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Codd, V.* ; Nelson, C.P.* ; Albrecht, E. ; Mangino, M.* ; Deelen, J.* ; Buxton, J.L.* ; Hottenga, J.J.* ; Fischer, K.* ; Esko, T.* ; Surakka, I.* ; Broer, L.* ; Nyholt, D.R.* ; Mateo Leach, I.* ; Salo, P.* ; Hägg, S.* ; Matthews, M.K.* ; Palmen, J.* ; Norata, G.D.* ; O'Reilly, P.F.* ; Saleheen, D.* ; Amin, N.* ; Balmforth, A.J.* ; Beekman, M.* ; de Boer, R.A.* ; Böhringer, S.* ; Braund, P.S.* ; Burton, P.R* ; Craen, A.J.* ; Denniff, M.* ; Dong, Y.* ; Douroudis, K.* ; Dubinina, E.* ; Eriksson, J.G.* ; Garlaschelli, K.* ; Guo, D.* ; Hartikainen, A.L.* ; Henders, A.K.* ; Houwing-Duistermaat, J.J.* ; Kananen, L.* ; Karssen, L.C.* ; Kettunen, J.* ; Klopp, N. ; Lagou, V.* ; van Leeuwen, E.M.* ; Madden, P.A.* ; Mägi, R.* ; Magnusson, P.K.* ; Männistö, S.* ; McCarthy, M.I.* ; Medland, S.E.* ; Mihailov, E.* ; Montgomery, G.W.* ; Oostra, B.A.* ; Palotie, A.* ; Peters, A. ; Pollard, H.* ; Pouta, A.* ; Prokopenko, I.* ; Ripatti, S.* ; Salomaa, V.* ; Suchiman, H.E.* ; Valdes, A.M.* ; Verweij, N.* ; Viñuela, A.* ; Wang, X.* ; Wichmann, H.-E. ; Widen, E.* ; Willemsen, G.* ; Wright, M.J.* ; Xia, K.* ; Xiao, X.* ; van Veldhuisen, D.J.* ; Catapano, A.L.* ; Tobin, M.D.* ; Hall, A.S.* ; Blakemore, A.I.* ; van Gilst, W.H.* ; Zhu, H.* ; CARDIoGRAM Consortium (Peters, A. ; Wichmann, H.-E. ; Döring, A. ; Meitinger, T. ; Illig, T. ; Klopp, N. ; Meisinger, C.) ; Erdmann, J.* ; Reilly, M.P.* ; Kathiresan, S.* ; Schunkert, H.* ; Talmud, P.J.* ; Pedersen, N.L.* ; Perola, M.* ; Ouwehand, W.* ; Kaprio, J.* ; Martin, N.G.* ; van Duijn, C.M.* ; Hovatta, I.* ; Gieger, C. ; Metspalu, A.* ; Boomsma, D.I.* ; Jarvelin, M.R.* ; Slagboom, P.E.* ; Thompson, J.R.* ; Spector, T.D.* ; van der Harst, P.* ; Samani, N.J.*

Identification of seven loci affecting mean telomere length and their association with disease.

Nat. Genet. 45, 422-427 (2013)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Interindividual variation in mean leukocyte telomere length (LTL) is associated with cancer and several age-associated diseases. We report here a genome-wide meta-analysis of 37,684 individuals with replication of selected variants in an additional 10,739 individuals. We identified seven loci, including five new loci, associated with mean LTL (P < 5 × 10(-8)). Five of the loci contain candidate genes (TERC, TERT, NAF1, OBFC1 and RTEL1) that are known to be involved in telomere biology. Lead SNPs at two loci (TERC and TERT) associate with several cancers and other diseases, including idiopathic pulmonary fibrosis. Moreover, a genetic risk score analysis combining lead variants at all 7 loci in 22,233 coronary artery disease cases and 64,762 controls showed an association of the alleles associated with shorter LTL with increased risk of coronary artery disease (21% (95% confidence interval, 5-35%) per standard deviation in LTL, P = 0.014). Our findings support a causal role of telomere-length variation in some age-related diseases.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Coronary-artery-disease ; Cardiovascular-disease ; Risk ; Cancer ; Atherosclerosis ; Susceptibility ; Fibroblasts ; Dysfunction ; Variants ; Stress
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 45, Heft: 4, Seiten: 422-427 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology II (EPI2)
Research Unit Molecular Epidemiology (AME)
Institute of Epidemiology (EPI)