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J Neurol Neurosurg Psychiatry doi:10.1136/jnnp.2009.173120

A diffusion tensor MRI study of cervical cord damage in benign and secondary progressive MS patients

  1. Beatrice Benedetti
  1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
    1. Maria A Rocca
    1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
      1. Rovaris Marco
      1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
        1. Domenico Caputo
        1. Multiple Sclerosis Center, Scientific Institute Don Gnocchi, Milan, Italy
          1. Mauro Zaffaroni
          1. Multiple Sclerosis Center, Ospedale di Gallarate, Gallarate, Italy
            1. Ruggero Capra
            1. Multiple Sclerosis Center, Spedali Civili, Brescia, Italy
              1. Antonio Bertolotto
              1. Multiple Sclerosis Center, Ospedale San Luigi, Orbassano, Italy
                1. Vittorio Martinelli
                1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
                  1. Giancarlo Comi
                  1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
                    1. Massimo Filippi (filippi.massimo{at}hsr.it)
                    1. Scientific Institute and University Ospedale San Raffaele, Milan, Italy
                      • Published Online First 21 June 2009

                      Abstract

                      Background: Diffusion tensor (DT) MRI enables to quantify the severity of brain and cervical cord pathology in MS.

                      Objective: To investigate the DT MRI patterns of cervical cord damage in benign MS (BMS) and secondary progressive MS (SPMS) patients, in order to achieve a better understanding of the mechanisms underlying the development of irreversible disability in MS.

                      Methods: Conventional and DT MRI scans of the cervical cord and brain were acquired from 40 BMS patients, 28 SPMS patients and 18 healthy individuals. Cervical cord and brain mean diffusivity (MD) and fractional anisotropy (FA) maps were created and average MD and FA were calculated. Cross-sectional cord area (CSA) was also computed.

                      Results: Thirty-seven (92%) BMS patients and all (100%) SPMS patients had macroscopic cervical cord lesions. Compared to healthy individuals, BMS patients had higher average cord MD, while SPMS patients had higher average cord MD, lower average cord FA and lower average CSA. Compared to BMS patients, SPMS patients had lower cord average FA and lower average CSA. In MS patients, expanded disability status scale (EDSS) was correlated with CSA (r=-0.47, p<0.0001), average cord FA (r=-0.37, p=0.002) and brain T2 lesion volume (LV) (r=0.34, p=0.005). A multivariate regression model identified CSA, average cord FA and brain T2 LV as variables influencing independently the EDSS score (r=0.58, p<0.0001).

                      Conclusions: Cervical cord damage outside focal macroscopic lesions is limited in patients with BMS. The assessment of cord and brain pathology provides complementary information to improve the understanding of disability accumulation in MS.

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