DURATION OF AMYOTROPHIC-LATERAL-SCLEROSIS IS AGE-DEPENDENT

被引:110
作者
EISEN, A
SCHULZER, M
MACNEIL, M
PANT, B
MAK, E
机构
[1] UNIV BRITISH COLUMBIA,NEUROMUSCULAR DIS UNIT,VANCOUVER V6T 1W5,BC,CANADA
[2] UNIV BRITISH COLUMBIA,DIV NEUROL,NEURODEGENERAT DISORDERS CTR,VANCOUVER V6T 1W5,BC,CANADA
关键词
AMYOTROPHIC LATERAL SCLEROSIS; YOUNG ONSET ALS; SURVIVAL PREDICTION;
D O I
10.1002/mus.880160107
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Since 1985, we prospectively followed 246 patients with ALS. The relationship between the age of developing neurological impairment and disease duration was analyzed in 138 patients (86 men and 52 women) who died. Mean disease duration was 4.0 +/- 3.8 years for men and 3.2 +/- 2.5 years for women. There was an inverse, exponential, relationship between onset age and duration (goodness-of-fit P > 0.05). Mean duration at onset age less-than-or-equal-to 40 years was 8.2 +/- 5.0 years compared with 2.6 +/- 1.4 years for patients aged 61 to 70 years (P > 0.001). The ratio of young (less-than-or-equal-to 40 years) men to women was 3.6:1. When matched for age, disease duration was the same for patients with bulbar and nonbulbar onsets. We conclude that onset age, but not sex, is the most significant predictor determining disesae duration in ALS. Longer survival in younger patients probably reflects their greater neuronal reserve.
引用
收藏
页码:27 / 32
页数:6
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