在智利,肌缩侧面硬化症的发病率
Patricia Lillo1,2,3, Pedro Zitko4, Gladys Godoy-Reyes1,5
1Departamento de Neurología Sur, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Amyotrophic lateral sclerosis & frontotemporal degeneration
|March 20, 2024
概括
这项研究估计了智利的肌缩侧面硬化症 (ALS) 发病率和存活率. 每10万人中ALS发病率为0.97,诊断后平均存活时间为2.3年.
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.
- 了解区域发病率和生存率对于公共卫生规划至关重要.
- 智利关于ALS流行病学的数据有限.
研究的目的:
- 估计智利大都会地区的ALS发病率.
- 为了确定该地区ALS患者的生存率.
- 为拉丁美洲的ALS研究提供基于人口的数据.
主要方法:
- 从2016-2019年进行了一项队列研究.
- 219个ALS病例从国家注册和合作的神经病学家中招募.
- 使用统计模型计算出发病率,生存率和危险比率.
主要成果:
- 总体ALS发病率为每10万居民0.97例.
- 发病率在70-79岁年龄组达到顶峰,男性与女性的比例为1.23.
- 诊断后的中位生存时间为2.3年,症状发作后的3.1年.
结论:
- 这是智利大都会地区对ALS发病率和存活率的首次基于人口的研究.
- 这些发现与拉丁美洲观察到的较低的ALS发病率一致.
- 结果为该地区的ALS提供了重要的流行病学数据.
相关概念视频
Cross-bridge Cycle
117.4K
As muscle contracts, the overlap between the thin and thick filaments increases, decreasing the length of the sarcomere—the contractile unit of the muscle—using energy in the form of ATP. At the molecular level, this is a cyclic, multistep process that involves binding and hydrolysis of ATP, and movement of actin by myosin.
117.4K
Amyloid Fibrils
9.5K
Amyloid fibrils are aggregates of misfolded proteins. Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils.
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
9.5K


