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Genetic Epidemiology of Musculoskeletal Aging

Genetic Epidemiology of Musculoskeletal Aging
肌肉骨骼衰老的遗传流行病学
批准号:
6948588
负责人:
Robert Edward Ferrell
金额:
$70.85万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-15 至 2007-08-31

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EXCEED THE SPACE PROVIDED. Age related declines in lean body mass become pathologically significant as osteoporosis, leading to fractures, and sarcopenia, leading to muscle weakness and loss of function. These changes in body composition are ultimately associated with declines in physical function and the ability to perform tasks of daily living. The Health ABC study is a longitudinal study of 3,075 men and women aged 70-79 (52% women and 42% African American) with state of the art measures of body composition, strength and function. In Health ABC, we will estimate the contribution of variation of 50 physiological candidate genes to interindividual variation in bone (bone mineral density and bone quality) and muscle (muscle mass, strength and quality phenotypes. We will: 1) Evaluate the association of muscle and bone phenotypes with variation in loci involved in sex steroid metabolism and action in growth factor and cytokine structure and action; 2) Evaluate the association between candidate gene variation and annualized changes in quantitative measures of muscle and bone phenotypes; 3) Evaluate the interaction between genes and between genes and environments in influencing muscle and bone phenotypes and 4) Examine the associations between variation at candidate genes and measures of performance. High throughput genotyping will use the recently developed fluorescence polarization technique. To examine the relationship between musculoskeletal phenotypes and genetic polymorphisms, we will use statistical models appropriate for cross- sectional and longitudinal data. For cross-sectional analyses, our major tools will be general linear model (regression, ANOVA, and MANOVA). Main effects, interactions and planned contrast will be assessed. Residuals, outliers and influential points will be examined and sensitivity analyses performed. For longitudinal data analysis of continuous outcomes, will employ standards random effects models. The models account for heterogeneity between subjects and consequently increased the precision with which genetics effects are measured. We will employ a general analytic method for association studies, genomic controls, to make our conclusions robust against the impact of population substructure. These studies will contribute to our knowledge of the mechanisms of age related loss of lean body mass and may identify individuals at elevated risk who are candidates for preventive interventions. i PERFORMANCE SITE ========================================Section End===========================================
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CORE--BASIC GENOMICS AND PROTEOMICS FACILITY
Genetic Epidemiology of Musculoskeletal Aging
Genetic Epidemiology of Musculoskeletal Aging
Genetic Epidemiology of Musculoskeletal Aging
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