Association of inflammatory markers and poor outcome in diabetic patients presenting with ST segment elevation

Yulia Belenkova1, Viktoria Karetnikova1, Aleksey Diachenko2

  • 1Federal State Budgetary Institution Research Institute for Complex Issues of Cardiovascular Diseases, Siberian Branch of the Russian Academy of Medical Sciences, Kemerovo, Russian Federation ; State Budgetary Educational Institution of Higher Professional Education Kemerovo State Medical Academy of the Russian Ministry of Health, Kemerovo, Russian Federation.

Insights

Carbohydrate metabolism disorders worsen ischemic heart disease outcomes. Inflammation, particularly in diabetic patients with ST-elevation myocardial infarction (STEMI), predicts poor prognosis despite revascularization.

Area of Science:

  • Cardiology
  • Metabolic Disorders
  • Inflammation Research

Background:

  • Carbohydrate metabolism disorders (CMD) are linked to ischemic heart disease (IHD) progression.
  • Inflammation acts as a key pathogenetic factor connecting CMD and IHD.

Purpose of the Study:

  • To investigate the impact of CMD on 1-year outcomes in ST-segment elevation myocardial infarction (STEMI) patients.
  • To analyze the role of inflammation markers in STEMI patients with and without CMD.

Main Methods:

  • Registry study of 601 STEMI patients admitted within 24 hours.
  • Measurement of inflammation markers (IL-6, sCD40L, IL-12) at days 10-14 post-MI.
  • 1-year follow-up to assess outcomes, including the impact of percutaneous coronary intervention.

Main Results:

  • Percutaneous coronary intervention improved 1-year prognosis for STEMI patients, irrespective of CMD status.
  • Higher IL-6 and sCD40L levels were observed in MI patients with diabetes mellitus and impaired glucose tolerance.
  • Impaired glucose tolerance correlated with higher IL-12 levels; high Killip classification indicated poor outcomes in diabetic MI patients.

Conclusions:

  • Persistent inflammation in STEMI patients with CMD may lead to vascular complications within 1 year post-MI.
  • Comorbid diabetes or impaired glucose tolerance exacerbates the inflammatory response and adverse outcomes.
Abstract

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