TY - JOUR
T1 - Effects of citalopram on neuropsychiatric symptoms in Alzheimer's dementia
T2 - Evidence from the CitAD study
AU - For the CitAD Research Group
AU - Leonpacher, Anne K.
AU - Peters, Matthew E.
AU - Drye, Lea T.
AU - Makino, Kelly M.
AU - Newell, Jeffery A.
AU - Devanand, D. P.
AU - Frangakis, Constantine
AU - Munro, Cynthia A.
AU - Mintzer, Jacobo E.
AU - Pollock, Bruce G.
AU - Rosenberg, Paul B.
AU - Schneider, Lon S.
AU - Shade, David M.
AU - Weintraub, Daniel
AU - Yesavage, Jerome
AU - Lyketsos, Constantine G.
AU - Porsteinsson, Anton P.
N1 - Funding Information:
Supported by National Institute on Aging (NIA) and NIMH grant R01AG031348, and in part by NIH grant P50-AG05142 (to University of Southern California and Dr. Schneider).
PY - 2016/5/1
Y1 - 2016/5/1
N2 - 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 symptomdomainsassessedbytheNeuropsychiatricInventory (NPI). They compared caregiver-reported NPI scores at week 9 in patients receiving citalopram(30mg/day) or placebowith regard to both the presence or absence of individual neuropsychiatric symptoms and individualdomain 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.
AB - 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 symptomdomainsassessedbytheNeuropsychiatricInventory (NPI). They compared caregiver-reported NPI scores at week 9 in patients receiving citalopram(30mg/day) or placebowith regard to both the presence or absence of individual neuropsychiatric symptoms and individualdomain 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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U2 - 10.1176/appi.ajp.2016.15020248
DO - 10.1176/appi.ajp.2016.15020248
M3 - Article
C2 - 27032628
AN - SCOPUS:84965156027
SN - 0002-953X
VL - 173
SP - 473
EP - 480
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 5
ER -