Ageing BIOmarker Study in Singaporeans (ABIOS)

May 28, 2026 updated by: Andrea Maier, National University of Singapore

Ageing BIOmarker Study in Singaporeans (ABIOS)

The Ageing BIOmarker Study in Singaporeans (ABIOS) aims to understand the biological aging processes and how they affect health among people in Singapore. As people grow older, their risk of developing chronic diseases increases. This study aims to better understand the biological changes that come with age, particularly in three major ethnic groups: Chinese, Malay, and Indian adults over 21 years old. By examining a range of health indicators such as DNA methylation, inflammation, metabolism, cardiovascular health, physical function, and physical activity (i.e., molecular, physiological, and digital biomarkers of ageing), the study seeks to identify how ethnicity, lifestyle, and socioeconomic factors influence ageing. This unique study focuses on an all-Asian population, aiming to enhance our understanding of healthy aging across different ethnic groups.

Study Overview

Status

Active, not recruiting

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

Observational

Enrollment (Actual)

378

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Singapore, Singapore, 159964
        • Centre for Healthy Longevity at Alexandra Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Adults 21 years of age or greater who has lived in Singapore for at least 5 consecutive years and is of Chinese, Malay, or Indian ethnicity

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Singaporean adults
Adults greater than 21 years of age living in Singapore of Chinese, Malay, or Indian ethnicity.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
blood DNA methylation
Time Frame: Baseline
DNA methylation ageing clock, years
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Carotid-femoral Pulse Wave Velocity
Time Frame: Baseline
Arterial stiffness measured by pulse wave velocity, m/s
Baseline
Handgrip strength
Time Frame: Baseline
Handgrip strength measured by dynamometer, kg
Baseline
8-repetition maximal strength
Time Frame: Baseline
Lower body strength measured by maximum weight for 8 leg extension repetitions, kg
Baseline
Objective physical activity
Time Frame: Baseline
Objective physical activity measured by an activity tracking monitor
Baseline
Facial age
Time Frame: Baseline
Facial ageing clock based on 3D face morphometry, years
Baseline
Complete red blood cell (RBC) count
Time Frame: Baseline
Clinical blood parameters, RBC x 10^12/L
Baseline
Total white blood cell (WBC) count
Time Frame: Baseline
Clinical blood parameters, WBC x 10^9/L
Baseline
Total cholesterol
Time Frame: Baseline
Lipid profile panel, mmol/L
Baseline
HDL cholesterol
Time Frame: Baseline
Lipid profile panel, mmol/L
Baseline
LDL cholesterol
Time Frame: Baseline
Lipid profile panel, mmol/L
Baseline
Triglycerides
Time Frame: Baseline
Lipid profile panel, mmol/L
Baseline
Fasting blood glucose
Time Frame: Baseline
Clinical blood parameters, mmol/L
Baseline
Total protein
Time Frame: Baseline
Liver profile panel, mmol/L
Baseline
Total bilirubin
Time Frame: Baseline
Liver profile panel, umol/L
Baseline
Alkaline phosphatase (ALP)
Time Frame: Baseline
Clinical blood parameters, U/L
Baseline
Insulin
Time Frame: Baseline
Clinical blood parameters, Roche immunoassay, mU/L
Baseline
HbA1c
Time Frame: Baseline
Clinical blood parameters, %
Baseline
Skin advanced glycation endproducts
Time Frame: Baseline
Skin advanced glycation endproducts measured by autofluorescence
Baseline

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood pressure
Time Frame: Baseline
Central and brachial blood pressure measurements, mmHg
Baseline
Waist-to-hip ratio
Time Frame: Baseline
Waist-to-hip circumference ratio
Baseline
Bone mineral density
Time Frame: Baseline
Bone mineral density measured by DEXA scan, g/cm^2
Baseline
Fat-free mass
Time Frame: Baseline
Fat-free mass measured by DEXA scan, kg
Baseline
Fat mass
Time Frame: Baseline
Fat mass measured by DEXA scan, kg
Baseline
Arm curl repetitions
Time Frame: Baseline
Number of arm curl repetitions at a certain weight in 30 seconds
Baseline
Backscratch test
Time Frame: Baseline
Backscratch test to assess upper body flexibility, distance between fingers in cm
Baseline
Sit-to-stand repeitions
Time Frame: Baseline
Number of chair sit-to-stand repetitions in 30 seconds
Baseline
4-metre walk
Time Frame: Baseline
Time it takes for the participant to walk 4 metres, seconds
Baseline
Habitual physical activity
Time Frame: Baseline
Habitual physical activity patterns reflected by the Global Physical Activity Questionnaire
Baseline
Frailty
Time Frame: Baseline
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)
Baseline
Risk of malnutrition
Time Frame: Baseline
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)
Baseline
Saliva DNA methylation status
Time Frame: Baseline
DNA methylation ageing clock, years
Baseline
Cognitive function
Time Frame: Baseline
Cognitive function test assessed by the Montreal Cognitive Assessment (MoCA), ranging from 0 to 30
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Andrea Maier, MD, PhD, National University of Singapore

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 12, 2021

Primary Completion (Actual)

July 4, 2024

Study Completion (Estimated)

December 31, 2028

Study Registration Dates

First Submitted

August 8, 2024

First Submitted That Met QC Criteria

August 12, 2024

First Posted (Actual)

August 15, 2024

Study Record Updates

Last Update Posted (Actual)

June 1, 2026

Last Update Submitted That Met QC Criteria

May 28, 2026

Last Verified

May 1, 2026

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

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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