Changes in Migraine Patients With T 2-Visible Lesions A 3T MRI Study

Background and Purpose—In migraine patients, functional imaging studies have shown changes in several brain gray matter (GM) regions. However, 1.5-T MRI has failed to detect any structural abnormality of these regions. We used a 3-T MRI scanner and voxel-based morphometry (VBM) to assess whether GM density abnormalities can be seen in patients with migraine with T2-visible abnormalities and to grade their extent. Methods—In 16 migraine patients with T2-visible abnormalities and 15 matched controls, we acquired a T2-weighted and a high-resolution T1-weighted sequence. Lesion loads were measured on T2-weighted images. An optimized version of VBM analysis was used to assess regional differences in GM densities on T1-weighted scans of patients versus controls. Statistical parametric maps were thresholded at P 0.001, uncorrected for multiple comparisons. Results—Compared with controls, migraine patients had areas of reduced GM density, mainly located in the frontal and temporal lobes. Conversely, patients showed increased periacqueductal GM (PAG) density. Compared with patients without aura, migraine patients with aura had increased density of the PAG and of the dorsolateral pons. In migraine patients, reduced GM density was strongly related to age, disease duration, and T2-visible lesion load (r ranging from 0.84 to 0.73). Conclusions—Structural GM abnormalities can be detected in migraine patients with brain T2-visible lesions using VBM and a high-field MRI scanner. Such GM changes comprise areas with reduced and increased density and are likely related to the pathological substrates associated with this disease. (Stroke. 2006;37:1765-1770.)

[1]  Karl J. Friston,et al.  A positron emission tomographic study in spontaneous migraine. , 2005, Archives of neurology.

[2]  M. Moskowitz,et al.  Migraine as an inflammatory disorder , 2005, Neurology.

[3]  A. Apkarian,et al.  Chronic Back Pain Is Associated with Decreased Prefrontal and Thalamic Gray Matter Density , 2004, The Journal of Neuroscience.

[4]  Karl J. Friston,et al.  A PET study exploring the laterality of brainstem activation in migraine using glyceryl trinitrate. , 2004, Brain : a journal of neurology.

[5]  T. Bartsch,et al.  Activation of 5‐HT1B/1D receptor in the periaqueductal gray inhibits nociception , 2004, Annals of neurology.

[6]  A. Dale,et al.  Thinning of the cerebral cortex in aging. , 2004, Cerebral cortex.

[7]  M. Ferrari,et al.  Migraine as a risk factor for subclinical brain lesions. , 2004, JAMA.

[8]  Bogdan Draganski,et al.  Neuroplasticity: Changes in grey matter induced by training , 2004, Nature.

[9]  W. Heindel,et al.  Magnetic resonance imaging protocols for examination of the neurocranium at 3 T , 2003, European Radiology.

[10]  C D Good,et al.  No change in the structure of the brain in migraine: a voxel‐based morphometric study , 2003, European journal of neurology.

[11]  K. Svoboda,et al.  Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex , 2002, Nature.

[12]  J. Grafman,et al.  Imaging cortical anatomy by high‐resolution MR at 3.0T: Detection of the stripe of Gennari in visual area 17 , 2002, Magnetic resonance in medicine.

[13]  V. Nagesh,et al.  Functional MRI-BOLD of brainstem structures during visually triggered migraine , 2002, Neurology.

[14]  T. Bartsch,et al.  P/Q-Type Calcium-Channel Blockade in the Periaqueductal Gray Facilitates Trigeminal Nociception: A Functional Genetic Link for Migraine? , 2002, The Journal of Neuroscience.

[15]  N Gelman,et al.  Periaqueductal Gray Matter Dysfunction in Migraine: Cause or the Burden of Illness? , 2001, Headache.

[16]  Karl J. Friston,et al.  A Voxel-Based Morphometric Study of Ageing in 465 Normal Adult Human Brains , 2001, NeuroImage.

[17]  M. Preul The Human Brain: Surface, Blood Supply, and Three-Dimensional Sectional Anatomy , 2001 .

[18]  R. Frackowiak,et al.  Brainstem activation specific to migraine headache , 2001, The Lancet.

[19]  A. May,et al.  Hypothalamic involvement and activation in cluster headache , 2001, Current pain and headache reports.

[20]  Karl J. Friston,et al.  Voxel-Based Morphometry—The Methods , 2000, NeuroImage.

[21]  S. Resnick,et al.  One-year age changes in MRI brain volumes in older adults. , 2000, Cerebral cortex.

[22]  G. Comi,et al.  A magnetization transfer imaging study of the brain in patients with migraine , 2000, Neurology.

[23]  Karl J. Friston,et al.  Correlation between structural and functional changes in brain in an idiopathic headache syndrome , 1999, Nature Medicine.

[24]  K. Welch,et al.  MRI of the occipital cortex, red nucleus, and substantia nigra during visual aura of migraine , 1998, Neurology.

[25]  Christian Büchel,et al.  Hypothalamic activation in cluster headache attacks , 1998, The Lancet.

[26]  Krishna Kumar,et al.  Headache Secondary to Deep Brain Implantation , 1998, Headache.

[27]  C Büchel,et al.  Experimental cranial pain elicited by capsaicin: a PET study , 1998, Pain.

[28]  C. Weiller,et al.  Brain stem activation in spontaneous human migraine attacks , 1995, Nature Medicine.

[29]  F. Fazekas,et al.  The Prevalence of Cerebral Damage Varies With Migraine Type: A MRI Study , 1992, Headache.

[30]  Richard S. J. Frackowiak,et al.  Central neuromodulation in chronic migraine patients with suboccipital stimulators: a PET study. , 2004, Brain : a journal of neurology.

[31]  Karl J. Friston,et al.  Statistical parametric maps in functional imaging: A general linear approach , 1994 .

[32]  H. Wolff Headache and Other Head Pain , 1972 .