The Effect of Fructooligosaccharides with Various Degrees of Polymerization on Calcium Bioavailability in the Growing Rat

2003 ◽  
Vol 228 (6) ◽  
pp. 683-688 ◽  
Author(s):  
Marlena C. Kruger ◽  
Katherine E. Brown ◽  
Gabrielle Collett ◽  
Lee Layton ◽  
Linda M. Schollum
Keyword(s):  
Bone Mass ◽  
Bone Mineral ◽  
Peak Bone Mass ◽  
Calcium Absorption ◽  
Bone Fractures ◽  
Ex Vivo ◽  
Later Life ◽  
Male Rat ◽  
Mineral Density ◽  
Calcium Bioavailability

Maximizing peak bone mass during adolescence may be the key to postponing and perhaps preventing bone fractures due to osteoporosis in later life. One mechanism to maximize peak bone mass is to maximize calcium absorption, and it has been suggested that inulin and oligofructose might be one of the ways of doing so. In this study, fructooligosaccharides with various degrees of polymerization have been compared in terms of impact on calcium absorption, bone density, and excretion of collagen cross-links in the young adult male rat. The various oligosaccharides were oligofructose (DP2-8), inulin (DP>23), and a mixture of 92% inulin and 8% short-chain oligofructose (DP2-8). Measuring ex vivo bone mineral density (BMD) and bone mineral content (BMC) showed that BMD was significantly higher in the group fed inulin (DP>23) in both femurs, whereas BMC was significantly higher in the spine. The excretion of fragments of Type 1 collagen decreased in all groups over the 4 weeks of feeding, but the decrease was most significant in the group fed inulin (DP>23). Several hypotheses have been offered to explain the effect of the fructooligosaccharides on calcium absorption and retention. These include the production of organic acids that would acidify the luminal contents and enhance solubility and hence absorption, or possibly a mechanism via calbindinD9k. This study is unique in that it compares the different fructooligosaccharides in the same model, and it clearly shows that the various fructans do not have the same effect. In our model, inulin (DP>23) had the most significant effect on calcium bioavailability.

scholarly journals Influence of Age at Menarche on Forearm Bone Microstructure in Healthy Young Women

2008 ◽  
Vol 93 (7) ◽  
pp. 2594-2601 ◽  
Author(s):  
Thierry Chevalley ◽  
Jean-Philippe Bonjour ◽  
Serge Ferrari ◽  
Rene Rizzoli
Keyword(s):  
Bone Mineral Density ◽  
Risk Factor ◽  
Bone Mass ◽  
Bone Mineral ◽  
Peak Bone Mass ◽  
Adult Women ◽  
Mineral Density ◽  
T Score ◽  
Estrogen Exposure ◽  
Volumetric Bmd

Abstract Background: Shorter estrogen exposure from puberty onset to peak bone mass attainment may explain how late menarche is a risk factor for osteoporosis. The influence of menarcheal age (MENA) on peak bone mass, cortical, and trabecular microstructure was studied in 124 healthy women aged 20.4 ± 0.6 (sd) yr. Methods: At distal radius, areal bone mineral density (aBMD) was measured by dual-energy x-ray absorptiometry, and volumetric bone mineral density (BMD) and microstructure were measured by high-resolution peripheral computerized tomography, including: total, cortical, and trabecular volumetric BMD and fraction; trabecular number, thickness, and spacing; cortical thickness (CTh); and cross-sectional area (CSA). Results: Median MENA was 12.9 yr. Mean aBMD T score of the whole cohort was slightly positive. aBMD was inversely correlated to MENA for total radius (R = −0.21; P = 0.018), diaphysis (R = −0.18; P = 0.043), and metaphysis (R = −0.19; P = 0.031). Subjects with MENA more than the median [LATER: 14.0 ± 0.7 (±sd) yr] had lower aBMD than those with MENA less than the median (EARLIER: 12.1 ± 0.7 yr) in total radius (P = 0.026), diaphysis (P = 0.042), and metaphysis (P = 0.046). LATER vs. EARLIER displayed lower total volumetric BMD (315 ± 54 vs. 341 ± 56 mg HA/cm3; P = 0.010), cortical volumetric BMD (874 ± 49 vs. 901 ± 44 mg HA/cm3; P = 0.003), and CTh (774 ± 170 vs. 849 ± 191 μm; P = 0.023). CTh was inversely related to CSA (R = −0.46; P < 0.001). In LATER reduced CTh was associated with 5% increased CSA. Conclusions: In healthy young adult women, a 1.9-yr difference in mean MENA was associated with lower radial aBMD T score, lower CTh without reduced CSA, a finding compatible with less endocortical accrual. It may explain how late menarche is a risk factor for forearm osteoporosis.

Bone mass, bone strength, and their relationship in developing CD-1 mice

2007 ◽  
Vol 85 (2) ◽  
pp. 274-279 ◽  
Author(s):  
Wendy E. Ward ◽  
Ana V. Piekarz ◽  
Debbie Fonseca
Keyword(s):  
Bone Mass ◽  
Bone Strength ◽  
Bone Mineral ◽  
Peak Load ◽  
Later Life ◽  
Strength Properties ◽  
Mineral Density ◽  
Effective Prevention ◽  
Nutritional Interventions ◽  
Skeletal Site

Optimizing nutrition during development may provide effective prevention strategies to protect against osteoporosis during later life. Because the mouse model is commonly used to test nutritional interventions on bone health, the overall objective of this study was to determine how bone develops during the first 4 months of life by assessing bone mass (bone mineral content (BMC) and bone mineral density (BMD)) and biomechanical strength properties such as peak load in male and female CD-1 mice. Bone outcomes were assessed at 1 month intervals from 1 to 4 months of age. Femur and spine BMC and BMD at 3 months were similar to 4 months, indicating that the accumulation of bone mass occurs primarily during the first 3 months of life. In contrast, the timing of changes in peak load, a measure of bone strength, varied by skeletal site. Regression analyses demonstrated that femur BMC is a significant predictor of femur peak load at the femur midpoint and neck. The study findings suggest that nutritional interventions aimed at optimizing peak bone mass to prevent osteoporosis may be most effective during pubertal growth.

scholarly journals Osteoporosis, Fractures, and Diabetes

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Peter Jackuliak ◽  
Juraj Payer
Keyword(s):  
Bone Mineral Density ◽  
Type 2 Diabetes ◽  
Bone Mass ◽  
Bone Mineral ◽  
Bone Fractures ◽  
Trabecular Bone Score ◽  
Bone Fragility ◽  
Mineral Density ◽  
Increased Risk

It is well established that osteoporosis and diabetes are prevalent diseases with significant associated morbidity and mortality. Patients with diabetes mellitus have an increased risk of bone fractures. In type 1 diabetes, the risk is increased by ∼6 times and is due to low bone mass. Despite increased bone mineral density (BMD), in patients with type 2 diabetes the risk is increased (which is about twice the risk in the general population) due to the inferior quality of bone. Bone fragility in type 2 diabetes, which is not reflected by bone mineral density, depends on bone quality deterioration rather than bone mass reduction. Thus, surrogate markers and examination methods are needed to replace the insensitivity of BMD in assessing fracture risks of T2DM patients. One of these methods can be trabecular bone score. The aim of the paper is to present the present state of scientific knowledge about the osteoporosis risk in diabetic patient. The review also discusses the possibility of problematic using the study conclusions in real clinical practice.

scholarly journals Cortical Consolidation due to Increased Mineralization and Endosteal Contraction in Young Adult Men: A Five-Year Longitudinal Study

2011 ◽  
Vol 96 (7) ◽  
pp. 2262-2269 ◽  
Author(s):  
Claes Ohlsson ◽  
Anna Darelid ◽  
Martin Nilsson ◽  
Johanna Melin ◽  
Dan Mellström ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Bone Mineral Density ◽  
Bone Mass ◽  
Bone Mineral ◽  
Peak Bone Mass ◽  
Volumetric Bone Mineral Density ◽  
Mineral Density ◽  
Site Specific ◽  
X Ray

Abstract Context: Peak bone mass is an important factor in the lifetime risk of developing osteoporosis. Large, longitudinal studies investigating the age of attainment of site-specific peak bone mass are lacking. Objective and Main Outcome Measures: The main outcome measures were to determine the site-specific development of peak bone mass in appendicular and axial skeletal sites and in the trabecular and cortical bone compartments, using both dual x-ray absorptiometry and peripheral computed tomography. Design, Setting, and Population: In total, 833 men [aged 24.1 ± 0.6 yr (mean ± sd)] from the original population-based Gothenburg Osteoporosis and Obesity Determinants Study (n = 1068) were included in this follow-up examination at 61.2 ± 2.3 months. Areal bone mineral density (aBMD) was measured with dual x-ray absorptiometry, whereas cortical and trabecular volumetric bone mineral density and bone size were measured by peripheral computed tomography at baseline and at the 5-yr follow-up. Results: During the 5-yr study period, aBMD of the total body, lumbar spine, and radius increased by 3.4, 4.2, and 7.8%, respectively, whereas a decrease in aBMD of the total hip of 1.9% was observed (P < 0.0001). Increments of 2.1 and 0.7% were seen for cortical volumetric bone mineral density of the radius and tibia, respectively (P < 0.0001), whereas cortical thickness increased by 3.8% at the radius and 6.5% at the tibia due to diminished endosteal circumference (radius 2.3% and tibia 4.6%, P < 0.0001). Conclusion: aBMD decreased at the hip but increased at the spine and radius, in which the increment was explained by continued mineralization and augmented cortical thickness due to endosteal contraction in men between ages 19 and 24 yr.

scholarly journals A COMPERATIVE STUDY ON RATIO OF CALCIUM AND PHOSPHORUS IN SERUM AND URINE AMONG PRE AND POSTMENOPAUSAL WOMEN.

2020 ◽  
pp. 1-5
Author(s):  
Ewanmihaka Pakma ◽  
Apurba Sarkar ◽  
Suresh Babu
Keyword(s):  
Bone Mass ◽  
Calcium Intake ◽  
Absorption Rate ◽  
Peak Bone Mass ◽  
Calcium Absorption ◽  
Later Life ◽  
Urinary Calcium ◽  
Calcium Excretion ◽  
Urinary Creatinine ◽  
Calcium And Phosphorus

Osteoporosis is a bone disease resulting in reduction in bone mass and the bone become susceptible for fracture. The major factor involved in the development of osteoporosis includes, low calcium intake or decrease in Calcium absorption rate in aged population, bone strength in later life depends on development of bones earlier in life, adequate calcium intake during youth is essential to achieve peak bone mass. The Serum Calcium and Phosphorus, Urinary Calcium and Phosphorus were estimated by spectrophotometrically by O-cresolphthalein and Phosphomolybdate method respectively. Urinary creatinine was estimated by Spectrophotometric Jaffe’s reaction. In our study, Urinary Calcium excretion was significantly increased with that of premenopausal woman of Indian sub population. Present study is an attempt to underscore urinary calcium quantification does increase diagnostic sensitivity by measuring it as derive parameter – CCR. It could as well be considered as an indicator for therapeutic intervention by studying large pre and postmenopausal woman population.

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