- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06555978
Ageing BIOmarker Study in Singaporeans (ABIOS)
Ageing BIOmarker Study in Singaporeans (ABIOS)
Study Overview
Status
Conditions
Detailed Description
Biological ageing is the primary driver of age-associated chronic diseases in older adults. Asian populations have been underrepresented in studies developing biological age predictors and understanding age-related diseases. Thus, the Ageing BIOmarker Study in Singaporeans (ABIOS) aims to characterise the biomarkers of ageing in Singaporeans, exploring associations between molecular, physiological, and digital biomarkers of ageing.
This is a single-centre, cross-sectional study that recruits healthy community-dwelling adults (≥ 21 years) from three different ethnic groups (Chinese, Malay, and Indian). Molecular biomarkers of ageing include a multi-omics approach, such as DNA methylation and metabolic and inflammatory parameters in blood, saliva, and stool. Physiological biomarkers of ageing include bone density, body composition, skin autofluorescence, arterial stiffness, physical performance (e.g., muscle strength and flexibility), cognition, and nutritional status. Digital biomarkers of ageing include three-dimensional facial morphology and objective physical activity. Additional factors such as habitual physical activity, dietary patterns, and medical history are also examined. The associations between the molecular, physiological, and digital phenotypes will be explored.
By examining diverse age-related biomarkers, clinical indicators, and lifestyle factors, ABIOS will offer unique insights into the ageing process within these ethnic groups to develop health policies and interventions for promoting healthy ageing in an all-Asian population.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Singapore, Singapore, 159964
- Centre for Healthy Longevity at Alexandra Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- ≥21 years of age
- Chinese, Malay, or Indian and has lived in Singapore for at least 5 consecutive years
- Apparently healthy and non-smokers
Having only 1 condition (if ≥45 and <65 years) or any condition (if ≥65 years), and all conditions were medication-controlled (if any):
- Hypertension
- Hyperlipidemia
- Hyperglycemia
- Osteopenia/osteoporosis
- Osteoarthritis
- Type 2 diabetes
Exclusion Criteria:
- Body mass index (BMI) ≥30 kg/m^2
- Pre-existing or history of major cardiovascular disease (e.g., coronary artery disease, heart failure, stroke, peripheral vascular disease)
- Any metal implants (excluding dental implants) in the body
- Pre-existing or history of cancer or chronic obstructive pulmonary disease (COPD)
- Pregnant women or planning pregnancy in the next 6-12 months
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Singaporean adults
Adults greater than 21 years of age living in Singapore of Chinese, Malay, or Indian ethnicity.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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blood DNA methylation
Time Frame: Baseline
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DNA methylation ageing clock, years
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Carotid-femoral Pulse Wave Velocity
Time Frame: Baseline
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Arterial stiffness measured by pulse wave velocity, m/s
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Baseline
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Handgrip strength
Time Frame: Baseline
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Handgrip strength measured by dynamometer, kg
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Baseline
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8-repetition maximal strength
Time Frame: Baseline
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Lower body strength measured by maximum weight for 8 leg extension repetitions, kg
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Baseline
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Objective physical activity
Time Frame: Baseline
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Objective physical activity measured by an activity tracking monitor
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Baseline
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Facial age
Time Frame: Baseline
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Facial ageing clock based on 3D face morphometry, years
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Baseline
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Complete red blood cell (RBC) count
Time Frame: Baseline
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Clinical blood parameters, RBC x 10^12/L
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Baseline
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Total white blood cell (WBC) count
Time Frame: Baseline
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Clinical blood parameters, WBC x 10^9/L
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Baseline
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Total cholesterol
Time Frame: Baseline
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Lipid profile panel, mmol/L
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Baseline
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HDL cholesterol
Time Frame: Baseline
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Lipid profile panel, mmol/L
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Baseline
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LDL cholesterol
Time Frame: Baseline
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Lipid profile panel, mmol/L
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Baseline
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Triglycerides
Time Frame: Baseline
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Lipid profile panel, mmol/L
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Baseline
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Fasting blood glucose
Time Frame: Baseline
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Clinical blood parameters, mmol/L
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Baseline
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Total protein
Time Frame: Baseline
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Liver profile panel, mmol/L
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Baseline
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Total bilirubin
Time Frame: Baseline
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Liver profile panel, umol/L
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Baseline
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Alkaline phosphatase (ALP)
Time Frame: Baseline
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Clinical blood parameters, U/L
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Baseline
|
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Insulin
Time Frame: Baseline
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Clinical blood parameters, Roche immunoassay, mU/L
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Baseline
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HbA1c
Time Frame: Baseline
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Clinical blood parameters, %
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Baseline
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Skin advanced glycation endproducts
Time Frame: Baseline
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Skin advanced glycation endproducts measured by autofluorescence
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Baseline
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Blood pressure
Time Frame: Baseline
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Central and brachial blood pressure measurements, mmHg
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Baseline
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Waist-to-hip ratio
Time Frame: Baseline
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Waist-to-hip circumference ratio
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Baseline
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Bone mineral density
Time Frame: Baseline
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Bone mineral density measured by DEXA scan, g/cm^2
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Baseline
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Fat-free mass
Time Frame: Baseline
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Fat-free mass measured by DEXA scan, kg
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Baseline
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Fat mass
Time Frame: Baseline
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Fat mass measured by DEXA scan, kg
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Baseline
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Arm curl repetitions
Time Frame: Baseline
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Number of arm curl repetitions at a certain weight in 30 seconds
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Baseline
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Backscratch test
Time Frame: Baseline
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Backscratch test to assess upper body flexibility, distance between fingers in cm
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Baseline
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Sit-to-stand repeitions
Time Frame: Baseline
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Number of chair sit-to-stand repetitions in 30 seconds
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Baseline
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4-metre walk
Time Frame: Baseline
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Time it takes for the participant to walk 4 metres, seconds
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Baseline
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Habitual physical activity
Time Frame: Baseline
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Habitual physical activity patterns reflected by the Global Physical Activity Questionnaire
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Baseline
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Frailty
Time Frame: Baseline
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Frailty assessed by the FRAIL scale (fatigue, resistance, aerobic capacity, illnesses, and loss of weight), with three categories: robust (score=0), prefrail (score=1-2), and frail (score=3-5)
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Baseline
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Risk of malnutrition
Time Frame: Baseline
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Risk of malnutrition assessed by the Mini Nutritional Assessment (MNA), with three categories: malnourished (0-7 points), at risk of malnutrition (8-11 points), normal nutritional status (12-14 points)
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Baseline
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Saliva DNA methylation status
Time Frame: Baseline
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DNA methylation ageing clock, years
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Baseline
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Cognitive function
Time Frame: Baseline
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Cognitive function test assessed by the Montreal Cognitive Assessment (MoCA), ranging from 0 to 30
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Baseline
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Andrea Maier, MD, PhD, National University of Singapore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NHG-DSRB-2019-00388
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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