Long-term Socioeconomic Outcomes Associated With Pediatric-Onset Multiple Sclerosis

• Published in: Archives of neurology (Chicago) Vol. 78; no. 4; p. 478
• Main Authors: McKay, Kyla A, Friberg, Emilie, Razaz, Neda, Alexanderson, Kristina, Hillert, Jan
• Format: Journal Article
• Language: English
• Published: United States American Medical Association 01.04.2021
• Subjects: Adult; Age; Age of Onset; Child; Cognitive ability; Cohort Studies; Disability pensions; Disabled Persons; Earnings; Education; Educational Status; Female; Humans; Income; Income - trends; Life span; Male; Middle Aged; Multiple sclerosis; Multiple Sclerosis, Relapsing-Remitting - economics; Multiple Sclerosis, Relapsing-Remitting - epidemiology; Pediatrics; Profits; Prospective Studies; Registries; Socioeconomic Factors; Socioeconomics; Sweden - epidemiology; Young Adult; Sweden
• ISSN: 2168-6149; 2168-6157
• DOI: 10.1001/jamaneurol.2020.5520

Pediatric-onset multiple sclerosis (PoMS) is associated with significant cognitive and physical disability. Whether this disability translates into differences in educational achievements and earnings is unknown. To evaluate the association between PoMS and educational level and income throughout adulthood. A prospective register-based cohort study of individuals with PoMS and a population-based matched reference cohort was conducted using nationwide microdata from linked registers in Sweden from January 1, 1990, to December 31, 2016; analyses were completed from May 1, 2019, to September 1, 2020. Of 772 persons with PoMS identified in the Swedish MS registry, 485 had an onset during the period from 1980 to 2014 and had socioeconomic data available. The general population reference cohort without multiple sclerosis (MS) (n = 4850) was randomly selected from the full Swedish population, matched 10:1 on age, sex, and country of birth. Pediatric-onset MS, diagnosed by a neurologist, with onset before 18 years of age. Highest educational level (elementary school, high school, or university) was assessed using logistic regression. Income, measured as the mean annual earnings from paid work in US dollars, was compared using Tobit models, and net annual sickness absence and disability pension days were compared using zero-inflated negative binomial regression. Earnings and days receiving disability benefits were compared within 4 age periods (19-24, 25-34, 35-44, and 45-54 years). The median age of the cohort with PoMS (n = 485) and the matched reference cohort (n = 4850) in 2016 was 32 years (interquartile range, 26-40 years), and most participants were women (348 [71.8%] in the PoMS cohort and 3480 [71.8%] in the matched reference cohort). Persons with PoMS were less likely than persons in the matched reference cohort to attend university (odds ratio, 0.80 [95% CI, 0.66-0.97]) and had significantly lower annual earnings than the reference cohort, ranging from -$1618 (95% CI, -$2558 to -$678) in the youngest age period to -$10 683 (95% CI, -$18 187 to -$3178) in the eldest. Persons with PoMS received higher rates of disability benefits, as sickness absence days in the youngest age period (rate ratio, 3.06 [95% CI, 2.08-4.52]) and disability pension days in the oldest age period (rate ratio, 1.43 [95% CI, 1.11-1.85]). This study suggests that having PoMS is associated with less educational achievement, lower earnings, and greater use of disability benefits throughout the working-age life span. As adults, persons with PoMS never earned as much as their counterparts without MS, and they exhibited a heavier reliance on disability benefits.