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20 岁前医院诊断的感染与随后多发性硬化症诊断风险的关系。

Hospital-diagnosed infections before age 20 and risk of a subsequent multiple sclerosis diagnosis.

机构信息

Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden.

Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden.

出版信息

Brain. 2021 Sep 4;144(8):2390-2400. doi: 10.1093/brain/awab100.

DOI:10.1093/brain/awab100
PMID:33693538
Abstract

The involvement of specific viral and bacterial infections as risk factors for multiple sclerosis has been studied extensively. However, whether this extends to infections in a broader sense is less clear and little is known about whether risk of a multiple sclerosis diagnosis is associated with other types and sites of infections such as the CNS. This study aims to assess if hospital-diagnosed infections by type and site before age 20 years are associated with risk of a subsequent multiple sclerosis diagnosis and whether this association is explained entirely by infectious mononucleosis, pneumonia, and CNS infections. Individuals born in Sweden between 1970 and 1994 were identified using the Swedish Total Population Register (n = 2 422 969). Multiple sclerosis diagnoses from age 20 years and hospital-diagnosed infections before age 20 years were identified using the Swedish National Patient Register. Risk of a multiple sclerosis diagnosis associated with various infections in adolescence (11-19 years) and earlier childhood (birth-10 years) was estimated using Cox regression, with adjustment for sex, parental socio-economic position, and infection type. None of the infections by age 10 years were associated with risk of a multiple sclerosis diagnosis. Any infection in adolescence increased the risk of a multiple sclerosis diagnosis (hazard ratio 1.33, 95% confidence interval 1.21-1.46) and remained statistically significant after exclusion of infectious mononucleosis, pneumonia, and CNS infection (hazard ratio 1.17, 95% confidence interval 1.06-1.30). CNS infection in adolescence (excluding encephalomyelitis to avoid including acute disseminated encephalitis) increased the risk of a multiple sclerosis diagnosis (hazard ratio 1.85, 95% confidence interval 1.11-3.07). The increased risk of a multiple sclerosis diagnosis associated with viral infection in adolescence was largely explained by infectious mononucleosis. Bacterial infections in adolescence increased risk of a multiple sclerosis diagnosis, but the magnitude of risk reduced after excluding infectious mononucleosis, pneumonia and CNS infection (hazard ratio 1.31, 95% confidence interval 1.13-1.51). Respiratory infection in adolescence also increased risk of a multiple sclerosis diagnosis (hazard ratio 1.51, 95% confidence interval 1.30-1.75), but was not statistically significant after excluding infectious mononucleosis and pneumonia. These findings suggest that a variety of serious infections in adolescence, including novel evidence for CNS infections, are risk factors for a subsequent multiple sclerosis diagnosis, further demonstrating adolescence is a critical period of susceptibility to environmental exposures that raise the risk of a multiple sclerosis diagnosis. Importantly, this increased risk cannot be entirely explained by infectious mononucleosis, pneumonia, or CNS infections.

摘要

特定病毒和细菌感染作为多发性硬化症的风险因素已经得到了广泛研究。然而,这种情况是否扩展到更广泛的感染范围尚不清楚,也不清楚多发性硬化症的诊断风险是否与中枢神经系统等其他类型和部位的感染有关。本研究旨在评估 20 岁之前按类型和部位诊断的医院感染是否与多发性硬化症诊断的风险相关,以及这种关联是否完全由传染性单核细胞增多症、肺炎和中枢神经系统感染解释。通过瑞典总人口登记册(n=2422969)识别 1970 年至 1994 年期间在瑞典出生的个体。通过瑞典国家患者登记册确定 20 岁以后的多发性硬化症诊断和 20 岁之前的医院感染。使用 Cox 回归估计青少年(11-19 岁)和更早的儿童(出生-10 岁)时期各种感染与多发性硬化症诊断风险的关系,并调整性别、父母社会经济地位和感染类型。10 岁之前的任何感染都与多发性硬化症诊断风险无关。任何青春期感染都会增加多发性硬化症诊断的风险(危险比 1.33,95%置信区间 1.21-1.46),并且在排除传染性单核细胞增多症、肺炎和中枢神经系统感染后仍然具有统计学意义(危险比 1.17,95%置信区间 1.06-1.30)。青春期中枢神经系统感染(排除脑炎以避免包括急性播散性脑脊髓炎)增加多发性硬化症诊断的风险(危险比 1.85,95%置信区间 1.11-3.07)。青春期病毒感染与多发性硬化症诊断风险增加相关,主要是由传染性单核细胞增多症引起的。青春期细菌感染会增加多发性硬化症诊断的风险,但在排除传染性单核细胞增多症、肺炎和中枢神经系统感染后,风险幅度降低(危险比 1.31,95%置信区间 1.13-1.51)。青春期呼吸道感染也会增加多发性硬化症诊断的风险(危险比 1.51,95%置信区间 1.30-1.75),但在排除传染性单核细胞增多症和肺炎后,这一关联不再具有统计学意义。这些发现表明,青春期的各种严重感染,包括中枢神经系统感染的新证据,是随后多发性硬化症诊断的风险因素,进一步证明青春期是对增加多发性硬化症诊断风险的环境暴露敏感的关键时期。重要的是,这种风险增加不能完全由传染性单核细胞增多症、肺炎或中枢神经系统感染解释。

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