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临床试验/NCT02750293
NCT02750293已完成3 期

The Effect of Vitamin D Supplementation on Cardiovascular Risk Factors in Subjects With Low Serum 25-hydroxyvitamin D Levels

University of Tromso1 个研究点 分布在 1 个国家目标入组 411 人开始时间: 2015年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
411
试验地点
1
主要终点
Change from baseline in systolic and diastolic blood pressure

研究概览

简要总结

Six-hundred subjects with vitamin D deficiency will be randomized to vitamin D 3000 IU per day versus placebo for 4 months, with effects on cardiovascular risk factors as main endpoint

详细描述

Vitamin D is a hormone with effects not only on the skeleton, but on most tissues in the body. Lack of vitamin D is associated with cardio-vascular disease (CVD) and type 2 diabetes, and also with risk factors for these diseases like hypertension, dyslipidemia, insulin resistance, and endothelial dysfunction. However, intervention studies with vitamin D have been inconclusive regarding diseases and risk factors. Most of these studies were done in white, Western populations in subjects fairly vitamin D sufficient, and accordingly, no benefits were to be expected. Also, in many studies the doses of vitamin D have been too low, and the studies underpowered. To firmly establish the role of vitamin D regarding CVD risk factors we will in the present study include 600 subjects with vitamin D deficiency (serum 25-hydroxyvitamin D (25(OH)D) < 30 nmol/L) and randomize to high dose vitamin D (3000 IU per day) versus placebo for four months. The subjects will be recruited based on 25(OH)D measurements in the forthcoming 7th survey in the Tromsø study where more than 20 000 subjects are expected to attend. If our hypotheses are correct and the vitamin D supplement has a positive effect, this will be of great importance not only in countries with low sun exposure, but particularly for subjects in developing countries where vitamin D deficiency is highly prevalent.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • participated in The 7th survey in The Tromsø study
  • vitamin D deficiency

排除标准

  • primary hyperparathyroidism
  • granulomatous disease
  • reduced kidney function
  • systolic blood pressure > 174 mmHg
  • diastolic blood pressure > 104 mmHg
  • renal stones last 5 years
  • use of solarium on regular basis
  • planned holidays in tropical areas
  • clinical depression
  • clinical signs of vitamin D deficiency (muscle weakness)
  • use of vitamin D supplements
  • serious illness

研究组 & 干预措施

cholecalciferol

Active Comparator

vitamin D (as a 20 000 IU capsule) will be given once a week for 4 months

干预措施: Cholecalciferol (Drug)

placebo

Placebo Comparator

placebo capsules (identical looking to the vitamin D capsules) will be given once a week for 4 months

干预措施: Placebo (Drug)

结局指标

主要结局

Change from baseline in systolic and diastolic blood pressure

时间窗: 4 months

次要结局

  • Change from baseline in score on Becks Depression Inventory(4 months)
  • Change from baseline in cognitive function evaluated with The Twelve Word Memory Test(4 months)
  • Change from baseline in cognitive function evaluated with The Digit Symbol Coding Test(4 months)
  • Change from baseline in cognitive function evaluated with The Tapping Test(4 months)
  • Change from baseline in arterial stiffness and endothelial function evaluated with pulse wave velocity(4 months)
  • Change from baseline in arterial stiffness and endothelial function evaluated with augmentation index (AIX)(4 months)
  • Change from baseline in arterial stiffness and endothelial function evaluated with the subendocardial viability ratio (SEVR)(4 months)
  • Change from baseline in hand-grip, quadriceps and biceps muscle strength measured by hand held dynamometry .(4 months)
  • Change from baseline in number of subjects with nasal staphylococcus aureus colonization(4 months)
  • Change from baseline in bone mass density measured with dual energy x-ray absorptiometry (DEXA) at the lumbar spine and hip(4 months)
  • Change from baseline in the bone turnover marker serum type 1 procollagen (P1NP)(4 months)
  • Change from baseline in the bone turnover marker serum collagen type 1 cross-linked C-telopeptide (CTX-1)(4 months)
  • Change from baseline in serum marker of interferon-γ mediated macrophage activation(4 months)
  • Change from baseline in serum vitamin B6 status.(4 months)
  • Change from baseline in the glycosylation marker HbA1c(4 months)
  • Change from baseline in the glycosylation marker the receptor for advanced glycosylation end products (s-RAGE)(4 months)
  • Change from baseline in the glycosylation marker carboxy-methyllysine(4 months)
  • Change from baseline in psoriasis Activity in subjects with psoriasis evaluated with the Self-Administered Psoriasis Area Severity Index (SAPASI)(4 months)
  • Change from baseline in number of subjects with nocturnal legg cramps(4 months)
  • Change from baseline in sleep pattern evaluated with the Tromsø Study 7th Survey sleep pattern questionnaire(4 months)
  • Change from baseline in the serum total cholesterol(4 months)
  • Change from baseline in the serum HDL-cholesterol(4 months)
  • Change from baseline in the serum LDL-cholesterol(4 months)
  • Change from baseline in psoriasis Activity in subjects with psoriasis, evaluated with the Dermatological Life Quality Index (DLQI)(4 months)
  • Change from baseline in psoriasis Activity in subjects with psoriasis, evaluated with the Psoriasis Area Severity Index (PASI)(4 months)
  • Change from baseline in transcriptomic profile (mRNA) in adipose tissue biopsies(4 months)
  • Change from baseline in the serum triglycerides(4 months)
  • Change from baseline in the serum Apolipoprotein A1(4 months)
  • Change from baseline in the serum Apolipoprotein B,(4 months)
  • Change from baseline in insulin resistance evaluated with the homeostasis model assessment (HOMA) index based on fasting serum glucose and serum insulin(4 months)
  • Change from baseline in proteomic profile with relative quantification in adipose tissue biopsies with the use of Liquid chromatography mass spectrometry Technology (LC-MS/MS)(4 months)
  • Change from baseline in metabolomic profile with relative quantification in adipose tissue biopsies with the use of Liquid chromatography mass spectrometry Technology (LC-MS/MS)(4 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rolf Jorde

Professor

University of Tromso

研究点 (1)

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