日晒与小儿多发性硬化复发风险的关系

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Gina Chang, Prince Sebastian, Akash Virupakshaiah, Vinicius A Schoeps, Nicolas Cherbuin, T Charles Casper, Mark P Gorman, Leslie A Benson, Tanuja Chitnis, Mary Rensel, Aaron W Abrams, Tim Lotze, Soe S Mar, Teri L Schreiner, Yolanda S Wheeler, John W Rose, Jennifer Graves, Lauren B Krupp, Amy T Waldman, Robyn Lucas, Emmanuelle Waubant
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引用次数: 0

摘要

背景和目的:低太阳和紫外线辐射(UVR)暴露与发生儿科发作的多发性硬化症(MS)的风险增加有关;然而,它们对病程的影响尚未被很好地表征。我们首先调查了儿童早期在阳光下的时间与儿童多发性硬化症复发风险之间是否存在关联,其次调查了近期阳光照射对复发风险的影响。方法:我们对2011年11月1日至2017年7月1日期间从美国18家儿科多发性硬化症诊所招募的儿科发病多发性硬化症患者进行了一项多中心队列研究。研究入组后对复发进行前瞻性识别;回顾研究入组前的复发情况。研究人员通过详细的环境调查问卷测量了不同时期在阳光下的时间,并通过邮政编码确定了环境紫外线辐射的暴露程度。使用多变量Cox回归模型来评估特定生命时期的日晒时间和UVR剂量与复发风险之间的关系。根据人口统计学、临床和日照相关特征对模型进行了调整。结果:在我们的334例多发性硬化症患儿队列中,206例(62%)从发病到随访结束至少复发一次。调整后,在生命的第一个夏天每天≥30分钟的阳光照射与复发风险降低相关(p = 0.01)。妊娠中期多晒太阳也与降低复发风险相关(aHR 0.68, CI 0.48-0.97, p = 0.04)。紫外线辐射剂量和晚年在阳光下的时间与复发风险没有显著相关。讨论:在这项针对多发性硬化症儿童的大型队列研究中,儿童早期和产前较长的阳光照射时间与较低的复发风险相关。需要进一步调查其他时期的阳光照射,以更好地表征其对疾病病程的影响,并指导潜在的未来干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between Sun Exposure and Risk of Relapse in Pediatric-Onset Multiple Sclerosis.

Background and objectives: Low sun and ultraviolet radiation (UVR) exposures have been associated with increased risk of developing pediatric-onset multiple sclerosis (MS); however, their effect on disease course has not been well characterized. We primarily investigated whether there was an association between time spent in the sun in early childhood and risk of relapse in pediatric MS. We secondarily investigated the effect of sun exposure during more recent periods on risk of relapse.

Methods: We conducted a multicenter cohort study of participants with pediatric-onset MS recruited from 18 pediatric MS clinics across the United States between November 1, 2011, and July 1, 2017. Relapses were identified prospectively after study enrollment; relapses preceding study enrollment were entered retrospectively. Time spent in the sun at various periods of life was measured using a detailed environmental questionnaire, and ambient UVR exposure was determined using zip codes. Multivariable Cox regression models were used to assess the association between time spent in the sun and UVR dose at specific periods of life and the risk of relapse. Models were adjusted for demographic, clinical, and sun exposure-related characteristics.

Results: In our cohort of 334 children with MS, 206 (62%) experienced at least one relapse from disease onset to the end of the follow-up period. After adjustment, ≥30 minutes of daily sun exposure during the first summer of life was associated with a lower risk of relapse compared with <30 minutes (adjusted hazard ratio [aHR] 0.67, CI 0.48-0.92, p = 0.01). Greater time spent in the sun during the second trimester of pregnancy was also associated with reduced risk of relapse (aHR 0.68, CI 0.48-0.97, p = 0.04). UVR dose and time spent in the sun later in life were not significantly associated with relapse risk.

Discussion: In this large cohort study of children with MS, greater early childhood and prenatal sun exposure time was associated with lower risk of relapse. Further investigation of sun exposure at other periods is needed to better characterize its impact on disease course and guide potential future interventions.

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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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