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A longitudinal uncontrolled study of cerebral gray matter volume in patients receiving natalizumab for multiple sclerosis.
Khalid, Fariha; Tauhid, Shahamat; Chua, Alicia S; Healy, Brian C; Stankiewicz, James M; Weiner, Howard L; Bakshi, Rohit.
Afiliação
  • Khalid F; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
  • Tauhid S; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
  • Chua AS; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
  • Healy BC; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
  • Stankiewicz JM; c c Biostatistics Center, Massachusetts General Hospital, Harvard Medical School , Boston, MA , USA.
  • Weiner HL; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
  • Bakshi R; a a Laboratory for Neuroimaging Research, Department of Neurology, Brigham and Women's Hospital, Partners MS Center, Harvard Medical School , Boston, MA , USA.
Int J Neurosci ; 127(5): 396-403, 2017 May.
Article em En | MEDLINE | ID: mdl-27143245
ABSTRACT

OBJECTIVE:

Brain atrophy in multiple sclerosis (MS) selectively affects gray matter (GM), which is highly relevant to disability and cognitive impairment. We assessed cerebral GM volume (GMV) during one year of natalizumab therapy. DESIGN/

METHODS:

Patients with relapsing-remitting (n = 18) or progressive (n = 2) MS had MRI ∼1 year apart during natalizumab treatment. At baseline, patients were on natalizumab for (mean ± SD) 16.6 ± 10.9 months with age 38.5 ± 7.4 and disease duration 9.7 ± 4.3 years.

RESULTS:

At baseline, GMV was 664.0 ± 56.4 ml, Expanded Disability Status Scale (EDSS) score was 2.3 ± 2.0, timed 25-foot walk (T25FW) was 6.1±3.4 s; two patients (10%) had gadolinium (Gd)-enhancing lesions. At follow-up, GMV was 663.9 ± 60.2 mL; EDSS was 2.6 ± 2.1 and T25FW was 5.9 ± 2.9 s. One patient had a mild clinical relapse during the observation period (0.052 annualized relapse rate for the entire cohort). No patients had Gd-enhancing lesions at follow-up. Linear mixed-effect models showed no significant change in annualized GMV [estimated mean change per year 0.338 mL, 95% confidence interval -9.66, 10.34, p = 0.94)], GM fraction (p = 0.92), whole brain parenchymal fraction (p = 0.64), T2 lesion load (p = 0.64), EDSS (p = 0.26) or T25FW (p = 0.79).

CONCLUSIONS:

This pilot study shows no GM atrophy during one year of natalizumab MS therapy. We also did not detect any loss of whole brain volume or progression of cerebral T2 hyperintense lesion volume during the observation period. These MRI results paralleled the lack of clinical worsening.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Substância Cinzenta / Natalizumab / Fatores Imunológicos / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Substância Cinzenta / Natalizumab / Fatores Imunológicos / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article