Relationship between Systemic Inflammatory Biomarkers and LAD Plaque Lesion Localization and Severity in Patients with Acute ST-segment Elevation Myocardial Infarction

Introduction: Acute ST-segment elevation myocardial infarction (STEMI) is a leading cause of mortality, driven by coronary artery disease and inflammation. Systemic inflammatory biomarkers, including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and C-reactive protein-to-albumin ratio (CAR), are linked to lesion severity and localization in the left anterior descending (LAD) artery, but local data from Pakistan are scarce. Objective: To assess the relationship between systemic inflammatory biomarkers (NLR, PLR, CAR) and the localization and severity of LAD plaque lesions in STEMI patients. Material and Methods: This retrospective study at Dr. Ruth K.M. Pfau Civil Hospital, Karachi from April, 2024 to September, 2024, included 87 STEMI patients with proximal or mid-LAD lesions. Biomarkers were correlated with angiographic findings using SPSS version 23.0. Results: Proximal LAD lesions (N=53) showed higher median NLR (3.00 vs. 1.50), PLR (109.75 vs. 70.00), and CAR (35.71 vs. 14.00) compared to mid-LAD lesions (N=33), indicating greater inflammatory burden (p<0.05). Conclusion: Elevated NLR, PLR, and CAR are associated with proximal LAD lesions, offering cost-effective risk stratification tools for STEMI patients in resource-limited settings.

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Journal
Indus journal of bioscience research.
Published
2025-08-01
DOI
https://doi.org/10.70749/ijbr.v3i8.1925
Primary Topic
Inflammatory Biomarkers in Disease Prognosis
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article
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article

Relationship between Systemic Inflammatory Biomarkers and LAD Plaque Lesion Localization and Severity in Patients with Acute ST-segment Elevation Myocardial Infarction

Faisal Ahmed, Syed Dilbahar Ali Shah, Arshad Ali Shah, Muhammad Hashim et al.
Indus journal of bioscience research.
Inflammatory Biomarkers in Disease Prognosis
article

Relationship between Systemic Inflammatory Biomarkers and LAD Plaque Lesion Localization and Severity in Patients with Acute ST-segment Elevation Myocardial Infarction

Faisal Ahmed, Syed Dilbahar Ali Shah, Arshad Ali Shah, Muhammad Hashim, Iqbal Khan, D. Shehwar
article en

Abstract

Introduction: Acute ST-segment elevation myocardial infarction (STEMI) is a leading cause of mortality, driven by coronary artery disease and inflammation. Systemic inflammatory biomarkers, including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and C-reactive protein-to-albumin ratio (CAR), are linked to lesion severity and localization in the left anterior descending (LAD) artery, but local data from Pakistan are scarce. Objective: To assess the relationship between systemic inflammatory biomarkers (NLR, PLR, CAR) and the localization and severity of LAD plaque lesions in STEMI patients. Material and Methods: This retrospective study at Dr. Ruth K.M. Pfau Civil Hospital, Karachi from April, 2024 to September, 2024, included 87 STEMI patients with proximal or mid-LAD lesions. Biomarkers were correlated with angiographic findings using SPSS version 23.0. Results: Proximal LAD lesions (N=53) showed higher median NLR (3.00 vs. 1.50), PLR (109.75 vs. 70.00), and CAR (35.71 vs. 14.00) compared to mid-LAD lesions (N=33), indicating greater inflammatory burden (p<0.05). Conclusion: Elevated NLR, PLR, and CAR are associated with proximal LAD lesions, offering cost-effective risk stratification tools for STEMI patients in resource-limited settings.

Indus journal of bioscience research.Vol. 3(8)
Jinnah University for Women (PK), Hamdard University (PK), Civil Hospital Karachi (PK), Dow University of Health Sciences (PK), Ziauddin University (PK)
Good health and well-being
Openalex Percentile: Top 71%
Inflammatory Biomarkers in Disease Prognosis
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Relationship between Systemic Inflammatory Biomarkers and LAD Plaque Lesion Localization and Severity in Patients with Acute ST-segment Elevation Myocardial Infarction — Faisal Ahmed, Syed Dilbahar Ali Shah, et al. · Indus journal of bioscience research. (2025) | TGRS Research Map | TGRS