首页> 美国卫生研究院文献>Frontiers in Neurology >Onset Symptoms Tobacco Smoking and Progressive-Onset Phenotype Are Associated With a Delayed Onset of Multiple Sclerosis and Marijuana Use With an Earlier Onset
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Onset Symptoms Tobacco Smoking and Progressive-Onset Phenotype Are Associated With a Delayed Onset of Multiple Sclerosis and Marijuana Use With an Earlier Onset

机译:发作症状吸烟和进行性表型与多发性硬化症的延迟发作和早期使用大麻有关

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>Background: Age at symptom onset (ASO) is a prognostic factor that could affect the accrual of disability in multiple sclerosis (MS) patients. Some factors are known to influence the risk of multiple sclerosis (MS), but their influence on the ASO is less well-investigated.>Objective: Examine the associations between known or emerging MS risk factors and ASO.>Methods: This was a multicenter study, incident cases (n = 279) with first clinical diagnosis of demyelinating event aged 18–59 years recruited at four Australian centres (latitudes 27°-43°S), from 1 November 2003 to 31 December 2006. Environmental/behavioral variables and initial symptoms were recorded at baseline interview. Linear regression was used to assess the association between risk factors and ASO.>Results: Five factors were significantly associated with ASO: a history of tobacco smoking was associated with 3.05-years later ASO (p = 0.002); a history of marijuana use was associated with 6.03-years earlier ASO (p < 0.001); progressive-onset cases had 5.61-years later ASO (p = 0.001); an initial presentation of bowel & bladder and cerebral dysfunctional were associated with 3.39 (p = 0.017) and 4.37-years (p = 0.006) later ASO, respectively. Other factors, including sex, offspring number, latitude of study site, history of infectious mononucleosis, HLA-DR15 & HLA-A2 genotype, 25(OH)D levels, and ultraviolet radiation exposure were not associated with ASO. Including all five significant variables into one model explained 12% of the total variance in ASO.>Conclusion: We found a novel association between a history of tobacco smoking and later onset, whereas marijuana use was associated with earlier onset. Behavioral factors seem important drivers of MS onset timing although much of the variance remains unexplained.
机译:>背景:症状发作年龄(ASO)是可能影响多发性硬化症(MS)患者残疾累积的预后因素。已知一些因素会影响多发性硬化症(MS)的风险,但对ASO的影响研究较少。>目的:检查已知或新兴的MS危险因素与ASO之间的关联。 strong>方法:这是一项多中心研究,从澳大利亚的4个中心(纬度27°-43°S)招募了首次临床诊断为18-59岁的脱髓鞘事件的病例(n = 279)。 2003年11月至2006年12月31日。在基线访谈中记录了环境/行为变量和初始症状。 >结果:有五个因素与ASO显着相关:吸烟史与3.05年后的ASO相关(p = 0.002);与吸烟相关的ASO与吸烟相关。大麻使用史与ASO提前6.03年相关(p <0.001);进展性病例的ASO为5.61年(p = 0.001);肠道和膀胱功能障碍以及脑功能障碍的最初表现分别与ASO发生后3.39(p = 0.017)和4.37年(p = 0.006)有关。其他因素,包括性别,后代数目,研究地点的纬度,传染性单核细胞增多症的病史,HLA-DR15和HLA-A2基因型,25(OH)D水平以及紫外线照射与ASO无关。将所有五个重要变量纳入一个模型可以解释ASO总变异的12%。>结论:我们发现吸烟史与晚发之间存在新型关联,而大麻的使用与早发相关。行为因素似乎是MS发病时机的重要驱动因素,尽管许多差异尚无法解释。

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