Summary
| Direction in Multiple Sclerosis | ↕ Inconsistent — reported as both higher and lower across studies, with no consistent direction |
|---|---|
| Category | Other |
| Compared against | postmortem MS cases with low levels of meningeal inflammation and GM demyelination |
| Associated symptoms | high levels of meningeal inflammation and GM demyelination |
| Source | Magliozzi et al. 2018 — doi:10.1002/ana.25197 |
| Condition atlas | Multiple Sclerosis Biomarker Atlas |
Related Other markers in Multiple Sclerosis
Full list: Multiple Sclerosis Biomarker Atlas.
Frequently asked questions
Is CXCL13 high or low in Multiple Sclerosis?
Mixed. Some studies report higher and others lower CXCL13 in Multiple Sclerosis compared with postmortem MS cases with low levels of meningeal inflammation and GM demyelination, so no single direction is established. Source: Magliozzi et al. 2018.
What symptoms is CXCL13 associated with in Multiple Sclerosis?
The cited literature associates this marker with high levels of meningeal inflammation and GM demyelination. These are population-level associations and do not mean the marker causes the symptoms.
Which test measures CXCL13?
The atlas record does not list a standardised clinical test code (LOINC) for CXCL13, which usually means it was measured with research assays or study-specific protocols rather than a routine clinical panel. Check the cited source for the exact method.
Is one abnormal CXCL13 result diagnostic of Multiple Sclerosis?
No. No single biomarker is diagnostic of Multiple Sclerosis. CXCL13 findings come from group comparisons, overlap considerably between patients and controls, and vary with study design, timing and comparison group. A result should be interpreted by a clinician alongside symptoms, history and other tests.
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Last reviewed: 2026-10-08 · Page generated from multiple-sclerosis.json · Browse: Multiple Sclerosis atlas · Biomarker Index · All marker pages
Disclaimer: This page is an educational synthesis of published, peer-reviewed research and is not medical advice. Biomarker findings vary across studies with case definitions, comparison groups, timing and assay methods. Direction of change reflects the predominant finding in the cited source and does not establish a diagnostic threshold. Discuss any test result with a qualified clinician.