Levodopa-induced dyskinesia

Levodopa-induced dyskinesia
SpecialtyNeurology

Levodopa-induced dyskinesia (LID) is a form of dyskinesia associated with levodopa (l-DOPA), used to treat Parkinson's disease. It often involves hyperkinetic movements, including chorea, dystonia, and athetosis.[1]

In the context of Parkinson's disease (PD), dyskinesia is often the result of long-term dopamine therapy. These motor fluctuations occur in up to 80% of PD patients after 5–10 years of l-DOPA treatment,[2] with the percentage of affected patients increasing over time.[3] Based on the relationship with levodopa dosing, dyskinesia most commonly occurs at the time of peak l-DOPA plasma concentrations and is thus referred to as peak-dose dyskinesia (PDD). As patients advance, they may present with symptoms of diphasic dyskinesia (DD), which occurs when the drug concentration rises or falls. If dyskinesia becomes too severe or impairs the patient's quality of life, a reduction in l-Dopa might be necessary, however this may be accompanied by a worsening of motor performance. Therefore, once established, LID is difficult to treat.[4] Amongst pharmacological treatments, N-methyl-D-aspartate (NMDA) antagonist, (a glutamate receptor), amantadine, has been proven to be clinically effective in a small number of placebo controlled randomized controlled trials, while many others have only shown promise in animal models.[5][6] Attempts to moderate dyskinesia by the use of other treatments such as bromocriptine (Parlodel), a dopamine agonist, appears to be ineffective.[7] In order to avoid dyskinesia, patients with the young-onset form of the disease or young-onset Parkinson's disease (YOPD) are often hesitant to commence l-DOPA therapy until absolutely necessary for fear of suffering severe dyskinesia later on.[citation needed] Alternatives include the use of DA agonists (i.e. ropinirole or pramipexole) in lieu of early l-DOPA treatment which delays the use of l-DOPA. Additionally, a review [8] shows that highly soluble l-DOPA prodrugs may be effective in avoiding the in vivo blood concentration swings that potentially lead to motor fluctuations and dyskinesia.

  1. ^ Gerlach, Manfred; Peter Riederer; Dieter Scheller (December 2011). "Mechanisms underlying and medical management of L-Dope-associated motor complications". Journal of Neural Transmission. 118 (12): 1659–1660. doi:10.1007/s00702-011-0728-0. PMID 22075781. S2CID 34936882.
  2. ^ Ahlskog JE, Muenter MD (2001). "Frequency of levodopa-related dyskinesias and motor fluctuations as estimated from the cumulative literature". Mov Disord. 16 (3): 448–458. doi:10.1002/mds.1090. PMID 11391738. S2CID 35936687.
  3. ^ Obeso JA; et al. (2000). "The evolution and origin of motor complications in Parkinson's disease". Neurology. 55 (S4): S13–S20. PMID 11147505.
  4. ^ Cite error: The named reference Thanvi was invoked but never defined (see the help page).
  5. ^ Rascol, Olivier; Goetz C.; Koller W.; Poewe W.; Sampaio C. (May 2002). "Treatment interventions for Parkinson's disease: an evidence based assessment". The Lancet. 359 (9317): 1589–1598. doi:10.1016/S0140-6736(02)08520-3. PMID 12047983. S2CID 24426198.
  6. ^ Wolf, Elisabeth; Seppi,K.; Katzenschlager, R.; Hochschorner, G.; Ransmayr, G.; Schwinenschuh, P.; Ott, E.; Kloiber, I.; Haubenberger, D.; Auff, E.; Poewe, W. (2010). "Long-term antidyskinetic efficacy of amantadine in Parkinson's Disease". Movement Disorders. 25 (10): 1357–1363. doi:10.1002/mds.23034. PMID 20198649. S2CID 10595065.
  7. ^ van Hilten J; Ramaker C; Stowe R; Nj Ives (2007). "Bromocriptine/levodopa combined versus levodopa alone for early Parkinson's disease". Cochrane Database Syst Rev. 4 (4): CD003634. doi:10.1002/14651858.cd003634.pub2. PMC 8724806. PMID 17943795.
  8. ^ Stocchi F, Marconi S (2010). "Factors associated with motor fluctuations and dyskinesia in Parkinson Disease: potential role of a new melevodopa plus carbidopa formulation (Sirio)". Clin Neuropharmacol. 33 (4): 198–203. doi:10.1097/WNF.0b013e3181de8924. PMID 20414107. S2CID 549658.

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