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  Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited

Deelen, J., Beekman, M., Uh, H. W., Helmer, Q., Kuningas, M., Christiansen, L., et al. (2011). Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. Aging Cell, 10(4), 686-98. doi:10.1111/j.1474-9726.2011.00705.x.

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Deelen, J.1, Author           
Beekman, M., Author
Uh, H. W., Author
Helmer, Q., Author
Kuningas, M., Author
Christiansen, L., Author
Kremer, D., Author
van der Breggen, R., Author
Suchiman, H. E., Author
Lakenberg, N., Author
van den Akker, E. B., Author
Passtoors, W. M., Author
Tiemeier, H., Author
van Heemst, D., Author
de Craen, A. J., Author
Rivadeneira, F., Author
de Geus, E. J., Author
Perola, M., Author
van der Ouderaa, F. J., Author
Gunn, D. A., Author
Boomsma, D. I., AuthorUitterlinden, A. G., AuthorChristensen, K., Authorvan Duijn, C. M., AuthorHeijmans, B. T., AuthorHouwing-Duistermaat, J. J., AuthorWestendorp, R. G., AuthorSlagboom, P. E., Author            more..
Affiliations:
1Deelen – Genetics and Biomarkers of Human Ageing, Research Groups, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394006              

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Free keywords: Adult Aged Aged, 80 and over Alzheimer Disease/genetics Apolipoproteins E/*genetics Case-Control Studies Cohort Studies Female Forkhead Box Protein O3 Forkhead Transcription Factors/genetics Genetic Loci Genetic Predisposition to Disease *Genome, Human Genome-Wide Association Study Humans Linkage Disequilibrium Longevity/*genetics Longitudinal Studies Male Middle Aged Polymorphism, Single Nucleotide Proto-Oncogene Proteins c-akt/genetics
 Abstract: By studying the loci that contribute to human longevity, we aim to identify mechanisms that contribute to healthy aging. To identify such loci, we performed a genome-wide association study (GWAS) comparing 403 unrelated nonagenarians from long-living families included in the Leiden Longevity Study (LLS) and 1670 younger population controls. The strongest candidate SNPs from this GWAS have been analyzed in a meta-analysis of nonagenarian cases from the Rotterdam Study, Leiden 85-plus study, and Danish 1905 cohort. Only one of the 62 prioritized SNPs from the GWAS analysis (P<1x10(-4) ) showed genome-wide significance with survival into old age in the meta-analysis of 4149 nonagenarian cases and 7582 younger controls [OR=0.71 (95% CI 0.65-0.77), P=3.39 x 10(-17) ]. This SNP, rs2075650, is located in TOMM40 at chromosome 19q13.32 close to the apolipoprotein E (APOE) gene. Although there was only moderate linkage disequilibrium between rs2075650 and the ApoE epsilon4 defining SNP rs429358, we could not find an APOE-independent effect of rs2075650 on longevity, either in cross-sectional or in longitudinal analyses. As expected, rs429358 associated with metabolic phenotypes in the offspring of the nonagenarian cases from the LLS and their partners. In addition, we observed a novel association between this locus and serum levels of IGF-1 in women (P=0.005). In conclusion, the major locus determining familial longevity up to high age as detected by GWAS was marked by rs2075650, which tags the deleterious effects of the ApoE epsilon4 allele. No other major longevity locus was found.

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 Dates: 2011-082011-03-23
 Publication Status: Issued
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 Identifiers: Other: 21418511
DOI: 10.1111/j.1474-9726.2011.00705.x
ISSN: 1474-9726 (Electronic)1474-9718 (Linking)
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Title: Aging Cell
Source Genre: Journal
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Pages: - Volume / Issue: 10 (4) Sequence Number: - Start / End Page: 686 - 98 Identifier: -