Evidence map›Paper›PMID 41199381›Full record

ArticleDiabetology & metabolic syndrome2025

Opportunistic AI-derived adiposity measures from coronary artery calcium scans predict new-onset type 2 diabetes in adults without obesity or hyperglycemia: insights from the AI-CVD study within MESA.

Morteza Naghavi, Amir Azimi, Kyle Atlas, Anthony P Reeves, Chenyu Zhang, Jakob Wasserthal, Seyed Reza Mirjalili, Mohammadhossein Mozafarybazargany, Ali Hashemi, Thomas Atlas and 18 more

Abstract read
In one paragraph

Article in Diabetology & metabolic syndrome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

28 authors.

Morteza NaghaviHeartLung.AI, Houston, 77021, TX, US. mn@vp.org.
Amir AzimiHeartLung.AI, Houston, 77021, TX, US.
Kyle AtlasHeartLung.AI, Houston, 77021, TX, US.
Anthony P ReevesDepartment of Electrical and Computer Engineering, Cornell University, Ithaca, 14853, NY, USA.
Chenyu ZhangHeartLung.AI, Houston, 77021, TX, US.
Jakob WasserthalClinic of Radiology and Nuclear Medicine, University Hospital Basel, Petersgraben 4, Basel, CH-4031, Switzerland.
Seyed Reza MirjaliliHeartLung.AI, Houston, 77021, TX, US.
Mohammadhossein MozafarybazarganyHeartLung.AI, Houston, 77021, TX, US.
Ali HashemiHeartLung.AI, Houston, 77021, TX, US.
Thomas AtlasTustin Teleradiology, Tustin, 92780, CA, USA.
Claudia I HenschkeDepartment of Diagnostic, Molecular, and Interventional Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
David F YankelevitzDepartment of Diagnostic, Molecular, and Interventional Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jeffrey I MechanickKravis Center for Clinical Cardiovascular Health, Mount Sinai Fuster Heart Hospital, New York, 10029, NY, USA.
Andrea D BranchDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Susan K FriedDiabetes Obesity and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Khurram NasirHouston Methodist Hospital, Houston, 77030, TX, USA.
Zahi A FayadBioMedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, 10029, NY, USA.
Michael V McConnellStanford Prevention Research Center, Stanford University School of Medicine, Stanford, 94305, CA, USA.
Rozemarijn VliegenthartDepartment of Radiology, University Medical Center, Groningen, 9713, GZ, Netherlands.
David J MaronStanford Prevention Research Center, Stanford University School of Medicine, Stanford, 94305, CA, USA.
Jagat NarulaUniversity of Texas Health-McGovern Medical School, Houston, 77030, TX, USA.
Kim A WilliamsUniversity of Louisville, Louisville, 40202, KY, USA.
Prediman K ShahCedars-Sinai Medical Center, Los Angeles, 90048, CA, USA.
Matthew J BudoffThe Lundquist Institute, Los Angeles, 90502, CA, USA.
Daniel LevyPopulation Sciences Branch, Division of Intramural Research, Lung, and Blood Institute, National Heart, National Institutes of Health, Bethesda, 20824, MD, USA.
Emelia J BenjaminBoston Medical Center and Chobanian & Avedisian School of Medicine and School of Public Health, Boston University, Boston, 02218, MA, USA.
Robert A KlonerHuntington Medical Research Institutes, Pasadena, 91105, CA, USA.
Nathan D WongHeart Disease Prevention Program, Mary and Steve Wen Cardiovascular Division, University of California Irvine, Irvine, 92697, CA, USA.

Funding

NHLBI NIH HHS UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420
6 · The paper itself

Abstract

backgroundThe AI-CVD initiative aims to maximize the value of coronary artery calcium (CAC) scans for cardiometabolic risk prediction by extracting opportunistic screening information. We investigated whether artificial intelligence (AI)-derived measures from CAC scans are associated with new-onset Type 2 diabetes mellitus (T2DM) in adults without obesity or hyperglycemia.

methodsBaseline CAC scans and up to 23 years of follow-up data were analyzed for participants without obesity (body mass index < 30 kg/m²) and hyperglycemia (fasting plasma glucose < 100 mg/dL) from the Multi-Ethnic Study of Atherosclerosis (MESA). AI-derived measures included liver attenuation index (LAI), subcutaneous fat index (SFI), total visceral fat index (TVFI), epicardial fat index (EFI), skeletal muscle index, and skeletal muscle mean density. Cox regression models compared highest vs. lowest quartiles of each AI-derived metric for T2DM risk. Multivariable models assessed adjusted predictive value using Wald chi-squared statistics. Subgroup analyses stratified participants by demographic and clinical factors.

resultsDuring a median follow-up of 19.7 years among 2,993 participants (baseline mean age 61.9 ± 10.5 years, 53% women), 257 participants (8.6%) developed T2DM. Key predictors included LAI (HR: 3.13, 95% CI: 2.15-4.55), SFI (HR: 2.85, 95% CI: 1.93-4.21), TVFI (HR: 2.49, 95% CI: 1.72-3.60), and EFI (HR: 1.59, 95% CI: 1.09-2.32). LAI remained the most robust predictor after adjusting for all metrics (Wald χ² = 38.24). Subgroup analyses confirmed LAI's consistent predictive performance.

conclusionAI-derived adiposity measures from CAC scans-especially liver fat-can identify adults without obesity or hyperglycemia at elevated risk for developing T2DM. These findings underscore the potential of AI-enabled opportunistic screening during CAC imaging to support early T2DM risk stratification in individuals not captured by current clinical guidelines.

Indexed as

AI-CVDArtificial intelligenceCoronary artery calcium (CAC) scansOpportunistic screeningType 2 diabetes mellitus

Identifiers

PMID41199381
PMCPMC12590910

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.