Evidence map›Paper›PMID 35109843›Full record

ArticleCardiovascular diabetology2022

Angiogenic content of microparticles in patients with diabetes and coronary artery disease predicts networks of endothelial dysfunction.

Isra Marei, Omar Chidiac, Binitha Thomas, Jennifer Pasquier, Soha Dargham, Amal Robay, Muneera Vakayil, Mohammad Jameesh, Christopher Triggle, Arash Rafii and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cardiovascular diabetology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. EndothelialCurrent diabetes reviews · 2025
    Review
  4. Endothelial-Derived Microparticles Associate with Hospital Major Adverse Cardiovascular Events but not with Long-Term Adverse Events in Acute Myocardial Infarction.The International journal of angiology : official publication of the International College of Angiology, Inc · 2024
    Article
  5. Review
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  8. Article
  9. Article
  10. Extracellular Vesicles in Atherosclerosis: State of the Art.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

13 authors at 3 institutions in 3 countries.

Isra Marei *Department of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Omar Chidiac *Department of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Binitha Thomas *Department of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Jennifer PasquierDepartment of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Soha DarghamBiostatistics Core, Weill Cornell Medicine-Qatar, Doha, Qatar.
Amal RobayDepartment of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Muneera VakayilDepartment of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Mohammad JameeshHeart Hospital, Hamad Medical Corporation, Doha, Qatar.
Christopher TriggleDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Arash RafiiDepartment of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar.
Amin JayyousiDepartment of Endocrinology, Hamad Medical Corporation, Doha, Qatar.
Jassim Al SuwaidiHeart Hospital, Hamad Medical Corporation, Doha, Qatar.
Charbel Abi KhalilDepartment of Genetic Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar. cha2022@med.cornell.edu.ORCID 0000-0002-1428-6324
Weill Cornell Medical College in Qatar · QAHamad Medical Corporation · QACornell University · US

Funding

Qatar National Research Fund NPRP 9-169-3-024Qatar National Research Fund PDRA4-0129-18003
6 · The paper itself

Abstract

backgroundElevated endothelial microparticles (EMPs) levels are surrogate markers of vascular dysfunction. We analyzed EMPs with apoptotic characteristics and assessed the angiogenic contents of microparticles in the blood of patients with type 2 diabetes (T2D) according to the presence of coronary artery disease (CAD).

methodsA total of 80 participants were recruited and equally classified as (1) healthy without T2D, (2) T2D without cardiovascular complications, (3) T2D and chronic coronary artery disease (CAD), and (4) T2D and acute coronary syndrome (ACS). MPs were isolated from the peripheral circulation, and EMPs were characterized using flow cytometry of CD42 and CD31. CD62E was used to determine EMPs' apoptotic/activation state. MPs content was extracted and profiled using an angiogenesis array.

resultsLevels of CD42- CD31 + EMPs were significantly increased in T2D with ACS (257.5 ± 35.58) when compared to healthy subjects (105.7 ± 12.96, p < 0.01). There was no significant difference when comparing T2D with and without chronic CAD. The ratio of CD42-CD62 +/CD42-CD31 + EMPs was reduced in all T2D patients, with further reduction in ACS when compared to chronic CAD, reflecting a release by apoptotic endothelial cells. The angiogenic content of the full population of MPs was analyzed. It revealed a significant differential expression of 5 factors in patients with ACS and diabetes, including TGF-β1, PD-ECGF, platelet factor 4, serpin E1, and thrombospondin 1. Ingenuity Pathway Analysis revealed that those five differentially expressed molecules, mainly TGF-β1, inhibit key pathways involved in normal endothelial function. Further comparison of the three diabetes groups to healthy controls and diabetes without cardiovascular disease to diabetes with CAD identified networks that inhibit normal endothelial cell function. Interestingly, DDP-IV was the only differentially expressed protein between chronic CAD and ACS in patients with diabetes.

conclusionOur data showed that the release of apoptosis-induced EMPs is increased in diabetes, irrespective of CAD, ACS patients having the highest levels. The protein contents of MPs interact in networks that indicate vascular dysfunction.

Indexed as

Neovascularization, PathologicAcute Coronary SyndromeAdultAgedAngiogenic ProteinsApoptosisBiomarkersCase-Control StudiesCell-Derived MicroparticlesCoronary Artery DiseaseDiabetes Mellitus, Type 2Endothelium, VascularFemaleFlow CytometryHumansMaleAngiogenic ProteinsBiomarkersAcute coronary syndromeCardiovascular diseaseCoronary artery diseaseDiabetesEndothelial dysfunctionMicroparticles

Identifiers

PMID35109843
PMCPMC8812242
OpenAlexW4210260007

What OpenQuestion 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 OpenQuestion graph.