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Associations between serum calcium, 25(OH)D level and bone mineral density in adolescents

Abstract

Backgrounds:

It is important to improve our understanding of the roles of calcium and vitamin D in bone health for preventing osteoporosis. We aimed at exploring the associations between serum calcium, vitamin D level, and bone mineral density (BMD) in adolescents included in the National Health and Nutrition Examination Survey (NHANES) 2001 – 2006.

Methods:

Weighted multivariate linear regression models were used to estimate the associations of serum calcium, 25(OH)D level with total BMD. Smooth curve fitting was used to explore the potential non-linear relationship.

Results:

A total of 5990 individuals aged between 12 and 19 years were included in this study. The fully-adjusted model showed serum calcium positively correlated with total BMD. However, an inverted U-shaped relationship was found when we performed the smooth curve fitting method, and the inflection point was calculated at 9.6 mg/dL using the two-piecewise linear regression model. In contrast, there was a positive correlation between serum 25(OH)D and total BMD after adjusting for potential confounders.

Conclusions:

The present study revealed a positive correlation between serum 25(OH)D level and total BMD, and an inverted U-shaped relationship between serum calcium and total BMD.

Keywords:
Calcium; Vitamin D; Bone health; Adolescent; NHANES

Introduction

Osteoporosis is a global health problem that is reported to originate during childhood or adolescence [11. Yang X, Zhai Y, Zhang J, Chen JY, Liu D, Zhao WH. Combined effects of physical activity and calcium on bone health in children and adolescents: a systematic review of randomized controlled trials. WJP. 2020;16(4):356-65.]. Adolescence is a critical period of skeletal development and peak bone mass (PBM) may be reached in late adolescence [22. Baxter-Jones AD, Faulkner RA, Forwood MR, Mirwald RL, Bailey DA. Bone mineral accrual from 8 to 30 years of age: an estimation of peak bone mass. J Bone Miner Res. 2011;26(8):1729–39.]. Evidence indicates that when PBM increases by 5% during childhood and adolescence, the risk of osteoporotic fracture reduces by 40%, while when PBM increases by 10%, this risk decreases by 50% [33. van der Sluis IM, de Muinck Keizer-Schrama SM. Osteoporosis in childhood: bone density of children in health and disease. J Pediatr Endocrinol Metab. 2001;14(7):817–32., 44. Goulding A, Jones IE, Taylor RW, Manning PJ, Williams SM. More broken bones: a 4-year double cohort study of young girls with and without distal forearm fractures. J Bone Miner Res. 2000;15(10):2011–8.]. Therefore, increased bone mass accumulation during this period is an effective way to maintain bone health in adulthood and prevent osteoporosis in older age [55. Rizzoli R, Bianchi ML, Garabedian M, McKay HA, Moreno LA. Maximizing bone mineral mass gain during growth for the prevention of fractures in the adolescents and the elderly. Bone. 2010;46(2):294–305.].

Calcium is an essential nutrient for skeletal development and maintenance [66. Rooney MR, Michos ED, Hootman KC, Harnack L, Lutsey PL. Trends in calcium supplementation, National Health and nutrition examination survey (NHANES) 1999-2014. Bone. 2018;111:23–7.]. Calcium supplementation is recommended for improving bone health in older adults. However, the effect of calcium supplementation on bone mineral density (BMD) remains controversial [77. Tai V, Leung W, Grey A, Reid IR, Bolland MJ. Calcium intake and bone mineral density: systematic review and meta-analysis. BMJ (Clinical research ed). 2015;h4183:351.], and it is uncertain whether an elevated serum calcium level is beneficial to bone health [88. Cerani A, Zhou S, Forgetta V, Morris JA, Trajanoska K, Rivadeneira F, Larsson SC, Michaelsson K, Richards JB. Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study. BMJ (Clinical research ed). 2019;l4410:366., 99. Dalemo S, Eggertsen R, Hjerpe P, Almqvist EG, Bostrom KB. Bone mineral density in primary care patients related to serum calcium concentrations: a longitudinal cohort study from Sweden. Scand J Prim Health Care. 2018; 36(2):198–206.]. Moreover, vitamin D is known to play an essential role in maintaining normocalcaemia, thus permitting normal skeletal mineralization [1010. Reid IR, Vitamin D. Effect on bone mineral density and fractures. Endocrinol Metab Clin N Am. 2017;46(4):935–45.]. In individuals with a low BMD or those at a high risk of osteoporotic fractures, calcium and vitamin D supplementation are suggested as adjuncts to osteoporosis therapies [1111. Shoback D, Rosen CJ, Black DM, Cheung AM, Murad MH, Eastell R. Pharmacological management of osteoporosis in postmenopausal women: an endocrine society guideline update. J Clin Endocrinol Metab. 2020;105(3).]. However, their effect on fracture risk is unclear [1212. Hauk L. Treatment of low BMD and osteoporosis to prevent fractures: updated guideline from the ACP. Am Fam Physician. 2018;97(5):352–3.]. Furthermore, whether serum calcium, and vitamin D independently correlate with BMD in the general population or certain population groups remains unclear [1313. Liu M, Yao X, Zhu Z. Associations between serum calcium, 25(OH)D level and bone mineral density in older adults. J Orthop Surg Res. 2019;14(1):458., 1414. Li GH, Robinson-Cohen C, Sahni S, Au PC, Tan KC, Kung AW, Cheung CL. Association of genetic variants related to serum calcium levels with reduced bone mineral density. J Clin Endocrinol Metab. 2020;105(3):e328-36.]. To the best of our knowledge, no large-sample study has been performed in adolescents. Moreover, the beneficial effect of vitamin D on bone health was reported to be associated with serum 25(OH)D level and not (1,25(OH)2D) [1515. Sharma DK, Sawyer RK, Robertson TS, Stamenkov R, Solomon LB, Atkins GJ, Clifton PM, Morris HA, Anderson PH. Elevated serum 25-Hydroxyvitamin D levels are associated with improved bone formation and micro-structural measures in elderly hip fracture patients. J Clin Med. 2019;8(11).], and serum 25(OH)D level has been used to assess vitamin D status [1616. Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357(3):266–81., 1717. Vieth R. Vitamin D supplementation, 25-hydroxyvitamin D concentrations, and safety. Am J Clin Nutr. 1999;69(5):842–56.]. Therefore, in this study, we examined the associations of serum calcium, and 25(OH)D level with total BMD among US adolescents using samples from a database of a multiracial population.

Methods

Study population

As a nationally representative survey, the National Health and Nutrition Examination Survey (NHANES) collected health examination data from the non-institutionalized US population [1818. Curtin LR, Mohadjer LK, Dohrmann SM, Montaquila JM, Kruszan-Moran D, Mirel LB, Carroll MD, Hirsch R, Schober S, Johnson CL. The National Health and Nutrition Examination Survey: Sample Design, 1999-2006. Vital Health Stat Ser 2 Data Eval Methods Res. 2012;(155):1–39.]. These data are released on a two-year cycle. We used the data from three cycles of NHANES 2001–2006 in this study. A total of 5990 individuals aged 12–19 years with available data on serum calcium, and 25(OH)D levels, and total BMD were included. The NHANES protocols were approved by the Institutional Review Board of the National Center for Health Statistics, and participants or their proxies (< 18 years) provided informed consent [1919. Zipf G, Chiappa M, Porter KS, Ostchega Y, Lewis BG, Dostal J. National health and nutrition examination survey: plan and operations, 1999-2010. Vital Health Stat Ser 1 Programs Collection Proced. 2013;(56):1–37.].

Variables

In this study, the dependent variable was total BMD, and the independent variables were serum calcium and 25(OH)D levels. All subjects included in the present study received dual-energy X-ray absorptiometry (DXA) total body scans. For the 2001–2006 cycles, total BMD was measured using the DXA scans obtained from a QDR-4500A fanbeam densitometer (Hologic, Inc., Bedford, Massachusetts) by trained and certified radiologic technologists. The Beckman Synchron LX20 (Beckman Coulter, Brea, CA) was used to determine serum calcium, and a radioimmunoassay kit (DiaSorin, Stillwater, Minnesota, USA) was used to determineserum 25(OH)D for the 2001–2006 cycles.

The following variables were selected as potential confounders: age, gender, race/ethnicity, physical activity (based on suggested metabolic equivalent rank) [2020. Patel CJ, Pho N, McDuffie M, Easton-Marks J, Kothari C, Kohane IS, Avillach P. A database of human exposomes and phenomes from the US National Health and nutrition examination survey. Sci Data. 2016;3: 160096.], income to poverty ratio, body mass index, and calcium supplementation use. Detailed information on serum calcium, and 25(OH)D levels, total BMD, and other variables can be found at www.cdc.gov/nchs/nhanes/.

Statistical analysis

We used sample weights in all analyses according to the stratified, multistage probability sampling design. The P-value was calculated using the weighted chi-square test for categorical variables, and the weighted linear regression model for continuous variables. The weighted multivariate linear regression model was used to investigate whether serum calcium and 25(OH)D levels independently correlated with total BMD. We used generalized additive models and smooth curve fitting to explore potential non-linear relationships. We further calculated the inflection points using the two-piecewise linear regression model. All analyses were conducted using R (version 3.5.3) and EmpowerStats software (http://www.empowerstats.com). P-value < 0.05 was considered statistically significant.

Results

The weighted characteristics of the study population according to gender are presented in Table 1. Most of the participants were racially/ethnically classified as “non-Hispanic white”. A total of 3086 boys and 2904 girls were included in this study: For boys and girls, respectively, the mean age was 15.46 ± 2.26 and 15.35 ± 2.23 years, mean serum calcium was 9.80 ± 0.30 mg/dL and 9.64 ± 0.30 mg/dL, mean serum 25(OH)D was 24.23 ± 8.63 ng/mL and 23.32 ± 10.02 ng/mL, and mean total BMD was 1.10 ± 0.14 g/cm2 and 1.06 ± 0.10 g/cm2.

Table 1
Participant characteristics

Association between serum calcium level and total BMD

There was a negative correlation between the serum calcium level and total BMD in the unadjusted model [− 0.0157 (− 0.0257, − 0.0058)] (Table 2), while after adjusting for all potential confounders, a positive correlation was found [0.0084 (0.0007, 0.0160)]. Compared to participants with the lowest serum calcium level in Q1, participants in other groups had a higher total BMD. The results of total BMD by quartiles of the serum calcium level, stratified by race/ethnicity and age, are shown in Table 3. Further more, we found an inverted U-shaped relationship between the serum calcium level and total BMD using the smooth curve fitting method (Fig. 1). We subsequently calculated that the inflection point was 9.6 mg/dL using the two-piecewise linear regression model (Table 4). In the subgroup analysis stratified by gender and race/ethnicity, this inverted U-shaped relationship existed in boys, Whites and Blacks (Figs. 3 and 4), whereas the serum calcium level positively correlated with total BMD in girls, Mexican Americans and other race/ethnicity. In addition, we calculated that the inflection points were 9.6 mg/dL in boys and Whites, and 9.2 mg/dL in Blacks.

Fig. 1
The association between serum calcium and total bone mineral density. a Each black point represents a sample. b Solid rad line represents the smooth curve fit between variables. Blue bands represent the 95% of confidence interval from the fit. Adjusted for age, gender, race/ethnicity, income to poverty ratio, education, physical activity, body mass index, calcium supplementation use
Table 2
Associations of serum calcium, 25(OH)D with total bone mineral density
Table 3
Total bone mineral density by quartiles of serum calcium, stratified by race/ethnicity and age
Table 4
Threshold effect analysis of serum calcium and 25(OH)D on total bone mineral density by using two-piecewise linear regression

Association between serum 25(OH)D level and total BMD

The serum 25(OH)D level negatively correlated with total BMD in the unadjusted model [0.0005 (− 0.0009, − 0.0002)] (Table 2). This association became positive after adjusting for all potential confounders [0.0006 (0.0003, 0.0008)] (Table 2, Fig. 2). Compared to participants with the lowest serum 25(OH)D level in Q1, participants in the other groups had a higher total BMD. The trend test remained significant (P < 0.001). The results of total BMD by quartiles of serum 25(OH)D, stratified by race/ethnicity and age. Are shown in Table 5. In the subgroup analysis stratified by gender and race/ethnicity, we found a U-shaped relationship in boys, and an inverted U-shaped relationship in girls and Whites (Figs. 3 and 4). The results of the inflection points are shown in Table 4.

Fig. 2
The association between serum 25(OH)D level and total bone mineral density. a Each black point represents a sample. b Solid rad line represents the smooth curve fit between variables. Blue bands represent the 95% of confidence interval from the fit. Adjusted for age, gender, race/ethnicity, income to poverty ratio, education, physical activity, body mass index, calcium supplementation use
Fig. 3
The associations between serum calcium (a), serum 25(OH)D (b) and total bone mineral density stratified by gender. Adjusted for age, race/ethnicity, income to poverty ratio, education, physical activity, body mass index, calcium supplementation use
Fig. 4
The associations between serum calcium (a), serum 25(OH)D (b) and total bone mineral density stratified by race/ethnicity. Adjusted for age, gender, income to poverty ratio, education, physical activity, body mass index, calcium supplementation use
Table 5
Total bone mineral density by quartiles of serum 25(OH)D level, stratified by race/ethnicity and age

Discussion

The aim of this study was to explore whether there are independent correlations between serum calcium, and 25(OH)D levels and total BMD among adolescents aged 12–19 years. The results showed that serum 25(OH)D was positively correlated with total BMD, and the relationship of serum calcium with total BMD assumed an inverted U-shaped (inflection point: 9.6 mg/dL).

Calcium plays an important role in many biological systems, most notably in bones. Thus, it is essential to ensure adequate calcium intake throughout life for building and maintaining bones [2121. Hodges JK, Cao S, Cladis DP, Weaver CM. Lactose intolerance and bone health: the challenge of ensuring adequate calcium intake. Nutrients. 2019; 11(4).]. However, a lower-than-recommended calcium intake has been reported for European and Brazilian populations [2222. Mensink GB, Fletcher R, Gurinovic M, Huybrechts I, Lafay L, Serra-Majem L, Szponar L, Tetens I, Verkaik-Kloosterman J, Baka A, et al. Mapping low intake of micronutrients across Europe. Br J Nutr. 2013;110(4):755–73., 2323. Pinheiro MM, Schuch NJ, Genaro PS, Ciconelli RM, Ferraz MB, Martini LA. Nutrient intakes related to osteoporotic fractures in men and women--the Brazilian osteoporosis study (BRAZOS). Nutr J. 2009;8:6.]. Several trials have suggested that supplementing by oral calcium salts is notably associated with bone attenuation [2424. Asmus HG, Braun J, Krause R, Brunkhorst R, Holzer H, Schulz W, Neumayer HH, Raggi P, Bommer J. Two year comparison of sevelamer and calcium carbonate effects on cardiovascular calcification and bone density. Nephrol Dial Transplant. 2005;20(8):1653–61., 2525. Raggi P, James G, Burke SK, Bommer J, Chasan-Taber S, Holzer H, Braun J, Chertow GM. Decrease in thoracic vertebral bone attenuation with calcium-based phosphate binders in hemodialysis. J Bone Miner Res. 2005;20(5):764–72.]. Some recent studies showed either no significant correlation or a negative association between serum calcium level with BMD [88. Cerani A, Zhou S, Forgetta V, Morris JA, Trajanoska K, Rivadeneira F, Larsson SC, Michaelsson K, Richards JB. Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study. BMJ (Clinical research ed). 2019;l4410:366., 99. Dalemo S, Eggertsen R, Hjerpe P, Almqvist EG, Bostrom KB. Bone mineral density in primary care patients related to serum calcium concentrations: a longitudinal cohort study from Sweden. Scand J Prim Health Care. 2018; 36(2):198–206., 1313. Liu M, Yao X, Zhu Z. Associations between serum calcium, 25(OH)D level and bone mineral density in older adults. J Orthop Surg Res. 2019;14(1):458.]; our results suggested an inverted U-shaped relationship in adolescents aged 12–19 years. There are some biological explanations for the findings of this study. It was found that a high calcium intake or an intake exceeding the optimal level, could reduce osteoblast differentiation and mineralization in vitro [2626. Eklou-Kalonji E, Denis I, Lieberherr M, Pointillart A. Effects of extracellular calcium on the proliferation and differentiation of porcine osteoblasts in vitro. Cell Tissue Res. 1998;292(1):163–71., 2727. Dvorak MM, Siddiqua A, Ward DT, Carter DH, Dallas SL, Nemeth EF, Riccardi D. Physiological changes in extracellular calcium concentration directly control osteoblast function in the absence of calciotropic hormones. Proc Natl Acad Sci U S A. 2004;101(14):5140–5.] and in some animals [2828. Al-Dujaili SA, Koh AJ, Dang M, Mi X, Chang W, Ma PX, McCauley LK. Calcium sensing receptor function supports osteoblast survival and acts as a co-factor in PTH anabolic actions in bone. J Cell Biochem. 2016;117(7):1556–67.]. Thus, there may be a narrow range of optimal calcium levels that promote bone growth, whereas elevated calcium levels may have deleterious effects on bone. The above evidence suggested that calcium intake is required to improve BMD in subjects with low serum calcium levels.

It has been shown that a low serum 25(OH)D level has an adverse effect on bone health [2929. Christakos S, Li S, DeLa Cruz J, Verlinden L, Carmeliet G. Vitamin D and bone. Handb Exp Pharmacol. 2020;262:47-63.]. Several cross-sectional studies reported a positive association between serum 25(OH)D level and BMD in adults [3030. von Muhlen DG, Greendale GA, Garland CF, Wan L, Barrett-Connor E, Vitamin D. Parathyroid hormone levels and bone mineral density in community-dwelling older women: the rancho Bernardo study. Osteoporos Int. 2005;16(12):1721–6.3232. Collins D, Jasani C, Fogelman I, Swaminathan R. Vitamin D and bone mineral density. Osteoporos Int. 1998;8(2):110–4.]. Vita-min D deficiency has been a global health problem in the general population, with a distinct lack of data in children and adolescents [3333. White Z, White S, Dalvie T, Kruger MC, Van Zyl A, Becker P. Bone health, body composition, and vitamin D status of black preadolescent children in South Africa. Nutrients. 2019;11(6).]. Recent studies showed that hypovitaminosis D is a common disease in children, and studies in an adult population regarding the aetiology of osteoporosis have somewhat linked the evidence to vitamin D deficiency during childhood and adolescence [3434. Guillemant J, Taupin P, Le HT, Taright N, Allemandou A, Peres G, Guillemant S. Vitamin D status during puberty in French healthy male adolescents. Osteoporos Int. 1999;10(3):222–5.]. The results of a cross-sectional study of 100 Indian healthy school-age children showed that the serum 25(OH)D level positively related to BMD [3535. Sharawat IK, Dawman L. Bone mineral density and its correlation with vitamin D status in healthy school-going children of Western India. Arch Osteoporos. 2019; 14(1):13.].

Our results also showed a positive association between the serum 25(OH)D level and total BMD. We performed subgroup analyses to describe the data in more detail following the STROBE guidelines [3636. von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet (London, England). 2007;370(9596):1453–7.]. A non-linear relationship between the 25(OH)D level and total BMD was found, and the inflection points were detected. These findings suggest a potentially optimal serum vita-min D level for BMD, while elevated 25(OH)D levels (beyond the turning point) may lead to a lower BMD in girls and Whites. The heterogeneity among these studies, including differences in participant selection, study size, study design, and controlled confounders, may provide a possible explanation for these conflicting conclusions.

To the best of our knowledge, this is the largest study investigating the relationships between serum calcium, and 25(OH)D levels and BMD in adolescents, and this representative sample of a multiracial population may be used as a general investigation of the whole population. Some limitations are worth noting. First, accurate data on puberty status were not included in our study. Although age was adjusted as a covariate in this study, the possible bias related to the unmeasured puberty status remained a limitation. Second, due to its cross-sectional design, this research had less power regarding the determination of causal relationships between serum calcium, and 25(OH)D levels and BMD.

Conclusions

We found that serum calcium level had an inverted U-shaped relationship with total BMD, while serum 25(OH)D level positively correlated with total BMD. Further studies are needed to assess whether increased serum 25 (OH) D or calcium levels may have a beneficial effect on BMD in adolescents with low serum 25 (OH) D or calcium levels.

  • Funding
    This study received no funding.
  • Availability of data and materials
    The survey data are publicly available on the internet for data users and researchers throughout the world (www.cdc.gov/nchs/nhanes/).
  • Declarations
    Ethics approval and consent to participate
    The ethics review board of the National Center for Health Statistics approved all NHANES protocols and written informed consents were obtained from all participants or their proxies (< 18 years).
  • Consent for publication
    Not applicable.
  • Publisher's Note
    Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Acknowledgements

The authors appreciate the time and effort given by participants during the data collection phase of the NHANES project.

References

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    Yang X, Zhai Y, Zhang J, Chen JY, Liu D, Zhao WH. Combined effects of physical activity and calcium on bone health in children and adolescents: a systematic review of randomized controlled trials. WJP. 2020;16(4):356-65.
  • 2
    Baxter-Jones AD, Faulkner RA, Forwood MR, Mirwald RL, Bailey DA. Bone mineral accrual from 8 to 30 years of age: an estimation of peak bone mass. J Bone Miner Res. 2011;26(8):1729–39.
  • 3
    van der Sluis IM, de Muinck Keizer-Schrama SM. Osteoporosis in childhood: bone density of children in health and disease. J Pediatr Endocrinol Metab. 2001;14(7):817–32.
  • 4
    Goulding A, Jones IE, Taylor RW, Manning PJ, Williams SM. More broken bones: a 4-year double cohort study of young girls with and without distal forearm fractures. J Bone Miner Res. 2000;15(10):2011–8.
  • 5
    Rizzoli R, Bianchi ML, Garabedian M, McKay HA, Moreno LA. Maximizing bone mineral mass gain during growth for the prevention of fractures in the adolescents and the elderly. Bone. 2010;46(2):294–305.
  • 6
    Rooney MR, Michos ED, Hootman KC, Harnack L, Lutsey PL. Trends in calcium supplementation, National Health and nutrition examination survey (NHANES) 1999-2014. Bone. 2018;111:23–7.
  • 7
    Tai V, Leung W, Grey A, Reid IR, Bolland MJ. Calcium intake and bone mineral density: systematic review and meta-analysis. BMJ (Clinical research ed). 2015;h4183:351.
  • 8
    Cerani A, Zhou S, Forgetta V, Morris JA, Trajanoska K, Rivadeneira F, Larsson SC, Michaelsson K, Richards JB. Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study. BMJ (Clinical research ed). 2019;l4410:366.
  • 9
    Dalemo S, Eggertsen R, Hjerpe P, Almqvist EG, Bostrom KB. Bone mineral density in primary care patients related to serum calcium concentrations: a longitudinal cohort study from Sweden. Scand J Prim Health Care. 2018; 36(2):198–206.
  • 10
    Reid IR, Vitamin D. Effect on bone mineral density and fractures. Endocrinol Metab Clin N Am. 2017;46(4):935–45.
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    Shoback D, Rosen CJ, Black DM, Cheung AM, Murad MH, Eastell R. Pharmacological management of osteoporosis in postmenopausal women: an endocrine society guideline update. J Clin Endocrinol Metab. 2020;105(3).
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    Hauk L. Treatment of low BMD and osteoporosis to prevent fractures: updated guideline from the ACP. Am Fam Physician. 2018;97(5):352–3.
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    Liu M, Yao X, Zhu Z. Associations between serum calcium, 25(OH)D level and bone mineral density in older adults. J Orthop Surg Res. 2019;14(1):458.
  • 14
    Li GH, Robinson-Cohen C, Sahni S, Au PC, Tan KC, Kung AW, Cheung CL. Association of genetic variants related to serum calcium levels with reduced bone mineral density. J Clin Endocrinol Metab. 2020;105(3):e328-36.
  • 15
    Sharma DK, Sawyer RK, Robertson TS, Stamenkov R, Solomon LB, Atkins GJ, Clifton PM, Morris HA, Anderson PH. Elevated serum 25-Hydroxyvitamin D levels are associated with improved bone formation and micro-structural measures in elderly hip fracture patients. J Clin Med. 2019;8(11).
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    Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357(3):266–81.
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    Vieth R. Vitamin D supplementation, 25-hydroxyvitamin D concentrations, and safety. Am J Clin Nutr. 1999;69(5):842–56.
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    Curtin LR, Mohadjer LK, Dohrmann SM, Montaquila JM, Kruszan-Moran D, Mirel LB, Carroll MD, Hirsch R, Schober S, Johnson CL. The National Health and Nutrition Examination Survey: Sample Design, 1999-2006. Vital Health Stat Ser 2 Data Eval Methods Res. 2012;(155):1–39.
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    Zipf G, Chiappa M, Porter KS, Ostchega Y, Lewis BG, Dostal J. National health and nutrition examination survey: plan and operations, 1999-2010. Vital Health Stat Ser 1 Programs Collection Proced. 2013;(56):1–37.
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    Patel CJ, Pho N, McDuffie M, Easton-Marks J, Kothari C, Kohane IS, Avillach P. A database of human exposomes and phenomes from the US National Health and nutrition examination survey. Sci Data. 2016;3: 160096.
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    Mensink GB, Fletcher R, Gurinovic M, Huybrechts I, Lafay L, Serra-Majem L, Szponar L, Tetens I, Verkaik-Kloosterman J, Baka A, et al. Mapping low intake of micronutrients across Europe. Br J Nutr. 2013;110(4):755–73.
  • 23
    Pinheiro MM, Schuch NJ, Genaro PS, Ciconelli RM, Ferraz MB, Martini LA. Nutrient intakes related to osteoporotic fractures in men and women--the Brazilian osteoporosis study (BRAZOS). Nutr J. 2009;8:6.
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    Asmus HG, Braun J, Krause R, Brunkhorst R, Holzer H, Schulz W, Neumayer HH, Raggi P, Bommer J. Two year comparison of sevelamer and calcium carbonate effects on cardiovascular calcification and bone density. Nephrol Dial Transplant. 2005;20(8):1653–61.
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    Raggi P, James G, Burke SK, Bommer J, Chasan-Taber S, Holzer H, Braun J, Chertow GM. Decrease in thoracic vertebral bone attenuation with calcium-based phosphate binders in hemodialysis. J Bone Miner Res. 2005;20(5):764–72.
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    Eklou-Kalonji E, Denis I, Lieberherr M, Pointillart A. Effects of extracellular calcium on the proliferation and differentiation of porcine osteoblasts in vitro. Cell Tissue Res. 1998;292(1):163–71.
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    Dvorak MM, Siddiqua A, Ward DT, Carter DH, Dallas SL, Nemeth EF, Riccardi D. Physiological changes in extracellular calcium concentration directly control osteoblast function in the absence of calciotropic hormones. Proc Natl Acad Sci U S A. 2004;101(14):5140–5.
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    Al-Dujaili SA, Koh AJ, Dang M, Mi X, Chang W, Ma PX, McCauley LK. Calcium sensing receptor function supports osteoblast survival and acts as a co-factor in PTH anabolic actions in bone. J Cell Biochem. 2016;117(7):1556–67.
  • 29
    Christakos S, Li S, DeLa Cruz J, Verlinden L, Carmeliet G. Vitamin D and bone. Handb Exp Pharmacol. 2020;262:47-63.
  • 30
    von Muhlen DG, Greendale GA, Garland CF, Wan L, Barrett-Connor E, Vitamin D. Parathyroid hormone levels and bone mineral density in community-dwelling older women: the rancho Bernardo study. Osteoporos Int. 2005;16(12):1721–6.
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    Collins D, Jasani C, Fogelman I, Swaminathan R. Vitamin D and bone mineral density. Osteoporos Int. 1998;8(2):110–4.
  • 33
    White Z, White S, Dalvie T, Kruger MC, Van Zyl A, Becker P. Bone health, body composition, and vitamin D status of black preadolescent children in South Africa. Nutrients. 2019;11(6).
  • 34
    Guillemant J, Taupin P, Le HT, Taright N, Allemandou A, Peres G, Guillemant S. Vitamin D status during puberty in French healthy male adolescents. Osteoporos Int. 1999;10(3):222–5.
  • 35
    Sharawat IK, Dawman L. Bone mineral density and its correlation with vitamin D status in healthy school-going children of Western India. Arch Osteoporos. 2019; 14(1):13.
  • 36
    von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet (London, England). 2007;370(9596):1453–7.

Publication Dates

  • Publication in this collection
    22 Mar 2021
  • Date of issue
    2021

History

  • Received
    01 Oct 2020
  • Accepted
    02 Mar 2021
  • Published
    10 Mar 2021
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