A 52 year old fully medicated Parkinsonian patient with severe disability (stage 4 on the Hoehn & Yahr disability scale) became asymptomatic 10 weeks after he received twice weekly transcranial treatments with AC pulsed electromagnetic fields (EMFs) of picotesla flux density. Prior to treatment with EMFs, his medication (Sinemet CR) was about 50% effective and he experienced end-of-dose deterioration and diurnal-related decline in the drug's efficacy. For instance, while his morning medication was 90% effective, his afternoon medication was only 50% effective and his evening dose was only 30% effective. Ten weeks after introduction of treatment with EMFs, there was 40% improvement in his response to standard Sinemet medication with minimal change in its efficacy during the course of the day or evening. These findings demonstrate that intermittent, AC pulsed applications of picotesla flux density EMFs improve Parkinsonian symptoms in part by enhancing the patient's response to levodopa. This effect may be related to an increase in the capacity of striatal DA neurons to synthesize, store and release DA derived from exogenously supplied levodopa as well as to increased serotonin (5-HT) transmission which has been shown to enhance the response of PD patients to levodopa. Since decline in the response to levodopa is a phenomenon associated with progression of the disease, this case suggests that intermittent applications of AC pulsed EMFs of picotesla flux density reverse the course of chronic progressive PD.
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UCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Royal Free Hosp, London NW3 2PF, EnglandUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Schapira, A. H. V.
Emre, M.
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Norol ABD, Istanbul Tip Fak, Istanbul Med Sch, Capa, TurkeyUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Emre, M.
Jenner, P.
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Kings Coll London, Neurodegenerat Dis Res Ctr, Sch Hlth & Biomed Sci, London WC2R 2LS, EnglandUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Jenner, P.
Poewe, W.
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Univ Innsbruck Hosp, Vorstand D Univ Klin F Neurol, A-6020 Innsbruck, AustriaUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England