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Abstract Details

Sex-specific Differences in Rim Appearance of Multiple Sclerosis Lesions on Quantitative Susceptibility Mapping
Multiple Sclerosis
P5 - Poster Session 5 (5:30 PM-6:30 PM)
15-023

To describe relationships between properties of multiple sclerosis (MS) lesions on quantitative susceptibility mapping (QSM) and several clinical metrics.

Susceptibility MRI studies have shown that techniques such as phase and QSM reveal lesion heterogeneity in MS, including the presence of lesions with outer rims suggestive of iron deposition. In this project, we aimed to evaluate possible correlations between clinical characteristics in MS patients and QSM lesion rims on 7 tesla (7T) MRI.

39 patients with MS underwent 7T brain MRIs and clinical evaluation. Lesions were identified on FLAIR. QSM images were reviewed for contrast patterns at the edge of these lesions. The proportions of lesion subtypes were compared to demographic characteristics and disability scores.

A total of 1279 lesions were identified on FLAIR MRI; 846 (66.15%) of these were visible on QSM, 119 of which had visible rims. Disability scores tended to be worse in those with rims, most of these relationships were not significant. Lesions visible on QSM were more likely to have rims in males (16.1%, vs 4.9% in females, p=0.009). Of the 18 participants (46.2%) with at least 1 rimmed lesion, 61.1% were male; only 19.0% without rims were male (p=0.006). In a logistic regression model accounting for the total number of lesions and age, male sex conferred a nearly 7-fold risk of having ≥1 rimmed lesion(s) (p=0.018).

These findings suggest that males with MS are prone to develop lesions with hyperintense rims on QSM – a lesion subtype consistent with pro-inflammatory, iron-laden macrophages at the outer rim of a chronically inflamed lesion on histopathology.   Our findings provide in vivo support for the body of pathologic literature indicating sex-specific differences in MS pathophysiology and suggest that 7T QSM can thus be used to study these sex differences in the future.
Authors/Disclosures
Besher Tolaymat
PRESENTER
No disclosure on file
Wei Zheng, MD (Penn Medicine) No disclosure on file
Huanwen Chen, MD (MedStar Georgetown University Hospital) Dr. Chen has nothing to disclose.
No disclosure on file
No disclosure on file
Daniel M. Harrison, MD, FAAN (University of Maryland School of Medicine) Dr. Harrison has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Horizon Therapeutics. Dr. Harrison has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for American College of Physicians. The institution of Dr. Harrison has received research support from Roche-Genentech. Dr. Harrison has received publishing royalties from a publication relating to health care.