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瑞典第一代和第二代移民中的嗜睡症:一项对总人口的研究。

Narcolepsy among first- and second-generation immigrants in Sweden: A study of the total population.

机构信息

Division of Family Medicine and Primary Care, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Huddinge, Sweden.

Center for Primary Health Care Research, Lund University, Malmö, Sweden.

出版信息

Acta Neurol Scand. 2022 Aug;146(2):160-166. doi: 10.1111/ane.13633. Epub 2022 May 11.

Abstract

AIMS

To study incident narcolepsy in first- and second-generation immigrant groups using Swedish-born individuals and native Swedes as referents.

METHODS

The study population included all individuals registered and alive in Sweden at baseline. Narcolepsy was defined as having at least one registered diagnosis of narcolepsy in the Swedish National Patient Register. The incidence of narcolepsy in different immigrant groups was assessed by Cox regression, with hazard ratios (HRs) and 95% confidence intervals (CI). The models were stratified by sex and adjusted for age, geographical residence in Sweden, educational level, marital status, co-morbidities, and neighbourhood socioeconomic status.

RESULTS

In the first-generation study, 1225 narcolepsy cases were found; 465 males and 760 females, and in the second-generation study, 1710 cases, 702 males and 1008 females. Fully adjusted HRs (95% CI) in the first-generation study was for males 0.83 (0.61-1.13) and females 0.83 (0.64-1.07), and in the second-generation study for males 0.76 (0.60-0.95) and females 0.91 (95% CI 0.76-1.09). Statistically significant excess risks of narcolepsy were found in first-generation males from North America, and second-generation males with parents from North America, and second-generation females with parents from Latin America.

CONCLUSIONS

There were only significant differences in incident narcolepsy between native Swedes and second-generation male immigrants. The observed differences can partly be explained by differences in Pandemrix® vaccinations and are probably not attributable to genetic differences between immigrants and natives.

摘要

目的

使用瑞典出生的个体和瑞典本地人作为参照,研究第一代和第二代移民群体中的偶发性嗜睡症。

方法

研究人群包括基线时在瑞典登记和存活的所有个体。嗜睡症的定义为在瑞典国家患者登记处至少有一次注册的嗜睡症诊断。使用 Cox 回归评估不同移民群体中嗜睡症的发病率,并用风险比(HR)和 95%置信区间(CI)表示。这些模型按性别分层,并根据年龄、在瑞典的地理居住位置、教育程度、婚姻状况、合并症和邻里社会经济地位进行调整。

结果

在第一代研究中,发现了 1225 例嗜睡症病例,其中男性 465 例,女性 760 例;在第二代研究中,发现了 1710 例病例,其中男性 702 例,女性 1008 例。第一代研究中完全调整后的 HR(95%CI)为男性 0.83(0.61-1.13)和女性 0.83(0.64-1.07),第二代研究中为男性 0.76(0.60-0.95)和女性 0.91(95%CI 0.76-1.09)。在第一代男性中,来自北美的移民以及第二代中来自北美的父母的男性和来自拉丁美洲的父母的第二代女性中,嗜睡症的发病风险存在统计学上的显著增加。

结论

只有在瑞典本地人与第二代男性移民之间观察到偶发性嗜睡症的发生率存在显著差异。观察到的差异部分可以用 Pandemrix®疫苗接种的差异来解释,而且不太可能归因于移民与本地人之间的遗传差异。

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