Epigenetics and NCD Prevention in Kazakhstan: Personalized Approaches and Biological Age Prediction
Epigenetics and Prevention of Non-communicable Diseases in Kazakhstan: a Personalized Approach and Biological Age Prediction
1 other identifier
observational
6,720
1 country
1
Brief Summary
This study aims to enhance personalized and preventive care for non-communicable diseases (NCDs) in Kazakhstan by examining epigenetic factors, predicting biological age and reproductive function using machine learning, and developing health improvement recommendations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 3, 2025
CompletedFirst Submitted
Initial submission to the registry
March 31, 2025
CompletedFirst Posted
Study publicly available on registry
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
ExpectedJuly 11, 2025
April 1, 2025
10 months
March 31, 2025
July 8, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Accuracy of Machine Learning Model for Predicting Biological Age
Evaluation of the model's performance (based on telomere length and DNA methylation) using Mean Absolute Error (MAE), Mean Squared Error (MSE), and R².
Within 10 months from start of data collection
Accuracy of Reproductive Function Prediction Model
Development and validation of machine learning model to predict reproductive function using biomarkers. Model performance evaluated via MAE, MSE, and R².
Within 10 months from start of data collection
Study Arms (1)
The study includes 1 cohort divided into 4 age subgroups.
The study follows a multistage cluster sampling design with age and gender stratification. A total of 1 cohorts have been identified, further divided into 4 age subgroups: 1. 18-29 years 2. 30-44 years 3. 45-59 years 4. 60-69 years Each age group is designed to have an equal distribution of men and women, ensuring gender balance across all subgroups.
Interventions
Investigation of telomere length (TL) and DNA methylation level analysis
Eligibility Criteria
The study population consists of 6,720 adult volunteers aged 18 to 69 years, residing across 17 regions of Kazakhstan. Participants are stratified by age and gender to ensure balanced representation within the following age groups: * 18-29 years * 30-44 years * 45-59 years * 60-69 years Each age group includes an equal proportion of men and women, ensuring gender balance. The selection follows a multistage cluster sampling design, incorporating various socioeconomic backgrounds and health statuses to enhance the generalizability of findings.
You may qualify if:
- Adults aged 18 to 69 years.
- Residents of 17 regions of Kazakhstan.
- Willingness to participate and provide informed consent.
You may not qualify if:
- Age less than 18 years old or over 69 years old.
- Failure to provide informed consent or incomplete participation in data collection procedures.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Asfendiyarov Kazakh National Medical University
Almaty, Kazakhstan, 050000, Kazakhstan
Biospecimen
Venous blood samples and peripheral blood mononuclear cells (PBMCs) will be collected. DNA will be extracted and analyzed for telomere length (via quantitative real-time polymerase chain reaction (qPCR)) and methylation patterns (using methylation-sensitive high-resolution melting (MS-HRM)). Only high-quality DNA (assessed by spectrophotometry and fluorometry) will be retained. Samples will be stored at -80°C.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Vice-rector
Study Record Dates
First Submitted
March 31, 2025
First Posted
May 1, 2025
Study Start
March 3, 2025
Primary Completion
January 1, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
July 11, 2025
Record last verified: 2025-04