Abstract
Background:
Vitamin D deficiency has been correlated with several diseases and injuries including diabetes, osteoporosis, fractures, and falls. In the Kingdom of Saudi Arabia (KSA), current data on vitamin D status are lacking.
Aims:
To inform Saudi public health authorities on the current status of blood levels vitamin D deficiency, we analyzed data from the Saudi Health Interview Survey.
Materials and Methods:
The Saudi Health Interview Survey (SHIS) is a cross-sectional national multistage survey of individuals aged 15 years and above on sociodemographic characteristics, tobacco consumption, diet, physical activity, health care utilization, different health-related behaviors, and self-reported chronic conditions. A total of 10,735 participants completed a health questionnaire and were invited to the local health clinics for biomedical exams.
Results:
62.65% of female Saudis and 40.6% of male Saudis aged 15 years and above are deficient in vitamin D. Out of them, less than 1% males and less than 2% females consume vitamin D supplements. Women who have never married and obese individuals are more likely to be deficient in vitamin D, compared to men who were currently married and nonobese individuals. Those consuming vitamin D supplements are less likely to be deficient in vitamin D.
Conclusions:
Our study showed a high prevalence of vitamin D deficiency among Saudi men and women, and the results call for an increased awareness to ensure adequate levels of vitamin D for better health in Saudi Arabia. Moreover, our findings are certainly relevant for other countries in the Gulf region or countries with similar cultures, clothing, and religions.
Keywords: Deficiency, Saudi Arabia, supplements, vitamin D
Introduction
The Kingdom of Saudi Arabia (KSA) is among the countries with the highest number of sunny days per year. Exposure to sunlight is an essential factor for vitamin D production by the skin.[1] Vitamin D deficiency has been correlated with osteoporosis, fractures, and falls.[2,3] It is also associated with some autoimmune diseases such as type 1 diabetes, rheumatoid arthritis, and osteoarthritis.[4,5,6]
Environment, tradition, and religion in KSA call for conservative clothing for both men and women. The traditional dress habits evolved around reducing sun exposure in the hot months and protection from the cold during nights in the desert and colder months. Thick clothing and head scarfs are used by the Saudi population. With reduced outdoor activities, the population is now less exposed to the sun. Previous studies showed low levels of vitamin D in KSA.[7,8] However, these studies had small sample sizes or were not nationally representative.
To examine the levels of vitamin D among the Saudi population, we conducted a large household survey including biomedical examinations.
Materials and Methods
The Saudi Ministry of Health and its Institutional Review Board (IRB) approved of the study protocol. The University of Washington IRB has deemed the study as exempt from IRB since the Institute for Health Metrics and Evaluation received de-identified data for this analyses. All the respondents consented and agreed to participate in the study. We used verbal consent that was captured by our computer program since it is commonly used and accepted in KSA. Two verbal consents were obtained: One for the household roster (obtained from the head of the household or the most knowledgeable person in the house) and another obtained from the randomly selected respondent. If the randomly selected respondent was between the ages of 15 years and 17 years, consent was obtained from his/her parent(s) or legal guardian on the individual's behalf for his/her participation in the study. The KSA Ministry of Health and The University of Washington IRB approved the verbal consents that were obtained in this study.
The Saudi Health Interview Survey (SHIS) is a national multistage survey of individuals aged 15 years and above. Households of Saudi citizens were randomly selected from a national sampling frame maintained and updated by the Census Bureau. The Ministry of Health divides KSA into 13 health regions, each with its own health department. We divided each region into subregions and blocks used by the KSA Department of Statistics. All regions were included, and a probability proportional to size was used to randomly select subregions and blocks. Households were randomly selected from each block. A roster of household members was collected and an individual aged 15 years or more was randomly selected to be surveyed. If the randomly selected adult was not present, our surveyors made an appointment to return, and a total of three visits were made before the household was classified as a nonresponse. Weight, height, and blood pressure of the randomly selected adult were measured at the household by a trained professional.
The survey included questions on sociodemographic characteristics, tobacco consumption, diet, physical activity, health care utilization, health-related behaviors, and self-reported chronic conditions. These conditions were hypertension, diabetes, hypercholesterolemia, stroke, cardiac arrest, myocardial infarction, congestive heart failure, chronic obstructive pulmonary disease, atrial fibrillation, renal failure, asthma, and cancer.[9,10,11,12]
We measured weight and height to calculate body mass index (BMI) as weight (kg)/height (m2). Participants were classified into four groups:
Underweight for a BMI less than 18.5;
Normal weight for a BMI within 18.5-24.9;
Overweight for a BMI within 25.0-29.9; or
Obese for a BMI greater than or equal to 30.[13]
Respondents were considered to be current smokers if they reported to be currently smoking. We used the International Physical Activity questionnaire[14] to classify respondents into four groups of physical activity:
Vigorous physical activity,
Moderate physical activity,
Insufficient physical activity, and
None.
To assess diagnosed blood pressure, prediabetes, diabetes, and hypercholesterolemia status, respondents were asked four separate questions: “Have you ever been told by a doctor, nurse, or other health professional that you had:
Hypertension, otherwise known as high blood pressure;
Prediabetes mellitus, otherwise known as prediabetes, borderline diabetes, impaired fasting glucose, impaired glucose tolerance, or impaired sugar tolerance;
Diabetes mellitus, otherwise known as diabetes, sugar diabetes, high blood glucose, or high blood sugar; and
Hypercholesterolemia, otherwise known as high or abnormal blood cholesterol?” Women diagnosed with diabetes or hypertension during pregnancy were not counted as having these conditions.
Those who reported diagnosis of any of these conditions were asked if they were currently receiving any treatment for their condition.
A total of three blood measurements were taken with the participant resting and at 5-min intervals. We followed the National Health and Nutrition Examination Survey (NHANES) for determining blood pressure levels.[15] Basically, respondents were considered to have hypertension if they met any of the following criteria:
Measured diastolic or systolic blood pressure exceeding 89 mmHg or 139 mmHg, respectively, or
Measured diastolic or systolic blood pressure not exceeding the appropriate threshold, but the respondent reported taking medications for hypertension.
Hence, respondents who were on drugs for hypertension were considered hypertensive even if their measured diastolic or systolic blood pressure did not exceed 89 mmHg or 139 mmHg, respectively. Respondents were considered to have borderline hypertension if:
They did not report taking drugs for hypertension and
Their measured diastolic blood pressure was between 80 mmHg and 89 mmHg or systolic blood pressure was between 120 mmHg and 139 mmHg.
Respondents who completed the questionnaire were invited to local primary health care clinics to provide blood samples for laboratory analysis. All blood samples were analyzed in a central laboratory at the King Fahd Medical City in Riyadh, Riyadh Province, Saudi Arabia. Respondents were considered to have a deficient level of vitamin D if blood work showed a vitamin D level below 28 ng/mL. Respondents were considered to have a sufficient level of vitamin D if blood work showed a vitamin D level between 28 ng/mL and 107 ng/mL. Respondents were considered to have a toxic level of vitamin D if blood work showed a vitamin D level above 107 ng/mL.
Respondents were considered to be hypercholesterolemic if they met any of the following criteria:
Measured cholesterol equal to or exceeding 6.2 mmol/L or
Measured cholesterol not exceeding 6.2 mmol/L but the respondent reported taking medications for hypercholesterolemia.
Respondents were considered to have borderline hypercholesterolemia if:
They did not report taking drugs for hypercholesterolemia and
Their measured blood cholesterol level was between 5.18 mmol/L and 6.2 mmol/L.
Respondents under treatment for hypercholesterolemia were considered controlled if their measured cholesterol levels were below 6.2 mmol/L.
We followed the National Health and Nutrition Examination Survey (NHANES) for determining diabetes status.[15] Respondents were considered to be diabetic if they met any of the following criteria:
Measured glycated hemoglobin (HbA1c) equal to or exceeding 6.5% (48.5 mmol/mol) or
Measured HbA1c not equaling or exceeding 6.5% (48.5 mmol/mol) but the respondent reported taking medications for diabetes.
Hence, the subgroup diabetic included those with measured HbA1c equal or above 6.5% or taking medication for diabetes. Respondents were considered to have borderline diabetes if: 1) they did not report taking drugs for diabetes, and 2) their measured HbA1c blood level was between 5.7% (35.3 mmol/mol) and less than 6.5% (48.5 mmol/mol).
Statistical analysis
We used a backward elimination multivariate logistic regression model to measure the association between vitamin D deficiency and consumption of vitamin D and all associated factors. All factors were first included in the models and variables and were eliminated based on a Wald chi-square test for analysis of effect. Variables were removed one by one based on the significance level of their effect on the model, starting with the variable with the highest P > 0.5 until all the variables kept had a P ≤ 0.5 in the analysis of effect. The logistic regression excluded cases with missing data. We used SAS 9.3 for the analyses and to account for the complex sampling design.
Results
Between April 2013 and June 2013, a total of 12,000 households were contacted and a total of 10,735 participants completed the survey (response rate of 89.4%). The remaining 1,265 participants completed part or all of the household enumeration but the selected individual did not complete the survey. A total of 5,590 individuals went to the local clinics and provided blood samples for analyses, which led to a response rate of 52.1%. Of these, there were missing data on blood vitamin D levels in 586 individuals and missing data on consumption of vitamin D supplements in 876 individuals.
Overall, 40.6% males and 62.7% females had insufficient levels of vitamin D. The sociodemographic characteristics of SHIS respondents by vitamin D blood levels are presented in Table 1. Young and unmarried individuals were more likely to have insufficient levels of vitamin D [Table 1].
Table 1.
Women [adjusted odds ratio (AOR)=2.69, 95% confidence interval (CI) = 2.09–3.47], individuals who had never married (AOR = 1.77, 95% CI=1.29-2.44), and obese individuals (AOR = 1.30, 95% CI= 1.01-1.67) were more likely to have deficient blood levels of vitamin D, compared to men who were currently married and nonobese individuals [Table 2].
Table 2.
Current smokers (AOR = 6.1, 95% CI = 1.31-27.48) were more likely to have toxic blood levels of vitamin D in comparison to those who were never smokers or previous smokers. Individuals with low levels of physical activity were less likely to have toxic levels of vitamin D (AOR = 0.21, 95% CI = 0.05-0.89) [Table 2].
The sociodemographic characteristics of SHIS respondents of vitamin D supplement consumption according to vitamin D sufficiency are presented in Table 3. Vitamin D supplement consumption was low [Table 3]. We found that the likelihood of consuming vitamin D supplements among those with an insufficient level of vitamin D was higher among individuals who had completed high school education (AOR = 3.85, 95% CI=1.43-10.39) or college or higher education (AOR = 4.62, 95% CI= 1.32-16.15) [Table 4]. Sun exposure was not associated with vitamin D supplement consumption among this group.
Table 3.
Table 4.
Discussion
Our study is the first national one to report blood levels of vitamin D and the consumption of vitamin D supplements among individuals in KSA. Our findings revealed high rates of vitamin D deficiency. These findings are surprising, given the amount of sunshine in KSA. Indeed, vitamin D deficiency may be overlooked as a health problem in the country due to this fact. Our study calls for a national plan to increase awareness of the importance of vitamin D and its sources and to encourage the monitoring of blood levels among those taking supplements.
The Saudi Ministry of Health developed its own guidelines and adopted them for the country. Vitamin D levels were assessed using Roche Hitachi COBAS 8000. No unique cutoffs exist for deficient, sufficient, and toxic serum levels of vitamin D. The Institute of Medicine defined vitamin D deficiency as blood levels less than 11 ng/mL for neonates, infants, and young children and less than 12 ng/mL for adults.[16] More recently, 25-hydroxyvitamin D (25(OH)D) serum levels between 20 ng/mL and 32 ng/mL have been defined as sufficient.[17] NHANES III defined vitamin D deficiency as serum levels below 15 ng/mL.[18] Others suggest that the most beneficial serum concentration of vitamin D begins at 30 ng/mL.[19] Some scientists agree on 20 ng/mL as a minimum desirable serum concentration of 25(OH)D.[20] Alshahrani et al. suggested that 25(OH)D serum levels between 20 ng/mL and 32 ng/mL were insufficient.[21] A common definition for high serum vitamin D concentrations is also lacking: serum levels above 100 ng/mL or 150 ng/mL have been suggested as indicative of toxicity.[22] We used the Saudi Ministry of Health guidelines for vitamin D for our cutoff points.
Our findings were in the range of the findings from previous studies in KSA on vitamin D deficiency. Sadat-Ali et al. reported a prevalence of vitamin D deficiency among healthy Saudi men in the range of 28% to 37% in Eastern KSA.[23] Elsammak et al. reported a prevalence of vitamin D deficiency of more than 65% among healthy young Saudis in the same region.[8] Naeem et al. reported a deficiency prevalence of 67.8% in the Quassim region.[24]
Inadequate amounts of vitamin D pose health risks for the entire age spectrum including rickets in children and osteopenia and osteoporosis in adults.[25] In addition, adequate vitamin D levels are needed to prevent complications from falls and fractures.[26]
Vitamin D deficiency is of more concern if present among postmenopausal women. These women are at an increased chance of falls and fractures due to hormone-related bone loss.[27] Although vitamin D alone has been proven ineffective in preventing fractures in postmenopausal women, vitamin D and calcium supplements may prevent fractures.[3,28] Our findings showed that 45.4% of women aged 50 years and above had vitamin D deficiency. Sadat-Ali et al. reported a vitamin D deficiency prevalence of 50-60% among Saudi postmenopausal women in 2002[29] while Al-Turki et al. reported a prevalence of 55% in 2008.[30]
Lack of sunlight exposure, lack of availability of vitamin D-fortified foods, and lack of or insufficient vitamin supplementations were the most likely factors explaining the high prevalence of vitamin D deficiency. In KSA, these three sources are lacking. Minimal sun exposure is mainly due to the use of protective clothing. Saudi men and women wear the abaya and the headscarf, minimizing any sun exposure outdoors. Hence, it is crucial to inform Saudis about the need for sun exposure and how it should be achieved while reducing the risks of melanoma and nonmelanoma skin cancer from sun exposure.
The amount of time for optimal vitamin D photosynthesis is uncertain. Even as little as 15 min of direct sunlight can generate up to 20,000 IU of vitamin D but many factors influence the synthesis of vitamin D: skin pigmentation, latitude, and amount of skin exposed, making it hard to assess how much 25-hydroxyvitamin D will be synthesized.[31] In addition, unprotected sun exposure has its health risks as well as benefits. Supplementation can provide a safe source of vitamin D.[32]
The current guidelines recommend daily supplementation of vitamin D for individuals at risk of vitamin D deficiency. The Endocrine Society and the American Academy of Pediatrics recommend a daily intake of 400 IU/day of vitamin D for children under 1 year of age, 600 IU/day for individuals aged 1-18 years, 600 IU/day for individuals aged 19-70 years, and 800 IU/day for individuals aged 70 years and above.[22] However, levels of 2,000 IU/day for children under 1 year of age, 4,000 IU/day for individuals aged 1-18 years, and 10,000 IU/d for individuals aged 19 years and above may be needed to correct vitamin D deficiency.[33] The optimal vitamin D levels for protection against cancer, autoimmune diseases, depression, and many other health problems are unknown. Clear guidelines are urgently needed to guide both the public and health officials to improve blood levels of vitamin D.
Few foods naturally contain vitamin D2 or D3. In the United States, milk, yogurt, cereal, and some bread products are fortified with vitamin D. Saadat-Ali et al. showed that food items consumed in the Eastern Province of KSA were not fortified.[34] Therefore, Saudi health officials should consider such an approach to improve vitamin D levels in the country.
Our study had some limitations. First, our data were from a cross-sectional study and therefore, we could not assess causality. Second, many of our behavioral data such as diet and physical activity were self-reported and subject to recall and social desirability biases. Third, we used Saudi cutoff points for vitamin D blood levels instead of international ones. Fourth, only 52% of the respondents completed the visit to a health clinic and had their blood drawn for analysis. However, our weighting methodology accounted for this bias by applying a poststratification adjustment using sociodemographic characteristics, health behaviors, previously diagnosed noncommunicable diseases, and anthropometric measurements of the respondents from the household survey. Finally, our study was based on a large sample and used a standardized methodology for all its measures.
Our study was of great importance, as it revealed that vitamin D levels in countries with plenty of sun such as Saudi Arabia were low and required action to improve them in order to decrease the burden of disease associated with the low levels of vitamin D. Moreover, our findings are certainly relevant for other countries in the Gulf region or countries with similar cultures, clothing, and religions. Awareness campaigns, taking into account the culture of the region, need to be developed and implemented in KSA to highlight the importance of vitamin D and educate residents about the best ways to improve vitamin D levels. Moreover, these programs should include monitoring of vitamin D levels in order to avoid toxicity.
Conclusion
Our study showed a high prevalence of vitamin D deficiency among Saudi men and women. Our results call for increased awareness to ensure adequate levels of vitamin D for better health in Saudi Arabia. Moreover, there is a need to inform the population about the importance of vitamin D and its sources in the Saudi diet. Our study also showed that very few Saudis use a supplement. Hence, it is crucial that those with low levels of vitamin D be encouraged to improve their diet and use supplements. At the same time, health professionals should caution individuals on supplement use to ensure that they do not reach toxic levels. In a country with plenty of sun, it is important to inform the public that vitamin D is an issue to monitor when outdoor exposure is minimal.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
Acknowledgments
We would like to thank Kathrine Muller at the Institute for Health Metrics and Evaluation for editing the manuscript. None of the authors declare a conflict of interest.
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