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Abstract Details

Rethinking Headache in Multiple Sclerosis as a Feature of Relapsing Disease Biology and Early Neuroinflammation
Multiple Sclerosis
P10 - Poster Session 10 (8:00 AM-9:00 AM)
19-006

To establish how headache intensity, prevalence, frequency, and precipitants differ by disability, gender, and MS subtypes, and if headache patterns are linked to early relapsing inflammatory or late progressive MS courses.

Headache is a common symptom among people with multiple sclerosis (MS), but its connection to disease process is incompletely characterized. New data indicate headache potentially serves as a marker for initial neuroinflammatory activity and cortical hyperexcitability, rather than progressive neurodegeneration. Describing headache across different disease stages potentially clarifies its connection between early inflammatory and progressive neurodegenerative processes.

We compared 294 MS patients’ headache frequency and intensity using a linked survey of headache, demographics, and Expanded Disability Status Scale (EDSS) at our center. Headache presence was self-reported by definition and intensity was determined using the Migraine Disability Assessment (MIDAS). Group comparisons were made by χ², t-tests, Mann–Whitney U, and Spearman correlation tests. Logistic modeling of predictors for sex, EDSS, and MS subtype was performed. Multiple comparisons were accounted for using false discovery rate correction.

Headaches were reported by 75% of participants and were more frequent in women (80.0%) than men (58.1%; χ² p=0.0007, surviving multiple-testing correction). Headache frequency declined with higher disability (mean EDSS 2.81 vs 3.40, p=0.039; OR 0.82 per point, p=0.0089) and was significantly lower in progressive compared with relapsing phenotypes (RRMS 79.1%, SPMS 53.6%, PPMS 46.7%; χ² p=0.00014; adjusted OR 0.29, p=0.006). Although less frequent in advanced disease, headache intensity correlated modestly with EDSS (ρ=0.175, p=0.012). 

Headache frequency in MS associates more with a relapsing–remitting pattern that is common in early, inflammatory stages and less frequent as the disease progresses and disability accrues. These results favor a paradigm of headache as reflective of cortical hyperexcitability and neuroinflammatory activity. Awareness of this relationship may improve understanding of disease biology, importance of symptomatic management, and timing of disease-modifying therapy.

Authors/Disclosures
Nara Michaelson, MD (Beth Israel Deaconess Medical Center)
PRESENTER
The institution of Dr. Michaelson has received research support from Biogen. The institution of Dr. Michaelson has received research support from the National Multiple Sclerosis Society (NMSS). Dr. Michaelson has received research support from Sanofi.
Alexandra R. Balshi Ms. Balshi has nothing to disclose.
Nova Manning Miss Manning has nothing to disclose.
John Dempsey, BA (SUNY Upstate Medical University) Mr. Dempsey has nothing to disclose.
Jacob A. Sloane, MD, PhD (Beth Israel Deaconess Medical Center) Dr. Sloane has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for biogen. Dr. Sloane has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genentech. Dr. Sloane has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi.