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Quantitative Measurement of Intrathecally Synthesized Proteins in Mice
Published on: November 29, 2019
Highly sensitive quantification of optic neuritis intrathecal biomarker CXCL13
M N Olesen1, A C Nilsson2, G Pihl-Jensen3
1Institutes of Regional Health Research and Molecular Medicine, University of Southern Denmark, Departments of Neurology, Slagelse Hospital & Biochemistry & Immunology, Lillebaelt Hospital, Vejle, Denmark.
Elevated CXCL13 levels in cerebrospinal fluid (CSF) can predict multiple sclerosis (MS) in patients with acute optic neuritis (ON). A highly sensitive assay shows promise for early MS diagnosis.
Area of Science:
- Neuroimmunology
- Biomarker Discovery
Background:
- CXCL13 is a key regulator of B-cell recruitment in cerebrospinal fluid (CSF) and is implicated in multiple sclerosis (MS).
- Elevated CXCL13 levels in CSF are associated with MS pathogenesis.
Purpose of the Study:
- To evaluate the predictive value of CXCL13 measurement using a highly sensitive assay for the development of MS in patients with acute optic neuritis (ON).
Main Methods:
- CXCL13 levels were measured using the Simoa assay in two independent treatment-naïve ON cohorts (training cohort: n=33, validation cohort: n=30).
- Patients were prospectively followed to determine progression to MS (MS-ON) or isolated ON (ION).
- Statistical analysis included logistic regression and ROC curve analysis.
Main Results:
- CXCL13 was detectable in all samples and higher in ON patients compared to healthy controls (HC).
- CSF CXCL13 levels were significantly higher in MS-ON patients compared to ION patients and HC in both cohorts.
- Logistic regression analysis showed an area under the ROC curve of 0.83, indicating good predictive value.
Conclusions:
- The highly sensitive Simoa assay for CXCL13 can identify ON patients.
- This assay can differentiate between MS-ON and ION, suggesting its potential as a predictive diagnostic tool for MS in ON patients.
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