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The Multiple Sclerosis Performance Test MSPT: An iPad-Based Disability Assessment Tool
Published on: June 30, 2014
Cardiovascular risk profiles among patients with multiple sclerosis and neuromyelitis optica spectrum disorder in
Chi-Ning Tsai1, Yi-Chih Wang2, Yi-Te Tsai3
1Department of Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
Background:
While cardiovascular comorbidities are well described in multiple sclerosis (MS), they remain poorly characterized in neuromyelitis optica spectrum disorder (NMOSD). We aimed to identify cardiovascular risk associations in a Taiwanese cohort and compare risk profiles between MS and NMOSD.
Methods:
A retrospective analysis was conducted using rigorously validated clinical records from a tertiary medical center in Taiwan (2016-2023). Patients diagnosed with MS (n = 48) or NMOSD (n = 17) were included. Standardized prevalence ratios (SPRs) were calculated to compare comorbidity rates with the general population. Pharmacological treatment patterns were analyzed to assess disease management burden.
Results:
MS patients exhibited a higher incidence of established cardiovascular events compared to NMOSD patients. SPR analysis revealed a significantly lower prevalence of dyslipidemia in both MS (SPR 0.45, 95% CI 0.18-0.93) and NMOSD (SPR 0.16, 95% CI 0.004-0.89) compared with the general population. However, dyslipidemia remained the strongest predictor of cardiovascular events in MS (p < 0.001). In NMOSD, despite a hypertension prevalence comparable to the general population (SPR 0.92), patients had significantly higher usage of angiotensin II receptor blockers (35.3% vs. 12.8%, p = 0.041) and direct oral anticoagulants (11.8% vs. 0%, p = 0.016), coinciding with universal corticosteroid use (100%).
Conclusion:
Taiwanese MS and NMOSD patients exhibit distinct cardiovascular phenotypes. MS is characterized by a "lipid paradox" where dyslipidemia, though less prevalent, serves as a high-potency risk trigger. In NMOSD, cardiovascular risk is treatment-related and masked by high medication burden. Comprehensive risk assessment must prioritize these specific metabolic and iatrogenic factors.
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