Genes, environment, and chance determine the course of human aging. This project focuses on the genetic contributions to longevity and healthy aging. Longevity is the phenotype we will use in this analysis, but it will be combined with functional outcome measures, to address hypotheses relating to the role of metabolism in aging. Associative genetics is the initial tool we will use. It will be applied to candidate genes that have been validated in model organisms as longevity genes, starting with HRAS1, LASS1, IGFIR, PPARG, and PRKAA2, followed by others. Genes such as APOE and LEPR are of particular interest in other projects of this Program Project, and they will be studied as well. All of the genes are involved in metabolism and stress resistance. Partial genomic scans will also be applied in this analysis, in particular in regions of the genome that are syntenic to mouse genome regions implicated in robust immune function coupled to longevity. The analysis will begin with an assessment of the genetic structure of our population in the genomic regions of interest, followed by a comparison of the level of variation in nonagenarians and younger controls. Next, we will test the detected variation in other populations, both non-preselected for age and age-selected (i.e. replication in other Iongevous cohorts). We will also apply a panel of ethnic affiliation markers to control for the confounding effects of population admixture. This analysis, in conjunction with the tests in other populations, may suggest the existence of Iongevous haplotypes in our population. This possibility will be explored further by searching for such haplotypes. Finally, we will examine the functional significance of any allelic variants detected at higher frequency in nonagenarians. This will be done by studying the effects on life span of homologous mutations using the yeast model system. It will also involve assays of antigen-induced T-cell death and transient transfection assays of transcription activity. The inclusion of this genetic study in the context of this Program Project with its focus on metabolism and functional outcome measures will help elucidate the attributes of healthy aging, and it provides the perspective of improvement of the quality of life in old age.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
1P01AG022064-01A1
Application #
6775162
Study Section
Special Emphasis Panel (ZAG1-ZIJ-8 (J3))
Project Start
2004-04-01
Project End
2009-03-31
Budget Start
2004-04-01
Budget End
2005-06-30
Support Year
1
Fiscal Year
2004
Total Cost
$170,924
Indirect Cost
Name
Louisiana State University Hsc New Orleans
Department
Type
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Jazwinski, S Michal; Jiang, James C; Kim, Sangkyu (2018) Adaptation to metabolic dysfunction during aging: Making the best of a bad situation. Exp Gerontol 107:87-90
Kim, Sangkyu; Jazwinski, S Michal (2018) The Gut Microbiota and Healthy Aging: A Mini-Review. Gerontology 64:513-520
Maffei, Vincent J; Kim, Sangkyu; Blanchard 4th, Eugene et al. (2017) Biological Aging and the Human Gut Microbiota. J Gerontol A Biol Sci Med Sci 72:1474-1482
Kim, Sangkyu; Myers, Leann; Wyckoff, Jennifer et al. (2017) The frailty index outperforms DNA methylation age and its derivatives as an indicator of biological age. Geroscience 39:83-92
Cherry, Katie E; Brown, Jennifer Silva; Kim, Sangkyu et al. (2016) Social Factors and Healthy Aging: Findings from the Louisiana Healthy Aging Study (LHAS). Kinesiol Rev (Champaign) 5:50-56
Kim, Sangkyu; Myers, Leann; Ravussin, Eric et al. (2016) Single nucleotide polymorphisms linked to mitochondrial uncoupling protein genes UCP2 and UCP3 affect mitochondrial metabolism and healthy aging in female nonagenarians. Biogerontology 17:725-36
Kim, Sangkyu; Simon, Eric; Myers, Leann et al. (2016) Programmed Cell Death Genes Are Linked to Elevated Creatine Kinase Levels in Unhealthy Male Nonagenarians. Gerontology 62:519-29
Kim, Sangkyu; Welsh, David A; Myers, Leann et al. (2015) Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival. Oncotarget 6:3600-12
Stanko, Katie E; Cherry, Katie E; Ryker, Kyle S et al. (2015) Looking for the Silver Lining: Benefit Finding after Hurricanes Katrina and Rita in Middle-Aged, Older, and Oldest-Old Adults. Curr Psychol 34:564-575
Kim, Sangkyu; Jazwinski, S Michal (2015) Quantitative measures of healthy aging and biological age. Healthy Aging Res 4:

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