International Journal of Endocrinology

International Journal of Endocrinology / 2013 / Article
Special Issue

Vitamin D and Kidney

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Clinical Study | Open Access

Volume 2013 |Article ID 164939 | 6 pages |

Vitamin D Status in Patients Operated for Primary Hyperparathyroidism: Comparison of Patients from Southern and Northern Europe

Academic Editor: Ibrahim Sahin
Received02 May 2013
Revised04 Jul 2013
Accepted08 Jul 2013
Published05 Aug 2013


Aim. The interaction between vitamin D deficiency and primary hyperparathyroidism (PHPT) is not fully understood. The aim of this study was to investigate whether patients with PHPT from Spain and Sweden differed in vitamin D status and PHPT disease activity before and after surgery. Methods. We compared two cohorts of postmenopausal women from Spain and Sweden that had first-time surgery for sporadic, uniglandular PHPT. Biochemical variables reflecting bone metabolism and disease activity, including levels of 25-hydroxy vitamin D3 (25(OH)D) and bone mineral density, BMD, were measured pre- and one year postoperatively. Results. Median preoperative 25(OH)D levels were lower, and adenoma weight, PTH, and urinary calcium levels were higher in the Spanish cohort. The Spanish patients had higher preoperative levels of PTH (13.5 versus 11.0 pmol/L, ), urinary calcium (7.3 versus 4.1 mmol/L, ), and heavier adenomas (620 versus 500 g, ). The mean increase in BMD was higher in patients from Spain and in patients with vitamin D deficiency one year after surgery. Conclusion. Postmenopasual women with PHPT from Spain had a more advanced disease and lower vitamin 25(OH)D levels. Improvement in bone density one year after surgery was higher in patients with preoperative vitamin D deficiency.

1. Introduction

Primary hyperparathyroidism (PHPT) is a common endocrine disorder affecting about 2-3% of all postmenopausal women [1] in Europe. PHPT and vitamin D deficiency coexist in elderly patients [2, 3]. The association between vitamin D and PHPT is complex and not fully understood [46]. It is not known if vitamin D deficiency could trigger PHPT or vitamin D deficiency is caused or worsened by PHPT. Patients with PHPT and low levels of 25-hydroxyvitamin D (25(OH)D) have a more severe bone disease [79]. Previous data has also suggested that suboptimal vitamin D nutrition is linked to parathyroid adenoma growth and that improved vitamin D nutrition might decrease PHPT disease activity [10].

Vitamin D status in general is influenced by sun exposure and nutrition, and data from previous studies have shown that vitamin D deficiency is common among elderly people both in northern and southern Europe [11, 12].

One study has actually shown that vitamin D deficiency is more common in southern than northern Europe indicating that not only the number of sun hours per year of a country is important in the context of vitamin D deficiency [13]. Comparisons between different cohorts of patients with PHPT from different part of Europe with assumed different sun exposure and/or different vitamin D nutrition are lacking. PHPT is associated with increased bone turnover and increased fracture risk [14, 15].

Thus, on average, BMD increases after successful surgery for pHPT, but not all patients experience improvement in BMD. One year after parathyroidectomy about half of the patients will have a significant remineralisation [16, 17]. Factors like the severity of primary hyperparathyroidism, age, and renal function has been found to influence bone recovery after surgery.

The aim of this study was to investigate if two cohorts of postmenopausal women with primary hyperparathyroidism with assumed low sun exposure (Sweden) and high sun exposure (Spain) differed preoperatively in vitamin D status, disease activity, and outcome after surgery measured as change in BMD and biochemical variables one year after surgery.

2. Methods

Data collected prospectively in two cohorts of patients with primary hyperparathyroidism from Spain and Sweden, respectively, were compared preoperatively, and at one year follow-up.

Informed consent for anonymous use of data was obtained from all patients.

All patients were postmenopausal and had successful first time surgery for sporadic PHPT.

The diagnosis of PHPT was histologically proven in all patients. Part of the Swedish cohort has been described in a previous paper [16], and data from the Spanish cohort was recently published [17].

2.1. Clinical and Biochemical Variables

Demographic data and history of fractures up to 10 years before surgery were recorded. Serum levels of calcium, phosphate, alkaline phosphatase, creatinine, intact PTH, 25(OH)D and 1,25(OH)2D3, urinary calcium output over 24 h, and GFR were determined before and 1 year after parathyroidectomy. In the Swedish population high performance liquid chromatography, HPLC, was used for assessment of the concentration of serum 25(OH)D (reference range >75 nmol/L), and 1,25(OH)2D3 (reference range 10–60 ng/L) was measured with a radio-receptor assay (Incstar, Stillwater, MN, USA). Concentration of plasma parathyroid hormone (PTH) was analysed by an immunoradiometric assay for intact PTH (Hitachi Modular-E), (reference range 1.6–6.9 pmol/L). The analysis has a total CV of 5% at 7 pmol/L and 5% at 100 pmol/L.

In the Spanish group intact PTH was analyzed by an immunoradiometric assay, (reference range 14–55 pg/mL), 25(OH)D with a chemiluminescence immunoassay, CLI, reference range 8–80 ng/mL and 1,25(OH)2D3 with a radioimmunoassay, (reference range 15–56 pg/mL). To convert from the conventional unit to the SI unit, we multiplied by the conversion factor 0.105 for PTH, 2.496 for 25(OH)D, and with 2.6 for 1,25(OH)2D3. In the Spanish cohort GFR was assessed according to the Modification of Diet in Renal Disease formula and in the Swedish cohort the iohexol clearance method was used [18]. Vitamin D deficiency was defined as 25(OH)D < 50 nmol/L [12, 18].

2.2. Bone Mineral Density

BMD was measured by dual-energy absorptiometry (DEXA) at three sites, the femoral neck, total hip, and lumbar spine. In the Spanish cohort the QDR 4500 SL (Hologic, Waltham, Massachusetts, USA) machine was used. This technique has an in vivo coefficient of variation, CV, of 1 per cent at the lumbar spine and 1.6 per cent at the femoral neck. In the Swedish cohort the Lunar Expert XL (Lunar Corp, Madison, Wis, USA) equipment was used, with an in vivo CV of 1 per cent. Results were expressed as grams per square centimetre and as age and gender specific standard deviations ( scores). BMD was measured preoperatively and one year after parathyroidectomy. A significant increase in BMD for an individual patient was calculated according to the formula 1.96 × 2 × CV. This formula generates the value that separates two independent samples with 95 per cent confidence. For an individual in the Spanish cohort, the BMD should increase by at least 3.7 per cent to be significant and for an individual in the Swedish cohort the corresponding figure was 2.8 per cent. Unfortunately   score was not assessed in all the Swedish patients and therefore not shown.

2.3. Surgery and Followup

Bilateral neck exploration or selective parathyroidectomy depending on preoperative localization studies was performed under general anaesthesia. All adenomas were confirmed by typical histological features. All patients were seen 2–6 weeks and 1 year after parathyroidectomy. At this time, BMD and biochemical variables were reassessed. In the Spanish cohort one gram of elemental calcium per day was prescribed during the follow-up period. In the Swedish cohort prescription of calcium and vitamin D was done on demand.

2.4. Statistics

Results are expressed as medians (interquartile range, IQR). Wilcoxon and Mann-Whitney tests were used when comparing continuous variables between groups. For categorical data statistical significance was analysed by the chi squared test . Statistical significance was set at . Data were analysed with STATA 11.0 (Stata corp., Texas, USA).

3. Results

3.1. Preoperative Data

254 patients with a median age of 65 (57–73) years were included in the study. The median serum calcium level was 2.74 (2.65–2.85) mmol/L, and the median serum intact PTH level was 12.0 (9.3–16.2) pmol/L. The median adenoma weight in all patients was 546 (300–1200) mg. 19 patients in the Spanish and 29 in the Swedish cohort had a history of fragility fracture before parathyroidectomy. 63 per cent of the Spanish and 39 per cent of the Swedish patients had biochemical vitamin D insufficiency preoperatively . There was no difference in age at surgery or preoperative calcium levels, but median preoperative levels of PTH, phosphate, urinary calcium, ALP, GFR, creatinine, 1,25(OH)2D3, and adenoma weight were all higher, and median preoperative 25(OH)D lower, in the Spanish cohort (see Table 1).

VariableAllSpanish cohort Swedish cohort P

Age (years)65 (57–73)64 (57–72)66 (58–74)0.33
p-Ca (mmol/L)2.74 (2.65–2.85)2.74 (2.65–2.85)2.74 (2.66–2.84)0.73
PTH (pmol/L)12 (9.3–16.2)13.5 (10.5–20.4)11.0 (8.4–14.0)<0.001
25-OH-D (nmol/L)44 (26–64)40 (25–58)51 (28–66)0.01
1,25-OH-D (pmol/L)55 (98–162)142 (99–198)56 (28–66)<0.001
Phosphate (mmol/L)0.85 (0.77–0.96)0.90 (0.80–1.0)0.82 (0.72–0.90)<0.001
ALP (unit)2.6 (1.6–3.8)3.0 (1.7–4.3)2.3 (1.5–3.4)0.002
GFR (mL/min)75 (63–89)70 (58–85)76 (65–93)0.01
Creatinine (umol/L)71 (62–81)80 (71–88)65 (56–73)<0.001
Urinary calcium (unit)5.9 (3.6–9)7.3 (3.9–10.0)4.1 (2.8–5.9)<0.001
Fracture (yes/no)48/19519/10729/990.002
Vitamin D deficiency (yes/no)130/9680/4250/540.007
Adenoma weight (mg)546 (300–1200)620 (290–1400)500 (320–1030)<0.001

3.2. Followup One Year after Surgery

At one year after surgery, all patients in both cohorts remained normocalcemic. However, median levels of 1,25(OH)2D3 were higher, and median levels of calcium and 25(OH)D were lower, in the Spanish cohort as compared to the Swedish (see Table 2).

VariableSpanish cohort Swedish cohort P

p-Ca (mmol/L)2.32 (2.24–2.42)2.37 (2.30–2.48)0.002
PTH (pmol/L)4.7 (3.8–6.9)4.7 (3.7–6)0.51
25-OH-D (nmol/L)45 (24–65)62 (49–84)<0.001
1,25-OH-D (pmol/L)84 (0–120)31 (38–50)<0.001
ALP1.2 (0.9–2.5)1.3 (1.0–2.1)0.35

BMD increased one year after surgery as compared to preoperatively at all sites in both cohorts, both in absolute terms (g/cm2) and as -scores (see Table 3). Preoperatively, BMD was higher in the Swedish cohort for lumbar spine and femoral neck in absolute terms, but not as -scores.

BMD siteSpanish cohort
Before surgery
Spanish cohort
One year postop
P Swedish cohort
Before surgery
Swedish cohort
One year postop
P P diff Spanish-swedish preop

Lumbar spine, absolute0.79 (0.70–0.88)0.83 (0.74–0.93)<0.001 1.00 (0.83–1.11)1.03 (0.88–1.14)<0.001 <0.001
Lumbar spine, -score−0.7 (−1.6–0.3)0.7 (0.4–1.3)<0.001 −0.4 (−1.6–0.6)0.7 (0.4–1.38)<0.001 0.75
Femoral neck, absolute0.62 (0.56–0.69)0.64 (0.57–0.70)<0.001 0.76 (0.69–0.85)0.79 (0.70–0.88)<0.001 <0.001
Femoral neck, -score−0.7 (−1.3 to −0.1)−0.4 (−1.1–0.2)<0.001 −0.5 (−1.1–0.1)−0.5 (−0.9–0.2)<0.001 0.11
Total hip, absolute0.76 (0.68–0.85)0.76 (0.70–0.87)<0.001 0.77 (0.56–0.88)0.84 (0.75–0.95)<0.001 0.40
Total hip, -score−0.5 (−0.9–0.3)−0.2 (−0.8–0.5)<0.001 −0.4 (1.0–0.4)0 (−0.7–0.7)<0.001 0.91

When the two cohorts were compared regarding change in BMD, the Spanish cohort improved more at the lumbar spine, in absolute terms, and at the femoral neck, as -score. For the other measurements, there was no difference between the two cohorts (see Table 4).

BMD siteSpanish cohortSwedish cohortP

Lumbar spine, absolute4.2 (1.0–6.9)1.3 (−0.9–6.8)0.009
Lumbar spine, -score0.4 (0.2–0.6)0.2 (0.0–0.6)0.18
Femoral neck, absolute2.8 (−0.9–7.3)2.1 (−1.1–5.8)0.46
Femoral neck, -score0.3 (0.0–0.5)0.1 (−0.1–0.4)0.004
Total hip, absolute2.8 (−0.3–5.7)1.9 (0.6–4.2)0.09
Total hip -score0.3 (0.1–0.5)0.2 (0.1–0.4)0.05

3.3. Vitamin D Status

Bone remineralisation after operation in patients with or without vitamin D deficiency (25(OH)D < 50 nmol/L) are shown in Table 5. Patients with vitamin D deficiency had higher remineralization one year after surgery at total hip compared to patients with sufficient vitamin D levels, but not at the lumbar spine and/or femoral neck.

BMD siteVitamin D-deficiencyVitamin D-sufficiencyP
(25-OH-D < 50 nmol/L) (25-OH-D ≥ 50 nmol/L)

Lumbar spine, absolute3.5 (−0.5–7.0)2.2 (−2.0–6.6)0.12
Lumbar spine, -score0.4 (0.1–0.6)0.3 (0.0–0.6)0.40
Femoral neck, absolute2.8 (−0.8–7.3)2.5 (−1.9–6.0)0.47
Femoral neck, -score0.3 (0–0.5)0.2 (−0.1–0.3)0.05
Total hip, absolute2.7 (0–5.7)1.00 (−1.4–4.8)0.03
Total hip, -score0.3 (0.1–0.5)0.2 (0.0–0.4)0.01

4. Discussion

In this study comparing postmenopausal Swedish and Spanish patients operated on for PHPT, the Spanish cohort had lower median levels of 25(OH)D whereas median PTH and urinary calcium levels were higher before surgery, compared to the Swedish group of patients. Median adenoma weight was also higher in the Spanish cohort, but preoperative calcium levels and age were similar in the two cohorts.

One year after surgery, we found no difference in median PTH levels between the two cohorts, but median levels of 25(OH)D were still lower in the Spanish than in the Swedish cohort, even though median levels of 25(OH)D were higher after surgery as compared to preoperatively in both cohorts.

A potential explanation for these findings could be a selection bias, that is, that patients in Spain are referred and accepted for surgery in a more advanced stage of the disease. If this is the case, the lower levels of 25(OH)D in the Spanish cohort preoperatively might be due to increased conversion of 25(OH)D into 1,25(OH2)D3 by PTH-mediated renal 1α-hydroxylation [19]. This phenomenon is supported by the fact that PTH and 25(OH)D are inversely correlated; thus, in a more severe PHPT disease higher PTH and lower 25(OH)D are expected [17]. Patients with PHPT might also have low levels of 25(OH)D because of poor nutrition and/or less sun exposure [20]. Whether the high serum calcium and PTH levels may interfere with the conversion of 7-dehydrocholesterol in the skin by UV-B to previtamin D, or with the hydroxylation of vitamin D in the liver to 25(OH)D remains to be determined.

We assumed that patients from Spain with PHPT had higher sun exposure than their Swedish counterparts [8]. However, sun exposure is not the only determinant of 25(OH)D levels. Hence, previous studies have shown a north-south gradient regarding serum 25(OH)D, with higher levels of 25(OH)D in Scandinavia and lower levels in Italy and Spain countries. This points to other determinants than sunshine, for example, nutrition, food fortification, and supplement use [13]. Unfortunately, information about nutrition was lacking in the present study. Thus, we cannot rule out that the Swedish patients were more inclined to take vitamin D supplementation and had a higher nutritional intake of vitamin D.

On the other hand the HELENA study has demonstrated that the winter half-year adolescents in Southern Europe have higher serum 25OHD levels compared to adolescents in Central Europe [21], so data about vitamin D status in different populations even without PHPT is conflicting.

Few studies have compared differences in preoperative status and outcome after PHPT surgery in two cohorts living in two countries that differ in distance from the equator, that is, different sun exposure and difference in preoperative D vitamin status [22, 23].

Silverberg compared two cohorts of patients with PHPT from New York City and Beijing, China. Patients from China had a more advanced PHPT disease and a more profound Vitamin D deficiency [23]. This could reflect the same findings we found between Swedish and Spanish patients, that is, patients from Spain and China come to surgery in a more advanced state of the PHPT disease.

However, in our study these mechanisms cannot account for the observed difference in 25(OH)D levels between the two cohorts after surgery, since at this point, both cohorts had similar levels of PTH and were normocalcemic, that is, cured of PHPT. Another explanation might instead be that low levels of 25(OH)D causes or at least worsens PHPT. One study suggests that low levels of 25(OH)D stimulate parathyroid adenoma growth [10].

It seems that it is very hard to define the mechanisms of interaction between vitamin D and PHPT exactly. We believe that the PHPT disease itself could worsen vitamin D deficiency but also the reverse situation, that is, vitamin D deficiency could worsen the PHPT disease.

Patients from Spain had preoperatively lower bone mineral density in lumbar spine and femoral neck probably because Spanish patients had a more advanced PHPT disease. The Spanish patients also gained more from the operation in terms of bone density suggesting that the remineralisation response is more pronounced in patients with lower BMD before parathyroidectomy [18].

Patients with vitamin D deficiency had higher increase in bone density in total hip. Previous studies have shown that patients with PHPT and vitamin D deficiency gain more in bone density after PHPT surgery [23]. This highlights the possible benefit of vitamin D supplementation in PHPT disease regarding gain in bone density. So far no convincing study has shown if postoperative vitamin D supplementation enhances increase in bone density after parathyroidectomy [9], and further studies are warranted.

The cohorts in the present study were homogeneous, and data was recorded in a prospective and consecutive manner. A limitation is that 25(OH)D was measured with different methods in Sweden and Spain, respectively. Previous results suggest that 25(OH)D levels measured with CLI, that is, the Spanish method in the present study yields lower levels than HPLC, that is, the Swedish method [24] Thus, the difference in 25(OH)D between the cohorts might be spurious and caused by the use of different methods. However, the other biochemical findings and bone density measurements support the conclusion that the Spanish patients suffered from a more severe PHPT disease. Another potential limitation is that we did not record season of blood sampling before PHPT surgery. However, there was no reason to suspect that distribution of season of operation differed between cohorts. Unfortunately, we did not have information about nutrition in the two cohorts.

In conclusion we found that postmenopausal women with PHPT from Spain had lower preoperative levels of 25(OH)D and more severe PHPT compared to Swedish patients, and patients with PHPT and vitamin D deficiency gained more in bone density at some sites one year after parathyroidectomy.


This work was presented orally at the 5th biennial ESES Congress in Gothenburg May 24–26, 2012.

Conflict of Interests

There is no conflict of interests that could be perceived as prejudicing the impartiality of the research reported.

Authors’ Contribution

Erik Nordenström and Antonio Sitges-Serra designed research. Erik Nordenström, Antonio Sithes-Serra, Joan Sancho, Mark Their, and Martin Almqvist conducted research. Erik Nordenström, Antonio Sitges-Serra, and Martin Almqvist analyzed data. Erik Nordenström, Antonio Sitges-Serra, Joan Sancho, Mark Their and Martin Almqvistwrote paper.


  1. E. Lundgren, E. G. Hagström, J. Lundin et al., “Primary hyperparathyroidism revisited in menopausal women with serum calcium in the upper normal range at population-based screening 8 years ago,” World Journal of Surgery, vol. 26, no. 8, pp. 931–936, 2002. View at: Publisher Site | Google Scholar
  2. W. Saliba, I. Lavi, H. S. Rennert, and G. Rennert, “Vitamin D status in primary hyperparathyroidism,” European Journal of Internal Medicine, vol. 23, no. 1, pp. 88–92, 2012. View at: Publisher Site | Google Scholar
  3. E. A. Yetley, “Assesing the vitamin D status of the US population,” The American Journal of Clinical Nutrition, vol. 88, no. 2, pp. 558–564, 2008. View at: Google Scholar
  4. R. Nuti, D. Merlotti, and L. Gennari, “Vitamin D deficiency and primary hyperparathyroidism,” Journal of endocrinological investigation, vol. 34, no. 7, pp. 45–49, 2011. View at: Google Scholar
  5. S. J. Silverberg, E. Shane, D. W. Dempster, and J. P. Bilezikian, “The effects of vitamin D insufficiency in patients with primary hyperparathyroidism,” American Journal of Medicine, vol. 107, no. 6, pp. 561–567, 1999. View at: Publisher Site | Google Scholar
  6. F. Bienaimé, D. Prié, G. Friedlander, and J. C. Souberbielle, “Vitamin D metabolism and activity in parathyroid gland,” Molecular and Cellular Endocrinology, vol. 347, no. 5, pp. 30–41, 2011. View at: Publisher Site | Google Scholar
  7. Y. Inoue, H. Kaji, I. Hisa et al., “Vitamin D status affects osteopenia in postmenopausal patients with primary hyperparathyroidism,” Endocrine Journal, vol. 55, no. 1, pp. 57–65, 2008. View at: Publisher Site | Google Scholar
  8. S. Weaver, D. B. Doherty, C. Jimenez, and N. D. Perrier, “Peer-reviewed, evidence-based analysis of vitamin D and primary hyperparathyroidism,” World Journal of Surgery, vol. 33, no. 11, pp. 2292–2302, 2009. View at: Publisher Site | Google Scholar
  9. E. Nordenström, J. Westerdahl, and A. Bergenfelz, “Effect on bone density of postoperative calcium and vitamin-D supplementation in patients with primary hyperparathyroidism: a retrospective study,” Langenbeck's Archives of Surgery, vol. 394, no. 3, pp. 461–467, 2009. View at: Publisher Site | Google Scholar
  10. D. Sudhaker Rao, M. Honasoge, G. W. Divine et al., “Effect of vitamin D nutrition on parathyroid adenoma weight: pathogenetic and clinical implications,” Journal of Clinical Endocrinology and Metabolism, vol. 85, no. 3, pp. 1054–1058, 2000. View at: Publisher Site | Google Scholar
  11. G. Isaia, R. Giorgino, G. B. Rini, M. Bevilacqua, D. Maugeri, and S. Adami, “Prevalence of hypovitaminosis D in elderly women in Italy: clinical consequences and risk factors,” Osteoporosis International, vol. 14, no. 7, pp. 577–582, 2003. View at: Publisher Site | Google Scholar
  12. R. Andersen, C. Mølgaard, L. T. Skovgaard et al., “Teenage girls and elderly women living in northern europe have low winter vitamin D status,” European Journal of Clinical Nutrition, vol. 59, no. 4, pp. 533–541, 2005. View at: Publisher Site | Google Scholar
  13. P. Lips, “Vitamin D status and nutrition in Europe and Asia,” Journal of Steroid Biochemistry and Molecular Biology, vol. 103, no. 3–5, pp. 620–625, 2007. View at: Publisher Site | Google Scholar
  14. S. Khosla and L. J. Melton III, “Fracture risk in primary hyperparathyroidism,” Journal of Bone and Mineral Research, vol. 17, no. 2, pp. N103–N107, 2002. View at: Google Scholar
  15. P. Vestergaard and L. Mosekilde, “Parathyroid surgery is associated with a decreased risk of hip and upper arm fractures in primary hyperparathyroidism: a controlled cohort study,” Journal of Internal Medicine, vol. 255, no. 1, pp. 108–114, 2004. View at: Publisher Site | Google Scholar
  16. E. Nordenström, J. Westerdahl, and A. Bergenfelz, “Recovery of bone mineral density in 126 patients after surgery for primary hyperparathyroidism,” World Journal of Surgery, vol. 28, no. 5, pp. 502–507, 2004. View at: Publisher Site | Google Scholar
  17. A. Sitges-Serra, L. García, R. Prieto, M. J. Peña, X. Nogués, and J. J. Sancho, “Effect of parathyroidectomy for primary hyperparathyroidism on bone mineral density in postmenopausal women,” British Journal of Surgery, vol. 97, no. 7, pp. 1013–1019, 2010. View at: Publisher Site | Google Scholar
  18. E. Krutzen, S. E. Back, I. Nilsson-Ehle, and P. Nilsson-Ehle, “Plasma clearance of a new contrast agent, iohexol: a method for the assessment of glomerular filtration rate,” Journal of Laboratory and Clinical Medicine, vol. 104, no. 6, pp. 955–961, 1984. View at: Google Scholar
  19. E. Kandil, A. P. Tufaro, K. A. Carson et al., “Correlation of plasma 25-hydroxyvitamin D levels with severity of primary hyperparathyroidism and likelihood of parathyroid adenoma localization on sestamibi scan,” Archives of Otolaryngology—Head and Neck Surgery, vol. 134, no. 10, pp. 1071–1075, 2008. View at: Publisher Site | Google Scholar
  20. L. O'Mahony, M. Stepien, M. J. Gibney, A. P. Nugent, and L. Brennan, “The potential role of vitamin D enhanced foods in improving vitamin D status,” Nutrients, vol. 3, no. 12, pp. 1023–1041, 2011. View at: Publisher Site | Google Scholar
  21. D. S. Rao, G. Agarwal, G. B. Talpos et al., “Role of vitamin D and calcium nutrition in disease expression and parathyroid tumor growth in primary hyperparathyroidism: a global perspective,” Journal of Bone and Mineral Research, vol. 17, no. 2, pp. N75–N80, 2002. View at: Google Scholar
  22. M. González-Gross, J. Valtueña, C. Breidenassel et al., “Vitamin D status among adolescents in Europe: The Healthy Lifestyle in Europe by Nutrition in Adolescence study,” British Journal of Nutrition, vol. 107, no. 5, pp. 755–764, 2012. View at: Publisher Site | Google Scholar
  23. S. J. Silverberg, “Vitamin D deficiency and primary hyperparathyroidism,” Journal of Bone and Mineral Research, vol. 22, no. 2, pp. V100–V104, 2007. View at: Publisher Site | Google Scholar
  24. G. Snellman, H. Melhus, R. Gedeborg et al., “Determining vitamin D status: a comparison between commercially available assays,” PLoS ONE, vol. 5, no. 7, article e11555, 2010. View at: Publisher Site | Google Scholar

Copyright © 2013 Erik Nordenström et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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