From the Pediatric Multiple Sclerosis and Related Disorders Program (S.K.G.J., S.C., L.A.B., M.P.G.), Department of Neurology, Boston Children's Hospital, Harvard Medical School; Boston College (S.K.G.J.), School of Social Work, MA; Stanford University School of Medicine (A.B.), Palo Alto, CA; Department of Pediatrics (M.W., T.C.C.), University of Utah, Salt Lake City; Pediatric Multiple Sclerosis Center (L.B.K., L.C., A.L.B.), NYU Grossman School of Medicine, New York; Pediatric Multiple Sclerosis Center at Loma Linda University Children's Hospital (G.S.A.), Loma Linda University, CA; Primary Children's Hospital (M.C.), University of Utah, Salt Lake City; Division of Child Neurology (T.C.), Department of Neurology, Massachusetts General Hospital, Boston; UCSD Pediatric MS Center (J.G.), San Diego, CA; Center for Pediatric-Onset Demyelinating Disease at the Children's of Alabama (Y.S.W.), University of Alabama, Birmingham; Children's National Medical Center (I.K.), Washington, DC; Baylor College of Medicine (T.E.L.), Houston, TX; Washington University Pediatric MS and other Demyelinating Disease Center (S.S.M.), Washington University in St. Louis, MO; Mellen Center for Multiple Sclerosis (M. Rensel), Cleveland Clinic, OH; Mayo Clinic (M. Rodriguez, J.-M.T.), Rochester, MN; Department of Neurology (J.W.R.), University of Utah, Salt Lake City; Ann and Robert H. Lurie Children's Hospital of Chicago (J.P.R.), IL; Division of Neurology (A.T.W.), Children's Hospital of Philadelphia, PA; The Pediatric MS Center at the Jacobs Neurological Institute (B.W.-G.), State University of New York at Buffalo; Division of Epidemiology and Genetic Epidemiology and Genomics Laboratory (L.F.B.), School of Public Health, University of California Berkeley; and UCSF Weill Institute for Neurosciences (E.W.), University of California San Francisco.
Neurol Neuroimmunol Neuroinflamm. 2024 Sep;11(5):e200282. doi: 10.1212/NXI.0000000000200282. Epub 2024 Aug 15.
Psychosocial adversity and stress, known to predispose adults to neurodegenerative and inflammatory immune disorders, are widespread among children who experience socioeconomic disadvantage, and the associated neurotoxicity and proinflammatory profile may predispose these children to multiple sclerosis (MS). We sought to determine associations of socioeconomic disadvantage and psychosocial adversity with odds of pediatric-onset MS (POMS), age at POMS onset, and POMS disease activity.
This case-control study used data collected across 17 sites in the United States by the Environmental and Genetic Risk Factors for Pediatric Multiple Sclerosis Study. Cases (n = 381) were youth aged 3-21 years diagnosed with POMS or a clinically isolated demyelinating syndrome indicating high risk of MS. Frequency-matched controls (n = 611) aged 3-21 years were recruited from the same institutions. Prenatal and postnatal adversity and postnatal socioeconomic factors were assessed using retrospective questionnaires and zip code data. The primary outcome was MS diagnosis. Secondary outcomes were age at onset, relapse rate, and Expanded Disability Status Scale (EDSS). Predictors were maternal education, maternal prenatal stress events, child separation from caregivers during infancy and childhood, parental death during childhood, and childhood neighborhood disadvantage.
MS cases (64% female, mean age 15.4 years, SD 2.8) were demographically similar to controls (60% female, mean age 14.9 years, SD 3.9). Cases were less likely to have a mother with a bachelor's degree or higher (OR 0.42, 95% CI 0.22-0.80, = 0.009) and were more likely to experience childhood neighborhood disadvantage (OR 1.04 for each additional point on the neighborhood socioeconomic disadvantage score, 95% CI 1.00-1.07; = 0.025). There were no associations of the socioeconomic variables with age at onset, relapse rate, or EDSS, or of prenatal or postnatal adverse events with risk of POMS, age at onset, relapse rate, or EDSS.
Low socioeconomic status at the neighborhood level may increase the risk of POMS while high parental education may be protective against POMS. Although we did not find associations of other evaluated prenatal or postnatal adversities with POMS, future research should explore such associations further by assessing a broader range of stressful childhood experiences.
心理社会逆境和压力会使成年人易患神经退行性和炎症性免疫疾病,而这些在经历社会经济劣势的儿童中普遍存在,其相关的神经毒性和促炎特征可能使这些儿童易患多发性硬化症(MS)。我们旨在确定社会经济劣势和心理社会逆境与儿科发病多发性硬化症(POMS)、POMS 发病年龄和 POMS 疾病活动的相关性。
本病例对照研究使用了在美国 17 个地点由环境和遗传风险因素儿科多发性硬化症研究收集的数据。病例(n=381)为年龄在 3-21 岁之间诊断为 POMS 或临床孤立性脱髓鞘综合征(提示 MS 风险高)的青少年。年龄在 3-21 岁之间、来自相同机构的频率匹配对照(n=611)被招募。使用回顾性问卷和邮政编码数据评估产前和产后逆境以及产后社会经济因素。主要结局是 MS 诊断。次要结局为发病年龄、复发率和扩展残疾状况量表(EDSS)。预测因素包括母亲教育程度、母亲产前应激事件、婴儿期和儿童期与照顾者分离、儿童期父母死亡以及儿童期邻里劣势。
MS 病例(64%为女性,平均年龄 15.4 岁,标准差 2.8)在人口统计学上与对照组(60%为女性,平均年龄 14.9 岁,标准差 3.9)相似。病例组母亲拥有学士学位或更高学历的可能性较低(OR 0.42,95%CI 0.22-0.80,p=0.009),更有可能经历儿童期邻里劣势(邻里社会经济劣势评分每增加 1 分,OR 1.04,95%CI 1.00-1.07,p=0.025)。社会经济变量与发病年龄、复发率或 EDSS 无关,产前或产后不良事件与 POMS、发病年龄、复发率或 EDSS 无关。
邻里水平的低社会经济地位可能会增加 POMS 的风险,而高父母教育程度可能对 POMS 具有保护作用。尽管我们没有发现其他评估的产前或产后逆境与 POMS 之间的关联,但未来的研究应该通过评估更广泛的压力童年经历来进一步探索这种关联。