Analysis of CSF D-Dimer to Identify Intrathecal Fibrin-Driven Autoimmunity in Patients With Multiple Sclerosis.

Neurol Neuroimmunol Neuroinflamm

From the Department of Neurology (M.A.S.-P., Y.Y., H.S., L.F., J.H.S., C.F.), University Hospital Frankfurt, Goethe-University; Institute of Neuroradiology (E.H.), University Hospital Frankfurt, Goethe-University, Frankfurt am Main; Department of Haemostaseology and Hemophilia Center (W.M.), Medical

Published: May 2022


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Article Abstract

Background And Objectives: Proteins of the coagulation system contribute to autoimmune inflammation in patients with multiple sclerosis (MS). On blood-brain barrier (BBB) disruption, fibrinogen enters the CNS and is rapidly converted to fibrin, unfolding pleiotropic autoimmune mechanisms. Fibrin accumulation leads to subsequent proteolytic degradation that results in D-dimer generation. The primary objective of this study was to determine intrathecal levels of D-dimer in CSF as a measure of intrathecal coagulation cascade activation and to evaluate its diagnostic utility in patients with MS in contrast to healthy subjects. Key secondary objectives included analysis of CSF D-dimer in differential diagnoses of MS and its relation to routine clinical markers of disease activity.

Methods: Patients admitted for the assessment of suspected MS were prospectively recruited from October 2017 to December 2020. Blood plasma and citrated CSF samples were analyzed using a highly sensitive luminescent oxygen channeling immunoassay. Intrathecal generation of D-dimer was analyzed by adjusting for CSF/serum albumin (Q) and CSF/plasma D-dimer quotients (Q), and corresponding CSF fibrinogen levels were determined. Final diagnoses after full evaluation and clinical data were recorded.

Results: Of 187 patients, 113 patients received a diagnosis of MS or clinically/radiologically isolated syndrome. We found increased intrathecal CSF D-dimer generation levels (Q/Q-index) for patients with relapsing-remitting MS (RRMS; n = 71, median 4.7, interquartile range [IQR] 2.5-8.0) when compared with those for disease controls (n = 22, median 2.6, IQR 2.1-4.8, = 0.031). Absolute CSF D-dimer values correlated with CSF fibrinogen levels (r = 0.463; < 0 .001) and CSF leukocytes (r = 0.273; = 0.003) and were elevated in MS patients with contrast enhancement (CE) compared with MS patients without CE on MRI (n = 48, median 6 ng/mL, and IQR 3-15.25 vs n = 41, median 4 ng/mL, and IQR 2-7; = 0.026). Exploratory subgroup analyses indicated a correlation of intrathecal inflammatory activity and CSF D-dimer levels.

Discussion: D-dimer in CSF can be reliably determined and correlates with markers of CNS inflammation and CSF fibrinogen levels. Adjusted for BBB dysfunction, CSF D-dimer may allow the identification of intrathecal coagulation cascade activation in patients with MS.

Classification Of Evidence: This study provides Class I evidence that CSF D-dimer levels are elevated in patients with RRMS.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906189PMC
http://dx.doi.org/10.1212/NXI.0000000000001150DOI Listing

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