Neuro Division, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Centre for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
JAMA Neurol. 2021 Apr 1;78(4):478-482. 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.
DESIGN, SETTING, AND PARTICIPANTS: 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.
儿科发病的多发性硬化症(PoMS)与显著的认知和身体残疾有关。这种残疾是否会转化为教育成就和收入方面的差异尚不清楚。
评估 PoMS 与整个成年期的教育水平和收入之间的关联。
设计、设置和参与者:这是一项使用瑞典全国微观数据进行的前瞻性基于登记的队列研究,纳入了来自瑞典多发性硬化症登记处的发病于 1990 年 1 月 1 日至 2016 年 12 月 31 日的 PoMS 患者和基于人群的匹配参考队列;分析于 2019 年 5 月 1 日至 2020 年 9 月 1 日完成。在瑞典 MS 登记处确定的 772 名 PoMS 患者中,有 485 名发病于 1980 年至 2014 年期间,且有社会经济数据。没有多发性硬化症(MS)的一般人群参考队列(n=4850)是从全瑞典人群中随机选择的,年龄、性别和出生国与 PoMS 患者 10:1 匹配。
儿科发病的多发性硬化症,由神经科医生诊断,发病年龄在 18 岁以下。
使用逻辑回归评估最高教育水平(小学、高中或大学)。使用 Tobit 模型比较收入,收入的衡量标准为带薪工作的年平均收入(以美元计),使用零膨胀负二项回归比较年净病假和残疾抚恤金天数。在 4 个年龄期(19-24 岁、25-34 岁、35-44 岁和 45-54 岁)内比较收益和残疾福利领取天数。
PoMS 队列(n=485)和匹配参考队列(n=4850)在 2016 年的中位年龄为 32 岁(四分位距,26-40 岁),大多数参与者为女性(PoMS 队列中 348 [71.8%]例,匹配参考队列中 3480 [71.8%]例)。与匹配参考队列相比,PoMS 患者更不可能上大学(优势比,0.80 [95%CI,0.66-0.97]),年收入明显低于参考队列,从最年轻年龄组的-1618 美元(95%CI,-2558 美元至-678 美元)到最年长年龄组的-10683 美元(95%CI,-18187 美元至-3178 美元)。PoMS 患者获得残疾福利的比例更高,最年轻年龄组的病假天数(比率比,3.06 [95%CI,2.08-4.52])和最年长年龄组的残疾抚恤金天数(比率比,1.43 [95%CI,1.11-1.85])。
这项研究表明,患有 PoMS 与整个工作年龄期间教育程度较低、收入较低和更多地依赖残疾福利有关。作为成年人,患有 PoMS 的人与没有 MS 的同龄人相比,从未有过那么高的收入,而且他们对残疾福利的依赖更重。