Long-term clinical evaluation in patients with Parkinson's disease and early autonomic involvement

• Published in: Parkinsonism & related disorders Vol. 12; no. 5; pp. 279 - 283
• Main Authors: Lucetti, Claudio, Gambaccini, Gianna, Dotto, Paolo Del, Ceravolo, Roberto, Logi, Chiara, Rossi, Giuseppe, Murri, Luigi, Bonuccelli, Ubaldo
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.06.2006
• Subjects: Aged; Antiparkinson Agents - therapeutic use; Autonomic nervous system; Autonomic Nervous System - physiopathology; Bromocriptine - therapeutic use; Disability Evaluation; Disease Progression; Dopamine Agonists - adverse effects; Dopamine Agonists - therapeutic use; Drug Therapy, Combination; Female; Follow-Up Studies; Hemodynamics - physiology; Humans; Levodopa - therapeutic use; Longitudinal Studies; Male; Middle Aged; Parkinson Disease - drug therapy; Parkinson Disease - physiopathology; Parkinson's disease; Pergolide - therapeutic use; Prognosis; Survival Analysis; Autonomic nervous system; Parkinson's disease; Disease progression
• ISSN: 1353-8020; 1873-5126
• DOI: 10.1016/j.parkreldis.2005.12.005

To evaluate in a prospective longitudinal study the evolution of functional disability and the response to dopaminergic therapy in PD patients with and without autonomic involvement. Sixty untreated consecutive patients with PD underwent autonomic cardiovascular function evaluation using the five autonomic tests of Ewing. An integrated index (Autonomic Score=AS), taking in account the results of all subtests, was calculated. Patients were treated with pergolide and bromocriptine during a 5-year follow-up until the level of functional disability was sufficient to warrant the initiation of levodopa therapy. Results of autonomic testing were compared with those of a group of age-matched healthy subjects. A value of AS>2 was considered as indicative of autonomic failure. Eighteen patients with PD (35%) showed AS>2 (autonomically impaired group=AI), the remaining 33 (65%) had AS<2 (nonautonomically impaired group=non-AI). During the follow-up levodopa was added to the treatment regimen of 10/18 (55%) patients in AI group, and 6/33 (18%) patients in non-AI group ( p<.01). The increased occurrence of levodopa adjunct in autonomically impaired PD suggests that there is a more rapid deterioration of functional performance in parkinsonian patients with early autonomic involvement.