4.6 Article

Effects of Citalopram on Neuropsychiatric Symptoms in Alzheimer's Dementia: Evidence From the CitAD Study

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AMERICAN JOURNAL OF PSYCHIATRY
卷 173, 期 5, 页码 473-480

出版社

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2016.15020248

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资金

  1. National Institute on Aging (NIA)
  2. NIMH [R01AG031348]
  3. NIH [P50-AG05142]
  4. Avanir
  5. NIA
  6. Office of the Federal Public Defender
  7. U.S. Attorney's Office
  8. Avanir Pharmaceuticals
  9. Transition Therapeutics
  10. Insys Therapeutics
  11. Takeda Global Research and Development Center
  12. Pfizer
  13. Genentech
  14. Merck
  15. Accera
  16. Elan
  17. Hoffmann-La Roche
  18. Novartis
  19. Baxter
  20. Eli Lilly
  21. Wyeth
  22. Janssen Alzheimer Initiative
  23. Alzheimer's Assocation
  24. Functional Neuromodulation
  25. Abbott
  26. AstraZeneca
  27. Bristol-Myers Squibb
  28. GlaxoSmithKline
  29. Johnson Johnson
  30. Lundbeck
  31. Roche
  32. AbbVie
  33. ACImmune
  34. Forest Laboratories
  35. Forum
  36. Merz
  37. Orion
  38. Otsuka
  39. Servier
  40. Takeda
  41. Toyama/FujiFilm
  42. Zinfandel
  43. Michael J. Fox Foundation for Parkinson's Research
  44. Department of Veterans Affairs
  45. Avid Radiopharmaceuticals
  46. Alzheimer's Disease Cooperative Study
  47. International Parkinson
  48. Movement Disorder Society
  49. Associated Jewish Federation of Baltimore
  50. Weinberg Foundation
  51. Forest
  52. Eisai
  53. Ortho-McNeil
  54. National Football League
  55. Biogen
  56. EnVivo
  57. Genentech/Roche
  58. Medivation
  59. MerckPfizer
  60. Toyama
  61. Department of Defense

向作者/读者索取更多资源

Objective: Citalopram has been shown to improve agitation in patients with Alzheimer's disease. The authors evaluated whether other neuropsychiatric symptoms improve with citalopram treatment compared with placebo. Method: In this planned secondary analysis of the Citalopram for Agitation in Alzheimer's Disease study, the authors evaluated the effect of citalopram on the 12 neuropsychiatric symptom domains assessed by the Neuropsychiatric Inventory (NPI). They compared caregiver-reported NPI scores at week 9 in patients receiving citalopram(30 mg/day) or placebo with regard to both the presence or absence of individual neuropsychiatric symptoms and individual domain scores (reflecting severity) in participants who had symptoms at week 9. Results: At week 9, participants treated with citalopram were significantly less likely to be reported as showing delusions (odds ratio=0.40), anxiety (odds ratio=0.43), and irritability/lability (odds ratio=0.38). A comparison of median scores of participants with symptoms present at week 9 showed significant differences favoring citalopram for hallucinations and favoring placebo for sleep/nighttime behavior disorders. Conclusions: While dosage constraints must be considered because of citalopram's adverse effect profile, this agent's overall therapeutic effects in patients with Alzheimer's disease and agitation, in addition to efficacy for agitation/aggression, included reductions in the frequency of irritability, anxiety, and delusions; among patients who had these symptoms at week 9, they included a reduction in the severity of hallucinations but an increase in the severity of sleep/nighttime behavior disorders.

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