AI Article Synopsis

  • The study aimed to determine if the use of oral contraceptives (OCs) affects the risk of a second attack and disability progression in women with clinically isolated syndrome (CIS) and early multiple sclerosis (MS).
  • Researchers analyzed data from a cohort of 495 women in Barcelona, focusing on their OC usage, and found that OC use did not significantly impact the risk of having a second attack or increased disability.
  • The conclusion suggests that oral contraceptive use does not alter the risk of relapse or disability in these patients, even when considering various factors that could influence the results.

Article Abstract

Objective: To evaluate whether oral contraceptive (OC) use is associated with the risk of a second attack and disability accrual in women with a clinically isolated syndrome (CIS) and early multiple sclerosis (MS).

Methods: Reproductive information from women included in the Barcelona CIS prospective cohort was collected through a self-reported cross-sectional survey. We examined the relationship of OC exposure with the risk of a second attack and confirmed Expanded Disability Status Scale of 3.0 using multivariate Cox regression models, adjusted by age, topography of CIS, oligoclonal bands, baseline brain T2 lesions, body size at menarche, smoking, and disease-modifying treatment (DMT). OC and DMT exposures were considered as time-varying variables. Findings were confirmed with sensitivity analyses using propensity score models.

Results: A total of 495 women were included, 389 (78.6%) referred to ever use OC and 341 (68.9%) started OC before the CIS. Exposure to OC was not associated with a second attack (adjusted hazard ratio (aHR) = 0.73, 95% confidence interval (CI) = 0.33-1.61) or disability accrual (aHR = 0.81, 95% CI = 0.17-3.76). Sensitivity analyses confirmed these results.

Conclusion: OC use does not modify the risk of second attack or disability accrual in patients with CIS and early MS, once considered as a time-dependent exposure and adjusted by other potential confounders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024022PMC
http://dx.doi.org/10.1177/13524585211053001DOI Listing

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