Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K)

被引:31
作者
Grubber, JM
Saunders, AM
Crane-Gatherum, AR
Scott, WK
Martin, ER
Haynes, CS
Conneally, PM
Small, GW
Roses, AD
Haines, JL
Pericak-Vance, MA
机构
[1] Duke Univ, Med Ctr, Ctr Human Genet, Dept Med, Durham, NC 27710 USA
[2] Glaxo Wellcome Inc, Res & Dev, GEnet Directorate, Res Triangle Pk, NC 27709 USA
[3] Indiana Univ, Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Psychiat, Los Angeles, CA 90024 USA
[5] Vanderbilt Univ, Program Human Genet, Nashville, TN 37232 USA
关键词
butyrylcholinesterase gene; apolipoprotein E; Alzheimer disease; transmission disequilibrium test; association; linkage disequilibrium;
D O I
10.1016/S0304-3940(99)00426-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Butyrylcholinesterase (BCHE) is an enzyme expressed in most human tissues. Recently, an increased odds of carrying the K variant of BCHE (BCHE-K) was reported among Alzheimer disease (AD) cases as compared with controls. We tested our data set of 245 sporadic AD cases and 241 controls for an association between BCHE-K, APOE4, and AD using logistic regression and chi-square analyses. The sib transmission disequilibrium test (S-TDT) was also used to test for differences in BCHE-K allele frequencies between 163 discordant sib-pairs selected from multiplex AD families. No statistically significant differences were noted between BCHE-K case and control allele frequencies even after stratifying by APOE4 status. S-TDT analysis between the BCHE-K variant and AD was also not significant (P = 0.52). We conclude that BCHE-K is not a major genetic risk factor for AD in our study population. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:115 / 119
页数:5
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