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Efficacy of a high dosage of donepezil for Alzheimer's disease as examined by single‐photon emission computed tomography imaging
Author(s) -
KANAYA Kiyoshi
Publication year - 2012
Publication title -
psychogeriatrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.647
H-Index - 32
eISSN - 1479-8301
pISSN - 1346-3500
DOI - 10.1111/j.1479-8301.2011.00399.x
Subject(s) - donepezil , single photon emission computed tomography , cerebral blood flow , alzheimer's disease , medicine , adverse effect , emission computed tomography , irritability , occipital lobe , psychology , nuclear medicine , dementia , disease , positron emission tomography , cognition , psychiatry , radiology
Background: The efficacy of donepezil 10 mg/day against Alzheimer's disease (AD) was examined, with a primary focus on changes in cerebral blood flow (CBF) as determined by single‐photon emission computed tomography imaging. Methods: The subjects were 24 outpatients who had been diagnosed with probable AD, which had progressed to advanced AD. Mini‐Mental State Examination and Alzheimer's Disease Assessment Scale (ADAS) scores were determined before and after the donepezil dosage increase. 99m Tc‐ethylcysteinate dimer single‐photon emission computed tomography was performed to evaluate changes in CBF. Then, a comparative study evaluated changes after the donepezil dosage increased. Results: After the donepezil dosage increase, adverse effects associated with gastrointestinal symptoms were observed in one patient, and irritability was observed in three. The average Mini‐Mental State Examination score changed from15.25 ± 6.24 to 14.67 ± 6.07; significant changes were not observed. Seventeen subjects were evaluated with the Alzheimer's Disease Assessment Scale‐cognitive subscale. After the dosage increase, the average subscale score decreased from 24.52 ± 13.39 to 21.56 ± 9.14, and significant improvement was observed ( P = 0.021). With respect to changes in the CBF, the values of all three indicators decreased after the higher dosage increased CBF. However, no significant differences were observed in CBF. Analysis performed after the donepezil dosage increase revealed significant increases in CBF in the right occipital and temporal lobes, left temporal lobe, right parietal lobe, and both parts of the posterior cerebellum. Conclusion: Increasing the donepezil dosage from 5 mg/day to 10 mg/day is effective for the treatment of AD.