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. 2014 Nov 19;69(6):707–711. doi: 10.1038/ejcn.2014.251

Vitamin D supplementation in obese type 2 diabetes subjects in Ajman, UAE: a randomized controlled double-blinded clinical trial

A Sadiya 1,*, S M Ahmed 1, M Carlsson 2, Y Tesfa 1, M George 1, S H Ali 1, H H Siddieg 1, S Abusnana 1
PMCID: PMC4458894  PMID: 25406966

Abstract

Objectives:

To study the effect of Vitamin D3 supplementation on metabolic control in an obese type 2 diabetes Emirati population.

Methods:

This randomized double-blind clinical trial was conducted with 87 vitamin D-deficient obese, type 2 diabetic participants. The vitamin D-group (n=45) and the placebo group (n=42) were matched for gender, age, HbA1c and 25-hydroxy vitamin D (25(OH) D) at the baseline. The study was divided into two phases of 3 months each; in phase 1, the vitamin D-group received 6000 IU vitamin D3/day followed by 3000 IU vitamin D3/day in phase 2, whereas the placebo group (n=42) received matching placebo.

Results:

After supplementation, serum 25(OH) D peaked in the vitamin D-group in phase 1 (77.2±30.1 nmol/l, P=0.003) followed by a decrease in the phase 2 (61.4±18.8 nmol/l, P=0.006), although this was higher compared with baseline. In the placebo group, no difference was observed in the serum 25(OH) D levels throughout the intervention. Relative to baseline serum, parathyroid hormone decreased 24% (P=0.003) in the vitamin D-group in phase 2, but remained unchanged in the placebo group. No significant changes were observed in blood pressure, fasting blood glucose, HbA1c, C-peptide, creatinine, phosphorous, alkaline phosphatase, lipids, C-reactive protein or thyroid stimulating hormone concentrations compared with baseline in either group.

Conclusions:

Six months of vitamin D3 supplementation to vitamin D-deficient obese type 2 diabetes patients in the UAE normalized the vitamin D status and reduced the incidence of eucalcemic parathyroid hormone elevation but showed no effect on the metabolic control.

Introduction

Vitamin D role in calcium homeostasis and bone metabolism is well established.1 However, in recent years, there has been numerous non-skeletal disease associations reported with vitamin D deficiency including type 2 diabetes mellitus (T2D). This additional evidence for the role of vitamin D in T2D comes from a number of epidemiological studies showing an inverse association between vitamin D status and hyperglycemia,2, 3 insulin resistance4 prevalence of T2D5, 6 and obesity.7

The prevalence of diabetes mellitus in the United Arab Emirates (UAE) has been reported to be ~20% in 2013 by the International Diabetes Federation,8 and this has been attributed to the rapid economic development coupled with ageing populations. This rapid urbanization, economic growth and technological advances have also contributed to the alarming rise of obesity in this region.9

Vitamin D deficiency is startlingly high in the UAE and other Gulf Cooperation Council countries, where the intensity and hours of sunlight is paradoxically proportional to the prevalence of vitamin D deficiency.10, 11

The demonstration of a causal relation between vitamin D and glucose metabolism needs evidence from randomized adequately powered placebo-controlled intervention trials. As reviewed recently, the studies published so far on T2D subjects have a number of methodological limitations and shortcomings, such as small sample sizes, heterogeneous regarding dose and formulation of vitamin D treatment, duration, inclusion–exclusion criteria and study populations. However, these studies have often yielded inconclusive results.12, 13

In the UAE, no randomized controlled trial has been reported in vitamin D-deficient obese T2D patients. The appropriate dosing regimen for improving vitamin D status in this population is insufficiently studied. The purpose of this study was to conduct a double-blind randomized trial in the Emirati population to clarify the relationship between vitamin D3 (cholecalciferol) supplementation and glycemic control. Also in our study, we aimed to give large enough doses of vitamin D3 to normalize (>50 nmol/l) serum 25-hydroxy vitamin D (25(OH) D).

Methodology

Participants

This trial was conducted between June 2012 and December 2012 at Rashid Center for Diabetes and Research, a tertiary diabetes care facility in Ajman, UAE. The criteria for eligibility were UAE nationality, male and female, age between 30 and 60 years, body mass index (BMI)⩾30 kg/m2, diagnosis of T2D and serum 25(OH) D<50 nmol/l. The participants were excluded if they were diagnosed with type 1 diabetes, taking vitamin D supplementation, serum creatinine >200 μmol/l, liver function tests (alkaline phosphates, alanine amino transferase and bilirubin) greater than three times the upper limit of the local reference range, possible primary hyperparathyroidism (plasma parathyroid hormone (PTH) >5.0 pmol/l combined with serum calcium >2.8 mmol/l), malabsorption syndrome, on hormone replacement therapy, corticosteroids or anti-convulsants. Pregnant or lactating women were also excluded.

Study design

The summary of the study design is illustrated in Figure 1. The recruited participants were randomized by a computer-generated random number sequence into one of the two groups—the vitamin D-group (D-group) and the placebo group (P-group)—with stratification according to age, gender and BMI by the Rashid Center for Diabetes and Research, Information Technology department. The participants and the research team remained blinded to treatment allocation until after the final analysis was completed. Vitamin D3 (Solgar, Leonia, NJ, USA) and placebo (starch) (Compound Pharmacy, Dubai, UAE) were in capsule form and identical in appearance. They were pre-packed in bottles and consecutively numbered to be dispensed by an independent pharmacist according to the randomization list.

Figure 1.

Figure 1

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Summary of study design.

The study was divided into two phases of 3 months each. In phase 1, the D-group (n=45) received unlabelled oral vitamin D3 6000 IU/day, whereas the P-group (n=42) received placebo capsules. In phase 2, the D-group (n=45) received 3000 IU/day of oral vitamin D3 and the P-group (n=42) continued with matching placebo capsules (Figure 1). Participants were advised to maintain their usual medical care and diets and avoid taking calcium or vitamin D supplements on their own while in the study period. They were also informed to report any interval morbidity including nausea, vomiting, excessive thirst, frequent urination, constipation, abdominal pain, weakness and confusion. A study staff contacted the participants by phone after 3 and 6 weeks of initiation of the trial to ensure that the study medication was taken correctly and to register any adverse events. Compliance was recorded in a questionnaire at 3 and 6 months and was assessed by measuring 25(OH) D concentrations after un-blinding.

Of the 366 patients who were screened for eligibility by the physician, 279 were excluded and 87 (23.8%) were recruited after a written informed consent was undertaken by the study staff. This study was conducted according to the guidelines laid down by the Declaration of Helsinki and all procedures involving the participants were approved by the Ethical committee of the Ministry of Health, UAE.

Measurements

A standard pretested questionnaire was completed by the participants to record information about outdoor sun exposure, use of sunscreen, clothing and skin colour (Fitzpatrick scale).14 Systolic and diastolic blood pressure was measured after 5–10 min rest, on the right arm in the sitting position. Fasting (12 h) venous blood sample (8 ml) was collected and assessed for fasting blood glucose, HbA1c, C-peptide, PTH, lipid profile (cholesterol, triglyceride, high-density lipoprotein-cholesterol and low-density lipoprotein-cholesterol), apolipoprotein A, Apolipoprotein B, phosphorous, calcium, C-reactive protein, creatinine, alkaline phosphatase and thyroid stimulating hormone in a Roche COBAS 6000 analyzer (Mannheim, Germany). Blood HbA1c was reported in the NGSP (%) unit, which is used in UAE. These results can be translated to SI (IFCC) units using the International Federation of Clinical Chemistry (IFCC)-National Glycohemoglobin Standardization Program (NGSP) ‘master equation' HbA1c (NGSP)=0.9148 × HbA1c (IFCC)+2.152.15 25(OH) D was measured using immunochemiluminescene, performed in Diasorin Liaison analyzer (Saluggia, Italy). The analyzing laboratory participated in the vitamin D external quality assessment scheme. The lab tests were repeated at the baseline end of phases 1 and 2.

Statistical analysis

The study was powered to detect 0.75% difference in HbA1c, 0.7 kg/m2 in BMI and 6 mm Hg in blood pressure between the groups. The estimated sample size of 50 subjects in each group would give a power of 90% with 95% confidence interval. Statistical evaluations were performed using SPSS 13.0 (IBM Corp, NY, USA. Released 2013). The biochemical variables that were non-normally distributed were normalized by logarithmic transformation. Comparison between the groups at baseline was done using Student's t-test and between baseline and phases 1 and 2 were done by repeated-measures analysis of variance in both the groups. The Post hoc least-square difference was performed to identify the significant group for each significant variable on the analysis of variance test. All statistical tests were performed two-sided, and P-value⩽0.05 was considered statistically significant. No data were attributed for missing data and analyzed for intent to treat. A secondary per-protocol analysis was also conducted for the accuracy of primary analysis and yielded results in similar significance and direction (not presented).

Results

Eighty-seven participants were randomly assigned into two groups—the D-group (n=45) and the P-group (n=42); there was no drop out reported at the end of phase 1 (3 months); in phase 2 (3 months) we lost three subjects in each arm as shown in Figure 1. At the end of the trial, 82 subjects—that is, D-group (n=43) and P-group (n=39)—were analyzed.

The baseline characteristics of the participants are presented in Table 1, and there was no significant difference (P<0.05) in age, BMI, serum 25(OH) D levels, HbA1c or duration of diabetes between randomly allocated groups. The oral anti-diabetic drugs included biguanides, thiazolidinediones, sulphonylureas and incretins. All participants wore traditional attire—kandoora (male) or Abaya (female)—when outdoor, which limits surface area exposure to direct sunlight. Less than 5 min/day exposure to direct sunlight was reported by 33 and 44% of participants in D and P-group. The average temperatures in the UAE were between 30 and 47 °C (maximum) and 17 and 27 °C (minimum) during the study period (June to December 2012).The Fitzpatrick scale assessed 84% of the participants between grade IV and V—that is, between minimally sun sensitive to sun insensitive, burns minimally to rarely burns and always tans to moderate brown to tans well.

Table 1. Baseline characteristics of the study participants.

Characteristics Vitamin D-group Mean±s.d. Placebo group Mean±s.d.
Subjects (Male) 45 (9) 42(7)
Age (years) 49±8 48±8
Body mass index (kg/m2) 37.9±6.1 37.6±7.7
Fitzpatrick skin score grade IV & V (%) 78 90
Oral anti-diabetic drugs (%) 69 50
Oral anti-diabetic drugs+insulin (%) 31 50
T2D duration of diagnosis (years) 9.5±6.2 9.1±5.5
Exposure to direct sunlight <15 min/day (%) 60 74
S-25(OH) vitamin D (nmol/l) 28.5±9.2 30.5±11.2
B-HbA1c (%) 8.3±1.3 8.3±1.9
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Abbreviations: s-25(OH)vitamin D, serum 25-hydroxy vitamin D; T2D, type 2 diabetes mellitus.

Values are Mean±s.d.

The Pearson correlation coefficient (r) at the baseline (n=87) showed an inverse relationship between serum 25(OH) D and fasting blood glucose (r=−0.27, P<0.01), HbA1c (r=−0.25, P<0.05), total cholesterol (r=−0.23, P<0.05) and triglycerides (r=−0.30, P<0.01).

The effect of vitamin D3 supplementation is shown in Table 2. Serum 25(OH) D increased (P=0.003) by the end of phase 1 followed by a decrease (P<0.01) in phase 2 but maintained a higher level compared with the baseline value (P<0.01), whereas serum PTH decreased in phase 2 (P=0.003) compared with the baseline. Concurrently, 25(OH) D and calcium decreased (P<0.05) after 6 months in the P-group.

Table 2. Effect of Vitamin D3 supplementation on obese type 2 diabetic subjects.

Variable Vitamin D-group
 Placebo group
  Baseline Phase 1 (6000 IU/day) Phase 2 (3000 IU/day) Baseline Phase 1 Phase 2
Weight (kg) 95.5±17.7 95.0±18.1 94.7±18.2 94.2±23.3 95.0±23.4 95.2±23.4
Systolic blood pressure (mm Hg) 128±20 133±16 133±12 131±18 132±19 133±19
Diastolic blood pressure (mm Hg) 70±12 74±9 73±9 73±9 73±10 73.±9
S-25(OH) vitamin D (nmol/l) 28.5±9.2 77.2±30.1a 62.3±20.8a,b 30.5±11.3 28.8±12.9 25.4±11.8a
P-calcium (mmol/l) 2.31±0.08 2.31±0.89 2.30±0.89 2.35±0.10 2.32±0.11 2.29±0.10a
P-phosporous (mmol/l) 1.16±0.18 1.21±0.16 1.17±0.13 1.17±.14 1.20±0.21 1.10±0.18
P-parathyroid hormone(pmol/l) 5.9±2.4 5.0±2.5 4.5±1.8a 5.4±2.3 5.4±2.4 5.5±2.4
P-alkaline phosphotase (IU/l) 73.9±17.7 69.4±16.7 69.5±16.0 81.2±22.6 76.3±22.5 77.9±24.6
P-fasting glucose (mmol/l) 9.3±2.8 9.8±3.1 9.5±2.9 8.9±3.2 9.2±3.4 9.7±3.7
B-HbA1c (%) 8.2±1.3 8.2±1.4 8.0±1.5 8.3±1.8 8.4±1.8 8.3±1.9
P-C-peptide (nmol/l) 1.2±0.5 1.3±0.5 1.2±0.5 1.0±0.4 1.0±0.4 1.0±0.4
P-CRP (mg/l) 7.4±7.6 7.8±10.8 8.0±9.5 8.0±9.2 9.5±10.4 10.0±13.0
P-creatinin (mmol/l) 55.5±14.3 57.1±20.3 54.3±13.1 54.0 ±16.1 51.6±13.6 53.0±15.2
P- cholesterol (mmol/l) 4.3±1.0 4.2±0.9 4.3±1.0 4.1±0.9 4.0±0.8 4.3±1.3
P-HDL-cholesterol (mmol/L) 1.1±0.2 1.1±0.2 1.1±0.2 1.1±0.3 1.1±0.2 1.1±0.2
P-LDL-cholesterol (mmol/l) 2.7±0.8 2.5±0.8 2.6±0.9 2.4±0.8 2.4±0.8 2.5±1.0
P-Triglyceride (mmol/l) 1.6±1.1 1.7±1.1 1.6±0.8 1.8±1.1 1.8±1.4 1.9±1.8
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Abbreviations: CRP, C-reactive protein; HDL, high-density lipoprotein; LDL, low-density lipoprotein.

Mean±s.d. (all such values).

a

Denotes significance compared with baseline.

b

Denotes significance compared with phase 1 (P<0.05). These comparisons were only performed when the group comparison P-value was <0.05.

Supplementation of vitamin D3 did not show statistical difference in glycemic control (fasting blood glucose, HbA1c and C-peptide), lipids, C-reactive protein, creatinine, (Table 2), apolipoproteins A and B and thyroid stimulating hormone (not shown in the table).

Sub analysis:

The observation remained consistent even after stratifying the groups according to BMI and serum 25(OH) D. The D-group was divided into two subgroups—that is, HbA1C⩽8% (n=22) and HbA1c >8% (n=23)—and compared baseline with phase 2, and none of the variables showed any statistical difference, except for an increase in 25(OH) D (P<0.001) in both the subgroups but a decrease (P<0.05) in PTH only in the group with HbA1C⩽8%.

The effect of vitamin D supplementation on a subgroup with serum 25(OH) D <30 nmol/l showed no improvement in any of the metabolic markers. The group (n=24) that achieved serum 25(OH) D ⩾75 nmol/l in phase 1 versus the placebo showed no changes in the metabolic markers either.

Discussion

This 6-month randomized double-blind placebo-controlled study in vitamin D-deficient obese T2D Emirati patients showed no effect of vitamin D3 supplementation on glycemic control.

The subjects recorded a strikingly low exposure to direct sunlight, although the climate of the UAE is generally hot and dry with ample sunlight throughout the year; the soaring temperatures in the summer (June–September average temperature 42 °C) restrict outdoor activities. Similar observation has been reported earlier in this region.16

At baseline, serum 25(OH) D was inversely related to glycemia (fasting blood glucose and HbA1C). From a theoretical point of view, there are several mechanisms whereby vitamin D may influence glycemic control, insulin secretion and sensitivity. For instance, the vitamin D receptor is expressed in the insulin producing beta cells. These cells also have the enzyme (CYP27B1) necessary for activating 25(OH) D to the active form 1,25 dihydroxy vitamin D. Added to this, the insulin secretion is also a calcium-dependent process and can consequently be indirectly influenced by vitamin D, which is a known regulator of calcium balance. Moreover, vitamin D may also stimulate the expression of the insulin receptor in peripheral tissues and thereby increase glucose transport.17, 18, 19

Another observation in our study was that the baseline C-reactive protein levels were high (8.0±7.6 mg/l), which is above the standard reference range (<4 mg/l). This was higher than participants of white, Hispanic, African-American and Asian ethnicity.20 Only four patients had C-reactive protein below 1.0 mg/l, and 20 patients had C-reactive protein levels >10.0 mg/l. This may indicate a high-grade inflammation in centrally obese diabetic subjects in the UAE.

On supplementation, we found neither dose (6000 or 3000 IU/day) of vitamin D3 could statistically influence the glycemic control (HbA1c, fasting blood glucose and c-peptide) nor was there any change in other metabolic markers (Table 2). However, there was an increase (P<0.01) in the serum 25(OH) D and a decrease in PTH in the D-group and alongside a decrease (P<0.05) in serum 25(OH) D and calcium in the P-group compared with baseline.

The results from small clinical trials and post hoc analyses of larger trials on the effect of vitamin D supplementation on glycemic control have been inconsistent. A systematic review of nine studies suggested a weak effect of vitamin D supplementation in reducing fasting blood glucose and improving insulin resistance and no change in HbA1c in subjects with T2D and impaired glucose tolerance.21 Three small underpowered randomized controlled trials in T2D patients show no change in fasting blood glucose, HbA1c or insulin resistance after a follow-up period of 8–26 weeks. This controversy, or at least part of it, might be due to the ethnicity differences in the study's population.22, 23, 24, 25

Detecting an increase in serum 25(OH) D in obese diabetic subjects following vitamin D supplementation is in agreement to all the supplementation studies.21 The significant (28.5±9.2 vs 77.2±30.1, P=0.003) but lower than anticipated rise in serum 25(OH) D may be because of ethnicity-related differences in vitamin D absorption and/or altered vitamin D metabolism in the obese subjects.26, 27

However, the supplementation dose was selected on the basis of the recommendations of Endocrine Society Clinical guidelines 2011,28 which suggested 6000–10 000 IU/day of vitamin D3 to treat vitamin D deficiency and maintain 25(OH)D level above 30 ng/ml (75 mmol/l), followed by maintenance therapy of 3000–6000 IU vitamin D3/d. Our findings show that 6000 IU vitamin D3/day for 3 months safely increased serum 25(OH) D, but was probably low to optimize all vitamin D-dependent functions. Some authors consider 75 nmol/l to be an adequate concentration to begin with, and the best to be between 90 and 100 nmol/l (36–40 ng/ml),29 although this is still controversial. Wortsman et al27 have reported that the obese participants were able to raise their blood levels of vitamin D by no more that 50% compared with the non-obese adults. Hence, we presume this could have also caused a suboptimal increase in the circulating 25(OH) D in our obese subjects.

The supplementation of vitamin D3 suppressed the PTH levels after phase 2 (5.9±2.4 vs 4.4±1.8), unlike in the P-group. which showed a small but insignificant increase in PTH. These results are in line with the fact that PTH decreases with increasing 25(OH) D concentrations as reported earlier.23 No significant change in blood pressure was recorded; this could be attributed to a well controlled baseline mean systolic and diastolic blood pressure. These results are supported by a meta-analysis where a small reduction in blood pressure was reported with vitamin D therapy but only in studies with a mean baseline systolic blood pressure of >140 mm Hg.24

In the present study, most of the patients were taking statins and angiotensin converting enzyme inhibitors at the baseline and the lipid profile was well controlled, and supplementation did not show any significant improvement. A meta-analysis of 12 clinical trials reported no significant effect of vitamin D supplementation on total cholesterol, high-density lipoprotein-cholesterol and triglyceride.30

To our knowledge, this is the first randomized double-blind placebo-controlled trial of vitamin D supplementation in obese T2D Emirati participants. In the current study, we have recorded a wide range of metabolic markers. There was a well-matched baseline group, and all the participants in the study were receiving medical care suggestive of current standards of care.31

The limitation of the study could be the inefficiency to raise and sustain the serum 25 (OH) D>75 nmol/l, attributing it to the compliance (85%) in both the groups, insufficiency of the dose of vitamin D3 and/or interaction with patient medication. However, in a recent study by Davidson et al32 a mean weekly dose of 89 000 IU in individuals with prediabetes and hypovitaminosis had no effect on the development of diabetes, insulin secretion or insulin sensitivity, although a slight reduction in HbA1c levels was observed. Therefore, we consider it unlikely that a higher dose of vitamin D or a better compliance would have changed the trial outcome significantly.

Conclusion

In conclusion, the present trial has indicated that, although there was an inverse baseline relationship between serum 25(OH) D and glycemic profile, the vitamin D3 supplementation in the obese T2D participants in the UAE did not improve glycaemic control or lipid concentrations. However, the treatment with vitamin D3 reduced the incidence of secondary hyperparathyroidism and normalized the PTH levels.

Acknowledgments

We acknowledge the support of the staff of the diabetes clinic for their support in data collection, Vijay Kumar and Ponnu Andrew Prem Kumar from the laboratory in specimen processing and Joseph George for IT support at Rashid Center for Diabetes and Research.

Clinical trial registry: ClinicalTrials.gov Identifier: NCT02101151

Funding: This clinical trial was supported by grants from Rashid Center for Diabetes and Research and Global Health Partner. Solgar, NJ, USA, supplied the vitamin D3 capsules and Compound Pharmacy, and Dubai, UAE, supplied placebo capsules used in the present study.

The authors declare no conflict of interest.

Footnotes

Authors' contribution

AS, SMA, MC, YT and SA designed the research, AS, SMA, YT, SHA, MG, HHS and SA conducted the research, AS and SA analyzed the data, AS wrote the paper and AS and SA had primary responsibility for the final content. All authors read and approved the final manuscript.

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