Perfusion weighted imaging during migraine: Spontaneous visual aura and headache

Cephalalgia

Volumn 19, Issue 8, 1999, Pages 701-707

  Sanchez Del Rio, Margarita ^a   Bakker, D ^a   Wu, O ^a   Agosti, R ^a   Mitsikostas, D D ^a   Ostergaard L ^a   Wells, W A ^b   Rosen, B R ^a   Sorensen, G ^a   Moskowitz, M A ^a   Cutrer, F M ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

FMRI; Hemodynamic changes; Migraine; Migraine aura; Perfusion weighted imaging

Indexed keywords

ADULT; ARTICLE; BRAIN BLOOD FLOW; BRAIN PERFUSION; BRAIN REGION; CLINICAL ARTICLE; FEMALE; HEADACHE; HUMAN; MALE; MIGRAINE; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCIPITAL CORTEX; OCCIPITAL LOBE;

ADULT; BRAIN MAPPING; CEREBROVASCULAR CIRCULATION; CONTRAST MEDIA; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; OCCIPITAL LOBE; PERFUSION; REPRODUCIBILITY OF RESULTS;

EID: 0032735428     PISSN: 03331024     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1468-2982.1999.019008701.x     Document Type: Article

References (37)

1. Fisher M, Prichard JW, Warach S. New magnetic resonance techniques for acute ischemic stroke. JAMA 1995;274:908-11
2. Cutrer FM, Sorensen AG, Weisskoff RM, et al. Perfusion-weighted imaging defects during spontaneous migrainous aura. Ann Neurol 1998;43:25-31
3. Headache Classification Committee of the International Headache Society. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988;Suppl 7:1-96
4. Villringer A, Rosen BR, Belliveau JW, et al. Dynamic imaging with lanthanide chelates in normal brain: contrast due to magnetic susceptibility effects. Magn Reson Med 1988;6:164-74
5. Rosen BR, Belliveau JW, Chien D. Perfusion imaging by nuclear magnetic resonance. Magn Reson Q 1989;5:263-81
6. Ostergaard L, Weisskoff RM, Chesler DA, Gyldensted C, Rosen BR. High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part I: Mathematical approach and statistical analysis. Magn Reson Med 1996;36:715-25
7. Ostergaard L, Sorensen AG, Kwong KK, Weisskoff RM, Gyldensted C, Rosen BR. High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part II: Experimental comparison and preliminary results. Magn Reson Med 1996;36:726-36
8. Porkka L, Neuder M, Hunter G. Arterial-input function measurement with MRI. Society of Magnetic Resonance in Medicine 10th Annual Meeting, 1991:120 (Abstract)
9. Stewart GN. Researches on the circulation time in organs and on the influences which affect it. J Physiol 1894;I-III
10. Damasio H, Damasio AR. Lesion analysis in neuropsychology. New York: Oxford University Press, 1989:184
11. Arndt S, Cizadlo T, O'Leary D, Gold S, Andreasen NC. Normalizing counts and cerebral blood flow intensity in functional imaging studies of the human brain. Neuroimage 1996;3:175-84
12. Lauritzen M, Olesen J. Regional cerebral blood flow during migraine attacks by Xenon-133 inhalation and emission tomography. Brain 1984;107:447-61
13. Andersen AR, Friberg L, Olsen TS, Olesen J. Delayed hyperemia following hypoperfusion in classic migraine. Single photon emission computed tomographic demonstration (see comments). Arch Neurol 1988;45:154-9
14. Olesen J, Larsen B, Lauritzen M. Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine. Ann Neurol 1981;9:344-52
15. Skyhoj OT, Friberg L, Lassen NA. Ischemia may be the primary cause of the neurologic deficits in classic migraine (see comments). Arch Neurol 1987;44:156-61
16. Lauritzen M, Olesen J. Regional cerebral blood flow during migraine attacks by Xenon-133 inhalation and emission tomography. Brain 1984;107:447-61
17. Skyhoj OT, Larsen B, Bech SE, Enevoldsen E, Lassen NA. Focal cerebral ischemia measured by the intra-arterial 133xenon method. Limitations of 2-dimensional blood flow measurements. Stroke 1981;12:736-44
18. Skyhoj OT, Friberg L, Lassen NA. Ischemia may be the primary cause of the neurologic deficits in classic migraine (see comments). Arch Neurol 1987;44:156-61
19. Andersson JL, Muhr C, Lilja A, Valind S, Lundberg PO, Langstrom B. Regional cerebral blood flow and oxygen metabolism during migraine with and without aura (see comments). Cephalalgia 1997;17:570-9
20. Merikangas KR, Fenton BT, Cheng SH, Stolar MJ, Risch N. Association between migraine and stroke in a large-scale epidemiological study of the United States. Arch Neurol 1997;54-362-8
21. Olesen J, Larsen B, Lauritzen M. Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine. Ann Neurol 1981;9:344-52
22. Olesen J, Friberg L, Olsen TS, et al. Timing and topography of cerebral blood flow, aura, and headache during migraine attacks. Ann Neurol 1990;28:791-8
23. Hachinski VC, Norris JW, Cooper PW, Larsen B, Lassen NA. Serial rCBF determinations during classic migraine. Acta Neurol Scand. Suppl 1977;64:198-9, 286:198-9, 286
24. Hachinski VC, Norris JW, Cooper PW, Larsen B, Lassen NA. Serial rCBF determinations during classic migraine. Acta Neurol Scand. Suppl 1977;64:198-9, 286:198-9, 286
25. Meyer JS, Zetusky W, Jonsdottir M, Mortel K. Cephalic hyperemia during migraine headaches. A prospective study. Headache 1986;26:388-97
26. Soriani S, Feggi L, Battistella PA, Arnaldi C, De CL, Stipa S. Interictal and ictal phase study with Tc 99m HMPAO brain SPECT in juvenile migraine with aura. Headache 1997;37:31-6
27. Welch KM, Cao Y, Aurora S, Wiggins G, Vikingstad EM. MRI of the occipital cortex, red nucleus, and substantia nigra during visual aura of migraine. Neurology 1998;51:1465-9
28. Hsieh JC, Belfrage M, Stone-Elander S, Hansson P, Ingvar M. Central representation of chronic ongoing neuropathic pain studied by positron emission tomography. Pain 1995;63:225-36
29. Weiller C, May A, Limmroth V, et al. Brain stem activation in spontaneous human migraine attacks. Nat Med 1995;1:658-60
30. Woods RP, Iacoboni M, Mazziotta JC. Bilateral spreading cerebral hypoperfusion during spontaneous migraine headache. N Engl J Med 1994;22:1689-92
31. Derbyshire SW, Jones AK, Gyulai F, Clark S, Townsend D, Firestone LL. Pain processing during three levels of noxious stimulation produces differential patterns of central activity. Pain 1997;73:431-45
32. May A, Kaube H, Buchel C, et al. Experimental cranial pain elicited by capsaicin: a PET study. Pain 1998;74:61-6
33. Ostergaard L, Smith DF, Vestergaard-Poulsen P, et al. Absolute cerebral blood flow and blood volume measured by magnetic resonance imaging bolus tracking: comparison with positron emission tomography values. J Cereb Blood Flow Metab 1998;18:425-32
34. 2O positron emission tomography in humans. J Cereb Blood Flow Metab 1998;18:935-40
35. Weisskoff RM, Zuo CS, Boxerman JL, Rosen BR. Microscopic susceptibility variation and transverse relaxation: theory and experiment. Magn Reson Med 1994;31:601-10
36. Sorensen AG, Rosen BR. Functional MRI of the brain. In: Scott W Atlas, editor. Magnetic resonance imaging of the brain and spine. 2nd ed. Philadelphia: Lippincott-Raven, 1996:1501-45
37. Moskowitz MA, Macfarlane R. Neurovascular and molecular mechanisms in migraine headaches. Cerebrovasc Brain Metab Rev 1993;5:159-77