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Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
Post-PCI Inflammation and Diastolic Dysfunction in Patients with Metabolic Risk Factors: A Retrospective
Alexandra Manuela Buzle1, Corina Cinezan1, Paul Sextil Sasu2
1Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410068 Oradea, Romania.
Insights
Systemic inflammation after percutaneous coronary intervention (PCI) showed weak, non-significant trends toward worsening left ventricular diastolic dysfunction (LVDD) in patients with acute coronary syndrome (ACS). Metabolic comorbidities were not independent predictors of LVDD severity post-PCI.
Area of Science:
- Cardiology
- Internal Medicine
- Biomarkers
Background:
- Left ventricular diastolic dysfunction (LVDD) precedes heart failure with preserved ejection fraction (HFpEF), especially with metabolic issues.
- Acute coronary syndrome (ACS) and percutaneous coronary interventions (PCI) can worsen LVDD through systemic inflammation.
Purpose of the Study:
- To investigate the link between post-PCI systemic inflammation and LVDD severity in ACS patients with metabolic comorbidities.
- To analyze inflammatory markers (leukocytes, neutrophils, C-reactive protein) and their association with diastolic function post-PCI.
Main Methods:
- Retrospective observational study of 181 ACS patients undergoing PCI.
- Echocardiography assessed diastolic dysfunction.
- Analyzed inflammatory markers (leukocytes, neutrophils, CRP) 24-48 hours post-PCI.
- Used multivariable ordinal logistic regression and correlation analyses.
Main Results:
- C-reactive protein (CRP) showed a non-significant trend (p=0.081) towards association with more severe LVDD.
- Metabolic comorbidities (hypertension, diabetes, dyslipidemia, obesity) were not independently predictive of LVDD.
- N-terminal pro-B-type natriuretic peptide (NT-proBNP) correlated significantly with high-sensitivity troponin (TrHS) at 48 hours, linking myocardial injury and wall stress.
Conclusions:
- Post-PCI systemic inflammation has a weak, non-significant association with diastolic dysfunction severity.
- Classical metabolic comorbidities are not independent predictors of LVDD post-PCI.
- Larger prospective studies are needed to confirm these modest trends.
Abstract:
Background and Objectives: Left ventricular diastolic dysfunction (LVDD) is a known precursor of heart failure with preserved ejection fraction (HFpEF), particularly in patients with metabolic comorbidities. Acute coronary syndrome (ACS) and percutaneous coronary interventions (PCI) may exacerbate LVDD via systemic inflammation. This study aimed to explore the association between post-procedural systemic inflammation and the severity of diastolic dysfunction in patients with ACS and metabolic comorbidities. Materials and Methods: A retrospective observational study was conducted in 181 patients with ACS who underwent PCI. Inflammatory markers (leukocytes, neutrophils, and C-reactive protein [CRP]) measured at 24-48 h post-intervention were analyzed in relation to diastolic dysfunction, assessed by echocardiography. Multivariable ordinal logistic regression and correlation analyses were performed. Results: CRP showed a non-significant trend toward association with more advanced diastolic dysfunction (p = 0.081). Hypertension had a positive but nonsignificant coefficient. Other metabolic comorbidities (diabetes, dyslipidemia, and obesity) were not significantly associated. The correlation between N-terminal pro-B-type natriuretic peptide (NT-proBNP) and troponin was exploratory. NT-proBNP was the only marker significantly correlated with high-sensitivity troponin (TrHS) at 48 h, indicating a link between myocardial injury and wall stress. Conclusions: CRP may be weakly associated with the severity of diastolic dysfunction post-PCI. However, classical metabolic comorbidities were not independently predictive. Post-PCI inflammation showed only modest, non-significant trends toward diastolic impairment, warranting confirmation in larger prospective studies.
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