Type 2 diabetes mellitus is the second cause of death in adults of both genders in Mexico, which presents it a as a high public interest pathology. As it is a chronic degenerative disease, it requires long-term treatments and not controlling it leads to the development of important macro and microvascular alterations and ultimately death. There is evidence indicating that the general population all over the world have vitamin D deficiency, which is known to intervene in inflammatory processes associated with most chronic degenerative disease. With respect to T2DM, prolonged low-grade chronic inflammation leads to these associated complications. We hypothesize that 6-month supplementation with 4000 IU/day during 6 months in adults with T2DM will have a positive effect on inflammatory markers, glucose metabolism and lipid profile.
Methods
* Study design Longitudinal study of 40 adults with Type 2 Diabetes Mellitus, with six-month follow-up of supplementation with 4000 IU of Vitamin D3/day, with pre and post measurements.
* Sample
A convenience sample of 40 patients with type 2 diabetes mellitus from community centers in the city of Toluca will be included, according to the following:
Inclusion criteria:
1. Patients medically diagnosed with type 2 diabetes mellitus
2. Patients controlled with diet, metformin or diet and metformin
3. Patients with less than five years of diagnosis
4. Patients with signed informed consent
5. Mexican born from Mexican parents and grandparents
6. Older than 18 years of age.
Elimination criteria:
1. Patients who do not complete the study for any reason
2. Patients that do not comply with the supplementation protocol.
* Study description
After obtaining approval from the Ethics and Research Committee and authorization from the State of Mexico's Health Institute, subjects from two community health centers will be invited to participate. If compliance with inclusion criteria es fulfilled (18-year-old or more adults with less than five-year medically diagnosed type 2 diabetes, controlled solely with diet, metformin or diet and metformin, Mexican born and being children and grandchildren of Mexican origin), subjects will be asked to sign an informed consent letter. Patients included in the study will be given an appointment for obtaining a finger-prick sample for glucose and a 10mL venous fasting blood sample for biochemical analysis (Insulin, Hb1Ac, Vitamin D, Vitamin D Binding Protein, C-reactive protein, IL-6, total and HDL cholesterol, HOMA-IR will be calculated from insulin and glucose), anthropometric measurements (weight and height for BMI), food-frequency questionnaires, systolic and diastolic blood pressure, as well as general and health information (age, sex, time of diagnosis, treatment, sun-exposure). Subjects will be then given a container with 60 capsules of 4000IU each and given the instructions to consume one daily, they will be given an appointment 60 days later to re-fill the Vitamin D container, this procedure will be repeated on day 120. Every 15 days subjects will receive a reminder phone-call, where compliance will be questioned. After 6 months, the anthropometric, biochemical, dietary and health measurements will be repeated.
After obtaining the blood samples and within one hour of obtention, blood will be centrifuged at 5000 RPM and plasma will be aliquoted into 10 five mL freezer tubes and stored at -70 C for further analysis. Analysis will be done after obtaining all pre- and post-supplementation samples to avoid any differences in the management of samples and to use the same kit for all samples. Insulin, Hb1Ac, Vitamin D, Vitamin D Binding Protein, C-reactive protein, IL-6, total and HDL cholesterol will be analyzed with commercial ELISA-kits.
Results of glucose, blood pressure and anthropometry will be individually given to the study subjects immediately after obtention; results of the intervention measurements will be individually given to patients after finalization of the trial. All data will be maintained confidential, subjects will be given a code number, and all personal information will be kept in a separate database. Any negative effect related to the supplementation will be recorded and reported immediately, in case of danger, supplementation will be suspended, and subject will be referred to their medical doctor.
Statistical analysis Data will be captured into a pre-designed 25.0 SPSS program, after cleaning of the data, we will proceed to analyze the information. Data will be initially described as means, standard deviations, percentiles, frequency or percentages. We will analyze the data with the Shapiro-Wilk test for normality; comparison of initial-final data will be undertaken with paired T-test in the case of parametric data and Wilcoxon for non-parametric data.
