Evidence map›Paper›PMID 39715147›Full record

ArticlePLOS digital health2024

Measurement of breast artery calcification using an artificial intelligence detection model and its association with major adverse cardiovascular events.

Suzanne J Rose, Josette Hartnett, Zachary J Estep, Daniyal Ameen, Shweta Karki, Edward Schuster, Rebecca B Newman, David H Hsi

Abstract read
In one paragraph

Article in PLOS digital health, 2024. 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. Review
  2. Article
  3. Observational
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

8 authors.

Suzanne J RoseDepartment of Research and Discovery, Stamford Hospital, Stamford, Connecticut, United States of America.ORCID https://orcid.org/0000-0001-5770-826X
Josette HartnettBurke Rehabilitation, Montefiore Health System.ORCID https://orcid.org/0000-0002-7475-4265
Zachary J EstepSidney Kimmel Medical College at Thomas Jefferson University/Deborah Heart and Lung Center, Browns Mills, New Jersey, United States of America.
Daniyal AmeenDepartment of Internal Medicine, Yale New Haven Health/Bridgeport Hospital, Bridgeport, Connecticut, United States of America.
Shweta KarkiDepartment of Research and Discovery, Stamford Hospital, Stamford, Connecticut, United States of America.
Edward SchusterStamford Health Medical Group, Stamford, Connecticut, United States of America.
Rebecca B NewmanDepartment of Internal Medicine, Stamford Hospital, Stamford, Connecticut, United States of America.
David H HsiHeart and Vascular Institute, Stamford Hospital, Stamford, Connecticut, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast artery calcification (BAC) obtained from standard mammographic images is currently under evaluation to stratify risk of major adverse cardiovascular events in women. Measuring BAC using artificial intelligence (AI) technology, we aimed to determine the relationship between BAC and coronary artery calcification (CAC) severity with Major Adverse Cardiac Events (MACE). This retrospective study included women who underwent chest computed tomography (CT) within one year of mammography. T-test assessed the associations between MACE and variables of interest (BAC versus MACE, CAC versus MACE). Risk differences were calculated to capture the difference in observed risk and reference groups. Chi-square tests and/or Fisher's exact tests were performed to assess age and ASCVD risk with MACE and to assess BAC and CAC association with atherosclerotic cardiovascular disease (ASCVD) risk as a secondary outcome. A logistic regression model was conducted to measure the odds ratio between explanatory variables (BAC and CAC) and the outcome variables (MACE). Out of the 99 patients included in the analysis, 49 patients (49.49%) were BAC positive, with 37 patients (37.37%) CAC positive, and 26 patients (26.26%) had MACE. One unit increase in BAC score resulted in a 6% increased odds of having a moderate to high ASCVD risk >7.5% (p = 0.01) and 2% increased odds of having MACE (p = 0.005). The odds of having a moderate-high ASCVD risk score in BAC positive patients was higher (OR = 4.27, 95% CI 1.58-11.56) than CAC positive (OR = 4.05, 95% CI 1.36-12.06) patients. In this study population, the presence of BAC is associated with MACE and useful in corroborating ASCVD risk. Our results provide evidence to support the potential utilization of AI generated BAC measurements from standard of care mammograms in addition to the widely adopted ASCVD and CAC scores, to identify and risk-stratify women who are at increased risk of CVD and may benefit from targeted prevention measures.

Identifiers

PMID39715147
PMCPMC11665981

What Socratic holds

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LicenceCC BY
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Registered trials

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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.