Disability threatens the independence of many older adults and results in substantial late-life health care needs and associated expenditures. Sarcopenia, defined as loss of muscle mass and strength, plays a central role in disability. Our long-term goals are to gain insight into the processes that underlie the development of sarcopenia and disability and to identify possible strategies for interventions that reduce the ris of sarcopenia and disability. In the first two cycles of this R01, we examined the hypothesis that oxidative stress contributes to loss of muscle strength, decline in physical performance, disability, and mortality in older adults, and our findings support this paradigm. We also showed that advanced glycation end products (AGEs) and receptor for AGEs (RAGE) were independently associated with poor muscle strength, disability, and mortality. In the third cycle, we propose to examine the relationship between the """"""""anti-aging"""""""" hormone klotho and sarcopenia in older adults. Klotho is a recently discovered hormone that plays a role in suppressing oxidative stress and is implicated in the pathogenesis of sarcopenia. We hypothesize that adults with low serum klotho levels have (1) lower skeletal muscle mass and strength and slower walking speed, and (2) greater decline of skeletal muscle mass and strength and walking speed, and (3) higher risk of mobility limitation, disability, and death. To address these hypotheses, we will study the relationship between serum klotho concentrations and the above outcomes in 2734 adults in the Health, Aging, and Body Composition (Health ABC) Study, a community-based prospective study of aging. We will measure serum klotho at baseline and examine the relationship between serum klotho and skeletal muscle mass, muscle strength, walking speed, mobility limitation, disability, and mortality over follow-up. Our propose studies will expand the knowledge of klotho into a novel area of investigation that focuses on sarcopenia and aging in community-dwelling adults.

Public Health Relevance

This project is relevant to public health as it aims to characterize the relationship between klotho, a recently discovered hormone, with decline of muscle mass, muscle strength, physical performance, disability, and mortality in older US adults.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
2R01AG027012-07
Application #
8293786
Study Section
Special Emphasis Panel (ZRG1-PSE-K (04))
Program Officer
Dutta, Chhanda
Project Start
2005-09-30
Project End
2015-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
7
Fiscal Year
2012
Total Cost
$232,470
Indirect Cost
$88,970
Name
Johns Hopkins University
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Tanaka, Toshiko; Biancotto, Angelique; Moaddel, Ruin et al. (2018) Plasma proteomic signature of age in healthy humans. Aging Cell 17:e12799
Ahmad, Meleha T; Zhang, Pingbo; Dufresne, Craig et al. (2018) The Human Eye Proteome Project: Updates on an Emerging Proteome. Proteomics 18:e1700394
Semba, Richard D; Gonzalez-Freire, Marta; Moaddel, Ruin et al. (2018) Altered Plasma Amino Acids and Lipids Associated With Abnormal Glucose Metabolism and Insulin Resistance in Older Adults. J Clin Endocrinol Metab 103:3331-3339
Buta, Brian; Choudhury, Parichoy Pal; Xue, Qian-Li et al. (2017) The Association of Vitamin D Deficiency and Incident Frailty in Older Women: The Role of Cardiometabolic Diseases. J Am Geriatr Soc 65:619-624
Drew, David A; Katz, Ronit; Kritchevsky, Stephen et al. (2017) Association between Soluble Klotho and Change in Kidney Function: The Health Aging and Body Composition Study. J Am Soc Nephrol 28:1859-1866
Semba, Richard D; Zhang, Pingbo; Zhu, Min et al. (2017) A targeted proteomic assay for the measurement of plasma proteoforms related to human aging phenotypes. Proteomics 17:
Zhang, Pingbo; Zhu, Min; Zhao, Yuming et al. (2017) A proteomic approach to understanding the pathogenesis of idiopathic macular hole formation. Clin Proteomics 14:37
Semba, Richard D; Trehan, Indi; Li, Ximin et al. (2017) Environmental Enteric Dysfunction is Associated with Carnitine Deficiency and Altered Fatty Acid Oxidation. EBioMedicine 17:57-66
Zhu, Min; Zhang, Pingbo; Geng-Spyropoulos, Minghui et al. (2017) A robotic protocol for high-throughput processing of samples for selected reaction monitoring assays. Proteomics 17:
Semba, Richard D; Gonzalez-Freire, Marta; Moaddel, Ruin et al. (2017) Environmental Enteric Dysfunction Is Associated With Altered Bile Acid Metabolism. J Pediatr Gastroenterol Nutr 64:536-540

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