Reduced Short-Latency Afferent Inhibition in Prefrontal but not Motor Cortex and Its Association With Executive Function in Schizophrenia: A Combined TMS-EEG Study. (1st April 2017)

• Record Type: Journal Article
• Authors: Noda, Yoshihiro; Barr, Mera S; Zomorrodi, Reza; Cash, Robin F H; Rajji, Tarek K; Farzan, Faranak; Chen, Robert; George, Tony P; Daskalakis, Zafiris J; Blumberger, Daniel M
• Is Part Of: Schizophrenia bulletin. Volume 44:Number 1(2018:Jan.)
• Page Start: 193
• Page End: 202
• Publication Date: 2017-04-01
• Subjects: short-latency afferent inhibition -- dorsolateral prefrontal cortex -- executive function -- TMS-EEG study -- TMS-evoked potentials -- schizophrenia; Schizophrenia -- Periodicals; Schizophrenia -- Research -- Periodicals; 616.898005
• DOI: 10.1093/schbul/sbx041
• Languages: English
• ISSNs: 0586-7614

Abstract

Abstract: Background: Cholinergic dysfunction is increasingly assumed to be involved in the pathophysiology of schizophrenia. Short-latency afferent inhibition (SAI) is a transcranial magnetic stimulation (TMS) paradigm that has been shown to assay central cholinergic activity from the motor cortex (M1). Recently, we established a method to index SAI from the dorsolateral prefrontal cortex (DLPFC), an area implicated in the pathophysiology of schizophrenia. We investigated SAI in M1 and DLPFC in schizophrenia. We hypothesized that modulation of N100 on TMS-evoked potentials (TEPs) from the DLPFC would be attenuated in patients with schizophrenia compared to healthy controls. Methods: SAI was examined in 12 patients, whose age was matched to controls, using TMS combined with electroencephalography (EEG). SAI was recorded with TMS applied to left M1 (M1-SAI) and DLPFC (DLPFC-SAI). For group comparison, we used the SAI data of healthy participants in our previous study. Results: In patients, N100 TEP was significantly attenuated with DLPFC-SAI, whereas P180 TEP was significantly increased with M1-SAI. Between patients and controls, there were significant differences in modulation of P180 TEP by M1-SAI ( t 22 = −2.748, P = .012; patients > controls) and N100 TEP by DLPFC-SAI ( t 22 = 5.456, P < .0001; patients < controls). Further, modulation of N100 TEP by DLPFC-SAI significantly correlated with executive function ( r = −.740, P = .006, N = 12). Conclusion: Our findings suggest that DLPFC-SAI but not M1-SAI were reduced in patients with schizophrenia and this was linked to deficits in cognition. This may reflect prefrontal cholinergic deficits and represent a biomarker for cholinergic and executive dysfunction in patients with schizophrenia.