Project 7: Determinants of Extreme Longevity in a Plant Species Senescence is defined demographically as an increase in mortality after reproductive maturity. Our current understanding of mortality patterns may be limited by the fact that most studies have been made with short-lived model organisms under laboratory conditions. This project uses a new model system, with a relatively long lifespan and unique trajectories of growth and reproduction with age. At the foundation of this project is a population of 30,000 individuals of Plantago lanceolata, a perennial plant species. Results from an earlier study suggest that continued growth after maturity might allow this species to minimize, or even escape, the aging process. This preliminary project showed that there are many determinants of mortality in this species including extrinsic environmental factors, spatial location, genetics, reproduction, cohort history, and most importantly size of an individual. This new project will expand this analysis to another population and to later years. It will test whether the importance of size, and the minimal importance of age, will continue to the latest ages. Data will be collected to test some of the assumptions in our covariate regression model that we have written to explore age-specific mortality in this species. We also have an established population of P. lanceolata that has been growing for over five years under the controlled conditions of the greenhouse. Few individuals, in the natural environment, live to this late age but under these protected conditions, the majority of the population has survived and is beginning to show an increase in mortality. This protected population offers a unique opportunity to study the mortality dynamics of a species at extremely late ages and it will test the hypothesis that patterns of senescence are only apparent at ages that are much later than individuals would survive in their natural environment.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG008761-19
Application #
7677404
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
19
Fiscal Year
2008
Total Cost
$258,605
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Mengel-From, Jonas; Rønne, Mette E; Carlsen, Anting L et al. (2018) Circulating, Cell-Free Micro-RNA Profiles Reflect Discordant Development of Dementia in Monozygotic Twins. J Alzheimers Dis 63:591-601
Saunders, Gretchen R B; Elkins, Irene J; Christensen, Kaare et al. (2018) The relationship between subjective well-being and mortality within discordant twin pairs from two independent samples. Psychol Aging 33:439-447
Debrabant, Birgit; Soerensen, Mette; Christiansen, Lene et al. (2018) DNA methylation age and perceived age in elderly Danish twins. Mech Ageing Dev 169:40-44
Dato, Serena; Soerensen, Mette; De Rango, Francesco et al. (2018) The genetic component of human longevity: New insights from the analysis of pathway-based SNP-SNP interactions. Aging Cell 17:e12755
Svane, Anne Marie; Soerensen, Mette; Lund, Jesper et al. (2018) DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins. Genes (Basel) 9:
Jensen, Magnus T; Wod, Mette; Galatius, Søren et al. (2018) Heritability of resting heart rate and association with mortality in middle-aged and elderly twins. Heart 104:30-36
Pahlen, Shandell; Hamdi, Nayla R; Dahl Aslan, Anna K et al. (2018) Age-Moderation of Genetic and Environmental Contributions to Cognitive Functioning in Mid- and Late-Life for Specific Cognitive Abilities. Intelligence 68:70-81
Pedersen, Jacob K; Elo, Irma T; Schupf, Nicole et al. (2017) The Survival of Spouses Marrying Into Longevity-Enriched Families. J Gerontol A Biol Sci Med Sci 72:109-114
Flachsbart, Friederike; Dose, Janina; Gentschew, Liljana et al. (2017) Identification and characterization of two functional variants in the human longevity gene FOXO3. Nat Commun 8:2063
Fagan, Erin; Sun, Fangui; Bae, Harold et al. (2017) Telomere length is longer in women with late maternal age. Menopause 24:497-501

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