effect was found for FAA. Relatively greater right frontal alpha (less cortical activity) in women only was associated with a favorable response to the Selective Serotonin Reuptake Inhibitors escitalopram and sertraline. No such effect was found for venlafaxine-extended release. Conclusions: FAA does not differentiate between MDD and controls, but is associated with antidepressant treatment response and remission in a gender and drug-class specific manner. Significance: Future studies investigating EEG alpha measures in depression should a-priori stratify by gender.

Original languageEnglish
Pages (from-to)509-519
Number of pages11
JournalClinical Neurophysiology
Volume127
Issue number1
DOIs
Publication statusPublished - 1 Jan 2016

Funding

We acknowledge the iSPOT-D Investigators Group, the contributions of iSPOT-D principal investigators at each site and the central management team (global coordinator Claire Day) as well as the support from William Rekshan for running the mixed models analyses. We acknowledge the editorial support of Jon Kilner, MS, MA (Pittsburgh, PA, USA). JMG is currently supported by a NHMRC CDF Fellowship APP1062495. We acknowledge the contribution of Dr Leanne Williams as academic principal investigator for iSPOT-D from 2008 to 2013. Appendix A

Keywords

  • Alpha
  • Alpha asymmetry
  • Antidepressant
  • Depression
  • EEG
  • Gender
  • ISPOT-D
  • Major depressive disorder
  • Personalized medicine
  • QEEG

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