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根据发病年龄的特点肌无力:日本全国性调查。

Characteristics of myasthenia gravis according to onset-age: Japanese nationwide survey.

机构信息

Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

J Neurol Sci. 2011 Jun 15;305(1-2):97-102. doi: 10.1016/j.jns.2011.03.004. Epub 2011 Mar 26.

Abstract

OBJECTIVE

To clarify the prevalence and clinical characteristics of myasthenia gravis (MG) in Japan.

METHODS

We performed a nationwide epidemiological survey of MG in Japan. The clinical features were compared among five groups of patients, divided according to onset age. A generalized additive model (GAM) was used to assess the linearity of these relationships.

RESULTS

A total of 8542 patients were reported, and detailed data were analyzed for 3141 patients. The estimated number of MG patients in Japan was 15,100, giving a prevalence of 11.8 per 100,000. Elderly-onset MG (≥ 65 years) accounted for 7.3% in 1987 (adjusted for population in 2005), but this had increased to 16.8% in 2006. Infantile-onset MG (0-4 years) accounted for 10.1% in 1987, and was still as high as 7.0% in 2006. The rate of ocular MG was highest (80.6%) in infantile-onset and lowest (26.4%) in early-onset disease, but the rate rose again in the late-onset group. GAM analysis of the ocular form showed a U-shaped curve, with a dip in the 20s. Anti-acetylcholine receptor antibodies were positive in only 50% of infantile-onset, but nearly 90% of elderly-onset patients. GAM analyses assessing the concurrence of thymoma and hyperplasia both showed reversed U-shapes, with peaks in the 50s and 20s-40s, respectively.

CONCLUSIONS

Persistent high incidence of infantile-onset disease and clinical heterogeneity according to onset age are characteristic features of MG in Japan.

摘要

目的

阐明日本重症肌无力(MG)的流行情况和临床特征。

方法

我们在日本进行了一项MG 的全国性流行病学调查。根据发病年龄将患者分为五组,比较各组的临床特征。采用广义加性模型(GAM)评估这些关系的线性。

结果

共报告了 8542 例患者,对 3141 例患者进行了详细数据分析。日本估计 MG 患者人数为 15100 人,患病率为 11.8/10 万。老年发病型 MG(≥65 岁)在 1987 年占 7.3%(按 2005 年人口调整),但在 2006 年已增至 16.8%。婴儿发病型 MG(0-4 岁)在 1987 年占 10.1%,在 2006 年仍高达 7.0%。眼肌型 MG 发病率最高(婴儿发病型 80.6%,发病年龄较早 26.4%),但在发病年龄较晚的患者中再次升高。眼肌型 MG 的 GAM 分析呈 U 型曲线,在 20 多岁时出现一个凹陷。抗乙酰胆碱受体抗体仅在 50%的婴儿发病型中阳性,但近 90%的老年发病型患者阳性。评估胸腺瘤和增生共存的 GAM 分析均呈反向 U 型,分别在 50 多岁和 20-40 多岁出现峰值。

结论

婴儿发病型疾病持续高发和发病年龄相关的临床异质性是日本 MG 的特征。

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