No association of α1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients

被引:3
作者
Bass, MP
Yamaoka, LH
Scott, WK
Gaskell, PC
Welsh-Bohmer, KA
Roses, AD
Saunders, AM
Haines, JL
Pericak-Vance, MA
机构
[1] Duke Univ, Med Ctr, Med Genet Sect, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Joseph & Kathleen Bryan Alzheimer Dis Res Ctr, Durham, NC 27710 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med Phys & Biophys, Program Human Genet, Nashville, TN 37232 USA
关键词
alpha-antichymotrypsin; Alzheimer disease; candidate gene; polymorphism; association study;
D O I
10.1016/S0304-3940(98)00398-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The alpha(1)-antichymotrypsin (AACT)-155 allele was found elsewhere to have a significant effect on Alzheimer disease (AD) risk in individuals with at least one APOE-4 allele, We compared AACT genotypes of 284 cases of sporadic AD and 172 controls. The frequency of the AACT-155 allele did not differ significantly between cases and controls, either overall or when restricted to subjects with at least one APOE-LF allele. Logistic regression controlling for age and sex failed to show an effect due to AACT either alone or acting with APOE. There was no evidence of an interaction between APOE-4 and the AACT-155 allele to reduce age at onset. Thus, our data do not support an association of AACT-155 with risk or age at onset in AD. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:79 / 82
页数:4
相关论文
共 24 条
[1]   PROTECTIVE EFFECT OF APOLIPOPROTEIN-E TYPE-2 ALLELE FOR LATE-ONSET ALZHEIMER-DISEASE [J].
CORDER, EH ;
SAUNDERS, AM ;
RISCH, NJ ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
RIMMLER, JB ;
LOCKE, PA ;
CONNEALLY, PM ;
SCHMADER, KE ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
NATURE GENETICS, 1994, 7 (02) :180-184
[2]  
DeKosky ST, 1996, ANN NY ACAD SCI, V802, P27
[3]  
Fallin D, 1997, AM J MED GENET, V74, P192, DOI 10.1002/(SICI)1096-8628(19970418)74:2<192::AID-AJMG15>3.0.CO
[4]  
2-D
[5]  
Farrer LA, 1997, JAMA-J AM MED ASSOC, V278, P1349, DOI 10.1001/jama.1997.03550160069041
[6]  
Fleiss JL, 1981, STAT METHODS RATES P
[7]   SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE [J].
GOATE, A ;
CHARTIERHARLIN, MC ;
MULLAN, M ;
BROWN, J ;
CRAWFORD, F ;
FIDANI, L ;
GIUFFRA, L ;
HAYNES, A ;
IRVING, N ;
JAMES, L ;
MANT, R ;
NEWTON, P ;
ROOKE, K ;
ROQUES, P ;
TALBOT, C ;
PERICAKVANCE, M ;
ROSES, A ;
WILLIAMSON, R ;
ROSSOR, M ;
OWEN, M ;
HARDY, J .
NATURE, 1991, 349 (6311) :704-706
[8]   No genetic effect of alpha(1)-antichymotrypsin in Alzheimer disease [J].
Haines, JL ;
Pritchard, ML ;
Saunders, AM ;
Schildkraut, JM ;
Growdon, JH ;
Gaskell, PC ;
Farrer, LA ;
Auerbach, SA ;
Gusella, JF ;
Locke, PA ;
Rosi, BL ;
Yamaoka, L ;
Small, GW ;
Conneally, PM ;
Roses, AD ;
PericakVance, MA .
GENOMICS, 1996, 33 (01) :53-56
[9]  
HAYNES CS, 1995, 45 ANN AM SOC HUM GE
[10]   APOE-ASTERISK-4-ASSOCIATED ALZHEIMERS-DISEASE RISK IS MODIFIED BY ALPHA-1-ANTICHYMOTRYPSIN POLYMORPHISM [J].
KAMBOH, MI ;
SANGHERA, DK ;
FERRELL, RE ;
DEKOSKY, ST .
NATURE GENETICS, 1995, 10 (04) :486-488