Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/36843
Title: Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Authors: Deelen, J.
Beekman, M.
Uh, H. W.
Broer, L.
Ayers, K. L.
Tan, Q.
Kamatani, Y.
Bennet, A. M.
Tamm, R.
Trompet, S.
Guðbjartsson, D. F.
Flachsbart, F.
Rose, G.
Viktorin, A.
Fischer, K.
Nygaard, M.
Cordell, H. J.
Crocco, P.
van den Akker, E. B.
Böhringer, S.
Helmer, Q.
Nelson, Christopher Paul
Saunders, G. I.
Alver, M.
Andersen-Ranberg, K.
Breen, M. E.
van der Breggen, R.
Caliebe, A.
Capri, M.
Cevenini, E.
Collerton, J. C.
Dato, S.
Davies, K.
Ford, I.
Gampe, J.
Garagnani, P.
de Geus, E. J.
Harrow, J.
van Heemst, D.
Heijmans, B. T.
Heinsen, F. A.
Hottenga, J. J.
Hofman, A.
Jeune, B.
Jonsson, P. V.
Lathrop, M.
Lechner, D.
Martin-Ruiz, C.
Mcnerlan, S. E.
Mihailov, E.
Montesanto, A.
Mooijaart, S. P.
Murphy, A.
Nohr, E. A.
Paternoster, L.
Postmus, I.
Rivadeneira, F.
Ross, O. A.
Salvioli, S.
Sattar, N.
Schreiber, S.
Stefánsson, H.
Stott, D. J.
Tiemeier, H.
Uitterlinden, A. G.
Westendorp, R. G.
Willemsen, G.
Samani, Nilesh J.
Galan, P.
Sørensen, T. I.
Boomsma, D. I.
Jukema, J. W.
Rea, I. M.
Passarino, G.
de Craen, A. J.
Christensen, K.
Nebel, A.
Stefánsson, K.
Metspalu, A.
Magnusson, P.
Blanché, H.
Christiansen, L.
Kirkwood, T. B.
van Duijn, C. M.
Franceschi, C.
Houwing-Duistermaat, J. J.
Slagboom, P. E.
First Published: 31-Mar-2014
Publisher: Oxford University Press (OUP)
Citation: Human Molecular Genetics, 2014, 23 (16), pp. 4420-4432
Abstract: The genetic contribution to the variation in human lifespan is ∼ 25%. Despite the large number of identified disease-susceptibility loci, it is not known which loci influence population mortality. We performed a genome-wide association meta-analysis of 7729 long-lived individuals of European descent (≥ 85 years) and 16 121 younger controls (<65 years) followed by replication in an additional set of 13 060 long-lived individuals and 61 156 controls. In addition, we performed a subset analysis in cases aged ≥ 90 years. We observed genome-wide significant association with longevity, as reflected by survival to ages beyond 90 years, at a novel locus, rs2149954, on chromosome 5q33.3 (OR = 1.10, P = 1.74 × 10(-8)). We also confirmed association of rs4420638 on chromosome 19q13.32 (OR = 0.72, P = 3.40 × 10(-36)), representing the TOMM40/APOE/APOC1 locus. In a prospective meta-analysis (n = 34 103), the minor allele of rs2149954 (T) on chromosome 5q33.3 associates with increased survival (HR = 0.95, P = 0.003). This allele has previously been reported to associate with low blood pressure in middle age. Interestingly, the minor allele (T) associates with decreased cardiovascular mortality risk, independent of blood pressure. We report on the first GWAS-identified longevity locus on chromosome 5q33.3 influencing survival in the general European population. The minor allele of this locus associates with low blood pressure in middle age, although the contribution of this allele to survival may be less dependent on blood pressure. Hence, the pleiotropic mechanisms by which this intragenic variation contributes to lifespan regulation have to be elucidated.
DOI Link: 10.1093/hmg/ddu139
eISSN: 1460-2083
Links: http://hmg.oxfordjournals.org/content/23/16/4420
http://hdl.handle.net/2381/36843
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © The Author 2014. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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