Cognitive deficits in patients with obsessive-compulsive disorder - electroencephalography correlates
Status PubMed-not-MEDLINE Language English Country New Zealand Media electronic-ecollection
Document type Journal Article
PubMed
27226716
PubMed Central
PMC4866747
DOI
10.2147/ndt.s93040
PII: ndt-12-1119
Knihovny.cz E-resources
- Keywords
- electroencephalography, frontal areas, low-frequency sources, obsessive-compulsive disorder, standardized low-resolution electromagnetic tomography,
- Publication type
- Journal Article MeSH
BACKGROUND: Obsessive-compulsive disorder (OCD) is associated with cognitive dysfunction. Although there are several studies focused on the neurobiology of OCD, little is known about the biological correlates of the cognitive deficit linked to this disorder. The aim of our study was to examine the association between cognitive impairment and current source density markers in patients with OCD. METHODS: Resting-state eyes-closed electroencephalography (EEG) data were recorded in 20 patients with OCD and 15 healthy controls who were involved in the study. Cortical EEG sources were estimated by standardized low-resolution electromagnetic tomography in seven frequency bands: delta (1.5-6 Hz), theta (6.5-8 Hz), alpha-1 (8.5-10 Hz), alpha-2 (10.5-12 Hz), beta-1 (12.5-18 Hz), beta-2 (18.5-21 Hz), and beta-3 (21.5-30 Hz). Cognitive performance was measured by the Trail-Making Test (versions A and B), Stroop CW Test, and D2 Test. RESULTS: Frontal delta and theta EEG sources showed significantly higher activity in the whole group of patients with OCD (N=20) than in control subjects (N=15). Subsequent analysis revealed that this excess of low-frequency activity was present only in the subgroup of eleven patients with cognitive impairment (based on the performance in the Trail-Making Test - A). The subgroup of patients with normal cognitive functions (N=9) did not differ in cortical EEG sources from healthy controls. CONCLUSION: The present results suggest that frontal low-frequency cortical sources of resting-state EEG rhythms can distinguish groups of cognitively impaired and cognitively intact patients with OCD. Based on our results, future studies should consider whether the present methodological approach provides clinically useful information for the revelation of cognitive impairment in patients with OCD.
See more in PubMed
Saxena S, Rauch SL. Functional neuroimaging and the neuroanatomy of obsessive–compulsive disorder. Psychiatr Clin North Am. 2000;23:563–584. PubMed
Nakao T, Okada K, Kanba S. Neurobiological model of obsessive-compulsive disorder: evidence from recent neuropsychological and neuroimaging findings. Psychiatry Clin Neurosci. 2014;68:587–605. PubMed
Strobel A, Dreisbach G, Müller J, Goschke T, Brocke B, Lesch KP. Genetic variation of serotonin function and cognitive control. J Cogn Neurosci. 2007;19:1923–1931. PubMed
Bechara A. Neurobiology of decision-making: risk and reward. Semin Clin Neuropsychiatry. 2001;6:205–216. PubMed
Cavedini P, Gorini A, Bellodi L. Understanding obsessive–compulsive disorder: focus on decision making. Neuropsychol Rev. 2006;16:3–15. PubMed
Yücel M, Harrison BJ, Wood SJ, et al. Functional and biochemical alterations of the medial frontal cortex in obsessive–compulsive disorder. Arch Gen Psychiatry. 2007;64:946–955. PubMed
Menzies L, Achard S, Chamberlain SR, et al. Neurocognitive endopheno-types of obsessive–compulsive disorder. Brain. 2007;130:3223–3236. PubMed
Kim MS, Jang KM, Kim BN. The neuropsychological profile of a subclinical obsessive-compulsive sample. J Int Neuropsychol Soc. 2009;15(2):286–290. PubMed
Moritz S, Birkner C, Kloss M, et al. Executive functioning in obsessive-compulsive disorder, unipolar depression, and schizophrenia. Arch Clin Neuropsychol. 2002;17(5):477–483. PubMed
Penadés R, Catalán R, Andrés S, Salamero M, Gastó C. Executive function and nonverbal memory in obsessive-compulsive disorder. Psychiatry Res. 2005;133(1):81–90. PubMed
Lawrence NS, Wooderson S, Mataix-Cols D, David R, Speckens A, Phillips ML. Decision making and set shifting impairments are associated with distinct symptom dimensions in obsessive–compulsive disorder. Neuropsychology. 2006;20:409–419. PubMed
Sachdev PS, Malhi GS. Obsessive–compulsive behaviour: a disorder of decision-making. Aust N Z J Psychiatry. 2005;39:757–763. PubMed
Nakao T, Nakatani E, Nabeyama M, Yoshioka K, Tomita M, Nakagawa A. Duration effect on neuropsychological function and treatment response of OCD. Seishin Shinkeigaku Zasshi. 2005;107:1286–1298. PubMed
Ischebeck M, Endrass T, Simon D, Kathmann N. Altered frontal EEG asymmetry in obsessive-compulsive disorder. Psychophysiology. 2014;51:596–601. PubMed
Karadag F, Oguzhanoglu NK, Kurt T, Oguzhanoglu A, Ateşci F, Ozdel O. Quantitative EEG analysis in obsessive compulsive disorder. Int J Neurosci. 2003;113:833–847. PubMed
Kopřivová J, Congedo M, Horáček J, et al. EEG source analysis in obsessive-compulsive disorder. Clin Neurophysiol. 2011;122:1735–1743. PubMed
Kopřivová J, Horáček J, Raszka M, Brunovský M, Praško J. Standardized low-resolution electromagnetic tomography in obsessive-compulsive disorder – a replication study. Neurosci Lett. 2013;548:185–189. PubMed
Pogarell O, Juckel G, Mavrogiorgou P, et al. Symptom-specific EEG power correlations in patients with obsessive-compulsive disorder. Int J Psychophysiol. 2006;62:87–92. PubMed
Sherlin L, Congedo M. Obsessive-compulsive dimension localized using low-resolution brain electromagnetic tomography (LORETA) Neurosci Lett. 2005;387:72–74. PubMed
Velikova S, Locatelli M, Insacco C, Smeraldi E, Comi G, Leocani L. Dysfunctional brain circuitry in obsessive-compulsive disorder: source and coherence analysis of EEG rhythms. Neuroimage. 2010;48:977–983. PubMed
World Health Organisation . ICD-10: The ICD-10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. Geneva: Word Health Organisation; 1992.
Lecrubier Y, Sheehan DV, Weiller E, et al. The MINI-international neuropsychiatric interview (M.I.N.I.): a short diagnostic structured interview: reliability and validity according to the CIDI. Eur Psychiatry. 1997;12:224–231.
Wen SL, Cheng MF, Cheng MH, Yue JH, Li JF, Xie LJ. Neurocognitive dysfunction and regional cerebral blood flow in medically naïve patients with obsessive-compulsive disorder. Dev Neuropsychol. 2014;39:37–50. PubMed
Reitan RM. Validity of the Trail Making Test as an indicator of organic brain damage. Percept Mot Skills. 1958;8:271–276.
EMEA . Guideline for good clinical practice. London: EMEA; 2002. 2002. [Accessed March 20, 2009]. Available from: http://www.edctp.org/fileadmin/documents/EMEA_ICH-GCP_Guidelines_July_2002.pdf.
Kubicki S, Herrmann WM, Fichte K, Freund G. Reflections on the topics: EEG frequency bands and regulation of vigilance. Pharmakopsychiatr Neuropsychopharmakol. 1979;12:237–245. PubMed
Pascual-Marqui RD. Standardized low-resolution brain electromagnetic tomography (sLORETA): technical details. Methods Find Exp Clin Pharmacol. 2002;24:5–12. PubMed
Holmes AP, Blair RC, Watson JD, Ford I. Nonparametric analysis of statistic images from functional mapping experiments. J Cereb Blood Flow Metab. 1996;16:7–22. PubMed
Reitan RM. Trail Making Test: Manual for Administration and Scoring. Tucson, AZ: Reitan Neuropsychology Laboratory; 1992.
Beucke JC, Sepulcre J, Eldaief MC, Sebold M, Kathmann N, Kaufmann C. Default mode network subsystem alterations in obsessive-compulsive disorder. Br J Psychiatry. 2014;205(5):376–382. PubMed
Hou J, Song L, Zhang W, et al. Morphologic and functional connectivity alterations of corticostriatal and default mode network in treatment-naïve patients with obsessive-compulsive disorder. PLoS One. 2013;8:e83931. PubMed PMC
Nakamae T, Sakai Y, Abe Y, et al. Altered fronto-striatal fiber topography and connectivity in obsessive-compulsive disorder. PLoS One. 2014;9:e112075. PubMed PMC
Buzsaki G. Theta oscillations in the hippocampus. Neuron. 2002;33:325–340. PubMed
Başar-Eroğlu C, Başar E, Demiralp T, Schürmann M. P300-response: possible psychophysiological correlates in delta and theta frequency channels: a review. Int J Psychophysiol. 1992;13:161–179. PubMed
Lavoie S, Schafer MR, Whitford TJ, et al. Frontal delta power associated with negative symptoms in ultra-high risk individuals who transitioned to psychosis. Schizophr Res. 2012;138:206–211. PubMed
Sponheim SR, Clementz BA, Iacono WG, Beiser M. Clinical and biological concomitants of resting state EEG power abnormalities in schizophrenia. Biol Psychiatry. 2000;48:1088–1097. PubMed
Leuchter AF, Cook IA, Hunter AM, Cai C, Horvath S. Resting-state quantitative electroencephalography reveals increased neurophysiological connectivity in depression. PLoS One. 2012;7:e32508. PubMed PMC
Meerwijk EL, Ford JM, Weiss SJ. Resting-state EEG delta power is associated with psychological pain in adults with a history of depression. Biol Psychol. 2015;105:106–114. PubMed PMC
Sachs G, Anderer P, Dantendorfer K, Saletu B. EEG mapping in patients with social phobia. Psychiatry Res. 2004;131:237–247. PubMed
Babiloni C, Frisoni G, Steriade M, et al. Frontal white matter volume and delta EEG sources negatively correlate in awake subjects with mild cognitive impairment and Alzheimer’s disease. Clin Neurophysiol. 2006;117:1113–1129. PubMed
Vandborg SK, Hartmann TB, Bennedsen BE, Pedersen AD, Thomsen PH. Can memory and executive functions in patients with obsessive-compulsive disorder predict outcome of cognitive behavioural therapy? Nord J Psychiatry. 2015;2:1–7. PubMed