Whether vitamin D3 is effective in reducing proteinuria in type 2 diabetic patients?

BACKGROUND: Nowadays Vitamin D deficiency is a notable medical condition world-wide and also in Iran. Since, vitamin D can have renoprotective effect by inhibiting the renin-angiotensin system; it appears that low vitamin D level can worsen the renal injury in diabetic patients. This study demonstrates the effect of vitamin D3 therapy on reducing proteinuria in diabetic patients with concomitant diabetic nephropathy and vitamin D deficiency after controlling hypertension and use of angiotensin converting enzyme inhibitors (ACEIs) or angiotensin II type receptor blockers (ARBs).
MATERIALS AND METHODS: In this randomized double blinded parallel groups clinical trial, 51 diabetic patients with proven nephropathy and vitamin D deficiency/insufficiency and stable hypertension, dyslipidemia, and hyperglycemic treatment were enrolled. The patients were divided randomly into two groups (treatment and placebo group). Patients received oral vitamin D3 (pearl 50000 IU) or placebo one pearl every week for 12 weeks. Patients were assessed at baseline and 12 weeks after intervention from the point of 25(OH) D level, and urine albumin/creatinine ration (UACR).
RESULTS: Mean serum 25(OH) D concentrations were 14.06 ng/ml and 16.05 ng/ml before treatment. Furthermore, after intervention, its levels were risen to 71.23 and 17.63 in drug and placebo groups, respectively. Whereas, UACR as the main variable did not change significantly after intervention in both groups (P = 0.919).
CONCLUSION: According to our finding, there was not a decrease in proteinuria in diabetic patients who received vitamin D for a period of 3 months.

RCT Entities:   Population Interventions Outcomes

INTRODUCTION

Nowadays Vitamin D deficiency is a notable medical condition world-wide. It seems that the limitation of sun exposure is the main cause of vitamin D deficiency.[12] The process of vitamin D photosynthesis begins in the sun exposed skin and then vitamin D will be activated by hydroxylase enzymes in the liver and kidney respectively. In Iran, vitamin D deficiency is also prevalent. A study by Hovsepian et al. in Isfahan (center of Iran) showed high prevalence of vitamin D deficiency (50.8%) and insufficiency (19.6%) among the adult population.[3] Another study by Kaykhaei et al. showed that the prevalence of vitamin D deficiency and insufficiency is about 94.7% in Zahedan.[4]

Vitamin D has the prominent role more than calcium and phosphate metabolism in the different organ. It can affect musculoskeletal and cardiovascular system; innate immunity and body metabolism. It also has a renoprotective effect.[56789101112] Vitamin D can also inhibit the renin-angiotensin system (RAS) as shown in Li et al. study.[1314] A study by Zhang et al. confirmed the effective role of vitamin D on RAS to protect from kidney injury.[15] In the other hand, Diabetic nephropathy is a problematic challenge as a leading cause of end stage renal disease (ESRD) world-wide. In the pathogenesis of diabetic nephropathy, multiple pathways are engaged, and the intrarenal RAS is also activated. It is proved that drugs that inhibit the RAS, can prevent from renal damage and proteinuria.[16] As the traditional management, treatment with angiotensin converting enzyme inhibitors (ACEIs) or Angiotensin II type receptor blockers (ARBs) can reduces the progression of proteinuria in diabetic patients.

Due to mentioned role for vitamin D, it appears that low vitamin D level can worsen the renal injury in the diabetic patients. Many of the studies showed the effect of activated forms of vitamin D on the diabetic nephropathy, but little information is available using vitamin D3.[1718192021] This study demonstrates the effect of vitamin D3 therapy on reducing proteinuria in diabetic patients with concomitant diabetic nephropathy and vitamin D deficiency after controlling hypertension and use of ACEIs or ARBs.

MATERIALS AND METHODS

Study design and patients

In this randomized double blinded parallel groups clinical trial, 60 diabetic patients with proven nephropathy and vitamin D deficiency/insufficiency were enrolled. In our study, the sample size was calculated by considering a 90% statistical power for detecting an effect size of 0.8 in urine albumin/creatinine ration (UACR) (based on percentage changes from the baseline between treatment and placebo groups) and 5% as a type one error rate.[19] All of them were selected randomly among patients who regularly followed-up in the Isfahan endocrine and metabolism research center during 2011. The Ethics Committee of the Isfahan Medical University approved the study (project number: 390287) and all participants signed a written informed consent. Vitamin D deficiency and vitamin D insufficiency is defined as 25(OH) D levels below 20 ng/mL and 20 to 29 ng/mL respectively.[22] Plasma levels of 25(OH) D were determined by direct competitive chemiluminescence as a routine laboratory test carried out in diabetic patients followed in Isfahan endocrine and metabolism disease research center.

In this study, nephropathy was defined as proteinuria determined in fasting urine sample by a UACR more than 30 mg/g Consistent with American Diabetes Association guidelines.

Other inclusion criteria included age older than 20 years; stable hypertension, dyslipidemia, and hyperglycemic treatment that not changed at least 3 months before the examination and the patients were receiving permanent doses of ACEIs or ARBs for 3 months or more. Glomerular filtration rate (GFR) was assessed by Cockcroft equation and patients with stable GFR were eligible for enrollment. Patients were excluded if there they had glomerulonephritis, serum phosphorus level greater than 5.2 mg/dl, serum calcium level (adjusted for albumin) greater than 10.5 mg/dl, malignancy, uncontrolled hypertension or chronic heart failure.

Procedure and measurements

A total of 60 patients were divided randomly into two groups (30 patients in treatment and plcebo). The randomization was carried out using permutated random blocks. Patients in the treatment group received oral vitamin D3 (pearl 50,000 IU) one pearl every week for 12 weeks. Furthermore, participants in the control group received placebo, one pearl weekly for 12 weeks; finally 51 patients completed the treatment period. 9 of the enrolled patients did not follow the prescribed study's protocol. The vitamin D and placebo pearls were formulated in Zahravi pharmaceutical company. The placebo pearls were completely identical in appearance to vitamin D pearl.

Detailed history was taken and physical examination was carried out at the beginning of the study. Patients were assessed at baseline and 12 weeks after intervention from the point of 25(OH) D level, lipid profile, hemoglobin A1C (Hb A1C) and UACR. The patients’ blood pressure and body mass index were also evaluated. At the end of follow-up period, 28 patients in the drug group and 23 patients in the placebo group completed the study.

Statistical analysis

Quantitative variables are represented as Mean ± SD (standard deviation) and qualitative ones as number (percentage). Normality of quantitative studied variables was assessed using Kolmogorov-Smirnov test and p-p plot. Logarithmic transformation was conducted for normalizing the distribution of variables as required. In our study, the transformation was conducted for Bun, serum Cr and 25(OH) D. Accordingly between groups comparisons, based on the absolute percentage changes, were conducted using two-independent samples t-test. The absolute percentage change for each variable was calculated by the formula |(E-B/B)×100|, where E was the end of treatment value and B was the baseline value and within group comparisons using the paired samples t-test. Between groups comparisons based on qualitative variables were done using Chi-square statistical test. P < 0.05 was considered as a statistically significant level. All statistical analyses were done using SPSS software version 16 (SPSS, Chicago IL).

RESULTS

From 51 diabetic patients included in study, 34 (66.7%) patients used oral hypoglycemic drugs and 17 (33.3%) were on insulin injection. Hypertension was determined from the patients’ medical history documents. All patients received ACEI or ARBs. 30 (58.8%) patients of 51 participants had the history of hypertension and all of them used ACEI or ARBs as anti-hypertensive drugs. Patients without hypertension also received ACEI or ARBs drugs as reno-protective agent. 20 (39.9%) patients had the history of diabetic retinopathy in the recent ophthalmologic examination and were treated properly. Among 51 patients, 18 (35.3%) had the history of thyroid dysfunction but all of them had normal thyroid function test before the study. The demographic and basic clinical characteristics of all study participants were evaluated at the start and end of the study period. No statistically significant differences were seen in terms of basic clinical characteristics in each studied groups as well as between case and control groups [Table 1].

Table 1

basic and clinical characteristics of participants in drug and placebo groups before intervention

Table 2 presents the results of within and between groups’ comparisons in terms of studied variables. As can be seen from Table 2, within groups’ comparisons only statistically significant is for vitamin D. The mean of calcium before and after intervention was 9.22 ± 0.4 mg/dl and 9.75 ± 0.32 mg/dl (P < 0.0001) and the mean of phosphorous was 3.70 ± 0.84 mg/dl and 4.02 ± 0.62 mg/dl (P < 0.05) respectively. However, between groups comparisons in terms of absolute percentage changes for these variables were not statistically significant. Mean systolic blood pressures changed significantly throughout the course of study in the treatment group. Mean systolic blood pressure in the vitamin D group was 125.35 ± 15.51 mm Hg at baseline and at last evaluation, it was 119.67 ± 16.74 mm Hg (P = 0.033). In the placebo group, the mean systolic blood pressure was 122.86 ± 12.8 and 118.17 ± 17.25 before and after intervention (P = 0.022). However, it showed no significant differences between two groups before and after treatment changes. In the control group, neither baseline nor final differences were statistically significant. Mean serum 25(OH) D concentrations were 14.06 ng/ml and 16.05 ng/ml before treatment, which was in the range of vitamin D deficiency and insufficiency in both groups. However, after intervention, its levels were risen to 71.23 and 17.63 in drug and placebo groups, respectively. Between groups comparison in terms of absolute percentage changes was statistically significant at P < 0.0001. Whereas, UACR as the main variable did not change significantly after intervention in both groups (P = 0.919). The studied groups did not show significant differences in terms of lipid profile, Hb A1C and GFR. None of the patients had the albumin-corrected calcium above 10.5 or phosphorous above 5.2 after treatment. No adverse events were reported in the placebo and drug groups.

Table 2

Results of within and between group comparisons in terms of studied variables

DISCUSSION

25(OH) D is not only a vitamin, but also known as a hormone in different pathological pathways. The anti-inflammatory role of 25(OH) D in addition to its effect on decreasing the cytokines is becoming evident on daily bases. In National Health And Nutrition Examination Study (NHANES) III study, there is a relationship between the increase in albuminuria and decrease in plasma 25(OH) D.[23] Zehnder et al. studied the relationship between inflammatory markers in chronic kidney disease (CKD) with the level of 1, 25(OH) D.[24] They found out that there is a relationship between the CKD and the level of 1, 25(OH) D. The higher levels of 25(OH) D consequently results in lower inflammation. On the other hand, in CKD patients, a decrease in vitamin D metabolites is related to increase in inflammation. The active metabolites of vitamin D directly influence the endothelial function and inversely related to the degree of arterial calcification in CKD patients. Therefore, decrease in 25(OH) D in CKD patients leads to poor prognosis and eventually progression to ESRD.[25]

There are evidences demonstrating that vitamin D decreases the renal fibrosis progression.[26] The mechanism might be due to decrease in podocytes and increase in glomerulosclerosis, which both increase the risk of albuminuria.[17] There are many studies showing that active forms of vitamin D such as calcitriol and paricalcitrol decreases the albuminuria rate in patients with type 2 diabetes mellitus. The mechanism might be due to decrease in renal expression of renin as well as curbing the Tumor necrosis alpha effect. The vitamin D analogues are known to have reno-protective effect.

As far as our investigation there is no clinical trial that has studied the effect of 25(OH) D on decreasing the proteinuria in patients with type 2 diabetes.

In this study, patients with stable hypertension, dyslipidemia and hyperglycemic treatment, and vitamin D deficiency have been treated with Pearl 50,000 IU vitamin D3 on weekly bases. The patients were compared with placebo groups. Although, the level of 25(OH) D in patients receiving the treatment significantly increased, there was no significant decrease in proteinuria or a change in GFR after 3 months of treatment was observed. The short period of follow-up and small population under study might be the result of insignificant albuminuria in these patients. However, the patients will be evaluated in periods of 6 months and 1 year after receiving the treatment. There are evidences showing that taking vitamin D is beneficial in decreasing the systolic and diastolic blood pressures. However, the difference between the two groups was not significant.

CONCLUSION

According to our finding, there was not a decrease in proteinuria in diabetic patients who have been receiving vitamin D for a period of 3 months.