Baltadjieva Rossitza, Giladi Nir, Gruendlinger Leor, Peretz Chava, Hausdorff Jeffrey M
Laboratory for Gait & Neurodynamics, Movement Disorders Unit and NPF Center for Parkinson's Disease, Department of Neurology, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, 64239, Israel.
Eur J Neurosci. 2006 Sep;24(6):1815-20. doi: 10.1111/j.1460-9568.2006.05033.x.
Little is known about the gait characteristics of subjects with de novo Parkinson's disease (PD). We hypothesized that alterations in the spatio-temporal characteristics of gait will already be quantifiable in these patients. The gait of 35 patients with idiopathic PD (mean age 60 years) who were in the early stages of the disease (Hoehn and Yahr stage 1.8 +/- 0.5, median 2.0, range 1.0-2.5) and were not yet treated with any anti-parkinsonian medications were compared with the gait of age- and sex-matched healthy controls (n = 22). The patients walked more slowly and with reduced swing times while also exhibiting increased left/right swing asymmetry and marked inconsistencies in the timing of gait. By contrast, significant group differences in the peak forces at heel-strike and in the stride-to-stride variability of the ground reaction forces (a reflection of muscle output consistency) were not observed. These findings indicate that in de novo PD, an altered gait pattern is observed, even though dramatic changes in the gait pattern may not yet be apparent visually (e.g. fairly intact gait speed). Furthermore, the results demonstrate that the observed alterations are not just side-effects of treatments or complications of the disease. Instead, there is evidence for motor programming deficits in gait, as revealed by increased gait variability and asymmetry in timing. PD apparently impinges on the regulation of a consistent gait rhythm, even early in the course of the disease when observed alterations are not the result of any pharmacologic treatment.
对于初发帕金森病(PD)患者的步态特征,人们了解甚少。我们推测,这些患者步态的时空特征改变在此时已可量化。将35例处于疾病早期(Hoehn和Yahr分期为1.8±0.5,中位数为2.0,范围为1.0 - 2.5)且尚未接受任何抗帕金森药物治疗的特发性PD患者(平均年龄60岁)的步态,与年龄和性别匹配的健康对照者(n = 22)的步态进行比较。患者行走速度较慢,摆动时间缩短,同时左右摆动不对称性增加,且步态时间存在明显不一致。相比之下,未观察到足跟撞击时的峰值力以及地面反作用力的步间变异性(反映肌肉输出一致性)存在显著组间差异。这些发现表明,在初发PD中,即使步态模式的显著变化在视觉上可能尚不明显(例如步态速度相当正常),也可观察到步态模式的改变。此外,结果表明观察到的改变并非仅仅是治疗的副作用或疾病的并发症。相反,有证据表明步态存在运动编程缺陷,表现为步态变异性增加和时间不对称。即使在疾病早期,当观察到的改变并非任何药物治疗的结果时,PD显然也会影响一致步态节律的调节。