Polysomnographic and pharmacokinetic findings in levodopa-induced augmentation of restless legs syndrome.
Identifieur interne : 001450 ( Ncbi/Curation ); précédent : 001449; suivant : 001451Polysomnographic and pharmacokinetic findings in levodopa-induced augmentation of restless legs syndrome.
Auteurs : Roberto Vetrugno [Italie] ; Manuela Contin ; Agostino Baruzzi ; Federica Provini ; Giuseppe Plazzi ; Pasquale MontagnaSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2006.
English descriptors
- KwdEn :
- Aged, Antiparkinson Agents (administration & dosage), Antiparkinson Agents (adverse effects), Antiparkinson Agents (pharmacokinetics), Disease Progression, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Humans, Levodopa (administration & dosage), Levodopa (adverse effects), Levodopa (pharmacokinetics), Metabolic Clearance Rate (physiology), Polysomnography, Restless Legs Syndrome (blood), Restless Legs Syndrome (chemically induced), Restless Legs Syndrome (diagnosis), Restless Legs Syndrome (drug therapy), Spasm (blood), Spasm (chemically induced), Spasm (diagnosis).
- MESH :
- chemical , administration & dosage : Antiparkinson Agents, Levodopa.
- chemical , adverse effects : Antiparkinson Agents, Levodopa.
- chemical , pharmacokinetics : Antiparkinson Agents, Levodopa.
- blood : Restless Legs Syndrome, Spasm.
- chemically induced : Restless Legs Syndrome, Spasm.
- diagnosis : Restless Legs Syndrome, Spasm.
- drug therapy : Restless Legs Syndrome.
- physiology : Metabolic Clearance Rate.
- Aged, Disease Progression, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Humans, Polysomnography.
Abstract
Augmentation, defined as a loss of circadian recurrence with progressively earlier daily onset and increase in the duration, intensity, and anatomy of symptoms, not compatible with the half-life of the drug, is associated with dopaminergic treatment in restless legs syndrome (RLS) patients. The pathogenesis of augmentation is unclear. We describe a patient with idiopathic RLS who developed augmentation after 8 months of levodopa treatment. Videopolysomnographic and pharmacokinetic studies with monitoring of plasma levodopa levels demonstrated marked motor hyperactivity during augmentation, with anarchic discharges of motor unit potentials, tonic grouped discharges and flexor spasms, associated with painful dysesthesia. Symptoms and signs of augmentation were related to low plasma levodopa levels, abating 75 minutes after oral levodopa administration and reappearing after 3 hours, closely mirroring the rapid rise and fall of plasma levodopa concentration. This case is the first report in which RLS augmentation is shown to be characterized by motor hyperkinesias paralleling levodopa plasma pharmacokinetic profile.
DOI: 10.1002/mds.20677
PubMed: 16200540
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pubmed:16200540Le document en format XML
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<front><div type="abstract" xml:lang="en">Augmentation, defined as a loss of circadian recurrence with progressively earlier daily onset and increase in the duration, intensity, and anatomy of symptoms, not compatible with the half-life of the drug, is associated with dopaminergic treatment in restless legs syndrome (RLS) patients. The pathogenesis of augmentation is unclear. We describe a patient with idiopathic RLS who developed augmentation after 8 months of levodopa treatment. Videopolysomnographic and pharmacokinetic studies with monitoring of plasma levodopa levels demonstrated marked motor hyperactivity during augmentation, with anarchic discharges of motor unit potentials, tonic grouped discharges and flexor spasms, associated with painful dysesthesia. Symptoms and signs of augmentation were related to low plasma levodopa levels, abating 75 minutes after oral levodopa administration and reappearing after 3 hours, closely mirroring the rapid rise and fall of plasma levodopa concentration. This case is the first report in which RLS augmentation is shown to be characterized by motor hyperkinesias paralleling levodopa plasma pharmacokinetic profile.</div>
</front>
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