Nucleus Accumbens Stimulation Modulates Inhibitory Control by Right Prefrontal Cortex Activation in Obsessive-Compulsive Disorder

Abstract Inhibitory control is considered a compromised cognitive function in obsessive-compulsive (OCD) patients and likely linked to corticostriatal circuitry disturbances. Here, 9 refractory OCD patients treated with deep brain stimulation (DBS) were evaluated to address the dynamic modulations o...

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Published inCerebral cortex (New York, N.Y. 1991) Vol. 31; no. 5; pp. 2742 - 2758
Main Authors Lopez-Sosa, Fernando, Reneses, Blanca, Sanmartino, Florencia, Galarza-Vallejo, Ana, Garcia-Albea, Julia, Cruz-Gomez, Alvaro J, Yebra, Mar, Oliviero, Antonio, Barcia, Juan A, Strange, Bryan A, Gonzalez-Rosa, Javier J
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 31.03.2021
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ISSN1047-3211
1460-2199
1460-2199
DOI10.1093/cercor/bhaa397

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Summary:Abstract Inhibitory control is considered a compromised cognitive function in obsessive-compulsive (OCD) patients and likely linked to corticostriatal circuitry disturbances. Here, 9 refractory OCD patients treated with deep brain stimulation (DBS) were evaluated to address the dynamic modulations of large-scale cortical network activity involved in inhibitory control after nucleus accumbens (NAc) stimulation and their relationship with cortical thickness. A comparison of DBS “On/Off” states showed that patients committed fewer errors and exhibited increased intraindividual reaction time variability, resulting in improved goal maintenance abilities and proactive inhibitory control. Visual P3 event-related potentials showed increased amplitudes during Go/NoGo performance. Go and NoGo responses increased cortical activation mainly over the right inferior frontal gyrus and medial frontal gyrus, respectively. Moreover, increased cortical activation in these areas was equally associated with a higher cortical thickness within the prefrontal cortex. These results highlight the critical role of NAc DBS for preferentially modulating the neuronal activity underlying sustained speed responses and inhibitory control in OCD patients and show that it is triggered by reorganizing brain functions to the right prefrontal regions, which may depend on the underlying cortical thinning. Our findings provide updated structural and functional evidence that supports critical dopaminergic-mediated frontal-striatal network interactions in OCD.
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ISSN:1047-3211
1460-2199
1460-2199
DOI:10.1093/cercor/bhaa397