Evidence map›Paper›PMID 42334801›Full record

ArticleGeroScience2026

Machine learning derived abdominal aortic calcification is associated with physical frailty in community-dwelling adults: the UK Biobank Imaging Study.

Abadi K Gebre, Marion Mundt, Elsa Dent, James Webster, Afsah Saleem, Syed Zulqarnain Gilani, Yuandan Zhang, Cassandra Smith, Parminder Raina, John P Kemp and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in GeroScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Abadi K GebreNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0002-1975-0085
Marion MundtNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia. m.mundt@ecu.edu.au.ORCID http://orcid.org/0000-0001-6624-2895
Elsa DentMenzies Institute for Medical Research, University of Tasmania, Hobart, Australia.ORCID http://orcid.org/0000-0002-4006-3992
James WebsterApplied Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-6999-6959
Afsah SaleemNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0001-7240-0837
Syed Zulqarnain GilaniNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0002-7448-2327
Yuandan ZhangMater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, QLD, Australia.ORCID http://orcid.org/0000-0002-1998-3313
Cassandra SmithNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0002-2517-2824
Parminder RainaMcMaster Institute for Research On Aging, McMaster University, Hamilton, ON, Canada.ORCID http://orcid.org/0000-0002-8107-3193
John P KempMater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, QLD, Australia.ORCID http://orcid.org/0000-0002-9105-2249
William D LeslieDepartment of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.ORCID http://orcid.org/0000-0002-1056-1691
John T SchousboePark Nicollet Clinic and HealthPartners Institute, HealthPartners, Minneapolis, USA.ORCID http://orcid.org/0000-0002-9329-0750
Nicholas C HarveyMRC Life Course Epidemiology Centre, University of Southampton, Southampton, UK.ORCID http://orcid.org/0000-0002-8194-2512
Joshua R LewisNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0003-1003-8443
Marc SimNutrition & Health Innovation Research Institute, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia.ORCID http://orcid.org/0000-0001-5166-0605

Funding

Institut National de la Santé et de la Recherche MédicaleNational Health and Medical Research Council of Australia GNT1158758Institut National de la Santé et de la Recherche MédicaleNational Health and Medical Research Council of Australia GNT1177938Medical Research Council MC_PC_21001Medical Research Council MC_PC_21003Medical Research Future Fund MRF2024225National Health and Medical Research Council of Australia APP1183570National Heart Foundation of Australia 107194National Heart Foundation of Australia 107323National Institute for Health Research NIHR203319National Institute for Health Research NIHR305844Royal Perth Hospital Medical Research Foundation RPHRF CAF 00/21Wellcome Trust 102817Western Australian Future Health and Innovation Fund, Government of Western Australia G1008388
6 · The paper itself

Abstract

Clinical cardiovascular disease (CVD) is often present in frail individuals. However, it remains unclear whether subclinical CVD, e.g., abdominal aortic calcification (AAC), is associated with frailty. This study investigated the cross-sectional relationship between AAC scored using a validated machine learning model (ML-AAC24) and physical frailty. 49,081 participants from the UK Biobank Imaging Study without atherosclerotic CVD (ASCVD) diagnosis were included. ML-AAC24 extent was categorised as low, moderate and high, based on established severity categories. Physical frailty was based on a modified Fried's frailty phenotype comprising weak hand grip strength, slow walking speed, weight loss, exhaustion, and physical inactivity. Individuals with three or more deficits were considered frail, while one or two deficits was considered pre-frail. Multivariable-adjusted multinominal logistic regression models were used to test the associations between ML-AAC24 extent and frailty status. One in five individuals had moderate or high ML-AAC24. Compared to individuals with low ML-AAC24, those with moderate and high ML-AAC24 had greater odds of being pre-frail (ORs 1.06 95%CI 1.00-1.12 moderate; 1.14 95%CI 1.04-1.26 high) or frail (ORs 1.27 95%CI 1.12-1.44 moderate; 1.58 95%CI 1.31-1.91 high), adjusted for multiple covariates. When stratified by sex, similar results for frailty were recorded. In a population, those with moderate and high ML-AAC24 were more likely to present as pre-frail and frail. AAC identified from lateral spine images obtained during routine bone density testing, could serve as a useful marker for the early detection of frailty, highlighting the importance of multimodality care.

Indexed as

Artificial IntelligenceCardiovascular DiseaseDual-energy X-ray AbsorptiometryVascular Calcification

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.