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Diagnostic methods used in searching for markers of atrophy in patients with multiple sclerosis.
Puz, Przemyslaw; Steposz, Arkadiusz; Lasek-Bal, Anetta; Bartoszek, Karina; Radecka, Patrycja; Karuga-Pierscienska, Aleksandra.
Afiliação
  • Puz P; a Department of Neurology , Medical University of Silesia, Professor Leszek Giec Upper Silesian Medical Centre , Katowice , Poland.
  • Steposz A; b School of Health Sciences in Katowice , Medical University of Silesia , Katowice , Poland.
  • Lasek-Bal A; a Department of Neurology , Medical University of Silesia, Professor Leszek Giec Upper Silesian Medical Centre , Katowice , Poland.
  • Bartoszek K; b School of Health Sciences in Katowice , Medical University of Silesia , Katowice , Poland.
  • Radecka P; a Department of Neurology , Medical University of Silesia, Professor Leszek Giec Upper Silesian Medical Centre , Katowice , Poland.
  • Karuga-Pierscienska A; b School of Health Sciences in Katowice , Medical University of Silesia , Katowice , Poland.
Neurol Res ; 40(2): 110-116, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29168666
The results of available studies on assessment of neurodegenerative lesions in multiple sclerosis (MS) patients using different approaches have not been conclusive. Currently, clinical assessment is the most commonly used (involving primarily mobility assessment), along with magnetic resonance imaging and electrophysiological testing. In this review we describe available clinical, neuroimaging, electrophysiological and laboratory tests used to assess the neurodegeneration in MS. Laboratory markers to determine the risk of disease, its conversion and prognosis in MS patients are being constantly sought. Cerebrospinal fluid (CSF) sample collection is invasive and constitutes a burden to a patient, so serum biomarkers are being investigated. Optimistic preliminary results of studies assessing neurofilament light chains (NFL) in serum of MS patients, encourage further research. The possibility to use such marker (or a group of markers) would significantly facilitate clinical decisions at the stage of diagnosis and treatment. Currently used treatments have limited efficacy and are associated with numerous adverse effects. Additional information from available clinical, imaging, electrophysiological or laboratory biomarker or a group of biomarkers, which predict the course and prognosis, will facilitate choosing optimal treatment and its escalation at the relevant stage. CONCLUSION: Using the diagnostic panel consisting of imaging, neurophysiology and serology testing along with clinical and neuropsychological assessment may improve the reliability of diagnostic instruments evaluating cerebral atrophy in MS patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article