Evidence map›Paper›PMID 36925713›Full record

ArticleBioengineering & translational medicine2023

SERS spectroscopy with machine learning to analyze human plasma derived sEVs for coronary artery disease diagnosis and prognosis.

Xi Huang, Bo Liu, Shenghan Guo, Weihong Guo, Ke Liao, Guoku Hu, Wen Shi, Mitchell Kuss, Michael J Duryee, Daniel R Anderson and 2 more

Full text read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Non-Contrasted CT Radiomics for SAH Prognosis Prediction.Bioengineering (Basel, Switzerland) · 2023
    Article
  9. Review
  10. 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

12 authors.

Xi HuangDepartment of Electrical and Computer Engineering University of Nebraska Lincoln Lincoln Nebraska USA.ORCID https://orcid.org/0000-0002-4477-3748
Bo LiuMary & Dick Holland Regenerative Medicine Program University of Nebraska Medical Center Omaha Nebraska USA.ORCID https://orcid.org/0000-0003-2455-2021
Shenghan GuoDepartment of Industrial and Systems Engineering Rutgers, The State University of New Jersey Piscataway New Jersey USA.
Weihong GuoDepartment of Industrial and Systems Engineering Rutgers, The State University of New Jersey Piscataway New Jersey USA.
Ke LiaoDepartment of Pharmacology and Experimental Neuroscience University of Nebraska Medical Center Omaha Nebraska USA.
Guoku HuDepartment of Pharmacology and Experimental Neuroscience University of Nebraska Medical Center Omaha Nebraska USA.
Wen ShiMary & Dick Holland Regenerative Medicine Program University of Nebraska Medical Center Omaha Nebraska USA.
Mitchell KussMary & Dick Holland Regenerative Medicine Program University of Nebraska Medical Center Omaha Nebraska USA.
Michael J DuryeeDivision of Rheumatology, Department of Internal Medicine University of Nebraska Medical Center Omaha Nebraska USA.
Daniel R AndersonDivision of Cardiovascular Medicine, Department of Internal Medicine University of Nebraska Medical Center Omaha Nebraska USA.
Yongfeng LuDepartment of Electrical and Computer Engineering University of Nebraska Lincoln Lincoln Nebraska USA.ORCID https://orcid.org/0000-0002-5942-1999
Bin DuanMary & Dick Holland Regenerative Medicine Program University of Nebraska Medical Center Omaha Nebraska USA.ORCID https://orcid.org/0000-0002-5647-3793

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronary artery disease (CAD) is one of the major cardiovascular diseases and represents the leading causes of global mortality. Developing new diagnostic and therapeutic approaches for CAD treatment are critically needed, especially for an early accurate CAD detection and further timely intervention. In this study, we successfully isolated human plasma small extracellular vesicles (sEVs) from four stages of CAD patients, that is, healthy control, stable plaque, non-ST-elevation myocardial infarction, and ST-elevation myocardial infarction. Surface-enhanced Raman scattering (SERS) measurement in conjunction with five machine learning approaches, including Quadratic Discriminant Analysis, Support Vector Machine (SVM), K-Nearest Neighbor, Artificial Neural network, were then applied for the classification and prediction of the sEV samples. Among these five approaches, the overall accuracy of SVM shows the best predication results on both early CAD detection (86.4%) and overall prediction (92.3%). SVM also possesses the highest sensitivity (97.69%) and specificity (95.7%). Thus, our study demonstrates a promising strategy for noninvasive, safe, and high accurate diagnosis for CAD early detection.

Indexed as

coronary artery diseasediagnosticsmachine learningsmall extracellular vesiclesspectrogram

Identifiers

PMID36925713
PMCPMC10013764

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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 OpenQuestion graph.