PMID- 17048979 OWN - NLM STAT- MEDLINE DCOM- 20070108 LR - 20240323 IS - 1549-1676 (Electronic) IS - 1549-1277 (Print) IS - 1549-1277 (Linking) VI - 3 IP - 10 DP - 2006 Oct TI - Anatomical alterations of the visual motion processing network in migraine with and without aura. PG - e402 LID - e402 AB - BACKGROUND: Patients suffering from migraine with aura (MWA) and migraine without aura (MWoA) show abnormalities in visual motion perception during and between attacks. Whether this represents the consequences of structural changes in motion-processing networks in migraineurs is unknown. Moreover, the diagnosis of migraine relies on patient's history, and finding differences in the brain of migraineurs might help to contribute to basic research aimed at better understanding the pathophysiology of migraine. METHODS AND FINDINGS: To investigate a common potential anatomical basis for these disturbances, we used high-resolution cortical thickness measurement and diffusion tensor imaging (DTI) to examine the motion-processing network in 24 migraine patients (12 with MWA and 12 MWoA) and 15 age-matched healthy controls (HCs). We found increased cortical thickness of motion-processing visual areas MT+ and V3A in migraineurs compared to HCs. Cortical thickness increases were accompanied by abnormalities of the subjacent white matter. In addition, DTI revealed that migraineurs have alterations in superior colliculus and the lateral geniculate nucleus, which are also involved in visual processing. CONCLUSIONS: A structural abnormality in the network of motion-processing areas could account for, or be the result of, the cortical hyperexcitability observed in migraineurs. The finding in patients with both MWA and MWoA of thickness abnormalities in area V3A, previously described as a source in spreading changes involved in visual aura, raises the question as to whether a "silent" cortical spreading depression develops as well in MWoA. In addition, these experimental data may provide clinicians and researchers with a noninvasively acquirable migraine biomarker. FAU - Granziera, Cristina AU - Granziera C AD - Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, United States of America. FAU - DaSilva, Alexandre F M AU - DaSilva AF FAU - Snyder, Josh AU - Snyder J FAU - Tuch, David S AU - Tuch DS FAU - Hadjikhani, Nouchine AU - Hadjikhani N LA - eng GR - P01 NS035611/NS/NINDS NIH HHS/United States GR - U54 EB005149/EB/NIBIB NIH HHS/United States GR - 5P01 NS 35611-09/NS/NINDS NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - PLoS Med JT - PLoS medicine JID - 101231360 SB - IM CIN - PLoS Med. 2006 Oct;3(10):e404. PMID: 17048980 MH - Adult MH - Brain/*pathology/physiopathology MH - Cerebral Cortex/pathology MH - *Diffusion Magnetic Resonance Imaging MH - Female MH - Geniculate Bodies/pathology MH - Humans MH - Male MH - Migraine with Aura/diagnosis/*physiopathology MH - Migraine without Aura/diagnosis/*physiopathology MH - *Motion Perception MH - Nerve Net/*pathology/physiopathology MH - Superior Colliculi/pathology MH - *Visual Perception PMC - PMC1609120 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2006/10/20 09:00 MHDA- 2007/01/09 09:00 PMCR- 2006/10/17 CRDT- 2006/10/20 09:00 PHST- 2006/02/23 00:00 [received] PHST- 2006/07/31 00:00 [accepted] PHST- 2006/10/20 09:00 [pubmed] PHST- 2007/01/09 09:00 [medline] PHST- 2006/10/20 09:00 [entrez] PHST- 2006/10/17 00:00 [pmc-release] AID - 06-PLME-RA-0158R4 [pii] AID - 10.1371/journal.pmed.0030402 [doi] PST - ppublish SO - PLoS Med. 2006 Oct;3(10):e402. doi: 10.1371/journal.pmed.0030402.