Acute Alteration in Bone Mineral Density and Biochemical Markers for Bone Metabolism in Nephrotic Patients Receiving High-Dose Glucocorticoid and One-Cycle Etidronate Therapy

2000 ◽  
Vol 66 (3) ◽  
pp. 195-199 ◽  
Author(s):  
T. Fujita ◽  
A. Satomura ◽  
M. Hidaka ◽  
I. Ohsawa ◽  
M. Endo ◽  
...  
Keyword(s):  
Bone Mineral Density ◽  
Bone Metabolism ◽  
Bone Mineral ◽  
Biochemical Markers ◽  
High Dose ◽  
Mineral Density

Effect of oxcarbazepine on bone mineral density and biochemical markers of bone metabolism in patients with epilepsy

2014 ◽  
Vol 108 (3) ◽  
pp. 442-447 ◽  
Author(s):  
Dae Lim Koo ◽  
Kyoung Jin Hwang ◽  
Suk Won Han ◽  
Ji Young Kim ◽  
Eun Yeon Joo ◽  
...  
Keyword(s):  
Bone Mineral Density ◽  
Bone Metabolism ◽  
Bone Mineral ◽  
Biochemical Markers ◽  
Mineral Density ◽  
Patients With Epilepsy

scholarly journals The influence of habitual salt intake on bone remodelling in young healthy people

2021 ◽  
pp. 1-10
Author(s):  
Erna Davidović-Cvetko ◽  
Anita Matić ◽  
Jasminka Milas-Ahić ◽  
Ines Drenjančević
Keyword(s):  
Bone Mineral Density ◽  
Vitamin D ◽  
Bone Metabolism ◽  
Bone Mineral ◽  
Biochemical Markers ◽  
Bone Remodelling ◽  
Sodium Intake ◽  
Healthy People ◽  
Type I ◽  
Mineral Density

Introduction: Sodium alters calcium metabolism by increasing calcium excretion, thus possibly influencing bone metabolism. The hypothesis of the present study is that amount of dietary sodium intake affects the bone remodelling. This study aimed to assess whether a habitual intake of sodium has an effect on peak bone mass and biochemical indicators of bone metabolism. Subjects and Methods: In a cross-sectional study that involved 41 young men and women, six biochemical markers were assessed from blood samples using ELISA: osteocalcin, C-terminal procollagen type I peptide, receptor activator kappa B ligand, pyridinoline, parathyroid hormone, and osteoprotegerin, while bone mineral density (BMD) and bone mineral content (BMC) were measured by dual x-ray absorptiometry. Subjects were divided into two groups according to habitual sodium intake (low-Na and high-Na group) assessed by questionnaire. Results: No difference was found between groups of low and high Na intake in BMD and BMC, or in biochemical markers of bone metabolism. Since the groups differed in Ca intake, energy and vitamin D, adjustments were made for those cofounders. Regression analysis showed that only the dietary intake of vitamin D was associated with dual femur BMD and BMC, and no correlation was found between bone remodelling indicators and Na intake after adjustment for vitamin D intake. Conclusion: The present results could not confirm that habitual sodium intake above recommended levels affects bone remodelling processes or decreases bone mineral density in young healthy people if combined with adequate calcium intake.

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