Post-polio syndrome (PPS) is the most common motor neuron disease in North America. It is a clinical syndrome characterized by new weakness, fatigue, and pain. It is probably caused by a distal degeneration of enlarged motor units, occuring through axonal sprouting, as a result of the recovery process following acute paralytic polio. New weakness is likely due to permanent denervation, whereas fatigue may be due to neuromuscular junction (NMJ) transmission defects as a result of motor unit degeneration and remodeling. The normal ageing process, with concomitant decreased growth hormone and insulin-like growth factor 1 (IGF-1) (which stimulate synthesis of protein and nucleic acids in muscle cells and regeneration/sprouting in peripheral nerves), are possible contributing factors. There is no specific treatment for PPS. Pyridostigmine is an anticholinesterase which inhibits the hydrolysis of acetylcholine at the NMJ and prolongs its effect. Pyridostigmine can also enhance growth hormone secretion in growth hormonr deficiency states. Preliminary work indicates that:: 1) NMJ transmission defects can be ameliorated with anticholinesterase agents in PPS, 2) fatigue in PPS may be due to NMJ transmission defects, and 3) about 60% of PPS patients responded to oral pyridostigmine 180 mg/d in an open-label trial. We hypothesize that pyridostigmine will produce an amelioration of NMJ transmission in motor units and an increase in IGF-1 levels, which will result in an improvement in general health status (as assessed by the short form health survey-36, [SF-36}), in fatigue, and in weakness in PPS patients. To test this hypothesis we will conduct a multicenter, randomized, double-blind, placebo-controlled treatment trial with the following onjectives: 1) to assess the clinical efficacy of a 6 month course of pyridostigmine by evaluating its effect on subjective physical functioning ( as measured by the SF-36 physical functional scale), on general health status (as measured by the 7 remaining subscales of the SF-36), on subjective fatigue (as measured by the Hare fatigue scale and the fatigue severity scale), and on isometric strength (as measured by the Tufts Quantitative Neuromuscular Exam); 2) to evaluate the effect of pyridostigmine on serum IGF-1 levels; and 3) to determine the incidence and severity of side effects from pyridostigmine treatment in PPS patienys. Patients will be recruited from 6 post-polio clinics in the USA and Canada. One hundred and twenty six patients (20 per center) will be randomly assigned to treatment with either pyridostigmine or matched placebo. There will be two baseline outcome assessments (within 4 weeks), and 3 trial assessments (after 6 weeks, 10 weeks, and 6 months of treatment). The primary outcome measure for the study will be the change in physical functioning as assessed by the SF-36 at basekine and after 6 months of treatment. The secondary outcome measures will be other indices on the SF-36 scale, Hare fatigue scale, fatigue severity scale, isometric muscle strength and IGF-1 levels. This trial may result in the identification of a safe and effective treatment for PPS. PROGRESS IN THE STUDY: This study was completed in July 1997 and enrolled a total of 126 patients. There was no beneficial effect of Mestinon in PPS: change in physical functioning as assessed by the SF-36; subjective fatigue as measured by the Hare Fatigue Scale and the Fatigue Severity Scale; and change in isometric strength as measured by the TQNE. There were no serious adverse effects seen in patients treated with Mestinon. The results of the study were presented at the annual American Academy of Physical Medicine & Rehabilitation Meeting in Atlanta, GA in November, 1997. From our center, 6 of the 9 enrolled patients entered the 6 months open-label phase of the study. The first patient entered the open-label study in June 1997 and the last patient finished in September 1998. FUTURE PLANS FOR THE STUDY: Further analyses are currently underway to see if any subgroup of patients, or individual measures constituting scales, showed benefit after Mestinon treatment. A manuscript relating to the study is in preparation for submission in the spring of 1998.
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