Pauri F, Boffa L, Cassetta E, Pasqualetti P, Rossini P M
AFaR-CRCCS Centro di Ricovero e Cura a Carattere Scientifico: Divisione di Neurologia, Ospedale Fatebenefratelli, Isola Tiberina 39, 00186, Roma, Italy.
J Neurol Sci. 2000 Dec 1;181(1-2):89-97. doi: 10.1016/s0022-510x(00)00439-1.
The aim of this study was to verify the action of Botulinum toxin type-A (BoNT-A) by means of neurophysiological techniques, in patients presenting lower limb spasticity and requiring BoNT-A injections in the calf muscles, due to the poor response to medical antispastic treatment.
Patients presenting paraparesis were enrolled. They underwent clinical evaluation for spasticity according to the Ashworth scale and neurophysiological recordings including: motor evoked potentials (MEPs) to transcranial magnetic stimulation (TMS) of the leg area; compound motor action potential (cMAP) to tibial nerve stimulation, F-wave, and H-reflex before the treatment and 24 h, 2 weeks and 1 month after the injection of BoNT-A. In all patients, gastrocnemius was treated and in some cases soleus or tibialis posterior muscles were also injected.
In all patients, BoNT-A injections induced a clear clinical improvement as showed by the reduced spasticity values of the Ashworth scale. A significant increment of MEP latency and central conduction time (CCT) duration were observed 2 weeks after the treatment only in the injected muscles.
Prolonged MEP latencies and CCT after BoNT-A injections is probably due to a central alteration in responsiveness of spinal motor neurons to descending impulses from the corticospinal tracts. Such changes represent objective parameters heralding clinical efficacy of treatment.
本研究旨在通过神经生理学技术,验证A型肉毒毒素(BoNT-A)对因药物抗痉挛治疗反应不佳而出现下肢痉挛且需要在小腿肌肉注射BoNT-A的患者的作用。
纳入表现为轻度截瘫的患者。他们接受了根据Ashworth量表进行的痉挛临床评估以及神经生理学记录,包括:对腿部区域进行经颅磁刺激(TMS)的运动诱发电位(MEP);治疗前以及注射BoNT-A后24小时、2周和1个月对胫神经刺激的复合运动动作电位(cMAP)、F波和H反射。所有患者均对腓肠肌进行了治疗,在某些情况下还对比目鱼肌或胫骨后肌进行了注射。
在所有患者中,BoNT-A注射均带来了明显的临床改善,如Ashworth量表的痉挛值降低所示。仅在治疗后2周,在注射的肌肉中观察到MEP潜伏期和中枢传导时间(CCT)持续时间显著增加。
BoNT-A注射后MEP潜伏期和CCT延长可能是由于脊髓运动神经元对皮质脊髓束下行冲动的反应性发生了中枢性改变。这些变化代表了预示治疗临床疗效的客观参数。