The skeletal response to a metabolic bone disease or a treatment regimen may be non-homogeneous. A particular disease or treatment may cause bone loss preferentially in the cortical or the trabecular bone, preserving one at the expense of the other. In the elderly osteoporotic population, we must be cognizant of the fact that a course of treatment with multiple therapies may have an effect on the skeleton which is not the sum of the individual parts. Non-invasive bone mass measurements can provide information about isolated regional skeletal responses, and this information can be used in a clinical setting to study the effects of specific disease processes or treatment regimens. The long-term goal of this program is to use information generated from patient studies to develop a comprehensive management plan for the treatment of the patient with multiple disorders. The experimental approach is designed to study """"""""isolated"""""""" processes in vivo which are known to affect the skeleton in diverse ways. This information will be used to predict the effects of treatment when multiple metabolic stimuli are present, and this will be tested initially in a single population. Concurrently, the capability of the various bone mass measurements (quantitative computed tomography, dual-photon and single-photon absorptiometry, radiogrammetry) will be assessed individually and in concert for their ability to predict the clinical consequence of bone loss, that is, fracture. This capabililty of skeletal assessment coupled with the knowledge of the effects of various metabolic stimuli will allow a coherent approach to the management of the older osteoporotic patient.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM027926-05
Application #
3151811
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Project Start
1980-12-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Gluer, C C; Reiser, U J; Davis, C A et al. (1988) Vertebral mineral determination by quantitative computed tomography (QCT): accuracy of single and dual energy measurements. J Comput Assist Tomogr 12:242-58
Ettinger, B; Genant, H K; Cann, C E (1987) Postmenopausal bone loss is prevented by treatment with low-dosage estrogen with calcium. Ann Intern Med 106:40-5
Richardson, M L; Pozzi-Mucelli, R S; Kanter, A S et al. (1986) Bone mineral changes in primary hyperparathyroidism. Skeletal Radiol 15:85-95
Reinbold, W D; Genant, H K; Reiser, U J et al. (1986) Bone mineral content in early-postmenopausal and postmenopausal osteoporotic women: comparison of measurement methods. Radiology 160:469-78
Genant, H K; Ettinger, B; Cann, C E et al. (1985) Osteoporosis: assessment by quantitative computed tomography. Orthop Clin North Am 16:557-68
Richardson, M L; Genant, H K; Cann, C E et al. (1985) Assessment of metabolic bone diseases by quantitative computed tomography. Clin Orthop Relat Res :224-38
Genant, H K; Cann, C E; Ettinger, B et al. (1985) Quantitative computed tomography for spinal mineral assessment: current status. J Comput Assist Tomogr 9:602-4
Marcus, R; Cann, C; Madvig, P et al. (1985) Menstrual function and bone mass in elite women distance runners. Endocrine and metabolic features. Ann Intern Med 102:158-63

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