Evidence map›Paper›PMID 39076491›Full record

ReviewReviews in cardiovascular medicine2024

UltraAIGenomics: Artificial Intelligence-Based Cardiovascular Disease Risk Assessment by Fusion of Ultrasound-Based Radiomics and Genomics Features for Preventive, Personalized and Precision Medicine: A Narrative Review.

Luca Saba, Mahesh Maindarkar, Amer M Johri, Laura Mantella, John R Laird, Narendra N Khanna, Kosmas I Paraskevas, Zoltan Ruzsa, Manudeep K Kalra, Jose Fernandes E Fernandes and 8 more

Abstract readReview
In one paragraph

Review in Reviews in cardiovascular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. 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

18 authors.

Luca SabaDepartment of Radiology, Azienda Ospedaliero Universitaria, 40138 Cagliari, Italy.
Mahesh MaindarkarSchool of Bioengineering Sciences and Research, MIT Art, Design and Technology University, 412021 Pune, India.
Amer M JohriDepartment of Medicine, Division of Cardiology, Queen's University, Kingston, ON K7L 3N6, Canada.
Laura MantellaDepartment of Medicine, Division of Cardiology, University of Toronto, Toronto, ON M5S 1A1, Canada.
John R LairdHeart and Vascular Institute, Adventist Health St. Helena, St Helena, CA 94574, USA.
Narendra N KhannaDepartment of Cardiology, Indraprastha APOLLO Hospitals, 110001 New Delhi, India.
Kosmas I ParaskevasDepartment of Vascular Surgery, Central Clinic of Athens, 106 80 Athens, Greece.
Zoltan RuzsaInvasive Cardiology Division, University of Szeged, 6720 Szeged, Hungary.
Manudeep K KalraDepartment of Radiology, Harvard Medical School, Boston, MA 02115, USA.
Jose Fernandes E FernandesDepartment of Vascular Surgery, University of Lisbon, 1649-004 Lisbon, Portugal.
Seemant ChaturvediDepartment of Neurology & Stroke Program, University of Maryland, Baltimore, MD 20742, USA.
Andrew NicolaidesVascular Screening and Diagnostic Centre and University of Nicosia Medical School, 2368 Agios Dometios, Cyprus.
Vijay RathoreNephrology Department, Kaiser Permanente, Sacramento, CA 95823, USA.
Narpinder SinghDepartment of Food Science and Technology, Graphic Era Deemed to be University, Dehradun, 248002 Uttarakhand, India.
Esma R IsenovicDepartment of Radiobiology and Molecular Genetics, National Institute of The Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Vijay ViswanathanMV Diabetes Centre, Royapuram, 600013 Chennai, Tamil Nadu, India.
Mostafa M FoudaDepartment of Electrical and Computer Engineering, Idaho State University, Pocatello, ID 83209, USA.
Jasjit S SuriStroke Monitoring and Diagnostic Division, AtheroPoint™, Roseville, CA 95661, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease (CVD) diagnosis and treatment are challenging since symptoms appear late in the disease's progression. Despite clinical risk scores, cardiac event prediction is inadequate, and many at-risk patients are not adequately categorised by conventional risk factors alone. Integrating genomic-based biomarkers (GBBM), specifically those found in plasma and/or serum samples, along with novel non-invasive radiomic-based biomarkers (RBBM) such as plaque area and plaque burden can improve the overall specificity of CVD risk. This review proposes two hypotheses: (i) RBBM and GBBM biomarkers have a strong correlation and can be used to detect the severity of CVD and stroke precisely, and (ii) introduces a proposed artificial intelligence (AI)-based preventive, precision, and personalized (

Indexed as

artificial intelligencebiascardiovascular diseasedeep learningexplainable AIgenomicspruningradiomicsstroke

Identifiers

PMID39076491
PMCPMC11267214

What Socratic holds

Textmetadata
LicenceCC BY
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.