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Vitamin D supplementation on surrogate markers of ageing, ageing-related genes, glycemic and metabolic markers in north Indian Individuals with the prediabetes

Randomized control trial of vitamin D supplementation on surrogate markers of ageing (leukocyte telomerase length and telomerase activity), association/interactions with selected ageing-related genes (including myostatin, α-Actinin-3, vitamin D receptor, Forkhead box O3 and Sirtuin1), glycemic and metabolic markers in north Indian Individuals with the prediabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/11/022106
Enrollment
200
Registered
2019-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Randomized control trial: Prediabetes is a substantial problem in India not only because it itself can be associated with morbidities such as coronary artery disease but also because it

Sponsors

Indian Councial of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cross-sectional Study: Inclusion Criteria: Individuals with prediabetes, aged 20-60 years. Prospective Intervention Study: Design: Randomized open labeled placebo-controlled trial. Inclusion Criteria: 1. Pre-diabetes: a. Fasting blood glucose >=100mg/dl and b. 2-h plasma glucose >=140mg/dl and 2. Baseline blood level of 25 hydroxy vitamin D 3. Aged 20-60 years

Exclusion criteria

Exclusion criteria: Cross sectional Exclusion Criteria: 1. Received Vitamin D or calcium supplementation in the previous six months. 2. On any medication within last one month which could potentially influence insulin secretion, insulin sensitivity, vitamin D or calcium metabolism and on any medication that activate steroid and xenobiotic receptors, and drugs used in transplantation. 3. Severe end organ damage or chronic diseases: renal/hepatic failure, any malignancy, major systemic illness etc. 4. Known case of diabetes mellitus, HIV infection and other endocrine disorders. Prospective Study 1. Received Vitamin D and/or calcium supplementation in the previous six months. 2. On any medication within last one month which could potentially influence insulin secretion, insulin sensitivity, vitamin D or calcium metabolism (e.g. metformin, thiazolidinediones, steroids etc) and on any medication that activate steroid and xenobiotic receptor and drugs used in transplantation (e.g. steroids, calcitonin etc.) 3. Severe end organ damage or chronic diseases: renal/ hepatic failure, any malignancy, nephrotic syndrome, malabsorption etc. 4. Known case of HIV infection. 5. Primary or tertiary hyperparathyroidism, granulomatous disorders (e.g. sarcoidosis) and any lymphomas. 6. Known case of diabetes mellitus.

Design outcomes

Primary

MeasureTime frame
Clinical and dietary profiles, blood pressure and phenotypic markers, sunlight exposure, anthropometric assessments [body mass index, circumferences and skinfolds, glycemic and lipid profile other metabolic parameters (serum Vitamin D, parathyroid hormone, calcium and phosphorus, fasting serum insulin and homeostasis model assessment, leukocyte telomerase length and telomerase activity and genetic polymorphismsTimepoint: Vitamin D supplementation could 1. Increase/preserve leucocyte telomerase length and activity, thus having positive effects on ageing. 2. Improve insulin action and glucose physiology, leading to lowering of blood glucose levels in persons with prediabetes.

Secondary

MeasureTime frame
2. If vitamin D addition leads to longer life span as indicated by aging-associated surrogate markers, it may be cost-effective and novel way to slow ageing in Indian population. Measurements same as in visit 1 except genetic polymorphismTimepoint: 2 years

Countries

India

Contacts

Public ContactDr Anoop Misra

Diabetes foundation India

anoopmisra@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026