Genetic association study on in and around the APOE in late-onset Alzheimer disease in Japanese
The ɛ 4 allele of APOE is a well-characterized genetic risk factor for late-onset Alzheimer disease (LOAD). Nevertheless, using high-density single nucleotide polymorphisms (SNPs), there have only been a few studies involving genetic association and linkage disequilibrium (LD) analyses of in and aro...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2009-05, Vol.93 (5), p.441-448 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The ɛ
4 allele of
APOE is a well-characterized genetic risk factor for late-onset Alzheimer disease (LOAD). Nevertheless, using high-density single nucleotide polymorphisms (SNPs), there have only been a few studies involving genetic association and linkage disequilibrium (LD) analyses of in and around the
APOE. Here, we report fine mapping of a genomic region (about 200 kb) including the
APOE in Japanese using 260 SNPs (mean intermaker distance, 0.77 kb). A case-control study demonstrated that 36 of these SNPs exhibited significance after adjustment for multiple testing. These SNPs are located in a genomic region including four genes,
PVRL2,
TOMM40,
APOE and
APOC1. Recombination rate estimation revealed that the associated region is firmly sandwiched between two recombination hotspots. Strong LD between these SNPs was observed (mean |
D′|
=
0.914). These data suggest that the three genes other than
APOE, i.e.
PVRL2,
TOMM40 and
APOC1, could also yield a predisposition to LOAD. |
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ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1016/j.ygeno.2009.01.003 |