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芬兰中部的肌萎缩侧索硬化症:一项流行病学研究。

Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study.

作者信息

Murros K, Fogelholm R

出版信息

Acta Neurol Scand. 1983 Jan;67(1):41-7. doi: 10.1111/j.1600-0404.1983.tb04543.x.

Abstract

Amyotrophic lateral sclerosis (ALS) was diagnosed in 36 patients in Middle-Finland Central Hospital District during 1976-1981. The annual incidence of ALS was 2.4 per 100,000 population and the prevalence rate was 6.4 per 100,000 population. The age-specific incidences of ALS were similar for men and women with a maximum of 14/100,000/year in the age group 60-69 years. The initial symptoms originated in 37% of the patients from bulbar and in 63% from spinal levels. Bulbar onset was more common in patients aged 60 years or more compared with younger patients. Patients with bulbar onset had a significantly poorer prognosis than those with spinal onset, which explained the poorer prognosis of older patients. 4 matched controls were chosen for each ALS patient from the files of the Central Hospital. There was no difference between the patients and the controls with respect to previous injuries, surgical operations, malignant neoplasms, or exposure to domestic animals. An earlier observation that evacuees from Karelia ceded to USSR after World War II should have a prevalence twice that of the remaining population was not substantiated.

摘要

1976年至1981年期间,芬兰中部中央医院区有36名患者被诊断为肌萎缩侧索硬化症(ALS)。ALS的年发病率为每10万人2.4例,患病率为每10万人6.4例。男性和女性的ALS年龄别发病率相似,在60 - 69岁年龄组中最高,为每年14/10万。37%的患者初始症状起源于延髓,63%起源于脊髓水平。与年轻患者相比,延髓起病在60岁及以上患者中更为常见。延髓起病的患者预后明显比脊髓起病的患者差,这解释了老年患者预后较差的原因。从中央医院档案中为每位ALS患者选择4名匹配对照。患者与对照在既往受伤、手术、恶性肿瘤或接触家畜方面没有差异。二战后从卡累利阿撤离到苏联的人员患病率应是其余人口两倍这一早期观察结果未得到证实。

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