CYP19 haplotypes increase risk for Alzheimer's disease

被引:45
作者
Huang, R.
Poduslo, S. E.
机构
[1] Med Coll Georgia, IMMAG, Augusta, GA 30912 USA
[2] VA Med Ctr, Dept Neurol, Inst Mol Med, Augusta, GA USA
关键词
D O I
10.1136/jmg.2005.039461
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cytochrome P450 aromatase, an enzyme that catalyses the conversion of androgens to oestrogen, is expressed at high levels in the gonads and in the brain. Aromatase activity is increased in the nucleus basalis of Meynert during aging and in Alzheimer's disease ( AD), making the gene (CYP19), at 15q21.1, a potential candidate risk factor. We examined 18 single nucleotide polymorphisms spanning the 59-untranslated region and the entire coding region of CYP19 in 227 patients with AD and 131 control spouses. We found that the gene region could be divided into two haplotype blocks; a haplotype in block 1 and a haplotype in block 2 increased the risk of developing the disease by twofold in APOE 4 carriers. The implication of two haplotypes conferring increased risk for AD warrants further investigation of the regulation of aromatase activity in brain.
引用
收藏
页数:6
相关论文
共 10 条
  • [1] The human CYP19 (aromatase P450) gene:: update on physiologic roles and genomic organization of promoters
    Bulun, SE
    Sebastian, S
    Takayama, K
    Suzuki, T
    Sasano, H
    Shozu, M
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 86 (3-5) : 219 - 224
  • [2] Mapping complex disease loci in whole-genome association studies
    Carlson, CS
    Eberle, MA
    Kruglyak, L
    Nickerson, DA
    [J]. NATURE, 2004, 429 (6990) : 446 - 452
  • [3] The structure of haplotype blocks in the human genome
    Gabriel, SB
    Schaffner, SF
    Nguyen, H
    Moore, JM
    Roy, J
    Blumenstiel, B
    Higgins, J
    DeFelice, M
    Lochner, A
    Faggart, M
    Liu-Cordero, SN
    Rotimi, C
    Adeyemo, A
    Cooper, R
    Ward, R
    Lander, ES
    Daly, MJ
    Altshuler, D
    [J]. SCIENCE, 2002, 296 (5576) : 2225 - 2229
  • [4] Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland
    Hiltunen, M
    Mannermaa, A
    Thompson, D
    Easton, D
    Pirskanen, M
    Helisalmi, S
    Koivisto, AM
    Lehtovirta, M
    Ryynänen, M
    Soininen, H
    [J]. NEUROLOGY, 2001, 57 (09) : 1663 - 1668
  • [5] NOVEL EXON-1 OF THE AROMATASE GENE-SPECIFIC FOR AROMATASE TRANSCRIPTS IN HUMAN BRAIN
    HONDA, S
    HARADA, N
    TAKAGI, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 198 (03) : 1153 - 1160
  • [6] Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease
    Iivonen, S
    Corder, E
    Lehtovirta, M
    Helisalmi, S
    Mannermaa, A
    Vepsäläinen, S
    Hänninen, T
    Soininen, H
    Hiltunen, M
    [J]. NEUROLOGY, 2004, 62 (07) : 1170 - 1176
  • [7] Diminished aromatase immunoreactivity in the hypothalamus, but not in the basal forebrain nuclei in Alzheimer's disease
    Ishunina, TA
    van Beurden, D
    van der Meulen, G
    Unmehopa, UA
    Hol, EM
    Huitinga, I
    Swaab, DF
    [J]. NEUROBIOLOGY OF AGING, 2005, 26 (02) : 173 - 194
  • [8] Multiplex automated primer extension analysis: Simultaneous genotyping of several polymorphisms
    Makridakis, NM
    Reichardt, JKV
    [J]. BIOTECHNIQUES, 2001, 31 (06) : 1374 - 1380
  • [9] MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
  • [10] The apolipoprotein CI A allele as a risk factor for Alzheimer's disease
    Poduslo, SE
    Neal, M
    Herring, K
    Shelly, J
    [J]. NEUROCHEMICAL RESEARCH, 1998, 23 (03) : 361 - 367