AI Article Synopsis

  • A recent study examined a condition called "pure spinal" MS, which features demyelination mainly in the spinal cord, potentially responding well to disease-modifying treatments (DMT).
  • Researchers analyzed data from around 8000 patients and identified 7 women with this condition, averaging 40 years old and having positive markers in their cerebrospinal fluid indicative of demyelination.
  • Treatment with DMT resulted in reduced relapse rates and stabilization of symptoms in these patients, suggesting that pure spinal MS may merit further study and could lead to updates in diagnostic criteria for MS.

Article Abstract

Background: Recent literature describes a condition similar to multiple sclerosis (MS) but with demyelinating lesions limited to the spinal cord. This condition, referred to as "pure spinal" MS, might benefit from disease-modifying treatment (DMT).

Methods: We screened the medical records of approximately 8000 patients with demyelinating diseases at the Isfahan MS clinic in Iran. Criteria for inclusion in the case series were adults with a demyelinating disease limited to the spinal cord, positive oligoclonal IgG bands in cerebrospinal fluid (CSF), and negative results for other potential diagnoses.

Results: Seven people with pure spinal MS were identified (all women, mean age [SD]: 40.14 [6.17] years at the first visit, mean follow-up duration [SD]: 98 [39.41] months). Two had a family history of conventional MS in their siblings. All patients exhibited lower limb weakness and tested negative for anti-MOG and anti-AQP4 antibodies. They experienced relapsing-remitting partial myelitis, with new spinal cord lesions on MRI but no extraspinal CNS lesions. DMT significantly reduced relapse rates in all patients, and two showed no increase in EDSS scores.

Conclusion: Pure spinal MS might be an atypical form of MS. Those affected may benefit from DMT; therefore, further investigation and consideration in the upcoming revisions of the McDonald criteria are recommended.

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Source
http://dx.doi.org/10.1016/j.jneuroim.2024.578429DOI Listing

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