Allelic association between the D10S1423 marker and Alzheimer's disease in a German population

被引:21
作者
Majores, M [1 ]
Bagli, M [1 ]
Papassotiropoulos, A [1 ]
Schwab, SG [1 ]
Jessen, F [1 ]
Rao, ML [1 ]
Maier, W [1 ]
Heun, R [1 ]
机构
[1] Univ Bonn, Dept Psychiat, D-53105 Bonn, Germany
关键词
Alzheimer's disease; chromosome; 10; D10S1423; marker; association;
D O I
10.1016/S0304-3940(00)01283-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recently a full genome survey detected an allelic association between Alzheimer's disease (AD) and the D10S1423 marker on chromosome 10p12-14 (40 cM from the telomere). in this study we examined the D10S1423 marker in an ethnically homogeneous German population of 80 AD patients and two groups of controls, 168 healthy subjects and 149 depressed patients. The 234-bp allele of the D10S1423 marker showed a significant association with AD (P = 0.033). In conclusion, our results support that the D10S1423 marker is associated with an increased AD risk and provides further evidence for an AD susceptibility locus on chromosome 10. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:224 / 226
页数:3
相关论文
共 10 条
[1]   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
[2]   A full genome scan for late onset Alzheimer's disease [J].
Kehoe, P ;
Wavrant-De Vrieze, F ;
Crook, R ;
Wu, WS ;
Holmans, P ;
Fenton, I ;
Spurlock, G ;
Norton, N ;
Williams, H ;
Williams, N ;
Lovestone, S ;
Perez-Tur, J ;
Hutton, M ;
Chartier-Harlin, MC ;
Shears, S ;
Roehl, K ;
Booth, J ;
Van Voorst, W ;
Ramic, D ;
Williams, J ;
Goate, A ;
Hardy, J ;
Owen, MJ .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :237-245
[3]   CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS [J].
LEVYLAHAD, E ;
WASCO, W ;
POORKAJ, P ;
ROMANO, DM ;
OSHIMA, J ;
PETTINGELL, WH ;
YU, CE ;
JONDRO, PD ;
SCHMIDT, SD ;
WANG, K ;
CROWLEY, AC ;
FU, YH ;
GUENETTE, SY ;
GALAS, D ;
NEMENS, E ;
WIJSMAN, EM ;
BIRD, TD ;
SCHELLENBERG, GD ;
TANZI, RE .
SCIENCE, 1995, 269 (5226) :973-977
[4]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[5]   Complete genomic screen in late-onset familial Alzheimer's disease [J].
Pericak-Vance, MA ;
Bass, ML ;
Yamaoka, LH ;
Gaskell, PC ;
Scott, WK ;
Terwedow, HA ;
Menold, MM ;
Conneally, PM ;
Small, GW ;
Saunders, AM ;
Roses, AD ;
Haines, JL .
NEUROBIOLOGY OF AGING, 1998, 19 (01) :S39-S42
[6]   APOLIPOPROTEIN-E-EPSILON-4 ALLELE DISTRIBUTIONS IN LATE-ONSET ALZHEIMERS-DISEASE AND IN OTHER AMYLOID-FORMING DISEASES [J].
SAUNDERS, AM ;
SCHMADER, K ;
BREITNER, JCS ;
BENSON, MD ;
BROWN, WT ;
GOLDFARB, L ;
GOLDGABER, D ;
MANWARING, MG ;
SZYMANSKI, MH ;
MCCOWN, N ;
DOLE, KC ;
SCHMECHEL, DE ;
STRITTMATTER, WJ ;
PERICAKVANCE, MA ;
ROSES, AD .
LANCET, 1993, 342 (8873) :710-711
[7]   GENETIC-LINKAGE EVIDENCE FOR A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-14 [J].
SCHELLENBERG, GD ;
BIRD, TD ;
WIJSMAN, EM ;
ORR, HT ;
ANDERSON, L ;
NEMENS, E ;
WHITE, JA ;
BONNYCASTLE, L ;
WEBER, JL ;
ALONSO, ME ;
POTTER, H ;
HESTON, LL ;
MARTIN, GM .
SCIENCE, 1992, 258 (5082) :668-671
[8]   APOLIPOPROTEIN-E - HIGH-AVIDITY BINDING TO BETA-AMYLOID AND INCREASED FREQUENCY OF TYPE-4 ALLELE IN LATE-ONSET FAMILIAL ALZHEIMER-DISEASE [J].
STRITTMATTER, WJ ;
SAUNDERS, AM ;
SCHMECHEL, D ;
PERICAKVANCE, M ;
ENGHILD, J ;
SALVESEN, GS ;
ROSES, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1977-1981
[9]   Clinical and neurobiological correlates of D10S1423 genotype in Alzheimer's disease [J].
Zubenko, GS ;
Hughes, HB ;
Stiffler, JS .
BIOLOGICAL PSYCHIATRY, 1999, 46 (06) :740-749
[10]   A genome survey for novel Alzheimer disease risk loci: Results at 10-cM resolution [J].
Zubenko, GS ;
Hughes, HB ;
Stiffler, JS ;
Hurtt, MR ;
Kaplan, BB .
GENOMICS, 1998, 50 (02) :121-128