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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Inflammatory and Hematological Indices as Simple, Practical Severity Predictors of Microdysfunction Following
Enyuan Zhang1, Mingdong Gao1, Jing Gao2
1Department of Coronary Care Unit, Tianjin Chest Hospital, Tianjin, China.
Insights
Higher levels of C-reactive protein (CRP) and certain blood cell ratios like neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) are linked to increased no-reflow incidence after procedures. Pre-procedure CRP/hsCRP can predict no-reflow and slow flow.
Area of Science:
- Cardiology
- Hematology
- Biomarkers
Background:
- No-reflow and slow-flow phenomena are complications in cardiovascular interventions.
- C-reactive protein (CRP), high-sensitivity CRP (hsCRP), and various hematological indices are implicated as potential predictors.
- Hematological indices include platelet-to-lymphocyte ratio (PLR), neutrophil-to-lymphocyte ratio (NLR), mean platelet volume (MPV), platelet distribution width (PDW), and red blood cell distribution width (RDW).
Purpose of the Study:
- To systematically evaluate the association between CRP, hsCRP, and hematological indices with the incidence of no-reflow and slow flow.
- To determine the predictive value of preangiographic CRP/hsCRP for these complications.
Main Methods:
- A meta-analysis was conducted on 21 clinical studies involving 7403 patients.
- Studies were retrieved from PubMed, EMBASE, Google Scholar, Clinical Trials, and Science Direct up to August 24, 2019.
- Pooled analysis was performed to calculate odds ratios (OR) and confidence intervals (CI) for various markers.
Main Results:
- Elevated hsCRP, NLR, PLR, and MPV were significantly associated with a higher incidence of no-reflow.
- No significant association was found between no-reflow risk and RDW or PDW.
- Higher CRP/hsCRP levels correlated with an increased rate of slow flow.
- Preangiographic CRP/hsCRP demonstrated independent predictive value for no-reflow and slow flow.
Conclusions:
- hsCRP, NLR, PLR, and MPV are significant predictors of no-reflow.
- CRP/hsCRP can independently predict both no-reflow and slow flow.
- These inflammatory and hematological markers offer valuable insights into predicting procedural outcomes in cardiology.
Abstract:
C-reactive protein (CRP) and high-sensitivity CRP (hsCRP), along with a series of hematological indices, platelet to lymphocyte ratio (PLR), neutrophil to lymphocyte ratio (NLR), mean platelet volume (MPV), platelet distribution width (PDW), and red blood cell distribution width (RDW), are regarded to be related to the incidence of no-reflow or slow flow. Clinical studies were retrieved from the electronic databases of PubMed, EMBASE, Google Scholar, Clinical Trials, and science direct from their inception to August 24, 2019. A total of 21 studies involving 7403 patients were included in the meta-analysis. Pooled analysis results revealed patients with higher hsCRP (odds ratio [OR] = 1.03, 95% confidence interval [CI], 1.01-1.05, P = .006), hsCRP (OR = 1.04, 95% CI: 1.0-1.08, P = .012), NLR (OR = 1.23, 95% CI: 1.11-1.37, P < .0001), PLR (OR = 1.13, 95% CI: 1.07-1.20, P < .0001), and MPV (OR = 2.13, 95% CI: 1.57-2.90, P < .0001) all exhibited significantly higher no-reflow incidence, but there was no significant association between no-reflow risk and RDW or PDW. Patients with higher CRP/hsCRP also performed higher rate of slow flow (OR = 1.06, 95% CI: 1.01-1.11, P = .018). Preangiographic CRP/hsCRP could independently predict no-reflow and slow flow. Moreover, some hematological indices are associated with no-flow.
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