4.6 Review

Early Versus Delayed Initiation of Pharmacotherapy in Parkinson's Disease

Journal

DRUGS
Volume 74, Issue 6, Pages 645-657

Publisher

ADIS INT LTD
DOI: 10.1007/s40265-014-0209-5

Keywords

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Funding

  1. Center for Regenerative Therapies Dresden
  2. Abbott
  3. Bayer Healthcare
  4. Boehringer Ingelheim
  5. Brittania
  6. Cephalon
  7. Desitin
  8. GSK
  9. Lundbeck
  10. Merck-Serono
  11. Novartis
  12. Orion
  13. Pfizer
  14. TEVA
  15. UCB Pharma
  16. Valeant

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Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease and pathologically is characterised by a progressive loss of dopaminergic cells of the nigrostriatal pathway. Clinically, PD is mainly defined by the presence of the motor symptoms of bradykinesia, rigidity, rest tremor and postural instability, but non-motor symptoms such as depression, dementia and autonomic disturbances are recognised as integral parts of the disease. Although pharmacotherapy for PD was introduced almost 50 years ago, and has improved significantly over the intervening period, the timing of initiation of treatment in newly diagnosed PD remains controversial. While some physicians favour an early start of pharmacotherapy at or soon after diagnosis, others prefer to delay pharmacological treatment until a certain degree of disability has developed. This article aims to discuss the advantages and disadvantages of both strategies by exploring their effects on symptoms, disease progression and quality of life. Although the data on putative disease-modifying effects of early pharmacological intervention in PD are still inconclusive, we believe that the most important indication for an early initiation of anti-parkinsonian treatment should be to maintain the quality of life of PD patients and to secure their socioeconomic status as long as possible.

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