The broad scope of this P01 is to test the hypothesis that human genotype influences energy metabolism, and as a consequence contributes to healthy aging. The objective of this project is to test the hypothesis that indicators of vascular status (e.g., brachial artery vasoreactivity and carotid intimal thickness) are associated with measures of physical function. This project of the P01 contributes to the overall scope of the program by exploring the biological plausibility that metabolism and oxidative stress exert an influence on function and consequently healthy aging via cardiovascular impairment. Therefore, this project specifically seeks funding for the inclusion of ultrasonographic imaging of carotid and brachial arteries. The investigators presently have funding for the assessment of physical function using the Continuous Scale-Physical Function Performance Task (CS-PFP), as well as handgrip strength, tapping speed, and ADL inventories. However, the investigators seek funding to enhance the information acquired during the functional assessment by collecting breath gas measures during the CS-PFP. This will allow the investigators to derive the oxygen uptake efficiency slope (DUES), which will serve as an index of cardiorespiratory capacity. Finally, the investigators propose to include a pilot exercise-training study to test the hypothesis that changes in vascular status will result in changes in physical function. While this project has important project specific hypotheses, the inclusion of measures of vascular and physical function will also provide numerous opportunities for synergy with the other projects, as described herein.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
1P01AG022064-01A1
Application #
6775171
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
2009-03-31
Support Year
1
Fiscal Year
2004
Total Cost
$150,248
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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