Is there a common pattern in the age-trajectory of mortality in developed countries at oldest-old ages? Does this pattern, albeit with different parameter values, hold for Medflies, Mexflies, West Indian fruitflies, and Drosophila? Do age trajectories of mortality for males vs. females converge or crossover? How much progress has been made in recent decades in reducing mortality after age 80? This research project is designed to address these questions through theory-based modeling and statistical analysis of data sets that will be rigorously checked for reliability and achieved and published in full to aid future researchers. Specifically, in the proposed research we will: (1) Extend, correct, archive, and publish in full (with public use files) a data set on sex-specific death counts, population counts, and death rates after age 50 and up to the highest ages attained by single year of age, by single year of time for several decades, and when possible, by year of birth, in at least 28 developed countries including the United States. (2) Apply various methods of checking data for reliability, including some innovative Lexis-map methods to these data sets. (3) Refine extinct-cohort methods so that mortality rates can be estimated for not-yet-extinct cohorts based only on death count data. (4) Analyze these data to determine trajectories of mortality over age and time, between sexes, and across countries, with a focus on mortality after age 80 and with emphasis on finding unifying, underlying patterns that aid understanding of the mechanisms of aging and death. (5) Analyze data on Medflies, Mexflies, and West Indian fruitflies with similar questions in mind. (6) Analyze data on Drosophila classified by genotype and by chromosomal markers to determine mortality trajectories for genotypes and for genes (i.e., for populations that share similar chromosomal regions), again with questions in mind similar to those in aim 4, and with the goal of determining whether """"""""inclusive"""""""" mortality models can be developed that hold across populations, species, and genotypes.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG008761-06
Application #
3726472
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
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

Showing the most recent 10 out of 445 publications