Association between stress hyperglycemia ratio and acute total occlusion in patients with non-ST-segment elevation

Shuai Wang1, Jiatong Li1, Shan Xie1

  • 1Department of Emergency, Xuanwu Hospital Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.

Insights

The stress hyperglycemia ratio (SHR) can help identify acute total occlusion (ATO) in non-ST-segment elevation myocardial infarction (NSTEMI) patients. Elevated admission SHR is independently linked to a higher likelihood of ATO, aiding in risk assessment.

Area of Science:

  • Cardiology
  • Metabolic Syndrome
  • Myocardial Infarction

Background:

  • Acute total occlusion (ATO) in non-ST-segment elevation myocardial infarction (NSTEMI) signifies a high-risk group, yet early identification is difficult.
  • The stress hyperglycemia ratio (SHR) quantifies acute glucose elevation against chronic glycemic status.

Purpose of the Study:

  • To investigate the association between admission SHR and ATO in NSTEMI patients.
  • To assess the discriminatory performance and independent association of SHR with ATO.

Main Methods:

  • Retrospective, single-center observational cohort study of 827 NSTEMI patients undergoing coronary angiography.
  • SHR calculated from fasting plasma glucose and glycated hemoglobin; ATO defined by Thrombolysis in Myocardial Infarction flow grade.
  • Statistical analyses included ROC, multivariable logistic regression, and restricted cubic spline analyses.

Main Results:

  • SHR demonstrated superior discriminatory performance for ATO (AUC, 0.743) compared to fasting plasma glucose or HbA1c.
  • An optimal SHR cutoff of 0.903 was identified.
  • Elevated SHR (>0.903) was independently associated with significantly higher odds of ATO (aOR, 5.09; P<0.001).

Conclusions:

  • Admission SHR is independently and nonlinearly associated with ATO in NSTEMI patients.
  • SHR may serve as a valuable adjunct to clinical assessment for identifying ATO.
  • Further external validation is necessary prior to clinical implementation.
Abstract

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