Neural correlates of behavioral variation in healthy adults' antisaccade performance

Psychophysiology

Volumn 50, Issue 4, 2013, Pages 325-333

  Schaeffer, David J ^a   Amlung, Michael T ^b   Li, Qingyang ^c   Krafft, Cynthia E ^b   Austin, Benjamin P ^d   Dyckman, Kara A ^b   Mcdowell, Jennifer E ^a,b  

^a UNIVERSITY OF GEORGIA   (United States)

^b Child Mind Institute ^*  (United States)

^c CHILD MIND INSTITUTE   (United States)

^d University of Wisconsin Cardiovascular Research Center   (United States)

Author keywords

Antisaccade; Cognitive control; Functional magnetic resonance imaging (fMRI)

Indexed keywords

EID: 84874729025     PISSN: 00485772     EISSN: 14698986     Source Type: Journal    
DOI: 10.1111/psyp.12030     Document Type: Article

References (30)

1. Beckmann, C. F., & Smith, S. M. (2004). Probabilistic independent component analysis for functional magnetic resonance imaging. IEEE Transactions on Medical Imaging, 23, 137-152. doi: 10.1109/tmi.2003.822821
2. Clementz, B. A., Brahmbhatt, S. B., McDowell, J. E., Brown, R., & Sweeney, J. A. (2007). When does the brain inform the eyes whether and where to move? An EEG study in humans. Cerebral Cortex, 17, 2634-2643. doi: 10.1093/cercor/bhl171
3. Clementz, B. A., Gao, Y., McDowell, J. E., Moratti, S., Keedy, S. K., & Sweeney, J. A. (2010). Top-down control of visual sensory processing during an ocular motor response inhibition task. Psychophysiology, 47, 1011-1018. doi: 10.1111/j.1469-8986.2010.01026.x
4. Connolly, J. D., Goodale, M. A., DeSouza, J. F., Menon, R. S., & Vilis, T. (2000). A comparison of frontoparietal fMRI activation during anti-saccades and anti-pointing. Journal of Neurophysiology, 84, 1645-1655. Retrieved from http://jn.physiology.org/content/84/3/1645.full
5. Cox, R. W. (1996). AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages. Computers and Biomedical Research, 29, 162-173.
6. Curtis, C. E., & D'Esposito, M. (2003). Success and failure suppressing reflexive behavior. Journal of Cognitive Neuroscience, 15, 409-418. doi: 10.1162/089892903321593126
7. Dale, A. M., & Buckner, R. L. (1997). Selective averaging of rapidly presented individual trials using fMRI. Human Brain Mapping, 5, 329-340. doi: 10.1002/(SICI)1097-0193(1997)5:5<329::AID-HBM1>3.0.CO;2-5
8. DeSouza, J. F., Menon, R. S., & Everling, S. (2002). Preparatory set associated with pro-saccades and anti-saccades in humans investigated with event-related fMRI. Journal of Neurophysiology, 89, 1016-1023. doi: 10.1152/jn.00562.2002
9. Dyckman, K. A., Camchong, J., Clementz, B. A., & McDowell, J. E. (2007). An effect of context on saccade-related behavior and brain activity. NeuroImage, 36, 774-784. doi: 10.1016/j.neuroimage.2007.03.023
10. Ettinger, U., Ffytche, D. H., Kumari, V., Kathmann, N., Reuter, B., Zelaya, F., & Williams, S. C. R. (2008). Decomposing the neural correlates of antisaccade eye movements using event-related fMRI. Cerebral Cortex, 18, 1148-1159. doi: 10.1093/cercor/bhm147
11. Fischer, B., Gezeck, S., & Hartnegg, K. (2000). On the production and correction of involuntary prosaccades in a gap antisaccade task. Vision Research, 40, 2211-2217. doi: 10.1016%2FS0042-6989%2800%2900082-1
12. Ford, K. A., Goltz, H. C., Brown, M. R., & Everling, S. (2005). Neural processes associated with antisaccade performance investigated with event-related fMRI. Journal of Neurophysiology, 94, 429-440. doi: 10.1152/jn.00471.2004
13. Hallett, P. E. (1978). Primary and secondary saccades to goals defined by instructions. Vision Research, 18, 1279-1296. doi: 10.1016/0042-6989(78)90218-3
14. Hill, S. Y., & Neiswanger, K. (1997). The value of narrow psychiatric phenotypes and "super" normal controls. Handbook of psychiatric genetics (Vol. 236). New York, NY: CRC Press.
15. Hutton, S. B., & Ettinger, U. (2006). The antisaccade task as a research tool in psychopathology: A critical review. Psychophysiology, 43, 302-313. doi: 10.1111/j.1469-8986.2006.00403.x
16. Johnston, K., & Everling, S. (2006). Neural activity in monkey prefrontal cortex is modulated by task context and behavioral instruction during delayed-match-to-sample and conditional prosaccade-antisaccade tasks. Journal of Cognitive Neuroscience, 18, 749-765. doi: 10.1162/jocn.2006.18.5.749
17. Klein, C., Rauh, R., & Biscaldi, M. (2010). Cognitive correlates of anti-saccade task performance. Experimental Brain Research, 203, 759-764. doi: 10.1007/s00221-010-2276-5
18. Krafft, C., Schwarz, N., Chi, L., Li, Q., Schaeffer, D., Rodrigue, A. L., ... McDowell, J. (2012). The location and function of parietal cortex supporting of reflexive and volitional saccades, a meta-analysis of over a decade of functional MRI data. In A. Costa & E. Villalba (Eds.), Horizons of neuroscience research, volume 9 (pp. 131-153). Hauppauge, NY: Nova Science Publishers.
19. Leigh, R. J., & Zee, D. S. (2006). The neurology of eye movements (Vol. 4). Oxford, UK: Oxford University.
20. Li, Q., Amlung, M. T., Valtcheva, M., Camchong, J., Austin, B. P., Dyckman, K. A., ... McDowell, J. E. (2012). Evidence from cluster analysis for differentiation of antisaccade performance groups based on speed/accuracy trade-offs. International Journal of Psychophysiology, 85, 274-277. doi: 10.1016/j.ipsycho.2012.03.008
21. McDowell, J. E., Brown, G. G., Paulus, M., Martinez, A., Stewart, S. E., Dubowitz, D. J., & Braff, D. L. (2002). Neural correlates of refixation saccades and antisaccades in normal and schizophrenia subjects. Biological Psychiatry, 51, 216-223. doi: 10.1016/S0006-3223(01)01204-5
22. McDowell, J. E., Dyckman, K. A., Austin, B. P., & Clementz, B. A. (2008). Neurophysiology and neuroanatomy of reflexive and volitional saccades: Evidence from studies of humans. Brain and Cognition, 68, 255-270. doi: 10.1016/j.bandc.2008.08.016
23. McDowell, J. E., Kissler J. M., Berg, P., Dyckman, K. A, Gao, Y., Rockstroh, B., & Clementz, B. A. (2005). Electroencephalography/magnetoencephalography study of cortical activities preceding prosaccades and antisaccades. NeuroReport, 16, 663-668. doi: 10.1097/00001756-200505120-00002
24. McKeown, M. J. (2000). Detection of consistently task-related activations in fMRI data with hybrid independent component analysis. NeuroImage, 11, 24-35. doi: 10.1006/nimg.1999.0518
25. Munoz, D. P., & Everling, S. (2004). Look away: The anti-saccade task and the voluntary control of eye movement. Nature Reviews Neuroscience, 5, 218-228. doi: 10.1038/nrn1345
26. Sharpe, J. A., Cheng, P., & Eizenman, M. (2011). Antisaccade generation is impaired after parietal lobe lesions. Annals of the New York Academy of Sciences, 1233, 194-199. doi: 10.1111/j.1749-6632.2011.06178.x
27. Talaraich, J., & Tournoux, P. (1998). Co-planar stereotaxic atlas of the human brain: A 3-dimensional proportional system, an approach to cerebral imaging. New York, NY: Thieme Medical Publishers.
28. Tu, P., Yang, T. H., Kuo, W. J., Hsieh, J. C., & Su, T. P. (2006). Neural correlates of antisaccade deficits in schizophrenia, an fMRI study. Journal of Psychiatric Research, 40, 606-612. doi: 10.1016/j.jpsychires.2006.05.012
29. Ward, B. D. (2000). Simultaneous inference for fMRI data, AlphaSim program documentation for AFNI. Milwaukee, WI: Medical College of Wisconsin.
30. Zhang, M., & Barash, S. (2000). Neuronal switching of sensorimotor transformations for antisaccades. Nature, 408, 971-975. doi: 10.1038/35050097