步态障碍与早期帕金森病胆碱能功能障碍相关

Y. Lim, J. Ham, A. Lee, E. Oh
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引用次数: 3

摘要

目的:早期帕金森病(PD)步态障碍的病理生理机制尚不完全清楚,但胆碱能功能障碍可能与步态障碍有关。中枢胆碱能活性与PD患者的嗅觉密切相关,可以通过短潜伏期传入抑制(SAI)来估计。我们假设胆碱能功能障碍,特别是嗅觉功能障碍,可能与早期PD的步态障碍有关。方法:共入组57例早期PD患者。嗅觉测试使用韩国版的嗅探棒(KVSS)测试。根据KVSS评分将PD患者分为嗅觉缺失症、嗅觉缺失症和正常缺失症。在10米的步态中检查步态参数。SAI是通过运动皮层单次磁刺激(TMS)引发的运动诱发电位来测量的,电刺激以N20至N20+4 ms的间隔传递给对侧正中神经。结果:在PD中,嗅觉缺失组和低嗅觉组的SAI反应(N20 ~ N20+4 ms)和综合SAI的抑制程度均低于正常嗅觉组(p<0.01)。PD嗅觉缺失组在10 m步中行走时间和步数均高于PD嗅觉缺失组(p=0.01, p<0.01)。PD嗅觉缺失组的步态速度较其他组慢,步幅较短(p=0.01, p<0.01)。TDI评分是PD患者的独立因素,与步态速度相关(R2=0.261, 0.257)。TDI评分降低是步态速度降低的独立决定因素,即使在纠正了与胆碱能功能障碍相关的各种因素后,也能解释25%的变异性。结论:中枢胆碱能系统影响帕金森病早期的认知、步态和嗅觉。
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Gait Disturbance Associated with Cholinergic Dysfunction in Early Parkinson's Disease
Objective: The pathophysiology of gait disturbance in early Parkinson’s disease (PD) is not fully understood, but cholinergic dysfunction may be associated with gait disturbance. Central cholinergic activity is closely related with olfaction in PD and it can be estimated with short-latency afferent inhibition (SAI). We hypothesize that cholinergic dysfunction, especially olfactory dysfunction, could be associated with gait disturbance in early PD. Methods: A total of 57 early PD patients were enrolled. Olfaction was examined using the Korean version of the Sniffin’ stick (KVSS) test. The PD patients were grouped as anosmia, hyposmia and normosmia according to the KVSS score. The gait parameters examined during 10 m of gait. SAI was measured by conditioning motor-evoked potentials, elicited by single transmagnetic stimulation (TMS) of the motor cortex, with electrical stimuli delivered to the contralateral median nerve at intervals ranging from N20 to N20+4 ms. Results: The SAI response (N20 to N20+4 ms) and integrated SAI were less inhibited in PD for the anosmia and hyposmia groups than for the normosmia group (for all values, p<0.01). In the PD anosmia group, the walking time was longer and more steps were taken during the 10 m gait than in the PD hyposmia and normosmia groups (p=0.01, p<0.01). In addition, gait speed was slower and stride length was shorter in the PD anosmia group than in the other groups (p=0.01, p<0.01). The TDI score was an independent factor that showed a correlation (R2=0.261, 0.257) with gait speed in PD patients. A reduced TDI score was an independent determinant of reduced gait speed, explaining 25% of the variability even after correction of various factors related to cholinergic dysfunction. Conclusion: Central cholinergic system influences cognition, gait, and olfaction in the early stage of PD.
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