Dr. Jones has received fees (less than $10,000) for service on the Speaker's Bureau for Pfizer. Dr. Bennett has received speaking fees (less than $10,000 each) from Eli Lilly, Pfizer, and Grünenthal.
A six-month randomized controlled trial of exercise and pyridostigmine in the treatment of fibromyalgia
Article first published online: 31 JAN 2008
Copyright © 2008 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 58, Issue 2, pages 612–622, February 2008
How to Cite
Jones, K. D., Burckhardt, C. S., Deodhar, A. A., Perrin, N. A., Hanson, G. C. and Bennett, R. M. (2008), A six-month randomized controlled trial of exercise and pyridostigmine in the treatment of fibromyalgia. Arthritis & Rheumatism, 58: 612–622. doi: 10.1002/art.23203
- Issue published online: 31 JAN 2008
- Article first published online: 31 JAN 2008
- Manuscript Accepted: 5 NOV 2007
- Manuscript Received: 18 JUN 2007
- NIH (National Institute of Nursing Research). Grant Numbers: 5R01-NR-8150-4, M01-RR-000334
A subset of fibromyalgia (FM) patients have a dysfunctional hypothalamic–pituitary–insulin-like growth factor 1 (IGF-1) axis, as evidenced by low serum levels of IGF-1 and a reduced growth hormone (GH) response to physiologic stimuli. There is evidence that pyridostigmine (PYD) improves the acute response of GH to exercise in FM patients. The purpose of this study was to evaluate the clinical effectiveness of 6 months of PYD and group exercise on FM symptoms.
FM patients were randomized to 1 of the following 4 groups: PYD plus exercise, PYD plus diet recall but no exercise, placebo plus exercise, and placebo plus diet recall but no exercise. The primary outcome measures were the visual analog scale (VAS) score for pain, tender point count, and total myalgic score. Secondary outcome measures were the total score on the Fibromyalgia Impact Questionnaire (FIQ) and FIQ VAS scores for individual symptoms (fatigue, poor sleep, stiffness, and anxiety), as well as quality of life (QOL) and physical fitness (lower body strength/endurance, upper and lower body flexibility, balance, and time on the treadmill).
A total of 165 FM patients completed baseline measurements; 154 (93.3%) completed the study. The combination of PYD and exercise did not improve pain scores. PYD groups showed a significant improvement in sleep and anxiety in those who completed the study and in QOL in those who complied with the therapeutic regimen as compared with the placebo groups. Compared with the nonexercise groups, the 2 exercise groups demonstrated improvement in fatigue and fitness. PYD was generally well tolerated.
Neither the combination of PYD plus supervised exercise nor either treatment alone yielded improvement in most FM symptoms. However, PYD did improve anxiety and sleep, and exercise improved fatigue and fitness. We speculate that PYD may have improved vagal tone, thus benefiting sleep and anxiety; this notion warrants further study.