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Cerebrospinal fluid camk2a levels at baseline predict long-term progression in multiple sclerosis.
Sohaei, Dorsa; Thebault, Simon; Avery, Lisa M; Batruch, Ihor; Lam, Brian; Xu, Wei; Saadeh, Rubah S; Scarisbrick, Isobel A; Diamandis, Eleftherios P; Prassas, Ioannis; Freedman, Mark S.
Afiliação
  • Sohaei D; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
  • Thebault S; Department of Medicine, The Ottawa Hospital, 01 Smyth Road, Box 601, Ottawa, ON, K1H 8L6, Canada.
  • Avery LM; The Ottawa Hospital Research Institute, Ottawa, Canada.
  • Batruch I; Biostatistics Division, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
  • Lam B; Department of Biostatistics, The Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
  • Xu W; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.
  • Saadeh RS; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, United States of America.
  • Scarisbrick IA; Biostatistics Division, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
  • Diamandis EP; Department of Biostatistics, The Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
  • Prassas I; Department of Physical Medicine and Rehabilitation, Center for Multiple Sclerosis and Autoimmune Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
  • Freedman MS; Department of Physical Medicine and Rehabilitation, Center for Multiple Sclerosis and Autoimmune Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
Clin Proteomics ; 20(1): 33, 2023 Aug 29.
Article em En | MEDLINE | ID: mdl-37644477
BACKGROUND: Multiple sclerosis (MS) remains a highly unpredictable disease. Many hope that fluid biomarkers may contribute to better stratification of disease, aiding the personalisation of treatment decisions, ultimately improving patient outcomes. OBJECTIVE: The objective of this study was to evaluate the predictive value of CSF brain-specific proteins from early in the disease course of MS on long term clinical outcomes. METHODS: In this study, 34 MS patients had their CSF collected and stored within 5 years of disease onset and were then followed clinically for at least 15 years. CSF concentrations of 64 brain-specific proteins were analyzed in the 34 patient CSF, as well as 19 age and sex-matched controls, using a targeted liquid-chromatography tandem mass spectrometry approach. RESULTS: We identified six CSF brain-specific proteins that significantly differentiated MS from controls (p < 0.05) and nine proteins that could predict disease course over the next decade. CAMK2A emerged as a biomarker candidate that could discriminate between MS and controls and could predict long-term disease progression. CONCLUSION: Targeted approaches to identify and quantify biomarkers associated with MS in the CSF may inform on long term MS outcomes. CAMK2A may be one of several candidates, warranting further exploration.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá