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The role of pontine lesion location in differentiating multiple sclerosis from vascular risk factor-related small vessel disease.
Geraldes, Ruth; Jurynczyk, Maciej; Dos Passos, Giordani Rodrigues; Pichler, Alexander; Chung, Karen; Hagens, Marloes; Ruggieri, Serena; Auger, Cristina; Sastre-Garriga, Jaume; Enzinger, Christian; Chard, Declan; Barkhof, Frederik; Gasperini, Claudio; Rovira, Alex; DeLuca, Gabriele; Palace, Jacqueline.
Afiliação
  • Geraldes R; Nuffield Department of Clinical Neurosciences, Oxford, UK.
  • Jurynczyk M; Nuffield Department of Clinical Neurosciences, Oxford, UK.
  • Dos Passos GR; Nuffield Department of Clinical Neurosciences, Oxford, UK.
  • Pichler A; Department of Neurology, Medical University of Graz, Graz, Austria/Division of Neuroradiology, Vascular & Interventional Radiology, Medical University of Graz, Graz, Austria.
  • Chung K; NMR Research Unit, Queen Square Multiple Sclerosis Centre, University College London Institute of Neurology, London, UK.
  • Hagens M; MS Center Amsterdam, Department of Neurology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Ruggieri S; Multiple Sclerosis Center, Department of Neurosciences, San Camillo-Forlanini Hospital, Rome, Italy.
  • Auger C; Section of Neuroradiology, Department of Radiology, Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Spain.
  • Sastre-Garriga J; Servei de Neurologia/Neuroimmunologia, Multiple Sclerosis Centre of Catalonia (Cemcat), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Enzinger C; Department of Neurology, Medical University of Graz, Graz, Austria/Division of Neuroradiology, Vascular & Interventional Radiology, Medical University of Graz, Graz, Austria.
  • Chard D; NMR Research Unit, Queen Square MS Centre, Department of Neuroinflammation, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK/National Institute for Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre, London, UK.
  • Barkhof F; MS Center Amsterdam, Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands/NMR Research Unit, Queen Square MS Centre, Department of Neuroinflammation, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, Lon
  • Gasperini C; Multiple Sclerosis Center, Department of Neurosciences, San Camillo-Forlanini Hospital, Rome, Italy.
  • Rovira A; Section of Neuroradiology, Department of Radiology, Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Spain.
  • DeLuca G; Nuffield Department of Clinical Neurosciences, Oxford, UK.
  • Palace J; Nuffield Department of Clinical Neurosciences, Oxford, UK.
Mult Scler ; 27(6): 968-972, 2021 05.
Article em En | MEDLINE | ID: mdl-32757905
ABSTRACT

BACKGROUND:

Differentiating multiple sclerosis (MS) from vascular risk factor (VRF)-small vessel disease (SVD) can be challenging. OBJECTIVE AND

METHODS:

In order to determine whether or not pontine lesion location is a useful discriminator of MS and VRF-SVD, we classified pontine lesions on brain magnetic resonance imaging (MRI) as central or peripheral in 93 MS cases without VRF, 108 MS patients with VRF and 43 non-MS cases with VRF.

RESULTS:

MS without VRF were more likely to have peripheral pons lesions (31.2%, 29/93) than non-MS with VRF (0%, 0/43) (Exp(B) = 29.8; 95% confidence interval (CI) = (1.98, 448.3); p = 0.014) but there were no significant differences regarding central pons lesions between MS without VRF (5.4%, 5/93) and non-MS with VRF patients (16.3%, 7/43) (Exp(B) = 0.89; 95% CI = (0.2, 3.94); p = 0.87). The presence of peripheral pons lesions discriminated between MS and VRF-SVD with 100% (95% CI = (91.8, 100)) specificity. The proportion of peripheral pons lesions in MS with VRF (30.5%, 33/108) was similar to that seen in MS without VRF (31.2%, 29/93, p = 0.99). Central lesions occurred in similar frequency in MS with VRF (8.3%, 9/108) and non-MS with VRF (16.3%, 7/43, p = 0.15).

CONCLUSION:

Peripheral pons lesion location is a good discriminator of MS from vascular lesions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article