4.3 Article

3D GRASE arterial spin labelling reveals an inverse correlation of cortical perfusion with the white matter lesion volume in MS

期刊

MULTIPLE SCLEROSIS JOURNAL
卷 18, 期 11, 页码 1570-1576

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458512441984

关键词

arterial spin labelling; multiple sclerosis; lesion load; cerebral blood flow; pulsed arterial spin labelling; cortical perfusion

资金

  1. GlaxoSmithKline
  2. Swiss MS Society
  3. German Federal Ministry of Education and Research (BMBF)
  4. Acorda
  5. Actelion
  6. Allozyne
  7. BaroFold
  8. Bayer HealthCare Pharmaceuticals
  9. Bayer Schering
  10. Bayhill
  11. Biogen Idec
  12. Boehringer Ingelheim
  13. Elan
  14. Genmab
  15. Glenmark
  16. Merck Serono
  17. Medicinova
  18. Novartis
  19. sanofi-aventis
  20. Santhera
  21. Shire
  22. Roche
  23. Teva
  24. UCB
  25. Wyeth
  26. Swiss National Research Foundation
  27. European Union
  28. Gianni Rubatto Foundation
  29. Novartis Research Foundation
  30. Roche Research Foundation
  31. TEVA Neurosciences

向作者/读者索取更多资源

Background: We hypothesized that in multiple sclerosis (MS) patients, reduced cortical perfusion is associated with chronic white matter injury. Objective: To investigate the influence of different clinical and magnetic resonance imaging characteristics on cortical perfusion. Methods: Cerebral blood flow (CBF) was assessed by applying a pulsed arterial spin labelling (ASL) technique combined with single-shot 3D-GRASE (gradient-spin echo) in a cohort of 165 MS patients with a relapsing-remitting (n=123) or secondary progressive disease course (n=42). Mean age was 45.4 years (20-68 years), mean disease duration was 14.2 years (1-48 years). Results: Mean cortical CBF was 45.6 ml/100g per min (SD: 7.8 ml/100g per min). Stepwise multiple linear regression models were calculated to investigate the relationship between different factor sets and mean CBF. The model with the highest adjusted coefficient of determination included T2 lesion load, age, gender and disease duration as significant factors. Post-hoc Spearman rank correlation revealed significant correlation of adjusted CBF with T2 lesion load (rho=-0.35, p=1*10(-6)), with age (rho =-0.34, p=4*10(-6)), and with disease duration (rho=0.16, p=0.03), while Expanded Disability Status Scale (EDSS) did not reach significance in either model. Conclusion: This study suggests that the amount of white matter lesions indicates a reduced metabolic demand and reduced perfusion at a cortical level.

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