application): The primary objective of this proposal is to identify and investigate genes that impact extreme longevity in human populations. The Iong-term goal is to maximize the potential for robust late-life health. The proposal is to conduct a candidate gene-association study based on cenenarians and octogenarians from China and Denmark. The first specific aim defines criteria for identifying candidate genes from categories of genes that are likely to have an effect on extreme longevity. The second specific aim describes the use of single strand conformation polymorphism methods to scan candidate genes for allelic variants. Aliele frequency differentials will be determined from analysis of Chinese and Danish centenarians and octogenarians. Candidate genes will be compared with respect to the magnitude of altele frequency differentials to decide which genes will beselected for DNA sequencing. The third specific aim focuses on sequencing regions of select candidate genes and analyzing these sequences to estimate haplotypes and evaluate the evolutionary history of genes. Sequencing is required to design genotype assays and sequence analysis is important for efficient logic-driven choices about which genotyinvestigatorng assays to conduct. The fourth specific aim describes the utility of an ELISA- oligonucleotide ligation assay to genotype thousands of very elderly individuals. This is one of the new generation of methods for genotyinvestigatorng single nucleotide substitutions and unique insertions/deletions. This assay is robust, cost efficient and high throughput which makes it ideal to genotype large numbers of Danes and Chinese, The sequential design of the specific aims and large sample sizes contribute to the rigor of this association study. The centenarian candidate gene study will be conducted in a collaborative matrix that includes demographic studies on Hart Chinese and Danes, as well as an analytical methods component of the larger program project.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
3P01AG008761-13S4
Application #
6594735
Study Section
Project Start
2002-06-01
Project End
2002-12-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
13
Fiscal Year
2002
Total Cost
$178,517
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

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