The Vitamin B Status in Type 2 Diabetes (VITA) Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Rima Obeid
- Enrollment
- 174
- Primary Endpoint
- The difference in serum vitamin B1 between cases and controls
Study Overview
Brief Summary
The objective of this study was to evaluate vitamin B deficiency (particularly vitamin B6 deficiency) in diabetic patients in Germany in relation to the presence or absence of proteinuria, and global vascular risk.
Detailed Description
This observational study recruited either control subjects or patients with type 2 diabetes for over 5 years and collected information on cardiovascular risk factors. Fasting blood samples and urine were collected and biomarkers of B-vitamins were measured and were related to renal function or to global cardiovascular risk. Global cardiovascular risk was calculated from established models that include Routine clinical and laboratory markers such as plasma lipids, smoking, hypertension, and BMI.
we measured the following markers: Glucose (fasting plasma glucose); HbA1C; serum creatinine; Glomerular filtration rate (GFR), urinary Albumin, C-reactive Protein, Soluble vascular cell adhesion molecule 1 (sVCAM-1), cystatin C, vitamin B1, vitamin B12, holotranscobalamin, methylmalonic acid, homocysteine, and different vitamin B6 forms.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Cross Sectional
Eligibility Criteria
- Ages
- 40 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Written informed consent before any study-related activities
- •Ambulatory subject >18 years of age
- •For patients with type 2 Diabetes:
- •Duration of diabetes ≥ 5 years
- •Glycated haemoglobin (HbA1C) <10%
- •Body mass index (BMI) 19-40 kg/m2
- •For healthy controls:
- •No diabetes (normal fasting glucose levels measured by stick)
Exclusion Criteria
- •End stage renal disease (creatinine clearance <10 mL/min)
- •Severe excess alcohol consumption (>50 units/week)
- •Severe co-morbidities
- •Renal and/or pancreatic transplant
- •Vitamin B1, B6 and/or B12 substitution (incl. multivitamin preparations)
- •Participation in an interventional study within 30 previous days;
- •Patient is female and pregnant or lactating
- •Patient is female in a childbearing age without adequate contraceptive precaution
Outcomes
Primary Outcomes
The difference in serum vitamin B1 between cases and controls
Time Frame: Baseline
Compare mean levels of the controls with those in the patients
The difference in serum vitamin B6 concentrations between cases and controls
Time Frame: Baseline
Compare mean levels of the controls with those in the patients
The difference in serum vitamin B12 levels between cases and controls
Time Frame: Baseline
Compare mean levels of the controls with those in the patients
Secondary Outcomes
- The difference in serum and urine vitamin B6 vitamers between patients with advanced global vascular risk versus those with a low vascular risk(Baseline)
- The difference in serum vitamin B12 between patients with and those without albuminuria(Baseline)
- The difference in serum and urine vitamin B1 between patients with and those without albuminuria(Baseline)
- The difference in serum and urine vitamin B6 vitamers between patients with and those without albuminuria(Baseline)
Investigators
Rima Obeid
Prof. Dr.
Universität des Saarlandes