Inam Shafqat, Vucic Steve, Brodaty Nina E, Zoing Margie C, Kiernan Matthew C
Prince of Wales Medical Research Institute, Barker Street, Randwick, Sydney, NSW 2031, Australia.
Amyotroph Lateral Scler. 2010 Dec;11(6):558-61. doi: 10.3109/17482961003792958. Epub 2010 Jun 2.
There remains a critical need to develop biomarkers of disease progression in amyotrophic lateral sclerosis (ALS). Mobility is a key determinant of disease status and quality of life. The present study assessed the utility of 10-metre gait speed as a functional biomarker of disability in ALS. The gait speed, ALSFRS-R score, body mass index (BMI) and forced vital capacity (FVC), measured in 50 consecutive ALS patients at the time of diagnosis were assessed. ALS patients were managed in the multidisciplinary clinic for up to three years. 10-metre gait speed was significantly reduced in ALS patients with lower limb-onset disease (0.9 ± 0.1 m/s) compared to those with upper limb (1.3 ± 0.1 m/s, p <0.01) and bulbar onset (1.2 ± 0.1 m/s, p <0.01) disease. The 10-metre gait speed correlated with the total ALSFRS-R score (R = 0.6) and the gross motor subscore (R = 0.8, p <0.001). As such, the 10-metre gait speed may serve as a robust marker of disability and disease progression in ALS.
在肌萎缩侧索硬化症(ALS)中,对于开发疾病进展生物标志物仍存在迫切需求。运动能力是疾病状态和生活质量的关键决定因素。本研究评估了10米步速作为ALS患者残疾功能生物标志物的效用。对50例连续诊断的ALS患者在诊断时测量的步速、ALS功能评定量表修订版(ALSFRS-R)评分、体重指数(BMI)和用力肺活量(FVC)进行了评估。ALS患者在多学科诊所接受治疗长达三年。与上肢发病(1.3±0.1米/秒,p<0.01)和延髓发病(1.2±0.1米/秒,p<0.01)的患者相比,下肢发病的ALS患者10米步速显著降低(0.9±0.1米/秒)。10米步速与ALSFRS-R总分(R=0.6)和粗大运动子评分(R=0.8,p<0.001)相关。因此,10米步速可能是ALS患者残疾和疾病进展的有力标志物。