PLoS ONE (Jan 2014)

Radiologically isolated syndrome: 5-year risk for an initial clinical event.

  • Darin T Okuda,
  • Aksel Siva,
  • Orhun Kantarci,
  • Matilde Inglese,
  • Ilana Katz,
  • Melih Tutuncu,
  • B Mark Keegan,
  • Stacy Donlon,
  • Le H Hua,
  • Angela Vidal-Jordana,
  • Xavier Montalban,
  • Alex Rovira,
  • Mar Tintoré,
  • Maria Pia Amato,
  • Bruno Brochet,
  • Jérôme de Seze,
  • David Brassat,
  • Patrick Vermersch,
  • Nicola De Stefano,
  • Maria Pia Sormani,
  • Daniel Pelletier,
  • Christine Lebrun,
  • Radiologically Isolated Syndrome Consortium (RISC),
  • Club Francophone de la Sclérose en Plaques (CFSEP)

DOI
https://doi.org/10.1371/journal.pone.0090509
Journal volume & issue
Vol. 9, no. 3
p. e90509

Abstract

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ObjectiveTo report the 5-year risk and to identify risk factors for the development of a seminal acute or progressive clinical event in a multi-national cohort of asymptomatic subjects meeting 2009 RIS Criteria.MethodsRetrospectively identified RIS subjects from 22 databases within 5 countries were evaluated. Time to the first clinical event related to demyelination (acute or 12-month progression of neurological deficits) was compared across different groups by univariate and multivariate analyses utilizing a Cox regression model.ResultsData were available in 451 RIS subjects (F: 354 (78.5%)). The mean age at from the time of the first brain MRI revealing anomalies suggestive of MS was 37.2 years (y) (median: 37.1 y, range: 11-74 y) with mean clinical follow-up time of 4.4 y (median: 2.8 y, range: 0.01-21.1 y). Clinical events were identified in 34% (standard error=3%) of individuals within a 5-year period from the first brain MRI study. Of those who developed symptoms, 9.6% fulfilled criteria for primary progressive MS. In the multivariate model, age [hazard ratio (HR): 0.98 (95% CI: 0.96-0.99); p=0.03], sex (male) [HR: 1.93 (1.24-2.99); p=0.004], and lesions within the cervical or thoracic spinal cord [HR: 3.08 (2.06-4.62); p=InterpretationThese data provide supportive evidence that a meaningful number of RIS subjects evolve to a first clinical symptom. An age <37 y, male sex, and spinal cord involvement appear to be the most important independent predictors of symptom onset.