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Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2 (DIMENSION)

2014年11月17日 更新者:Rinkoo Dalan、Tan Tock Seng Hospital

Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2 and Low 25(OH)D Concentrations: Does it Help to Improve Endothelial Function-The DIMENSION TRIAL

Background and Objectives :

The presence of vitamin D deficiency in patients with type 2 diabetes mellitus (T2DM) is associated with an increased risk of cardiovascular disease (CVD). We aim to see whether supplementation of vitamin D in these patients helps to improve the endothelial function (EF) a surrogate marker of CVD risk.

Hypothesis: Vitamin D supplementation in patients with T2DM and low serum 25(OH) D concentrations (<30ng/ml) will improve EF as measured by the Endo-PAT machine by 0.4 units (30% improvement over baseline) and/or will result in a increase of EPCs (CD133+/KDR+) and CD45dim CD34+/KDR.

The investigators will test this hypothesis by comparing 2 groups of T2DM patients randomized to placebo or vitamin D3 for 16 weeks.

Methods:

This is a 16 weeks trial in which 120 T2DM patients will be screened with the aim to recruit 60 T2DM patients with vitamin D deficiency or insufficiency. Out of these 60 patients , 30 patients will be started on vitamin D supplementation and 30 patients will be given a matched placebo. Endothelial function (EF) will be checked before and after supplementation to see a change in EF.

Significance of Project:

If this study shows a significant improvement of EF, it would justify larger scale studies to show that vitamin D supplementation in patients with T2DM mitigates CVD risk and vitamin D supplementation in patients with T2DM and vitamin D deficiency to improve CVD risk.

研究概览

详细说明

Overall Aims: Type 2 Diabetes Mellitus (T2DM) is increasingly more prevalent in Singapore and is a high cardiovascular diseases (CVD) risk factor (1,2). The presence of low serum 25(OH)D concentrations (<30ng/ml) has also been classified as an independent predictor of CVD(3,4) and has been seen to be more prevalent in T2DM (5-7). We aim to see whether replacement with vitamin D in these patients helps to mitigate CVD risk. Since endothelial dysfunction is one of the earliest manifestations of CVD and is a very robust surrogate marker, we aim to measure the endothelial function (EF) before and after vitamin D supplementation to evaluate for beneficial impact on this endpoint.

Specific Aims: Although, there are some small scale studies done with a single high dose replacement of vitamin D2/D3, no studies have been done using regular daily supplementation with vitamin D3 and with measurement of EF using the Endo-PAT machine or measurement of endothelial progenitor cells (EPCs).We are doing this pilot study to see whether replacement with vitamin D results in an improvement of EF as measured using the Endo-PAT and estimation of EPCs and some biomarkers as independent established surrogate markers of CVD risk. The estimation of endothelial progenitor cells has been proposed as a surrogate marker of vascular dysfunction and is known to be reduced in patients with cardiovascular risk factors (8). The no. of circulating endothelial cells (CECs) and endothelial microparticles have been seen to be elevated in patients with cardiovascular risk factors and DM and has also been proposed as a effective surrogate marker. We aim to quantify the no. of endothelial progenitor cells (EPCs) staining positive for CD133+/KDR (kinase insert domain-containing receptor),CD34+/KDR and CD45dim CD34+/KDR , CECs (CD 146+/CD45- ) and EMPs derived from endothelial progenitors (CD45-/CD146+/CD34+/CD117+) and from mature endothelial cells (CD45-/CD146+/CD34+/CD117-).using flow cytometry.

Primary Hypothesis:

Vitamin D supplementation in patients with T2DM and low serum 25(OH) D concentrations (<30ng/ml) will improve EF as measured by the Endo-PAT machine by 0.4 units (30% improvement over baseline) and/or will result in a increase of EPCs (CD133+/KDR+) and CD45dim CD34+/KDR. The investigators will test this hypothesis by comparing 2 groups of T2DM patients randomized to placebo or vitamin D3 for 16 weeks.

Secondary Objectives:

To explore the prevalence of low serum 25(OH) D concentrations (<30ng/ml) in T2DM patients and evaluate the difference in the EF in the two groups. To see whether vitamin D supplementation helps to further improve other parameters such as biomarkers, blood pressure, BMI, urine albumin-to-creatinine ratio (ACR), lipid profile of T2DM patients.

研究类型

介入性

注册 (实际的)

64

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Singapore、新加坡、308433
        • Tan Tock Seng Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

21年 至 80年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subjects with Type 2 Diabetes Mellitus
  • HbA1c : 6.0-10.0%
  • Male of female aged 21-80 years
  • Stable Diabetes, blood pressure and hyperlipidemia medications (a 25% dose adjustment is allowed) in the last three months
  • Baseline serum 25(0H)D concentration <30ng/ml for randomisation

Exclusion Criteria:

  • Baseline serum 25(OH)D concentration >30ng/ml
  • Baseline HbA1c>10.1%
  • Baseline hypercalcemia (Ca>2.58 mmol/L)
  • Known case of Primary Hyperparathyroidism
  • Known to be on bisphosphonates
  • Known to be on Vitamin D supplementation of 1000 units daily or more in the last one year.
  • Chronic renal failure with eGFR<30ml/min
  • Known to have cirrhosis of the liver or transaminitis with ALT/AST >3X ULN
  • Patients with h/o sarcoidosis, renal calculi or any malignancy
  • Patients on current treatment for tuberculosis
  • Pregnancy and Lactation
  • Women of childbearing potential not taking effective contraceptive measures.
  • Patients on long term glucocorticoids or anti-retroviral drugs
  • Patients on orlistat or other over the counter preparations that claim to block fat absorption.
  • A change in the type of medications for hypertension, diabetes mellitus and hyperlipidemia in the last three months
  • Patients who have undergone any form of bariatric surgery
  • Patients known to have any malabsorption disorders
  • Patients known to have osteoporosis or of baseline BMD scan shows osteoporosis as T score <-2.5SD (for randomisation)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂丸
Placebo pill supplied by oneNine 57 imported to Singapore with approval and import licence from HSA.
其他名称:
  • 安慰剂
有源比较器:Vitamin D supplementation
Vitamin D3 tablets (cholecalciferol)
Vitamin D3 marketed by oneNine57
其他名称:
  • Vitamin D3-Cholecalciferol 1000units per tablet.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Endothelial function as assessed by the reactive hyperemia index and endothelial progenitor cells
大体时间:16 weeks
Endothelial function will be tested by using the EndoPAT machine which measures the reactive hyperemia index and by estimating the no. of endothelial progenitor cells in the peripheral blood by flow cytometry.
16 weeks

次要结果测量

结果测量
措施说明
大体时间
Markers of endothelial cell activation and thrombogenesis
大体时间:16 weeks
Biomarkers measured include hsCRP, e-selectin,von-willebrand factor(vWF)
16 weeks
No. of circulating endothelial cells and endothelial microparticles
大体时间:16-20 weeks
The no. of circulating endothelial cells and endothelial microparticles will be estimated before and after intervention.
16-20 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Rinkoo Dalan, MBBS, FRCP、Tan Tock Seng Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年9月1日

初级完成 (实际的)

2014年11月1日

研究完成 (实际的)

2014年11月1日

研究注册日期

首次提交

2012年11月30日

首先提交符合 QC 标准的

2012年11月30日

首次发布 (估计)

2012年12月4日

研究记录更新

最后更新发布 (估计)

2014年11月18日

上次提交的符合 QC 标准的更新

2014年11月17日

最后验证

2014年11月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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