ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2026
Phenotyping healthcare use before pediatric-onset multiple sclerosis, including by sex and age: A matched cohort study.
Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundLittle is known about the prodrome in pediatric-onset multiple sclerosis (POMS), especially potential age and sex differences.
objectiveTo compare annual hospitalization and physician visit rates overall, and for physician visits, examine sex- and age-group (<12, 12-15, 16 to <18 years) differences, up to 18 years pre-first demyelinating event (pre-index) in 451 POMS and 1420 matched non-multiple sclerosis (MS) individuals.
methodUsing Ontario administrative data (1991-2020), we estimated rate ratios (RRs) by visit-related diagnosis, sex, and age using over-dispersed-Poisson models.
resultsThe POMS cohort showed elevated rates by year 1 pre-index ("year -1"), for ill-defined, other-health-contact, mental-, and respiratory-related hospitalizations (RRs ⩾ 3.6). Elevated physician visits began at year -14 for respiratory (RRs ⩾ 1.3), year -13 for endocrine (RRs ⩾ 2.4) and injury-related (RRs ⩾ 1.2), year -12 for ill-defined (RRs ⩾ 1.3), and year -11 for nervous system (RRs ⩾ 4.0) and mental-related (RRs ⩾ 2.0). Nervous system visits showed the largest sex-gap; males with (vs without) MS had elevated RRs from year -12 and females from year -6; both peaked the year pre-index (males: RR = 47.2; 95% confidence interval (CI): 17.3-128.3; females: RR = 17.0; 95% CI: 8.9-32.3). Among 12- to 15-year-olds, elevated rates were sustained for respiratory-related (from year -12, except year -5), injury-related, and ill-defined (from year -13); (all RR ⩾ 1.3), while findings were more sporadic in the other age groups.
conclusionFindings suggest prolonged, organ-specific healthcare use pre-POMS, with some sex- and age-related differences indicating pre-onset disease heterogeneity.
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