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Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

Authors :
Sarah Cubaynes
Joanne M. Murabito
Eric S. Orwoll
Iris E. Jansen
Joanna Collerton
Vilmundur Gudnason
Mikko Hurme
Paola Sebastiani
Carol Jagger
Carmen Martin-Ruiz
Douglas P. Kiel
Henne Holstege
Kenny Ye
Pilar Galan
Wolfgang Lieb
Diana van Heemst
Janina Dose
Wanlin Zheng
Ilkka Seppälä
Ashley van der Spek
Jessica D. Faul
Nir Barzilai
David R. Weir
James W. Vaupel
Wiesje M. van der Flier
Dan E. Arking
Terho Lehtimäki
Marja Jylhä
Thomas B. L. Kirkwood
Andrew Kingston
Marcel J. T. Reinders
Jean-François Deleuze
Cornelia M. van Duijn
Hélène Blanché
Anne B. Newman
Chao Nie
Elizabeth J. Becker
Daniel S. Evans
P. Eline Slagboom
Marianne Nygaard
Lene Christiansen
Jean Marie Robine
Junxia Min
Almut Nebel
Tamara B. Harris
Lenore J. Launer
Mary K. Wojczynski
Ellen A. Nohr
Alice M. Arnold
Olli T. Raitakari
Birgit Debrabant
Jerome I. Rotter
Thorkild I. A. Sørensen
André G. Uitterlinden
Steven R. Cummings
Kristin L. Ayers
Jennifer A. Smith
Joris Deelen
Yi Zeng
Chloé Sarnowski
Heather J. Cordell
Karen Davies
Kent D. Taylor
Mika Kähönen
Albert V. Smith
Najaf Amin
Rachel Duncan
Michael A. Province
Leo-Pekka Lyytikäinen
Kathryn L. Lunetta
Kaare Christensen
Sharon L.R. Kardia
Thomas T. Perls
Erin B. Ware
Martijn Huisman
Mary L. Biggs
Marian Beekman
Sven J. van der Lee
David Karasik
Niccolò Tesi
Xiaomin Liu
Gil Atzmon
Claudio Franceschi
Bruce M. Psaty
Source :
Nature Communications, Nature Communications, Vol 12, Iss 1, Pp 1-1 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group UK, 2021.

Abstract

Human longevity is heritable, but genome-wide association (GWA) studies have had limited success. Here, we perform two meta-analyses of GWA studies of a rigorous longevity phenotype definition including 11,262/3484 cases surviving at or beyond the age corresponding to the 90th/99th survival percentile, respectively, and 25,483 controls whose age at death or at last contact was at or below the age corresponding to the 60th survival percentile. Consistent with previous reports, rs429358 (apolipoprotein E (ApoE) ε4) is associated with lower odds of surviving to the 90th and 99th percentile age, while rs7412 (ApoE ε2) shows the opposite. Moreover, rs7676745, located near GPR78, associates with lower odds of surviving to the 90th percentile age. Gene-level association analysis reveals a role for tissue-specific expression of multiple genes in longevity. Finally, genetic correlation of the longevity GWA results with that of several disease-related phenotypes points to a shared genetic architecture between health and longevity.

Details

Language :
English
ISSN :
20411723
Volume :
12
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....103364f77ece1c12b726d16f73c47fd8