E. Oostra, W. L. Schipper, E. B. Tans, E. J. Regeer, Y. D. van der Werf, P. F. van Eijndhoven, O. A. van den Heuvel, E. van Exel, E. d'Angremont
Objective: Disruption of the excitation/inhibition balance may contribute to the pathophysiology of bipolar disorder, with post-mortem studies reporting abnormalities in GABA-receptors, interneurons and inhibitory signaling in prefrontal areas. Transcranial magnetic stimulation with electroencephalography (TMS-EEG) enables in vivo assessment of cortical excitability/inhibition. This study examined short-latency intracortical inhibition (SICI) after left- and right-dorsolateral prefrontal cortex (DLPFC) stimulation in bipolar depression (BDep, n=10) and healthy controls (HC, n=22). Methods: SICI (paired-pulse TMS) and excitability (single-pulse TMS) were quantified using local- and global-mean-field-power. Associations with lithium use and between-group differences in TMS-evoked potential amplitudes were also explored. Results: For left-DLPFC stimulation, BDep showed weaker SICI than HC (local: 3.7%{+/-}12.5 vs 9.0%{+/-}20.3, p=0.05; global: 1.5%{+/-}11.7 vs 8.8%{+/-}20.6, p=0.10), driven by larger ppTMS responses (weaker inhibition). For right-DLPFC stimulation, BDep showed stronger SICI than HC (local: 17.3%{+/-}16.1 vs 0.75%{+/-}27.1, p=0.36; global: 16.2%{+/-}14.6 vs -1.0%{+/-}21.8, p=0.03), driven by a larger spTMS response (enlarged excitability). Stronger right-hemispheric global-SICI was most pronounced in BDep patients not using lithium (17.9%{+/-}7.0) vs lithium users (3.9%{+/-}11.9) and HC (pFDR=0.03). Conclusions: BDep is characterized by reduced cortical inhibition after left DLPFC stimulation and enlarged cortical excitability after right DLPFC stimulation; the latter partly normalized by lithium. Significance: To our knowledge, this is the first study to apply TMS-EEG to the bilateral DLPFC in BDep, revealing distinct patterns of hemispheric dysfunction. These findings warrant replication in larger samples, to further elucidate the underlying pathophysiology and inform the mechanisms of action of neuromodulation treatments, such as rTMS.