Tenomodulin variants, APOE and Alzheimer's disease in a Finnish case-control cohort

3Citations
Citations of this article
30Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The tenomodulin gene (TNMD, locus Xq-22) encodes an angiogenesis inhibitor. It is an interesting candidate gene for Alzheimer's disease (AD), since it is expressed in brain, alterations in angiogenesis have been linked to AD and in our previous studies we have observed associations between TNMD and phenotypes, which are related to increased risk of AD. The common sequence variation in the TNMD was not associated with prevalence of AD among 526 cases and 672 controls. However, a significant interaction (p= 0.002) between rs5966709 and the APOE ε4-allele status was observed in women. Among the ε4-allele carriers, the women with rs5966709-TT genotype had smaller risk for having AD than those with other genotypes (odds ratio 0.47, p= 0.019, false discovery rate 10.4%). According to these results the sequence variation of TNMD is not associated with AD, but might modify the effect of APOE ε4-allele in women. © 2009 Elsevier Inc.

Cite

CITATION STYLE

APA

Tolppanen, A. M., Helisalmi, S., Hiltunen, M., Kolehmainen, M., Schwab, U., Pirttilä, T., … Soininen, H. (2011). Tenomodulin variants, APOE and Alzheimer’s disease in a Finnish case-control cohort. Neurobiology of Aging, 32(3), 546.e7-546.e9. https://doi.org/10.1016/j.neurobiolaging.2009.05.010

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free