Evidence map›Paper›PMID 37161453›Full record

ArticleBMC cardiovascular disorders2023

Relationship between inflammatory markers and coronary slow flow in type 2 diabetic patients.

Moataz Ali Hasan Ali Elsanan, Islam Hussein Hassan Hussein Tahoon, Ghada Ibrahim Mohamed, Shimaa Gamal ZeinElabdeen, Islam Elsayed Shehata

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Coronary Slow-Flow Syndrome: A Review on Natural History of Disease and Best Practices.Research in heart yield and translational medicine · 2025
    Review
  5. Article
  6. The predictors of coronary slow flow in patients undergoing coronary angiography.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2024
    Article
  7. Single Nucleotide Polymorphisms in Coronary Microvascular Dysfunction.Journal of the American Heart Association · 2024
    Review
  8. 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

5 authors at 1 institution in 1 country.

Moataz Ali Hasan Ali ElsananDepartment of Cardiology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Sharkia Governorate, Egypt.ORCID 0000-0002-8672-3159
Islam Hussein Hassan Hussein TahoonDepartment of Cardiology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Sharkia Governorate, Egypt.ORCID 0000-0002-6676-149X
Ghada Ibrahim MohamedDepartment of Cardiology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Sharkia Governorate, Egypt.ORCID 0000-0001-5016-9021
Shimaa Gamal ZeinElabdeenDepartment of Cardiology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Sharkia Governorate, Egypt.ORCID 0000-0001-7769-562X
Islam Elsayed ShehataDepartment of Cardiology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Sharkia Governorate, Egypt. iemshehata@zu.edu.eg.ORCID 0000-0002-3850-9027
Zagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetes is a serious and quickly expanding global health problem. Cardiovascular disease is the leading cause of mortality in type 2 diabetes mellitus (T2DM) patients. Coronary slow flow (CSF) is characterised by delayed distal perfusion during coronary angiography with normal coronary arteries. This study aimed to investigate the correlation between CSF and inflammatory markers regarding glycemic status in T2DM.

methodsThis cross-sectional study included 120 patients who were divided equally into 4 groups according to their glycemic control and presence or absence of coronary slow flow: Group I included patients with T2DM with good glycemic control without CSF; Group II included patients with T2DM with good glycemic control and CSF; Group III included patients with T2DM with poor glycemic control without CSF; and Group IV included patients with T2DM with poor glycemic control and CSF. The neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), C-reactive protein (CRP), platelets, hematocrit, and haemoglobin were also evaluated as risk factors for coronary slow flow.

resultsThis study showed that body mass index (BMI), hematocrit level, NLR, and CRP demonstrated a moderate but significant correlation (r = 0.53) with CSF in poorly controlled T2DM. NLR cutoff > 2.1 could predict CSF in poorly controlled T2DM with a modest sensitivity and specificity. A 1.9 increase in HbA1c increases the likelihood of coronary slow flow. Dylipidemia increases the likelihood of coronary slow flow by 0.18 times. Other predictors for coronary slow flow include NLR, PLR, CRP, platelets, hematocrit, and hemoglobin. The effect of the predictors is still statistically significant after being adjusted for glycemic status, age, and sex (p < 0.001).

conclusionsPoor glycemic control increases the incidence of CSF. This supports the hypothesis that CSF is related to endothelial dysfunction as poor glycemic control causes endothelial dysfunction due to inflammation.

trial registrationZU-IRB#9419-3-4-2022 Registered 3 April 2022, email.  IRB_123@medicine.zu.edu.eg .

Indexed as

Autoimmune DiseasesDiabetes Mellitus, Type 2Blood PlateletsC-Reactive ProteinCross-Sectional StudiesHumansRisk FactorsC-Reactive ProteinCoronary slow flowDiabetes type 2Inflammatory markers (NLR, PLR)

Identifiers

PMID37161453
PMCPMC10169369
OpenAlexW4376115907

What OpenQuestion holds

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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.