Ticagrelor improves systemic immune-inflammation index in acute coronary syndrome patients

Mehmet Koray Adali1, Ipek Buber1, Oguz Kilic2

  • 1Department of Cardiology, Pamukkale University, School of Medicine, Denizli, Turkey.

Acta Cardiologica
|September 8, 2021
PubMed

Insights

Ticagrelor demonstrated a significant reduction in key inflammatory markers, including neutrophil-to-lymphocyte ratio (NLR), monocyte-to-high-density lipoprotein ratio (MHR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII), compared to clopidogrel in acute coronary syndrome patients. These findings suggest ticagrelor may offer superior anti-inflammatory effects post-percutaneous coronary intervention.

Area of Science:

  • Cardiology
  • Immunology
  • Pharmacology

Background:

  • Inflammation is a key factor in the development of atherosclerosis.
  • Acute coronary syndrome (ACS) patients often exhibit elevated inflammatory markers.
  • Antiplatelet therapies are crucial in managing ACS post-percutaneous coronary intervention (PCI).

Purpose of the Study:

  • To compare the effects of ticagrelor and clopidogrel on inflammatory parameters in ACS patients.
  • To evaluate changes in complete blood count (CBC) and biochemical inflammatory markers.
  • To assess the potential anti-inflammatory benefits of ticagrelor versus clopidogrel.

Main Methods:

  • A study involving 100 ACS patients undergoing PCI, randomized to receive either ticagrelor or clopidogrel with aspirin.
  • Collection of CBC and biochemical data at baseline, 3 months, and 6 months post-ACS.
  • Calculation and comparison of neutrophil-to-lymphocyte ratio (NLR), monocyte-to-high-density lipoprotein ratio (MHR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII).

Main Results:

  • Patients treated with ticagrelor showed significantly lower NLR, PLR, and SII at 3 and 6 months compared to clopidogrel (p < 0.001).
  • The monocyte-to-high-density lipoprotein ratio (MHR) was also significantly lower in the ticagrelor group (p < 0.05).
  • Conversely, white blood cell (WBC) count was higher in the ticagrelor group (p < 0.001).

Conclusions:

  • Ticagrelor treatment was associated with lower levels of NLR, MHR, PLR, and SII in ACS patients compared to clopidogrel.
  • Ticagrelor may possess superior anti-inflammatory properties in ACS patients undergoing PCI.
  • These findings highlight potential differential impacts of P2Y12 inhibitors on systemic inflammation.
Abstract

Related Concept Videos

Acute Coronary Syndrome IV: Interprofessional Care01:28

Acute Coronary Syndrome IV: Interprofessional Care

IntroductionThe management of Acute Coronary Syndrome (ACS) aims to minimize myocardial damage, preserve myocardial function, and prevent complications.Initial ManagementInpatient management involves continuous cardiac monitoring, preferably in an ICU, focusing on blood pressure, serum sodium, potassium, and creatinine levels, and urine output. Ongoing pharmacologic management is crucial for stabilizing the patient.Supplemental Oxygen: Administer supplemental oxygen if oxygen saturation is...
55
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
48
Acute Coronary Syndrome I: Introduction01:30

Acute Coronary Syndrome I: Introduction

Acute Coronary Syndrome (ACS) encompasses a spectrum of heart conditions caused by sudden obstruction of coronary arteries, typically resulting from the rupture of an atherosclerotic plaque and subsequent thrombus (blood clot) formation. This obstruction can lead to partial or complete blockage of blood flow, causing varying degrees of myocardial ischemia or infarction.ACS includes the following clinical entities:Unstable Angina (UA)Non-ST-Elevation Myocardial Infarction (NSTEMI)ST-Elevation...
139
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations01:19

Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations

The pathophysiology of Acute Coronary Syndrome [ACD] involves several key processes:The main underlying cause of ACD is atherosclerosis, a chronic inflammatory disease characterized by the buildup of lipid-laden plaques within the coronary arteries.As the atherosclerotic plaque grows in the coronary artery, it may become unstable due to the formation of a lipid-rich core and a thin fibrous cap. Inflammatory cells within the plaque, such as macrophages, secrete enzymes that degrade the...
87
Acute Coronary Syndrome V: Nursing Management01:26

Acute Coronary Syndrome V: Nursing Management

Nursing Assessment:Nursing management of acute coronary syndrome (ACS) involves taking the patient's history, focusing on primary complaints such as chest pain, dyspnea, and excessive sweating (diaphoresis), as well as other symptoms like back or jaw pain, nausea, vomiting, palpitations, dizziness, and fatigue. The nurse also reviews the patient's history of cardiac events, risk factors such as hypertension, diabetes, smoking, family history, and current medications.In the objective assessment,...
74
Myocarditis III: Medical Management01:14

Myocarditis III: Medical Management

Myocarditis: Comprehensive Medical ManagementMyocarditis, the heart muscle inflammation, requires a comprehensive medical management strategy that addresses the underlying cause, provides supportive care, manages symptoms, and reduces cardiac workload.Infections and Autoimmune CausesAdminister appropriate antimicrobial therapy when an infectious agent causes myocarditis. For instance, penicillin treats infections caused by Group A Streptococcus. In cases where autoimmune processes are...
32