Journal article icon

Journal article

Comprehensive cross-sectional and longitudinal comparison of sixteen markers of biological aging from the Berlin Aging Study II

Abstract:
Background: The disproportionate increase in lifespan compared to healthspan over the past decades results in a growing proportion of life marked by diseases, even if incidence rates are falling in some cases. However, not everyone ages at the same pace and some people remain in good health and preserve physical and cognitive function into old age. To quantify inter-individual differences in the biological aging process, numerous indicators of biological age have been developed. Methods: In this study, we analyzed 16 measures of biological aging including epigenetic clocks, proteomics clock, telomere length, and SkinAge, laboratory composite markers (BioAge, Allostatic Load), psychological aging, and Brain Age. These age markers were evaluated cross-sectionally as well as longitudinally in the context of age-associated outcomes covering frailty, mobility, cognitive function, depressive symptoms, autonomy in daily life, nutrition, morbidity, and chronic disease in participants of the Berlin Aging Study II (BASE-II). Results: Here, we analyze longitudinal data from 1083 participants (mean age of 68.3 years at baseline, 52% women) with an average follow-up period of 7.4 years. Allostatic Load Index and DunedinPACE show the strongest and most consistent cross-sectional and longitudinal associations with age-associated phenotypes. Furthermore, both biomarkers individually increase the accuracy of a logistic regression model trained to predict incident cases of Metabolic Syndrome, high cardiovascular risk (Lifes’s Simple 7) as well as incident frailty (Fried’s frailty index) 7.4 years after baseline examination by up to 24 percentage points. Conclusions: Our findings support the previously shown distinction between indicators of aging and provide a comprehensive overview of their individual strengths and weaknesses in the context of wide variety of age-associated phenotypes.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Authors

More by this author
Role:
Author
ORCID:
0000-0001-5003-7766
More by this author
Role:
Author
ORCID:
0000-0002-3774-2169
More by this author
Role:
Author
ORCID:
0000-0003-2791-7065


More from this funder
Funder identifier:
10.13039/100007625
Grant:
CIR-CUITS
More from this funder
Funder identifier:
10.13039/501100002347
Grant:
#01UW0808; #16SV5536K, #16SV5537, #16SV5538, #16SV5837, #01GL1716A, and #01GL1716B
More from this funder
Funder identifier:
10.13039/100013278
Grant:
JPND2021-650-289
More from this funder
Funder identifier:
10.13039/501100001659
Grant:
460683900


Publisher:
Nature Research
Journal:
communications medicine More from this journal
Volume:
6
Issue:
1
Article number:
168
Publication date:
2026-03-27
Acceptance date:
2025-10-30
DOI:
EISSN:
2730-664X
ISSN:
2730-664X


Language:
English
Pubs id:
2407715
Local pid:
pubs:2407715
Source identifiers:
3894020
Deposit date:
2026-03-27
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP