Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease

被引:23
作者
Lin, P. I.
Martin, E. R.
Bronson, P. G.
Browning-Large, C.
Small, G. W.
Schmechel, D. E.
Welsh-Bohmer, K. A.
Haines, J. L.
Gilbert, J. R.
Pericak-Vance, M. A.
机构
[1] Duke Univ, Med Ctr, Ctr Human Genet, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC 27710 USA
[3] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA
[4] Vanderbilt Univ, Ctr Med, Ctr Human Genet Res, Nashville, TN 37232 USA
关键词
D O I
10.1212/01.wnl.0000223438.90113.4e
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Previous linkage studies have shown that chromosome 12 harbors susceptibility genes for late-onset Alzheimer disease (LOAD). However, association studies of several candidate genes on this chromosome region have produced ambiguous results. A recent study reported the association between the glyceraldehyde-3-phosphate dehydrogenase (GAPD) gene on chromosome 12p and the risk of LOAD. Methods: The authors conducted family-based and case-control association studies in two independent LOAD data sets on 12 single-nucleotide polymorphisms (SNPs) in the GAPD gene and its paralogs. Results: No association was found of the GAPD gene with LOAD in the family-based data set, but marginal evidence of association was seen in the later- onset subgroup when age at onset was stratified. The SNP rs2029721 in one GAPD pseudogene was also found to be associated with risk for LOAD in the unrelated case-control data set (p = 0.003). Conclusions: The GAPD gene and its pseudogene was also found to be associated with risk for LOAD in the unrelated case-control data set (p = 0.003). Conclusions: The GAPD gene and its pseudogene may play a role in the development of late-onset Alzheimer disease. However, the effect, if any, is likely to be limited.
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页码:64 / 68
页数:5
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