Abstract Details

Title Exploring New Imaging Biomarkers: 3D Conformational Analysis Of The Medulla And Upper Cervical Spinal Cord In People With Relapsing Multiple Sclerosis

Topic Multiple Sclerosis

Presentation(s) P11 - Poster Session 11 (11:45 AM-12:45 PM)

Poster/Presentation
Number 3-015

Objective Explore three-dimensional (3D) medulla-upper cervical spinal cord (MUCSC) conformational imaging metrics as biomarkers in multiple sclerosis (MS).

Background Measures of spinal cord atrophy are associated with MS disease progression but have yet to emerge as reliable biomarkers of treatment efficacy. 3D MUCSC conformational analysis is a new technique that may provide additional information about neurodegenerative changes in MS beyond conventional magnetic resonance imaging metrics. In the placebo-controlled Phase 3 TEMSO trial (NCT00134563), teriflunomide 14 mg/day lowered the risk of disability worsening and reduced brain volume loss in participants with relapsing MS. 3D MUCSC conformational analysis of the TEMSO dataset has not been explored.

Design/Methods TEMSO baseline and 2-year end of study follow-up 3D T1-Magnetization Prepared Rapid Gradient Echo (MP-RAGE) images acquired primarily at 1.5T were assessed for quality, then segmented and analyzed using in-house proprietary software. Change from baseline in MUCSC volume, local curvature and surface texture were summarized with descriptive statistics.

Results Quality assessments led to the exclusion of 481 of the 799 TEMSO participants, comprising 64.0%, 62.1%, and 54.5% of participants in the placebo, 7 mg/day, and 14 mg/day arms, respectively. Mean age and disease duration were lower for placebo participants versus teriflunomide arms. No between-group differences were apparent for mean (SD) change from baseline in MUCSC volume (-86±236, -85±218, and -75±218 mm_³ for placebo, 7 mg/day, and 14 mg/day arms, respectively), mean curvature (0.01±0.06, 0.02±0.07, and 0.02±0.07 mm), or surface texture (-15.6±28.0, -21.3±26.6, and -19.0±24.2 triangle count).

Conclusions 3D conformational analysis of MP-RAGE images from the TEMSO trial showed no discernable between-group differences for MUCSC surface features or volume; however, imbalanced exclusion of participants during quality assessment likely introduced attrition bias. Further development of 3D conformational metrics as MS biomarkers may better illuminate mechanisms related to neurodegenerative changes and treatment efficacy.

Authors/Disclosures
Tatum Moog (University of Texas Southwestern Medical Center) PRESENTER	Miss Moog has nothing to disclose.
Janneke Van Wingerden	Janneke Van Wingerden has received personal compensation for serving as an employee of Sanofi Genzyme.
Bruno Padrazzi, MD (Sanofi)	Dr. Sanofi has received personal compensation for serving as an employee of Sanofi. Dr. Sanofi has received personal compensation for serving as an employee of Sanofi. Dr. Sanofi has stock in Sanofi. Dr. Sanofi has stock in Sanofi.
Svend Geertsen, PhD (Sanofi)	Dr. Geertsen has received personal compensation for serving as an employee of Sanofi.
	No disclosure on file
Darin T. Okuda, MD, FAAN (UT Southwestern Medical Center)	Dr. Okuda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen. Dr. Okuda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Cortechs AI. Dr. Okuda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for EMD Serono. Dr. Okuda has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Genentech. Dr. Okuda has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Sanofi. Dr. Okuda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Octave Bioscience. Dr. Okuda has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Pfizer. Dr. Okuda has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Zenas BioPharma. The institution of Dr. Okuda has received research support from Novartis. The institution of Dr. Okuda has received research support from Alexion. Dr. Okuda has received intellectual property interests from a discovery or technology relating to health care.

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