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. 2013 Mar 7;17(4):732–738. doi: 10.1017/S136898001300030X

Predictors of vitamin D deficiency and insufficiency in adult Bahrainis: a cross-sectional study

Jamal Golbahar 1,*, Nida Al-Saffar 1, Diab Altayab Diab 1, Sara Al-Othman 1, Abdullah Darwish 2, Ghada Al-Kafaji 1
PMCID: PMC10282488  PMID: 23464685

Abstract

Objective

High prevalence of hypovitaminosis D has been reported to be common in different regions of the Middle East. The objective of the present study was to examine the predictors of vitamin D deficiency and insufficiency in Bahrainis.

Design

A cross-sectional study.

Setting

Blood transfusion volunteers at a blood bank.

Subjects

Serum levels of total 25-hydroxyvitamin D, bone markers and other parameters such age, sex, season and clothing style in the 500 healthy Bahrainis were investigated.

Results

In the entire cohort the prevalence of vitamin D deficiency was 49·4 % and the relative risk of vitamin D deficiency increased significantly by 1·1, 1·2, 1·5, 1·7 and 1·2 fold with younger age group (P = 0·03), hyperparathyroidism (P = 0·01), low serum Ca (P < 0·001), warm and hot months of the year (P < 0·0001) and female sex (P = 0·002), respectively. In females the prevalence of vitamin D deficiency was 67·6 % and the relative risk of vitamin D deficiency increased significantly by 1·1, 1·2, 1·2, 1·2 and 1·4 fold with younger age group (P = 0·04), hyperparathyroidism (P = 0·03), low serum Ca (P = 0·001), warm and hot months of the year (P = 0·001) and conservative clothing style (P = 0·04), respectively. In contrast, in males the prevalence of vitamin D deficiency was 31·2 % and the relative risk of vitamin D deficiency was increased by 1·6 fold in warm and hot months of the year (P < 0·0001).

Conclusions

High prevalence of low circulating levels of vitamin D and the relative risk factors associated with vitamin D deficiency and insufficiency observed in the present study suggest an urgent need for public health interventions including vitamin D food fortification in Bahrain.

Keywords: Vitamin D, Deficiency, Insufficiency, Predictors, Bahrainis


Prevalence of hypovitaminosis D has been reported to be high and is a public health issue in various regions around the Middle East, including the United Arab Emirates, Oman, Saudi Arabia, Jordan, Iran and Qatar. This major public health problem could affect all individuals across all life stages. The high prevalence of vitamin D deficiency in the region is suggested to be largely the result of limited sun exposure due to religious and cultural practices, prolonged breast-feeding without vitamin D supplementation( 1 7 ) and also the lack of food fortification policies( 8 ). The levels of serum 25-hydroxycholecalciferol (25(OH)D3) have also been reported to be <25 nmol/l in one-third of individuals in this region( 9 ).

There are a number of risk factors that are reported to be associated with vitamin D status in different populations. Generally, it has been reported that younger individuals have higher levels of vitamin D than older ones and males have slightly higher levels than females( 9 , 10 12 ). There are also reports to suggest that the prevalence of vitamin D deficiency is higher during the winter than during the summer months and that winter season is one of the risk factors associated with vitamin D deficiency( 13 , 14 ). In addition, biochemical markers such as plasma parathyroid hormone (PTH) and serum Ca have also been reported to be associated with vitamin D status( 15 , 16 ). Serum level of 25(OH)D3 plus 25-hydroxyergocalciferol (25(OH)D2), which is known as total 25-hydroxyvitamin D (25(OH)D), has been reported to be the most precise marker of vitamin D status as it reflects cutaneous synthesis as well as total intakes of vitamin D from foods and supplements( 17 ). Based on its review of data of vitamin D needs, a committee of the Institute of Medicine concluded that persons are at risk of vitamin D deficiency with serum total 25(OH)D concentrations of <30 nmol/l and inadequacy at levels ranging from 30 to 50 nmol/l. The committee stated that a serum total 25(OH)D level of 50 nmol/l (optimal) could cover the needs of 97·5 % of a population( 18 ).

In the present study, the associations of vitamin D deficiency and insufficiency with biometric and biochemical markers related to vitamin D metabolism in healthy adults were investigated for the first time in a Bahraini population.

Materials and methods

The present study was conducted between October 2010 and October 2011 among volunteers attending the blood bank centre in Bahrain Defense Force (BDF) Hospital, the second largest hospital in Bahrain. The volunteers were queried to assess their eligibility and willingness to participate in the study. All completed a questionnaire on age, gender, style of clothing, history of any chronic diseases (such as diabetes mellitus, hypertension, obesity, osteoporosis, osteomalacia, liver disease, renal disease, hypo- or hyperparathyroidism), vitamin and mineral deficiency, steroid therapy or any drugs that could interfere with vitamin D metabolism, or vitamin therapy including vitamin D and Ca intake by face-to-face interview. Out of 700 persons who attended the blood bank and were asked to participate in the study, sixty-six were non-Bahrainis. Of the remaining 634, 550 agreed with a response rate of 87 %; however, fifty persons were excluded because of obesity (BMI >25 kg/m2), history of liver, renal, gestational or endocrine disorder, and also taking medications that influence bone metabolism and current vitamin D and Ca intake. All study participants gave written informed consent after being fully informed of the study objectives and procedures and their right to withdraw from the study. The research protocol was approved by the Research and Ethics Committees of the College of Medicine and Medical Sciences, Arabian Gulf University, and the Research and Ethics Committee of BDF Hospital.

Conservative style of clothing was defined as women wearing a traditional long black garment called ‘abayah’ that covers the body from the shoulders down to the feet, with scarf-like cover that covers the hair but not the face.

A blood sample was collected from each participant and serum and plasma were prepared. Serum Ca and P were analysed immediately using a Cobas 6000 analyser system (Roche Ltd, Basel, Switzerland). Remaining serum and plasma samples were then stored at −70°C until further analysis of vitamin D and PTH. Plasma PTH was determined using commercially available ELISA kits (Creative Diagnostics, Shirley, NY, USA). The intra-assay and inter-assay CV for determination of PTH in plasma were <4·5 % and 7·1 % for low control and 3·2 % and 5·2 % for high control, respectively. Serum 25(OH)D3 and 25(OH)D2 concentrations were determined by ultra-performance liquid chromatography mass spectrometry (UPLC-MS/MS) using a commercially available kit (Chromsystem, Munich, Germany). The intra-assay and inter-assay CV for determination of 25(OH)D3 in serum for low control were <2·7 % and 3·9 %, and for high control were 4·2 % and 4·0 %, respectively. The intra-assay and inter-assay CV for determination of 25(OH)D2 in serum for low control were <3·9 % and 5·7 % and for high control were <4·3 % and 4·7 %, respectively.

Statistical analysis

Vitamin D status was assessed according to the 2011 recommendation of the Institute of Medicine that classifies vitamin D deficiency at serum 25(OH)D concentration of <30 nmol/l, insufficiency at levels ranging from 30 to 50 nmol/l and optimal at levels of ≥50 nmol/l( 18 ).

The normality of total 25(OH)D distribution was assessed using the Kolmogorov–Smirnov test. As the distribution was negatively skewed, logarithmic transformation was applied to reduce kurtosis before geometric means were calculated. Thus the logarithmic transformations were used in further statistical analysis.

Student's t test was used to compare the total 25(OH)D concentrations according to all other biometric and biochemical parameters between males and females. Pearson's correlation coefficient was used to examine the correlation between total 25(OH)D and other variables. ANOVA was used to compare the values of biometric and biochemical parameters between participants with optimal, insufficiency and deficiency of vitamin D.

Mantel–Haenszel relative risk analysis was used to determine the association of age, gender, season, hyperparathyroidism, low Ca and style of clothing with vitamin D deficiency and insufficiency in the entire cohort, males and females. Hyperparathyroidism was defined as plasma PTH levels of >65·0 pg/ml and hypocalcaemia was defined as serum Ca of <2·1 nmol/l. Receiver operating characteristic (ROC) curve analysis was used to determine the best biochemical marker to predict vitamin D deficiency. Participants with vitamin D deficiency were considered affected, and those with an optimal amount of vitamin D were considered as controls and not affected. Greater deviation toward the left upper corner of the curve indicates better detection of vitamin D deficiency.

All statistical inferences were made based on a two-sided significance level of P < 0·05 and all statistical analyses were performed using the statistical software package IBM SPSS version 19·0.

Results

Baseline biochemical and biometric characteristics of the entire cohort, males and females are illustrated in Table 1. Among all the variables, plasma PTH and serum P were significantly higher in females than males (P < 0·05), whereas serum total 25(OH)D and serum Ca were significantly lower in females than in males (P < 0·05).

Table 1.

Biochemical and biometric characteristics of the entire cohort, males and females; Bahrain, October 2010–October 2011

Entire cohort (n 500) Males (n 250) Females (n 250)
Characteristic Mean sd 95 % CI Mean sd 95 % CI Mean sd 95 % CI
Age (years) 33·7 10·1 32·4, 34·9 33·8 10·1 32·3, 35·4 33·5 10·4 31·5, 35·6
Serum total 25(OH)D (nmol/l) 27·9 19·3 26·9, 31·6 34·2* 23·7 26·9, 31·6 21·6 19·0 18·6, 24·2
Serum P (mmol/l) 1·2 0·3 1·1, 1·2 1·1 0·3 1·1, 1·2 1·3† 0·3 1·2, 1·3
Serum Ca (mmol/l) 2·3 0·2 2·2, 2·3 2·3* 0·2 2·3, 2·4 2·2 0·2 2·2, 2·3
Plasma PTH (pg/ml) 56·3 24·0 41·1, 71·4 46·5 37·4 29·4, 54·4 78·2† 38·5 45·1, 111·2

25(OH)D, 25-hydroxyvitamin D; PTH, parathyroid hormone.

Results are expressed as mean and standard deviation, except for total 25(OH)D which is expressed as geometric mean and standard deviation.

*Mean value was significantly higher in males than females (P < 0·05).

†Mean value was significantly higher in females than males (P < 0·05).

Results from the Pearson correlation analysis in the entire cohort showed that, among all variables, serum total 25(OH)D was significantly and positively correlated with age (r = 0·131, P = 0·003), serum Ca (r = 0·174, P = 0·001) and male sex (r = 0·388, P = 0·000) and negatively correlated with plasma PTH (r = −0·19, P = 0·03). In females, serum total 25(OH)D was significantly and positively correlated with age (r = 0·289, P = 0·001) and significantly and negatively correlated with plasma PTH (r = −0·21, P = 0·01); whereas in males among all variables serum total 25(OH)D was significantly and negatively correlated with plasma PTH (r = −0·134, P = 0·03).

Table 2 presents the serum levels of total 25(OH)D in the entire cohort, males and females according to age group, season and clothing style.

Table 2.

Serum levels of total 25(OH)D (nmol/l) in the entire cohort, males and females, according to age group, season and clothing style; Bahrain, October 2010–October 2011

Entire cohort (n 500) Males (n 250) Female (n 250)
Mean sd n Mean sd n Mean sd n
Age
<30 (15–29 years) 26·1 18·1 262 33·9 23·7 133 18·3* 12·5 129
>30 (30–68 years) 29·7 20·4 238 34·5 20·9 117 24·8* 19·9 121
P 0·004 0·07 0·001
Season
Apr–Sep 21·1 17·4 325 27·0 15·1 135 17·6* 14·5 190
Oct–Mar 34·7 21·2 175 41·4 32·3 115 25·6* 23·5 60
P <0·0001 <0·0001 <0·001
Clothing style
Conservative 20·0 18·9 224
Western style 23·2 19·1 16
P 0·03

25(OH)D, 25-hydroxyvitamin D.

All results are presented as geometric mean and standard deviation.

*Mean value was significantly lower than that of males (P ≤ 0·0001).

Biochemical and biometric parameters according to vitamin D status in the entire cohort, females and males are illustrated in Table 3. In the entire cohort, ANOVA showed that serum Ca (P = 0·02) was significantly decreased whereas plasma PTH (P = 0·03) was significantly increased between individuals with optimal, insufficiency and deficiency of vitamin D. In females, age (P = 0·04) and serum Ca (P = 0·04) were significantly decreased and plasma PTH (P = 0·004) was significantly increased between individuals with vitamin D insufficiency and deficiency compared with those with optimal total 25(OH)D.

Table 3.

Biochemical and biometric characteristics of the entire cohort, males and females, according to vitamin D status; Bahrain, October 2010–October 2011

Entire cohort (n 500) Females (n 250) Males (n 250)
Optimal (n 68) Insuf. (n 185) Defic. (n 247) P Optimal (n 20) Insuf. (n 61) Defic. (n 169) P Optimal (n 48) Insuf. (n 124) Defic. (n 78) P
Characteristic Mean sd Mean sd Mean sd ANOVA Mean sd Mean sd Mean sd ANOVA Mean sd Mean sd Mean sd ANOVA
Age (years) 35·5 10·7 35·2 10·7 33·5 10·6 0·164 38·4 13·6 38·1 11·9 33·1 10·6 0·04 34·3 9·1 33·8 9·8 34·5 10·0 0·892
Serum P (mmol/l) 1·2 0·31 1·1 0·29 1·2 0·28 0·07 1·4 0·41 1·3 0·29 1·3 0·29 0·154 1·0 0·21 1·1 0·27 1·1 0·23 0·863
Serum Ca (mmol/l) 2·5 0·27 2·3 0·18 2·2 0·21 0·02 1·9 0·41 2·1 0·19 2·3 0·20 0·04 2·4 0·16 2·3 0·17 2·1 0·21 0·435
Plasma PTH (pg/ml) 50·8 45·3 57·2 38·5 60·2 33·9 0·03 41·0 36·1 48·7 35·8 70·7 55·8 0·004 43·8 31·4 43·4 27·0 55·1 35·6 0·256

PTH, parathyroid hormone; 25(OH)D, 25-hydroxyvitamin D.

Vitamin D status: optimal, serum 25(OH)D ≥ 50 nmol/; insufficiency (Insuf.), serum 25(OH)D = 30–50 nmol/l; deficiency (Defic.), serum 25(OH)D < 30 nmol/l.

In Table 4, Mantel-Haenszel relative risk analysis showed that, in the entire cohort, the relative risk of vitamin D deficiency was significantly increased with younger age group (P = 0·03), low serum Ca (P < 0·001), warm and hot months of the year (P < 0·0001) and female sex (P = 0·002), while relative risk of hyperparathyroidism was significantly increased with vitamin D deficiency (P = 0·01). In females the relative risk of vitamin D deficiency was significantly increased with younger age group (P = 0·04), low serum Ca (P = 0·001), warm and hot months of the year (P = 0·001) and conservative clothing style (P = 0·04), and relative risk of hyperparathyroidism was significantly increased with vitamin D deficiency (P = 0·03). In males, the relative risk of vitamin D deficiency was increased by 1·6 fold with warm and hot months of the year (P < 0·0001). In the entire cohort (P = 0·03), females (P = 0·03) and males (P = 0·006), the relative risk of vitamin D insufficiency was also significantly increased in warm and hot months of the year.

Table 4.

Mantel–Haenszel relative risk analysis for the association of age, high plasma PTH and low serum calcium with vitamin D deficiency and insufficiency in the entire cohort, females and males; Bahrain, October 2010–October 2011

Entire cohort (n 500) Females (n 250) Males (n 250)
Insufficiency Deficiency Insufficiency Deficiency Insufficiency Deficiency
Optimal RRR 95 % CI P RRR 95 % CI P Optimal RRR 95 % CI P RRR 95 % CI P Optimal RRR 95 % CI P RRR 95 % CI P
Age <30 (15–29 years) 1·0 1·1 0·9, 1·3 0·169 1·1 1·0, 1·3 0·03 1·0 0·9 0·2, 1·2 0·634 1·1 1·0, 1·2 0·04 1·0 1·2 0·9, 1·5 0·113 1·2 0·9, 1·6 0·158
Plasma PTH > 65 ng/l 1·0 0·9 0·7, 1·2 0·839 1·2 1·1, 1·3 0·01 1·0 1·0 0·6, 1·3 0·784 1·2 1·1, 1·2 0·03 1·0 0·9 0·6, 1·2 0·772 1·3 0·9, 1·6 0·107
Serum Ca < 2·1 nmol/l 1·0 1·0 0·8, 1·2 0·552 1·5 1·2, 1·8 <0·001 1·0 0·6 0·3, 1·2 0·670 1·2 1·1, 1·4 0·001 1·0 1·0 0·8, 1·3 0·693 1·0 0·7, 1·3 0·974
Season (Apr–Sep) 1·0 1·2 1·0, 1·4 0·03 1·7 1·5, 2·1 <0·0001 1·0 1·3 1·0, 1·6 0·03 1·2 1·1, 1·4 0·001 1·0 1·3 1·1, 1·3 0·006 1·6 1·4, 1·9 <0·0001
Sex (female) 1·0 1·1 0·9, 2·2 0·249 1·2 1·1, 1·3 0·002
Conservative clothing 1·0 1·2 0·8, 1·4 0·210 1·4 1·0, 1·2 0·04

PTH, parathyroid hormone; RRR, relative risk ratio; 25(OH)D, 25-hydroxyvitamin D.

Vitamin D status: optimal, serum 25(OH)D ≥ 50 nmol/; insufficiency, serum 25(OH)D = 30–50 nmol/l; deficiency, serum 25(OH)D < 30 nmol/l.

As illustrated in Table 5, results from the ROC curve analyses used to examine the ability of biochemical parameters to detect vitamin D deficiency suggested that the best predictive markers for vitamin D deficiency were plasma PTH and serum Ca in the entire cohort and females.

Table 5.

ROC curve analysis for the best predictors of vitamin D deficiency

Entire cohort (n 500) Females (n 250) Males (n 250)
Test result variable AUC 95 % CI P AUC 95 % CI P AUC 95 % CI P
Plasma PTH 0·651 0·478, 0·708 0·03 0·592 0·430, 0·614 0·04 0·450 0·346, 0·553 0·333
Serum Ca 0·569 0·503, 0·636 0·04 0·573 0·492, 0·692 0·04 0·510 0·409, 0·612 0·843
Serum P 0·450 0·393, 0·517 0·145 0·542 0·441, 0·643 0·542 0·497 0·395, 0·600 0·959

ROC, receiver operating characteristic; AUC, area under the curve; PTH, parathyroid hormone.

Discussion

Vitamin D status has been investigated in different populations and its deficiency is increasingly recognized worldwide. The present study is the first one to assess vitamin D status in healthy men and women in relation to biochemical parameters including serum Ca and plasma PTH, and also other factors such as age, gender, women's style of clothing and season, in Bahrain.

In adult Bahrainis a clear association of gender with vitamin D status was observed, as total 25(OH)D was significantly lower in females than males and the results from Mantel–Haenszel relative risk analysis showed that female sex was one of the major risk factors associated with vitamin D deficiency. Results from the present study are consistent with published studies suggesting that female sex is one of the most common risk factors associated with vitamin D deficiency and insufficiency in developing countries( 7 , 8 , 17 , 19 21 ). This could be due to the fact that women tend to spend more time indoors than men, in addition to their style of clothing and sun protection and sun avoidance attitude, which could all attribute to the vitamin D deficiency in Bahraini women.

There are reports to suggest that age has an effect on vitamin D status due to the fact that skin production of vitamin D precursor declines with age( 22 ). However, in this Bahraini population, total 25(OH)D was significantly higher in older than in younger individuals. In addition, Pearson correlation coefficients and Mantel–Haenszel relative risk analysis suggested that age was positively and significantly associated with serum total 25(OH)D and the risk of vitamin D deficiency was associated with younger age (<30 years) in the entire cohort and in female participants. These findings are inconsistent with a large number of studies in Europe and the USA suggesting that vitamin D deficiency is associated with older populations rather than younger ones( 23 , 24 ). Nevertheless, consistent with the present study, some studies in the Middle East have reported an association of vitamin D deficiency with younger age groups( 20 , 25 ).

Globally, the prevalence of vitamin D deficiency has been found to be higher during the winter than during the summer months, and winter season has been reported to be one of the risk factors associated with vitamin D deficiency( 13 , 14 ). However, paradoxically, in the present study serum total 25(OH)D concentrations in the entire group of participants of all ages averaged 41·5 nmol/l in October–March and 21·1 nmol/l in April–September. Mantel–Haenszel relative risk analysis revealed that the risks of vitamin D insufficiency and deficiency were significantly associated with warm and hot months of the year, particularly in women, consistent with a number of studies in the Arabian Peninsula( 1 , 2 , 8 , 26 ). In winter there are lots of outdoor activities which can be seen from October to the end of March, whereas during summer these outdoor activities are very limited owing to the high humidity and extreme heat in Bahrain.

In the present study serum total 25(OH)D levels were significantly lower in women with conservative Middle Eastern clothing style than those with non-conservative style and Mantel–Haenszel relative risk analysis showed that conservative clothing style was another risk factor associated with vitamin D deficiency in women. Vitamin D status is reported to be associated with lifestyle, particularly with type of clothing, and consistent with the present results there are reports to suggest that vitamin D status is higher in women with European-style clothing than in women with conservative clothing style( 19 , 20 , 27 ). In addition to a marked gender difference in vitamin D levels, being significantly decreased in females compared with males, plasma PTH was also significantly higher in women than in men. The negative correlation of PTH with total 25(OH)D and the association of vitamin D deficiency with high PTH observed in the present study are consistent with a large number of reported studies( 27 29 ). When participants were stratified according to their vitamin D levels, Ca and PTH were decreased significantly in participants with vitamin D deficiency compared with those with insufficiency and optimal levels of vitamin D in the entire cohort and females, but not males. In addition, Mantel–Haenszel relative risk analysis showed a significant association of vitamin D deficiency with hyperparathyroidism. Vitamin D supplementation is reported to decrease serum PTH concentration and vitamin D insufficiency and deficiency-induced hyperparathyroidism have been reported to stimulate high bone turnover leading to bone loss( 30 33 ).

Furthermore, results from ROC curve analyses to examine the ability of biochemical parameters to detect vitamin D deficiency showed that the best predictive markers for vitamin D deficiency in the entire cohort and also females were plasma PTH and serum Ca. A low Ca intake has been reported to aggravate vitamin D deficiency whereas a high Ca intake may reduce the vitamin D requirement( 33 ). In addition, low Ca intake has also been reported to increase PTH secretion and effectively it may influence vitamin D metabolism. Animal studies suggest that a low Ca intake causes increases in serum PTH and 1,25-dihydroxyvitamin D (1,25(OH)2D) with increased metabolic clearance of 25(OH)D in rats. Therefore low Ca would lead to an increase in serum 1,25(OH)2D from hydroxylation of 25(OH)D, thereby decreasing serum 25(OH)D and inducing or aggravating vitamin D deficiency( 30 , 34 ).

Although the prevalence of vitamin D insufficiency and deficiency was very high in our study participants, one of the limitations of the study is that vitamin D status was investigated only in volunteers attending a blood bank. Therefore the study may not fully reflect the vitamin D status in Bahrain, as healthy volunteers attending a blood bank could have higher vitamin D levels than the general population.

Conclusion

The present study is the first one in Bahrainis highlighting the associations of vitamin D status and risk factors associated with vitamin D deficiency and insufficiency, as well as the best indices to investigate vitamin D status. Despite the abundance of sunshine in Bahrain that allows vitamin D synthesis all year round, the study revealed low levels of vitamin D and high prevalence of hypovitaminosis D in adult Bahrainis, mainly in women. This can be a major public health problem that can affect all life stages and all individuals. Urgent public health measures, including education to increase awareness of vitamin D supplements and the role of lifestyle, and also vitamin D fortification of foods, are strongly recommended in Bahrain.

Acknowledgements

Sources of funding: This research work received no specific grant from any funding agency in the public, commercial or not-for-profit sectors. Conflicts of interest: None to declare. Authors’ contributions: J.G. designed the study and wrote the article; N.A.-S. and D.A.D. carried out the collection and analysis of samples; G.A.-K. and A.D. contributed to the design of the study and recruited the volunteers from the blood bank.

References

  • 1. Al-Daghri NM, Al-Attas OS, Alokail MS et al. (2012) Increased vitamin D supplementation recommended during summer season in the Gulf region: a counterintuitive seasonal effect in vitamin D levels in adult, overweight and obese Middle Eastern residents. Clin Endocrinol (Oxf) 76, 346–350. [DOI] [PubMed] [Google Scholar]
  • 2. Al Anouti F, Thomas J, Abdel-Wareth L et al. (2011) Vitamin D deficiency and sun avoidance among university students at Abu Dhabi, United Arab Emirates. Dermatoendocrinol 3, 235–239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Al-Kindi MK (2011) Vitamin D status in healthy Omani women of childbearing age: study of female staff at the Royal Hospital, Muscat, Oman. Sultan Qaboos Univ Med J 11, 56–61. [PMC free article] [PubMed] [Google Scholar]
  • 4. Al-Turki HA, Sadat-Ali M, Al-Elq AH et al. (2008) 25-Hydoxyvitamin D levels among healthy Saudi Arabian women. Saudi Med J 29, 1765–1768. [PubMed] [Google Scholar]
  • 5. Gharaibeh MA & Stoecker BJ (2009) Assessment of serum 25(OH)D concentration in women of childbearing age and their preschool children in Northern Jordan during summer. Eur J Clin Nutr 63, 1320–1326. [DOI] [PubMed] [Google Scholar]
  • 6. Hashemipour S, Larijani B, Adibi H et al. (2006) The status of biochemical parameters in varying degrees of vitamin D deficiency. J Bone Miner Metab 24, 213–218. [DOI] [PubMed] [Google Scholar]
  • 7. Mahdy S, Al-Emadi SA, Khanjar IA et al. (2010) Vitamin D status in health care professionals in Qatar. Saudi Med J 31, 74–77. [PubMed] [Google Scholar]
  • 8. Bandeira F & Gris L (2006) Vitamin D deficiency a global perspective. Arq Bras Endocrinol Metab 50, 640–646. [DOI] [PubMed] [Google Scholar]
  • 9. Arabi A, El Rassi R & El-Hajj Fuleihan G (2010) Hypovitaminosis D in developing countries – prevalence, risk factors and outcomes. Nat Rev Endocrinol 6, 550–561. [DOI] [PubMed] [Google Scholar]
  • 10. Lips P, Hosking D & Lippuner K (2006) The prevalence of vitamin D inadequacy amongst women with osteoporosis: an international epidemiological investigation. J Intern Med 260, 245–254. [DOI] [PubMed] [Google Scholar]
  • 11. Dawodu A, Kochiyil J & Altaye N (2011) Pilot study of sunlight exposure and vitamin D status in Arab women of childbearing age. East Mediterr Health J 17, 570–574. [PubMed] [Google Scholar]
  • 12. Sharif EA & Rizk NM (2011) The prevalence of vitamin D deficiency among female college students at Qatar University. Saudi Med J 32, 964–965. [PubMed] [Google Scholar]
  • 13. Lund B & Sorensen OH (1979) Measurement of 25-hydroxyvitamin D in serum and its relation to sunshine, age and vitamin D intake in the Danish population. Scand J Clin Lab Invest 39, 23–30. [DOI] [PubMed] [Google Scholar]
  • 14. Scharla SH, Scheidt-Nave C, Leidig G et al. (1996) Lower serum 25-hydroxyvitamin D is associated with increased bone resorption markers and lower bone density at the proximal femur in normal females: a population-based study. Exp Clin Endocrinol Diabetes 104, 289–292. [DOI] [PubMed] [Google Scholar]
  • 15. Harkness L & Cromer B (2005) Low levels of 25-hydroxy vitamin D are associated with elevated parathyroid hormone in healthy adolescent females. Osteoporos Int 16, 109–113. [DOI] [PubMed] [Google Scholar]
  • 16. Lips P (2001) Vitamin D deficiency and secondary hyperparathyroidism in the elderly: consequences for bone loss and fractures and therapeutic implications. Endocr Rev 22, 477–501. [DOI] [PubMed] [Google Scholar]
  • 17. Meddeb N, Sahli H, Chahed M et al. (2005) Vitamin D deficiency in Tunisia. Osteoporos Int 16, 180–183. [DOI] [PubMed] [Google Scholar]
  • 18. Institute of Medicine, Food and Nutrition Board (2010) Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC: National Academy Press. [Google Scholar]
  • 19. Mishal AA (2001) Effects of different dress styles on vitamin D levels in healthy young Jordanian women. Osteoporos Int 12, 931–935. [DOI] [PubMed] [Google Scholar]
  • 20. Gannage-Yared MH, Chemali R, Yaacoub N et al. (2000) Hypovitaminosis D in a sunny country: relation to lifestyle and bone markers. J Bone Miner Res 15, 1856–1862. [DOI] [PubMed] [Google Scholar]
  • 21. MacLaughlin J & Holick MF (1985) Aging decreases the capacity of human skin to produce vitamin D3 . J Clin Invest 76, 1536–1538. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Holick MF (1995) Environmental factors that influence the cutaneous production of vitamin D3 . Am J Clin Chem 61, 638–645. [DOI] [PubMed] [Google Scholar]
  • 23. Haddad JG Jr, Chyu KJ, Hahn TJ et al. (1973) Serum concentrations of 25-hydroxyvitamin D in sex-linked hypophosphatemic vitamin D-resistant rickets. J Lab Clin Med 81, 22–27. [PubMed] [Google Scholar]
  • 24. Lips P, Hackeng WH, Jongen MJ et al. (1983) Seasonal variation in serum concentrations of parathyroid hormone in elderly people. J Clin Endocrinol Metab 57, 204–206. [DOI] [PubMed] [Google Scholar]
  • 25. Kashi Z, Saeedian F, Akha O et al. (2011) Vitamin D deficiency prevalence in summer compared to winter in a city with high humidity and a sultry climate. Endokrynol Pol 62, 249–251. [PubMed] [Google Scholar]
  • 26. Mithal A, Wahl DA, Bonjour JP et al. (2009) Global vitamin D status and determinants of hypovitaminosis D. Osteoporos Int 20, 1807–1820. [DOI] [PubMed] [Google Scholar]
  • 27. Alagol F, Shihadeh Y & Boztepe H (2000) Sunlight exposure and vitamin D deficiency in Turkish women. J Endocrinol Invest 23, 173–177. [DOI] [PubMed] [Google Scholar]
  • 28. Lips P, Wiersinga A, van Ginkel FC et al. (1988) The effect of vitamin D supplementation on vitamin D status and parathyroid function in elderly subjects. J Clin Endocrinol Metab 67, 644–650. [DOI] [PubMed] [Google Scholar]
  • 29. Ooms ME, Lips P, Roos JC et al. (1995) Vitamin D status and sex hormone binding globulin: determinants of bone turnover and bone mineral density in elderly women. J Bone Miner Res 10, 1177–1184. [DOI] [PubMed] [Google Scholar]
  • 30. Chapuy MC, Chapuy P & Meunier PJ (1987) Calcium and vitamin D supplements: effects on calcium metabolism in elderly people. Am J Clin Nutr 46, 324–328. [DOI] [PubMed] [Google Scholar]
  • 31. Parfitt AM, Gallagher JC, Heaney RP et al. (1982) Vitamin D and bone health in the elderly. Am J Clin Nutr 36, 1014–1031. [DOI] [PubMed] [Google Scholar]
  • 32. McKenna MJ (1992) Differences in vitamin D status between countries in young adults and the elderly. Am J Med 93, 69–77. [DOI] [PubMed] [Google Scholar]
  • 33. Strife CF & Hug G (1996) Effect of growth hormone on urine calcium and serum vitamin D metabolites in renal failure. Pediatr Nephrol 10, 648–650. [DOI] [PubMed] [Google Scholar]
  • 34. Clements MR, Johnson L & Fraser DR (1987) A new mechanism for induced vitamin D deficiency in calcium deprivation. Nature 325, 62–65. [DOI] [PubMed] [Google Scholar]

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