Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Effects of Cholecalciferol on Depressive Symptoms in Type 2 Diabetes Mellitus Patients: Study of Neurotrophin-3, Serotonin, and C-Peptide
One in eleven adults falls ill with Diabetes Mellitus (DM) and 90% of them suffered from type 2 DM. Depression in type 2 DM patients had a big impact, acting as a major barrier to self-care in type 2 DM patients. Depression in diabetes patients is also associated with decreasing quality of life. Poor self-care behavior and adherence, poor glycemic control, and increased risk of mortality about 36-38% from cardiovascular complications are other known debilitating results. Vitamin D receptors are present in many organ systems, namely the pancreas, intestine, musculoskeletal, and nervous systems. Vitamin D has pleiotropic effects, which were seen from its mechanism as an anti-inflammatory, anti-apoptotic, and immunomodulatory agent. Based on the mechanism of Vitamin D action in the nervous system, which also plays a role in depression pathogenesis, vitamin D is hypothesized to have a beneficial effect on depression, both for depression prevention and treatment. Few studies denote that Vitamin D can improve depression in type 2 DM patients. Vitamin D may become an important adjuvant therapy to ameliorate depression in type 2 DM patients. These clinical trials concerning vitamin D in type 2 DM are relevant, reminding that type 2 DM resulted in higher morbidity, mortality, and numerous high-risk complications in the population.
Status | Recruiting |
Enrollment | 90 |
Est. completion date | October 2021 |
Est. primary completion date | October 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Male or female subjects with aged 18 and over - Living in around Jakarta - Type 2 diabetes mellitus patients with depression symptom - Patients with Body mass index 20-30 m/kg2 - Patients are able and willing to maintain diet, physical activity, and lifestyle for 3 months - Patients are able and willing to control for follow up Exclusion Criteria: - - Presence of severe hepatic dysfunction, defined as cirrhosis hepatic - Presence of severe renal dysfunction, defined as chronic kidney disease stage 5 or e-GFR =15 or history of hemodialysis - Patients with acute coronary syndrome - Presence of acute systemic inflammatory response syndrome (SIRS). The term SIRS describes a clinical state arising from a non-specific cause, infective, or otherwise - Recent obtained vitamin D therapy within the last 3 months - Current or regular use of corticosteroids within immunosuppressant dosage - Presence of major depression - Presence of psychosis - Current or regular use of anti-depressant - Current or regular use of phenytoin or phenobarbital - For females: current pregnancy and lactation period - Patients who refuse the studies |
Country | Name | City | State |
---|---|---|---|
Indonesia | Cipto Mangunkusumo National General Hospital | Jakarta Pusat | DKI Jakarta |
Lead Sponsor | Collaborator |
---|---|
Indonesia University |
Indonesia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluating the effects of cholecalciferol for depression symptoms with BDI II score | Improvement rate on days 90 (end of study) as defined by a proportion of subjects with category of BDI II score below 13. The BDI II scale was a subjective measurement of depressive symptoms. Interpretation of BDI II were 0-13 for minimal depression, 14-19 for mild depression, 20-28 for moderate depression, and 29-63 for major depression. Cholecalciferol with doses of 4000 IU a day expected to demote BDI II scale or depressive symptoms in participants. | 90 days | |
Secondary | Evaluating the effects of cholecalciferol against neuroplasticity (NT-3) | NT-3 concentration (pg/ml) in the sample was determined by comparing the sample against the standard curve. Some studies have shown that neurotrophin-3 (NT-3 pg/ml) levels decreased in depression. Thus, cholecalciferol (for doses of 4000 IU a day) with expected could increase NT-3 pg/ml plasm levels. Furthermore, the enhancement of NT-3 pg/ml concentrates expected to had correlated with scale BDI II improvement. | 30 days | |
Secondary | Evaluating the effects of cholecalciferol against serotonin | Studies have shown that serotonin (ng/mL) in depressive patients had lower levels than patient without depressive syndrome. The serotonin levels were measured by the ELISA method. Cholecalciferol expected could increase levels of serotonin concentration (ng/mL) significantly 2-3 times after administrated. | 30 days | |
Secondary | Evaluating the effects of cholecalciferol against C-Peptide | C-peptide hormone is an indicator of insulin secretion. Specifically, a c-peptide level of less than 0.2 nmol/l is associated with a diagnosis of type 1 diabetes mellitus. C-peptide measured using ELISA at a minimal room temperature for 24 hours. Cholecalciferol expected could improve C-peptide levels concentration in type 2 Diabetes Mellitus. | 30 days |
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