Air pollution and the risk of multiple sclerosis relapses in the Paris region, the CONFISEP study

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17 Oct 2026 0 comments

Air pollution has been proposed as a short-term trigger of multiple sclerosis (MS) relapses, but delayed effects remain poorly studied in the era of modern disease-modifying therapies (DMTs). We investigated whether weekly air pollution exposure was associated with delayed MS relapse risk up to 15 weeks.

We conducted a bicentric retrospective cohort study in the Île-de-France region (2018–2021) including adults with relapsing MS from the Observatoire Francais de la Sclérose en Plaques registry. Weekly exposure to particulate matter (PM)10, PM2.5, nitrogen dioxide (NO2) and ozone (O3) was estimated using Airparif street-level modelling data. Associations (lags 0–15 weeks) were assessed using self-controlled case series and cohort analyses adjusted for time-varying DMTs, disease duration, number of relapses during the previous year, respiratory infections, temperature, sunlight exposure, lockdown and holiday periods and additionally for age, sex, deprivation index and urbanicity in cohort analyses.

Among 1152 patients (73.6% women; median age 37 years), 898 relapses occurred (0.20/patient-year). In self-controlled analyses, PM10 exposure was associated with increased relapse risk at 2-week (incidence rate ratio (IRR) 1.28, 95% CI 1.05 to 1.57) and 11-week lags (IRR 1.26, 95% CI 1.02 to 1.54), PM2.5 exposure was associated with increased risk at 2-week (IRR 1.20, 95% CI 1.03 to 1.39), while NO2 exposure was associated with increased risk at 2-week (IRR 1.21, 95% CI 1.02 to 1.44), 3-week (IRR 1.26, 95% CI 1.04–1.52) and 12-week lags (IRR 1.32, 95% CI 1.12 to 1.56). Cohort analyses showed similar but weaker associations for PM10 and PM2.5. DMTs were strongly associated with lower relapse risk, with effect sizes greater than those observed for air pollution exposure.

Weekly exposure to PM10, PM2.5 and NO2 was associated with increased MS relapse risk over delayed time windows ranging from 2– 3 weeks to 11–12 weeks. These temporal windows should be considered exploratory given the multiple lag-specific analyses. DMTs remained the strongest determinants of relapse risk.

NCT05033782.