Back

A Blood-Based Biological Age Model Derived from Routine Laboratory Biomarkers in the Singapore Longitudinal Ageing Study

Ye, J.; Lim, X.; Franck, M.; Li, W.; Goh, D.; Chen, H.; Chung, Z.; Yang, W.; Zhu, Z.; Sitjar, P. H.; Wang, T. O.; Wee, F.; Fincham, R. E. A.; Tan, D. S. W.; Chua, K.; Hong-Wen, T.; Goh, J.; Lim, D. W.-T.; Lim, E.; Cohen, A. A.; Ho, R. C. M.; Tan, M.-H.; Jia, G.; Fülöp, T.; Yeong, J.

2026-05-06 primary care research
10.64898/2026.05.05.26352428 medRxiv
Show abstract

Risk assessment in clinical practice depends largely on clinical phenotypes, including age, sex, body mass index, blood pressure and comorbidities. Routine laboratory data remain underutilised despite their accessibility and low cost. Using data from the Singapore Longitudinal Ageing Studies (n = 5,409; follow-up median 11.4 years), we developed a mortality prediction model based on routine laboratory biomarkers. We derived a biological age (age quotient, or AQ) score, and investigated its role as a mediator between lifestyle risk factors and mortality. Both models and association analyses were validated in the US National Health and Nutrition Examination Survey (n = 6,593) and UK Biobank (n = 290,949) cohorts. AQ was significantly elevated in deceased individuals (P<0.0001). AQ acceleration was also observed (P<0.0001). In overall survival discrimination, AQ outperformed chronological age (C-index 0.629 [SE 0.011] vs 0.606 [SE 0.011]), indicating superior prognostic prediction. Additionally, incorporation of AQ into a baseline model containing chronological age resulted in an improvement in model fit (likelihood ratio test, P<0.0001), consistent with incremental predictive value for mortality beyond chronological age alone. Mediation analysis supports a partial mediating role for AQ in the relationship between lifestyle factors and mortality. In a 57-patient subset, higher AQ was associated with increased TET2 clonal hematopoiesis burden ({beta}{approx}0.016 per +1 AQ year), suggesting a potential link between AQ acceleration, CH risk and diseases of aging, requiring validation in larger cohorts. We identified differential associations between lifestyle factors and groups of biological age components, indicating selective effects across biological systems. These findings provide an evidence-based framework for earlier and more accurate identification of high-risk individuals, offering a practical and easy-to-implement tool to inform preventive strategies.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

1
Aging Cell
144 papers in training set
Top 0.2%
23.6%
2
eLife
5422 papers in training set
Top 2%
15.1%
3
The Journals of Gerontology: Series A
25 papers in training set
Top 0.2%
7.2%
4
Nature Aging
51 papers in training set
Top 0.3%
6.6%
50% of probability mass above
5
Aging
69 papers in training set
Top 0.4%
5.1%
6
Advanced Science
249 papers in training set
Top 4%
4.6%
7
npj Aging
15 papers in training set
Top 0.2%
4.5%
8
Scientific Reports
3102 papers in training set
Top 29%
4.2%
9
Clinical Epigenetics
53 papers in training set
Top 0.2%
3.8%
10
GeroScience
97 papers in training set
Top 0.5%
3.8%
11
BMC Medicine
163 papers in training set
Top 2%
2.5%
12
Nature Communications
4913 papers in training set
Top 48%
2.0%
13
The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences
22 papers in training set
Top 0.1%
2.0%
14
Communications Medicine
85 papers in training set
Top 0.7%
0.9%
15
Communications Biology
886 papers in training set
Top 21%
0.8%
16
European Journal of Epidemiology
40 papers in training set
Top 0.7%
0.8%
17
eBioMedicine
130 papers in training set
Top 4%
0.8%
18
Frontiers in Medicine
113 papers in training set
Top 7%
0.8%
19
Nature Medicine
117 papers in training set
Top 5%
0.8%
20
Journal of Infection
71 papers in training set
Top 3%
0.7%
21
Frontiers in Aging
10 papers in training set
Top 0.5%
0.5%
22
Journal of Personalized Medicine
28 papers in training set
Top 2%
0.5%
23
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 48%
0.5%