爱尔兰的肌缩侧面硬化症的流行病学趋势,1996-2021年
Robert McFarlane1, Colm Peelo2, Miriam Galvin2
1From the Academic Unit of Neurology, Trinity College Dublin, Ireland. mcfarlro@tcd.ie.
Neurology
|September 25, 2023
概括
在爱尔兰,25年来,肌缩侧面硬化症 (ALS) 的发病率,患病率和发病年龄都在增加. 然而,尽管在治疗方面取得了进展,但ALS患者的生存率没有显著变化.
科学领域:
- 神经学 神经学
- 流行病学 流行病学
- 公共卫生 公共卫生
背景情况:
- 肌缩侧面硬化症 (ALS) 是一种进展性神经退行性疾病.
- 了解ALS发病率,流行率和生存率的趋势对于公共卫生规划和资源分配至关重要.
研究的目的:
- 检查爱尔兰共和国25年来ALS患者的发病率,流行率,发病年龄和存活率的变化.
主要方法:
- 利用基于人口的爱尔兰ALS注册 (1994年开始运行) 来识别事件和流行病例.
- 采用年龄标准化,卡普兰-梅尔曲线和考克斯回归模型来分析流行病学和生存数据.
- 使用克鲁斯卡尔-瓦利斯测试与邦费罗尼校正对非正常分布的组进行比较.
主要成果:
- 在25年内,确定了2,771名ALS患者;原始发病率从每10万人中从2.64上升到5.46,标准化发病率从每10万人中从2.64上升到3.1.
- 患病率从每10万人的5.83增加到8.10,发病时的中位数年龄从64岁增加到67岁.
- 不同时期观察到生存率没有显著变化;发病时的年龄较大是一个负面的生存预测因素,而Riluzole使用和较短的诊断延迟是积极的预测因素.
结论:
- 在过去的25年里,爱尔兰的ALS年龄标准化发病率,高峰发病率,流行率和发病年龄都在增加.
- 尽管在ALS治疗和管理方面有所改善,但爱尔兰人口的平均存活率保持不变.
- 发病时的年龄较大,Riluzole的使用和诊断延迟是影响ALS患者生存的关键因素.
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