fMRI evidence that precision ophthalmic tints reduce cortical hyperactivation in migraine
Jie Huang, Xiaopeng Zong, Arnold Wilkins, Brian Jenkins, Andrea Bozoki, Yue Cao, Jie Huang, Xiaopeng Zong, Arnold Wilkins, Brian Jenkins, Andrea Bozoki, Yue Cao
Abstract
Background: Certain patterns can induce perceptual illusions/distortions and visual discomfort in most people, headaches in patients with migraine, and seizures in patients with photosensitive epilepsy. Visual stimuli are common triggers for migraine attacks, possibly because of a hyperexcitability of the visual cortex shown in patients with migraine. Precision ophthalmic tints (POTs) are claimed to reduce perceptual distortions and visual discomfort and to prevent migraine headaches in some patients. We report an fMRI visual cortical activation study designed to investigate neurological mechanisms for the beneficial effects of POTs in migraine.
Methods: Eleven migraineurs and 11 age- and sex-matched non-headache controls participated in the study using non-stressful and stressful striped patterns viewed through gray, POT, and control coloured lenses.
Results: For all lenses, controls and migraineurs did not differ in their response to the non-stressful patterns. When the migraineurs wore gray lenses or control coloured lenses, the stressful pattern resulted in activation that was greater than in the controls. There was also an absence of the characteristic low-pass spatial frequency (SF) tuning in extrastriate visual areas. When POTs were worn, however, both cortical activation and SF tuning were normalized. Both when observing the stressful pattern and under more typical viewing conditions, the POTs reduced visual discomfort more than either of the other two lenses.
Conclusion: The normalization of cortical activation and SF tuning in the migraineurs by POTs suggests a neurological basis for the therapeutic effect of these lenses in reducing visual cortical hyperactivation in migraine.
Figures
References
- Campbell FW, Robson JG. Application of Fourier analysis to the visibility of gratings. J Physiol. 1968;197:551–566.
- Wilkins AJ. Visual stress. Oxford University Press; Oxford: 1995.
- Huang J, Cooper TG, Satana B, Kaufman DI, Cao Y. Visual distortion provoked by a stimulus in migraine associated with hyperneuronal activity. Headache. 2003;43:664–671.
- Wilkins AJ, Bonanni P, Porciatti V, Guerrini R. Physiology of human photosensitivity. Epilepsia. 2004;45:7–13.
- Aurora SK, Cao Y, Bowyer SM, Welch KMA. The occipital cortex is hyperexcitable in migraine: experimental evidence. Headache. 1998;39:469–476.
- Irlen H. Reading by the colors: overcoming dyslexia and other reading disabilities through the Irlen method. Avery Publishing Group; New York: 1991.
- Wilkins A, Milroy R, Nimmo-Smith I, Wright A, Tyrrell R, Holland K, et al. Preliminary observations concerning treatment of visual discomfort and associated perceptual distortion. Ophthalmic Physiol Opt. 1992;12:257–263.
- Wilkins AJ, Patel R, Adjamian R, Evans BJW. Tinted spectacles and visually sensitive migraine. Cephalalgia. 2002;22:711–719.
- Wilkins AJ, Lewis E, Smith F, Rowland E, Tweedie W. Coloured overlays and their benefit for reading. J Res Read. 2001;24:41–64.
- Hunt RWG. Measuring color. Fountain Press Ltd; London: 2001.
- Wilkins AJ, Sihra N, Myers A. Increasing reading speed using colours: issues concerning reliability and specificity, their theoretical and practical implications. Perception. 2005;34:109–120.
- Wilkins AJ, Sihra N. A colorizer for use in determining an optimal ophthalmic tint. Color Res Applic. 2000;26:246–253.
- Sereno MI, Dale AM, Reppas JB, Kwong KK, Belliveau JW, Brady TJ, et al. Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging. Science. 1995;268:889–893.
- Tootell RBH, Mendola JD, Hadjikhani NK, Ledden PJ, Liu AK, Reppas JB, et al. Functional analysis of V3A and related areas in human visual cortex. J Neurosci. 1997;17:7060–7078.
- Boynton GM, Engel SA, Glover GH, Heeger DJ. Linear systems analysis of functional magnetic resonance imaging in human V1. J Neurosci. 1996;16:4207–4221.
- Singh KD, Smith AT, Greenlee MW. Spatiotemporal frequency and direction sensitivities of human visual areas measured suing fMRI. NeuroImage. 2000;12:550–564.
- von der Heydt R, Peterhans E. Mechanisms of contour perception in monkey visual cortex. I. lines of pattern discontinuity. J Neuroscience. 1989;9:1731–1748.
- Foster KH, Gaska JP, Nagler M, Pollen DA. Spatial and temporal frequency selectivity of neurons in visual cortical areas V1 and V2 of the macaque monkey. J Physiol. 1985;365:331–363.
- Lund JS, Hendrickson AE, Ogren MP, Tobin EA. Anatomic organization of primate visual cortex area VII. J Comp Neurol. 1981;202:19–45.
- Levitt JB, Kiper DC, Movshon JA. Receptive fields and functional architecture of macaque V2. J Neurophysiol. 1994;71:2517–2542.
- Levitt JB, Yoshioka T, Lund JS. Intrinsic cortical connections in macaque visual area V2: evidence for interaction between different functional streams. J Comp Neurol. 1994;342:551–570.
- Xiao Y, Wang Y, Felleman DJ. A spatially organized representation of color in macaque cortical area V2. Nature. 2003;2003;421:535–539.
- Leao AAP. Spreading depression of activity in cerebral cortex. J Neurophysiol. 1944;7:359–390.
- Olesen J, Larsen B, Lauritzen M. Focal hyperemia followed by spreading oligemia and impaired activation of rcbf in classic migraine. Ann Neurol. 1981;9:344–352.
- Cao Y, Welch KMA, Aurora S, Vikingstad SE. Functional MRI-BOLD of visually triggered headache in patients with migraine. Arch Neurol. 1999;56:548–554.
- Hadjikhani N, Sanchez del Rio M, Wu O, Schwartz D, Bakker D, Fischl B, et al. Mechanisms of migraine aura revealed by functional MRI in human visual cortex. Proc Natl Acad Sci USA. 2001;98:4687–4692.
- Hall SD, Barnes GR, Hillebrand A, Furlong PL, Singh KD, Holliday IE. Spatio-temporal imaging of cortical desynchronization in migraine visual aura: a magnetoencephalography case study. Headache. 2004;44:204–208.
- Van Harreveld A, Stamm JS. Cortical responses to metrazol and sensory stimulation in the rabbit. Electroencephalogr Clin Neurophysiol. 1955;7:363.
- Noseda R, Kainz V, Jakubowski M, Gooley JJ, Saper CB, Digre K, Burstein R. A neural mechanism for exacerbation of headache by light. Nat Neurosci. 2010;13:239–245.
Source: PubMed