Impaired Response Inhibition in Patients with Obsessive-Compulsive Disorder

강박장애 환자의 반응억제 결함

  • Boo, Young Jun (Department of Medicine, Yonsei University College of Medicine) ;
  • Kim, Se Joo (Department of Psychiatry and Institute of Behavioral Science in Medicine, Yonsei University College of Medicine) ;
  • Kang, Jee In (Department of Psychiatry and Institute of Behavioral Science in Medicine, Yonsei University College of Medicine)
  • 부영준 (연세대학교 의과대학 의학과) ;
  • 김세주 (연세대학교 의과대학 정신과학교실, 의학행동과학연구소) ;
  • 강지인 (연세대학교 의과대학 정신과학교실, 의학행동과학연구소)
  • Received : 2015.02.09
  • Accepted : 2015.04.02
  • Published : 2015.04.30

Abstract

Objective : Impaired response inhibition has been suggested to play an important role in the pathophysiology of obsessive-compulsive disorder (OCD). The aim of this study was to evaluate the response inhibition in patients with OCD, by using the Go/NoGo paradigm, and to better understand its associations with clinical symptoms. Methods : The participants included 63 OCD patients and 80 healthy volunteers matched in age and sex. response inhibition was evaluated using computerized Go/NoGo task, in which their commission error rates, omission error rates, and mean response times were measured. The severity of clinical symptoms in the OCD patients was assessed using Montgomery-Asberg Depression Scale and Yale-Brown Obsessive Compulsive Scale. Result : OCD patients showed significantly impaired inhibition and higher omission errors rates despite their slower response time, compared to normal controls. Clinical symptoms were not correlated with commission errors and omission errors. Conclusion : The present results indicate that impairment in response inhibition may play a critical role in the pathophysiology of OCD as a trait. These findings suggest that deficit of response inhibition may contribute to developing and maintaining clinical symptoms such as compelling need to repeat certain actions in patients with OCD.

Keywords

References

  1. Ting JT, Feng G. Neurobiology of obsessive-compulsive disorder: insights into neural circuitry dysfunction through mouse genetics. Curr Opin Neurobiol 2011;21:842-848. https://doi.org/10.1016/j.conb.2011.04.010
  2. Menzies L, Chamberlain SR, Laird AR, Thelen SM, Sahakian BJ, Bullmore ET. Integrating evidence from neuroimaging and neuropsychological studies of obsessive-compulsive disorder: the orbitofronto-striatal model revisited. Neurosci Biobehav Rev 2008;32:525-549. https://doi.org/10.1016/j.neubiorev.2007.09.005
  3. Chamberlain SR, Menzies L, Hampshire A, Suckling J, Fineberg NA, del Campo N, et al. Orbitofrontal dysfunction in patients with obsessive-compulsive disorder and their unaffected relatives. Science 2008;321:421-422. https://doi.org/10.1126/science.1154433
  4. Ahmari SE, Spellman T, Douglass NL, Kheirbek MA, Simpson HB, Deisseroth K, et al. Repeated cortico-striatal stimulation generates persistent OCD-like behavior. Science 2013;340:1234-1239. https://doi.org/10.1126/science.1234733
  5. Bari A, Robbins TW. Inhibition and impulsivity: behavioral and neural basis of response control. Prog Neurobiol 2013;108:44-79. https://doi.org/10.1016/j.pneurobio.2013.06.005
  6. Aycicegi A, Dinn WM, Harris CL, Erkmen H. Neuropsychological function in obsessive-compulsive disorder: effects of comorbid conditions on task performance. Eur Psychiatry 2003;18:241-248. https://doi.org/10.1016/S0924-9338(03)00065-8
  7. Bannon S, Gonsalvez CJ, Croft RJ, Boyce PM. Response inhibition deficits in obsessive-compulsive disorder. Psychiatry Res 2002;110:165-174. https://doi.org/10.1016/S0165-1781(02)00104-X
  8. Bohne A, Savage CR, Deckersbach T, Keuthen NJ, Wilhelm S. Motor inhibition in trichotillomania and obsessive-compulsive disorder. J Psychiatr Res 2008;42:141-150. https://doi.org/10.1016/j.jpsychires.2006.11.008
  9. First MB. User's guide for the structured clinical interview for DSMIV-TR axis I disorders: SCID-I;2002.
  10. Penades R, Catalan R, Rubia K, Andres S, Salamero M, Gasto C. Impaired response inhibition in obsessive compulsive disorder. Eur Psychiatry 2007;22:404-410. https://doi.org/10.1016/j.eurpsy.2006.05.001
  11. Rubia K, Russell T, Overmeyer S, Brammer MJ, Bullmore ET, Sharma T, et al. Mapping motor inhibition: conjunctive brain activations across different versions of go/no-go and stop tasks. Neuroimage 2001;13:250-261.
  12. Rubia K, Taylor E, Smith AB, Oksanen H, Overmeyer S, Newman S. Neuropsychological analyses of impulsiveness in childhood hyperactivity. Br J Psychiatry 2001;179:138-143. https://doi.org/10.1192/bjp.179.2.138
  13. Brunner JF, Hansen TI, Olsen A, Skandsen T, Haberg A, Kropotov J. Long-term test-retest reliability of the P3 NoGo wave and two independent components decomposed from the P3 NoGo wave in a visual Go/NoGo task. Int J Psychophysiol 2013;89:106-114. https://doi.org/10.1016/j.ijpsycho.2013.06.005
  14. Covey TJ, Shucard JL, Violanti JM, Lee J, Shucard DW. The effects of exposure to traumatic stressors on inhibitory control in police officers: a dense electrode array study using a Go/NoGo continuous performance task. Int J Psychophysiol 2013;87:363-375. https://doi.org/10.1016/j.ijpsycho.2013.03.009
  15. Goodman WK, Price LH, Rasmussen SA, Mazure C, Fleischmann RL, Hill CL, et al. The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability. Arch Gen Psychiatry 1989;46:1006-1011. https://doi.org/10.1001/archpsyc.1989.01810110048007
  16. Montgomery SA, Asberg M. A new depression scale designed to be sensitive to change. Br J Psychiatry 1979;134:382-389. https://doi.org/10.1192/bjp.134.4.382
  17. Menzies L, Achard S, Chamberlain SR, Fineberg N, Chen CH, del Campo N, et al. Neurocognitive endophenotypes of obsessive-compulsive disorder. Brain 2007;130:3223-3236. https://doi.org/10.1093/brain/awm205
  18. Chamberlain SR, Fineberg NA, Blackwell AD, Robbins TW, Sahakian BJ. Motor inhibition and cognitive flexibility in obsessive-compulsive disorder and trichotillomania. Am J Psychiatry 2006;163:1282-1284. https://doi.org/10.1176/ajp.2006.163.7.1282
  19. Di Russo F, Zaccara G, Ragazzoni A, Pallanti S. Abnormal visual event-related potentials in obsessive-compulsive disorder without panic disorder or depression comorbidity. J Psychiatr Res 2000;34:75-82. https://doi.org/10.1016/S0022-3956(99)00030-8
  20. Johannes S, Wieringa BM, Nager W, Rada D, Dengler R, Emrich HM, et al. Discrepant target detection and action monitoring in obsessive-compulsive disorder. Psychiatry Res 2001;108:101-110. https://doi.org/10.1016/S0925-4927(01)00117-2
  21. Herrmann MJ, Jacob C, Unterecker S, Fallgatter AJ. Reduced response-inhibition in obsessive-compulsive disorder measured with topographic evoked potential mapping. Psychiatry Res 2003;120:265-271. https://doi.org/10.1016/S0165-1781(03)00188-4
  22. Kim MS, Kim YY, Yoo SY, Kwon JS. Electrophysiological correlates of behavioral response inhibition in patients with obsessive-compulsive disorder. Depress Anxiety 2007;24:22-31. https://doi.org/10.1002/da.20195
  23. Tolin DF, Witt ST, Stevens MC. Hoarding disorder and obsessive-compulsive disorder show different patterns of neural activity during response inhibition. Psychiatry Res 2014;221:142-148. https://doi.org/10.1016/j.pscychresns.2013.11.009
  24. Drewe EA. Go-no go learning after frontal lobe lesions in humans. Cortex 1975;11:8-16. https://doi.org/10.1016/S0010-9452(75)80015-3
  25. Grane VA, Endestad T, Pinto AF, Solbakk AK. Attentional control and subjective executive function in treatment-naive adults with attention deficit hyperactivity disorder. PLoS One 2014;9:e115227. https://doi.org/10.1371/journal.pone.0115227