Madrazo I, Franco-Bourland R, Aguilera M, Ostrosky-Solis F, Madrazo M, Cuevas C, Catrejon H, Guizar-Zahagun G, Magallon E
Department of Clinical Research in Neurology and Neurosurgery, Hospital de Especialidades, Mexico City, Mexico.
J Neural Transplant Plast. 1991;2(3-4):157-64. doi: 10.1155/NP.1991.157.
We report on the clinical status of 5 patients with Parkinson's disease (PD) 3 years after autologous adrenal medullary (AM)-to-caudate nucleus (CN) implantation, and of 2 PD patients, 2 years after fetal ventral mesencephalon (VM)- and fetal adrenal (A)-to-CN homotransplantation. Current clinical evaluation of 4 of the AM grafted patients revealed sustained bilateral amelioration of their PD signs, most notably of rigidity, postural imbalance and gait disturbances, resulting in a substantial improvement in their quality of life. The disease-related dystonia of one of them disappeared only 2 years after surgery. The levodopa requirements of 2 of these patients and the anticholinergic therapy of another have been reduced. In agreement with the satisfactory clinical evaluation of these 4 patients, their neuropsychological and electrophysiological improvements, initially registered 3 months after surgery, have been maintained for 3 years. After 1 year of significant recovery, the 5th patient of this group has almost returned to her preoperative state. The 2 homotransplanted patients also showed sustained bilateral improvement of their PD signs. Two years after surgery, the most improved signs of the fetal VM case were rigidity, bradykinesia, postural imbalance, gait disturbances and facial expression. The fetal A case has only shown amelioration of rigidity and bradykinesia. Neither of them has shown significant neuropsychological changes. Their current levodopa requirements are less than before surgery. The improvements shown here by PD patients after brain tissue grafts go beyond those obtained using any other therapeutic approach, when levodopa fails. Although more studies and the development of these procedures are obviously required, these initial human trials appear to be resisting the test of time.
我们报告了5例帕金森病(PD)患者自体肾上腺髓质(AM)移植到尾状核(CN)3年后的临床状况,以及2例PD患者在接受胎儿腹侧中脑(VM)和胎儿肾上腺(A)移植到CN 2年后的临床状况。对4例接受AM移植的患者进行的当前临床评估显示,其PD症状持续双侧改善,最明显的是僵硬、姿势失衡和步态障碍,从而使其生活质量得到显著提高。其中1例患者与疾病相关的肌张力障碍在手术后2年才消失。其中2例患者的左旋多巴需求量减少,另1例患者的抗胆碱能治疗量减少。与对这4例患者的满意临床评估一致,他们在术后3个月首次记录到的神经心理学和电生理改善一直维持了3年。在显著恢复1年后,该组的第5例患者几乎恢复到了术前状态。2例接受同种移植的患者也显示出PD症状持续双侧改善。手术后2年,胎儿VM移植患者改善最明显的症状是僵硬、运动迟缓、姿势失衡、步态障碍和面部表情。胎儿A移植患者仅显示僵硬和运动迟缓有所改善。他们均未出现明显的神经心理学变化。他们目前的左旋多巴需求量低于手术前。当左旋多巴治疗无效时,PD患者脑组织移植后所显示的改善超过了使用任何其他治疗方法所获得的改善。尽管显然需要更多的研究和这些手术方法的改进,但这些初步的人体试验似乎经受住了时间的考验。