Longevity defined as top 10% survivors and beyond is transmitted as a quantitative genetic trait

作者: Niels van den Berg , Mar Rodríguez-Girondo , Ingrid K. van Dijk , Rick J. Mourits , Kees Mandemakers

DOI: 10.1038/S41467-018-07925-0

关键词:

摘要: Survival to extreme ages clusters within families. However, identifying genetic loci conferring longevity and low morbidity in such longevous families is challenging. There debate concerning the survival percentile that best isolates component longevity. Here, we use three-generational mortality data from two large datasets, UPDB (US) LINKS (Netherlands). We study 20,360 unselected containing index persons, their parents, siblings, spouses, children, comprising 314,819 individuals. Our analyses provide strong evidence transmitted as a quantitative trait among survivors up top 10% of birth cohort. subsequently show advantage, mounting 31%, for individuals with surviving first second-degree relatives both databases across generations, even presence non-longevous parents. To guide future studies, suggest base case selection on cohort equally long-lived family members.

参考文章(63)
Semyonova Vg, Evdokushkina Gn, Gavrilova Ns, Evdokushkina Nn, Gavrilov La, Kushnareva Ye, Kroutko Vn, Gavrilova Al, Andreyev AYu, Evolution, mutations, and human longevity: European royal and noble families. Human Biology. ,vol. 70, pp. 799- 804 ,(1998)
Jennifer A. Deluty, Gil Atzmon, Jill Crandall, Nir Barzilai, Sofiya Milman, The influence of gender on inheritance of exceptional longevity Aging (Albany NY). ,vol. 7, pp. 412- 418 ,(2015) , 10.18632/AGING.100763
Carolien A. Wijsman, Maarten P. Rozing, Trea C. M. Streefland, Saskia le Cessie, Simon P. Mooijaart, P. Eline Slagboom, Rudi G. J. Westendorp, Hanno Pijl, Diana van Heemst, , Familial longevity is marked by enhanced insulin sensitivity Aging Cell. ,vol. 10, pp. 114- 121 ,(2011) , 10.1111/J.1474-9726.2010.00650.X
Leonid A. Gavrilov, Natalia S. Gavrilova, Predictors of Exceptional Longevity: Effects of Early-Life and Midlife Conditions, and Familial Longevity The North American Actuarial Journal. ,vol. 19, pp. 174- 186 ,(2015) , 10.1080/10920277.2015.1018390
Friederike Flachsbart, Amke Caliebe, Rabea Kleindorp, Hélène Blanché, Huberta von Eller-Eberstein, Susanna Nikolaus, Stefan Schreiber, Almut Nebel, Association of FOXO3A variation with human longevity confirmed in German centenarians Proceedings of the National Academy of Sciences of the United States of America. ,vol. 106, pp. 2700- 2705 ,(2009) , 10.1073/PNAS.0809594106
T. T. Perls, J. Wilmoth, R. Levenson, M. Drinkwater, M. Cohen, H. Bogan, E. Joyce, S. Brewster, L. Kunkel, A. Puca, Life-long sustained mortality advantage of siblings of centenarians Proceedings of the National Academy of Sciences of the United States of America. ,vol. 99, pp. 8442- 8447 ,(2002) , 10.1073/PNAS.122587599
Ariane Kemkes-Grottenthaler, Parental effects on offspring longevity—evidence from 17th to 19th century reproductive histories Annals of Human Biology. ,vol. 31, pp. 139- 158 ,(2004) , 10.1080/03014460410001663407
B. J. Willcox, T. A. Donlon, Q. He, R. Chen, J. S. Grove, K. Yano, K. H. Masaki, D. C. Willcox, B. Rodriguez, J. D. Curb, FOXO3A genotype is strongly associated with human longevity Proceedings of the National Academy of Sciences of the United States of America. ,vol. 105, pp. 13987- 13992 ,(2008) , 10.1073/PNAS.0801030105
Rune Lindahl-Jacobsen, Heidi A. Hanson, Anna Oksuzyan, Geraldine P. Mineau, Kaare Christensen, Ken R. Smith, The male–female health-survival paradox and sex differences in cohort life expectancy in Utah, Denmark, and Sweden 1850–1910 Annals of Epidemiology. ,vol. 23, pp. 161- 166 ,(2013) , 10.1016/J.ANNEPIDEM.2013.02.001
Hjalti Gudmundsson, Daniel F Gudbjartsson, Augustine Kong, Hákon Gudbjartsson, Mike Frigge, Jeffrey R Gulcher, Kári Stefánsson, Inheritance of human longevity in Iceland. European Journal of Human Genetics. ,vol. 8, pp. 743- 749 ,(2000) , 10.1038/SJ.EJHG.5200527