It is believed that peak bone mass is a critical element in the determination of risk for osteoporotic fractures. At the time of peak bone there is a 1 SD black-white difference in bone mass which must contribute greatly to the 50% reduction in osteoporotic fractures among elderly black men and women in the U.S. This difference in peak bone mass must reflect processes which differ in black and white children during skeletal growth, and it is the purpose of Part A of this proposed research to investigate: l) the black-white differences in rates of gain in bone mass in children aged 5-14; 2) the relationship between markers of skeletal turnover and rates of gain in bone mass in black and white children, and whether such differences account for differences in skeletal growth; and 3) factors which might influence bone mass either through effects on skeletal modeling and remodeling during growth, or through other mechanisms, including sex steroids, growth hormone and other growth factors. In Part B we propose to also study the role of skeletal remodeling in bone mass and bone loss differences among black and white adults. We will examine both differences in bone mass and rates of change in bone mass in older black and white men and women, and investigate whether changes in rates of skeletal remodeling are associated with rates of change in skeletal mass. We will also test whether there are differences in sex steroids which are associated with differences in bone mass, bone loss, markers of remodeling, or other potential influences on the skeletal mass (e.g. muscle mass).

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
2P01AG005793-11
Application #
3726349
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Hui, Siu L; Perkins, Anthony J; Harezlak, Jaroslaw et al. (2010) Velocities of bone mineral accrual in black and white American children. J Bone Miner Res 25:1527-35
Ruppel, Meghan E; Burr, David B; Miller, Lisa M (2006) Chemical makeup of microdamaged bone differs from undamaged bone. Bone 39:318-24
Mashiba, T; Hui, S; Turner, C H et al. (2005) Bone remodeling at the iliac crest can predict the changes in remodeling dynamics, microdamage accumulation, and mechanical properties in the lumbar vertebrae of dogs. Calcif Tissue Int 77:180-5
McCabe, Linda D; Martin, Berdine R; McCabe, George P et al. (2004) Dairy intakes affect bone density in the elderly. Am J Clin Nutr 80:1066-74
Day, J S; Ding, M; Bednarz, P et al. (2004) Bisphosphonate treatment affects trabecular bone apparent modulus through micro-architecture rather than matrix properties. J Orthop Res 22:465-71
Ding, M; Day, J S; Burr, D B et al. (2003) Canine cancellous bone microarchitecture after one year of high-dose bisphosphonates. Calcif Tissue Int 72:737-44
Burr, David B; Miller, Lisa; Grynpas, Marc et al. (2003) Tissue mineralization is increased following 1-year treatment with high doses of bisphosphonates in dogs. Bone 33:960-9
Burr, D B (2002) Targeted and nontargeted remodeling. Bone 30:2-4
Mashiba, T; Turner, C H; Hirano, T et al. (2001) Effects of high-dose etidronate treatment on microdamage accumulation and biomechanical properties in beagle bone before occurrence of spontaneous fractures. Bone 29:271-8
Turner, C H; Wang, T; Burr, D B (2001) Shear strength and fatigue properties of human cortical bone determined from pure shear tests. Calcif Tissue Int 69:373-8

Showing the most recent 10 out of 42 publications