Risk of cardiovascular and autoimmune disease in people with multiple sclerosis on long-term interferon-β therapy

Chronically elevated type I interferons (-β and -α) can induce atherosclerosis and autoimmunity but whether this link translates into adverse events in interferon-β users with multiple sclerosis is unknown. We therefore aimed to determine whether long-term interferon-β exposure increases the risk of cardiovascular and autoimmune disease in a Canadian population-based cohort with linked hospital/physician visits and filled prescriptions. People with multiple sclerosis were included from the most recent of (i) first diagnostic code or disease-modifying therapy or (ii) prescription data availability (1/JAN/1996), and followed until the earliest of outcome, emigration, death or study end (31/DEC/2017). Associations were tested using stratified Cox regressions with time-dependent covariates. The cohort included 19 360 people with multiple sclerosis followed for a median duration of 11.2 years (Q1-Q3: 5.1-18.7), of whom 3138 (16.2%) ever used an interferon-β. Longer interferon-β therapy was associated with a higher incidence of cardiovascular disease (per 5-year longer treatment: hazard ratio = 1.18; 95% confidence interval: 1.02, 1.37; <i>P</i> = 0.026) but not with autoimmunity (hazard ratio = 0.74; 95% confidence interval: 0.49, 1.11; <i>P</i> = 0.139). This new safety signal should encourage clinicians to optimize cardiovascular prevention in people with multiple sclerosis and may be considered when discussing treatment options in interferon-β users who are at high risk or with established cardiovascular disease.

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Publication Details

Journal
Brain Communications
Published
2025-01-01
DOI
https://doi.org/10.1093/braincomms/fcaf363
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Risk of cardiovascular and autoimmune disease in people with multiple sclerosis on long-term interferon-β therapy

David Hunt, Helen Tremlett, Bastien Rioux, Huah Shin Ng et al.
Brain Communications
Systemic Sclerosis and Related Diseases
article

Risk of cardiovascular and autoimmune disease in people with multiple sclerosis on long-term interferon-β therapy

David Hunt, Helen Tremlett, Bastien Rioux, Huah Shin Ng, Thomas M. Caparrotta, William Whiteley, Feng Zhu, Yinshan Zhao
article en

Abstract

Chronically elevated type I interferons (-β and -α) can induce atherosclerosis and autoimmunity but whether this link translates into adverse events in interferon-β users with multiple sclerosis is unknown. We therefore aimed to determine whether long-term interferon-β exposure increases the risk of cardiovascular and autoimmune disease in a Canadian population-based cohort with linked hospital/physician visits and filled prescriptions. People with multiple sclerosis were included from the most recent of (i) first diagnostic code or disease-modifying therapy or (ii) prescription data availability (1/JAN/1996), and followed until the earliest of outcome, emigration, death or study end (31/DEC/2017). Associations were tested using stratified Cox regressions with time-dependent covariates. The cohort included 19 360 people with multiple sclerosis followed for a median duration of 11.2 years (Q1-Q3: 5.1-18.7), of whom 3138 (16.2%) ever used an interferon-β. Longer interferon-β therapy was associated with a higher incidence of cardiovascular disease (per 5-year longer treatment: hazard ratio = 1.18; 95% confidence interval: 1.02, 1.37; <i>P</i> = 0.026) but not with autoimmunity (hazard ratio = 0.74; 95% confidence interval: 0.49, 1.11; <i>P</i> = 0.139). This new safety signal should encourage clinicians to optimize cardiovascular prevention in people with multiple sclerosis and may be considered when discussing treatment options in interferon-β users who are at high risk or with established cardiovascular disease.

Brain CommunicationsVol. 7(5)
NHS Lothian (GB), University of British Columbia (CA), Flinders University (AU), Government of South Australia (AU), British Heart Foundation (GB), MRC Centre for Regenerative Medicine (GB), SA Health (AU), Adelaide Institute for Sleep Health (AU), UK Dementia Research Institute (GB), Health Data Research UK (GB), University of Edinburgh (GB)
Wellcome Trust, Multiple Sclerosis Scientific Research Foundation, Scottish Government, Alzheimer's Society, National Institute for Health and Care Research, Multiple Sclerosis Society, University of Edinburgh, UK Dementia Research Institute, National Institutes of Health, Canadian Institutes of Health Research, Cancer Council South Australia
Openalex Percentile: Top 63%
Systemic Sclerosis and Related Diseases
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