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The Effect of Choline Acetyltransferase Genotype on Donepezil Treatment Response in Patients with Alzheimer’s Disease

Authors :
Seungho Ryu
Kang Uk Lee
Jin Hyeong Jhoo
Dong Young Lee
Jeong Lan Kim
Bong Jo Kim
Jong Chul Youn
Jong Inn Woo
Do Hoon Kim
Sung Man Chang
Ki Woong Kim
Chang-Uk Lee
Hae Kook Lee
Nam Jin Lee
Jung Hie Lee
Seok Woo Moon
Young Hoon Kim
Moon Doo Kim
Source :
Clinical Psychopharmacology and Neuroscience
Publication Year :
2015
Publisher :
Korean College of Neuropsychopharmacology, 2015.

Abstract

OBJECTIVE We examined the difference in responses to donepezil between carriers and non-carriers of the A allele at the +4 position of the choline acetyltransferase (ChAT) gene in Koreans. METHODS Patients who met the criteria for probable Alzheimer's disease (AD) (n=199) were recruited. Among these, 145 completed the 12-week follow-up evaluation and 135 completed the 26-week scheduled course. Differences and changes in the Korean version of the mini-mental state examination (MMSE-KC) score, Korean version of the Consortium to Establish a Registry for Alzheimer's Disease Neuropsychological Assessment Battery (CERAD-K[N]) wordlist subtest score (WSS), CERAD-K(N) total score (TS), and the Korean version of geriatric depression scale (GDS-K) score between baseline and 12 weeks or 26 weeks were assessed by the Student's t-test. RESULTS At 12 weeks, the changes in the MMSE-KC score, CERAD-K(N) WSS, and CERAD-K(N) TS from baseline were not significant between ChAT A allele carriers and non-carriers; however, at 26 weeks, these changes were significantly larger in ChAT A allele carriers than in non-carriers (p=0.02 for MMSE-KC and p=0.03 for CERAD-K(N) WSS respectively). CONCLUSION Our findings in this study suggested that presence of the A allele at the +4 position of ChAT might positively influence the treatment effect of donepezil in the early stages of AD in Koreans.

Details

Language :
English
ISSN :
20934327 and 17381088
Volume :
13
Issue :
2
Database :
OpenAIRE
Journal :
Clinical Psychopharmacology and Neuroscience
Accession number :
edsair.doi.dedup.....9c6b3d7c918a950a47c35ef79231793c