Evidence map›Paper›PMID 33858484›Full record

ArticleBioData mining2021

Machine learning and statistical approaches for classification of risk of coronary artery disease using plasma cytokines.

Seema Singh Saharan, Pankaj Nagar, Kate Townsend Creasy, Eveline O Stock, James Feng, Mary J Malloy, John P Kane

Open access · goldAbstract read
In one paragraph

Article in BioData mining, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Machine Learning-Based Model for Predicting Coronary Heart Disease Using Preβ HDL and Cytokines as Plasma Biomarkers.Proceedings. International Conference on Computational Science and Computational Intelligence · 2025
    Article
  3. Article
  4. Smoking Classification Using Novel Plasma Cytokines by implementing Machine Learning and Statistical Methods.Proceedings. International Conference on Computational Science and Computational Intelligence · 2023
    Article
  5. Article
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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

7 authors at 3 institutions in 3 countries.

Seema Singh SaharanDepartment of Statistics, University of Rajasthan, Jaipur, India. ssaharan9@gmail.com.ORCID http://orcid.org/0000-0001-7294-6573
Pankaj NagarDepartment of Statistics, University of Rajasthan, Jaipur, India.
Kate Townsend CreasyDepartment of Medicine, Cardiovascular Research Institute, University of California, San Francisco, USA.
Eveline O StockDepartment of Medicine, Cardiovascular Research Institute, University of California, San Francisco, USA.
James FengDepartment of Medicine, Cardiovascular Research Institute, University of California, San Francisco, USA.
Mary J MalloyDepartments of Medicine and Pediatrics, Cardiovascular Research Institute, University of California, San Francisco, USA.
John P KaneDepartment of Medicine, Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, USA.
University of California, San Francisco · USBerkeley College · USUniversity of Rajasthan · IN

Funding

MOLECULAR AND CELLULAR BASIS OF CARDIOVASCULAR DISEASET32HL007731 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian L Black · 1992 to 2026
$12.4M
NHLBI NIH HHS T32 HL007731U.S. Public Health Service 2T32HL007731-26
6 · The paper itself

Abstract

backgroundAs per the 2017 WHO fact sheet, Coronary Artery Disease (CAD) is the primary cause of death in the world, and accounts for 31% of total fatalities. The unprecedented 17.6 million deaths caused by CAD in 2016 underscores the urgent need to facilitate proactive and accelerated pre-emptive diagnosis. The innovative and emerging Machine Learning (ML) techniques can be leveraged to facilitate early detection of CAD which is a crucial factor in saving lives. The standard techniques like angiography, that provide reliable evidence are invasive and typically expensive and risky. In contrast, ML model generated diagnosis is non-invasive, fast, accurate and affordable. Therefore, ML algorithms can be used as a supplement or precursor to the conventional methods. This research demonstrates the implementation and comparative analysis of K Nearest Neighbor (k-NN) and Random Forest ML algorithms to achieve a targeted "At Risk" CAD classification using an emerging set of 35 cytokine biomarkers that are strongly indicative predictive variables that can be potential targets for therapy. To ensure better generalizability, mechanisms such as data balancing, repeated k-fold cross validation for hyperparameter tuning, were integrated within the models. To determine the separability efficacy of "At Risk" CAD versus Control achieved by the models, Area under Receiver Operating Characteristic (AUROC) metric is used which discriminates the classes by exhibiting tradeoff between the false positive and true positive rates.

resultsA total of 2 classifiers were developed, both built using 35 cytokine predictive features. The best AUROC score of .99 with a 95% Confidence Interval (CI) (.982,.999) was achieved by the Random Forest classifier using 35 cytokine biomarkers. The second-best AUROC score of .954 with a 95% Confidence Interval (.929,.979) was achieved by the k-NN model using 35 cytokines. A p-value of less than 7.481e-10 obtained by an independent t-test validated that Random Forest classifier was significantly better than the k-NN classifier with regards to the AUROC score. Presently, as large-scale efforts are gaining momentum to enable early, fast, reliable, affordable, and accessible detection of individuals at risk for CAD, the application of powerful ML algorithms can be leveraged as a supplement to conventional methods such as angiography. Early detection can be further improved by incorporating 65 novel and sensitive cytokine biomarkers. Investigation of the emerging role of cytokines in CAD can materially enhance the detection of risk and the discovery of mechanisms of disease that can lead to new therapeutic modalities.

Indexed as

AUROCCADClassificationConfidence intervalDistance metricsk-fold cross validationk-NNMLPlasma cytokinesRandom ForestROSE

Identifiers

PMID33858484
PMCPMC8050889
OpenAlexW3113140258

What OpenQuestion 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 OpenQuestion graph.