A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease

被引:41
作者
Harold, Denise
MacGregor, Stuart [2 ]
Patterson, Cathryn E. [3 ]
Hollingworth, Paul
Moore, Pamela
Owen, Michael J.
Williams, Julie
O'Donovan, Michael
Passmore, Peter [3 ]
Mcllroy, Stephen [3 ]
Jones, Lesley [1 ]
机构
[1] Cardiff Univ, Wales Sch Med, Dept Psychol Med, Cardiff CF14 4XN, S Glam, Wales
[2] Cardiff Univ, Biostat & Biomath Unit, Cardiff CF14 4XN, S Glam, Wales
[3] Queens Univ Belfast, Dept Geriatr Med, Belfast, Antrim, North Ireland
基金
英国医学研究理事会;
关键词
pharmacogenetics; acetylcholinesterase inhibitors; Alzheimer's disease; choline acetyltransferase;
D O I
10.1097/01.fpc.0000189799.88596.04
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Background Alzheimer's disease ( AD) is a devastating neurodegeneration with a characteristic deficit in cholinergic neurotransmission. Treatment with acetylcholinesterase ( AChE) inhibitors aims to reverse this deficit and does ameliorate the decline in cognition in some AD patients, although response is variable. Objective To examine whether sequence variation in the gene encoding choline acetyltransferase ( CHAT), which encodes the major catalytic enzyme of the cholinergic pathway, predicts response to AChE inhibitors. Methods Alzheimer's disease patients ( 121) were treated with cholinesterase inhibitors and the effect of treatment on cognition was measured using the Mini Mental State Examination ( MMSE). Six polymorphisms in CHAT were analysed for association with change in MMSE score. Results After correction for multiple testing, we found one SNP, rs733722, in a promoter region of CHAT, is associated with response of AD patients to cholinesterase inhibitors ( P = 0.03) and accounts for 6% of the variance in response to AChE inhibitors. Conclusion Rs733722 represents a putative marker of response to AChE inhibitors in AD patients.
引用
收藏
页码:75 / 77
页数:3
相关论文
共 16 条
[1]
A general test of association for quantitative traits in nuclear families [J].
Abecasis, GR ;
Cardon, LR ;
Cookson, WOC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :279-292
[2]
NEUROTRANSMITTER-RELATED ENZYMES AND INDEXES OF HYPOXIA IN SENILE DEMENTIA AND OTHER ABIOTROPHIES [J].
BOWEN, DM ;
SMITH, CB ;
WHITE, P ;
DAVISON, AN .
BRAIN, 1976, 99 (SEP) :459-496
[3]
Candidate gene association studies of genes involved in neuronal cholinergic transmission in Alzheimer's disease suggests choline acetyltransferase as a candidate deserving further study [J].
Cook, LJ ;
Ho, LW ;
Wang, L ;
Terrenoire, E ;
Brayne, C ;
Evans, JG ;
Xuereb, J ;
Cairns, NJ ;
Turic, D ;
Hollingworth, P ;
Moore, PJ ;
Jehu, L ;
Archer, N ;
Walter, S ;
Foy, C ;
Edmondson, A ;
Powell, J ;
Lovestone, S ;
Williams, J ;
Rubinsztein, DC .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 132B (01) :5-8
[4]
NEUROTRANSMITTER-RELATED ENZYMES IN SENILE DEMENTIA OF THE ALZHEIMER TYPE [J].
DAVIES, P .
BRAIN RESEARCH, 1979, 171 (02) :319-327
[5]
DAVIES P, 1976, LANCET, V2, P1403
[6]
Pedigree disequilibrium tests for multilocus haplotypes [J].
Dudbridge, F .
GENETIC EPIDEMIOLOGY, 2003, 25 (02) :115-121
[7]
ERICKSON JD, 1994, J BIOL CHEM, V269, P21929
[8]
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease [J].
Harold, D ;
Peirce, T ;
Moskvina, V ;
Myers, A ;
Jones, S ;
Hollingworth, P ;
Moore, P ;
Lovestone, S ;
Powell, J ;
Foy, C ;
Archer, N ;
Walter, S ;
Edmonson, A ;
McIlroy, S ;
Craig, D ;
Passmore, PA ;
Goate, A ;
Hardy, J ;
O'Donovan, M ;
Williams, J ;
Liddell, M ;
Owen, MJ ;
Jones, L .
HUMAN GENETICS, 2003, 113 (03) :258-267
[9]
Lynch M., 1998, GENETICS ANAL QUANTI
[10]
McCarten JR, 2004, J ALZHEIMERS DIS, V6, P11