Correlation Between QTc Dispersion and Soluble Growth-stimulating Gene 2 Protein on the Early Prognosis of Acute Carbon Monoxide Poisoning Heart Disease

J Cardiovasc Pharmacol. 2021 Oct 1;78(4):572-580. doi: 10.1097/FJC.0000000000001090.

Abstract

This study aimed to explore the correlation between QTc dispersion (QTcd) and soluble growth-stimulating gene 2 protein (sST2) after heart rate correction in patients with acute carbon monoxide poisoning heart disease. Among the 150 patients, 35 cases had severe toxic heart disease. The concentrations of sST2, cardiac troponin I, and creatine kinase-MB in the severe group began to increase from admission, 24 hours, and 2 days, respectively, and their detected values were all higher than those in the nonsevere group and the normal control group. There were statistically significant differences in sST2 and QTcd between the poisoning, nonsevere, and normal control groups before the treatment. There was a statistically significant difference between the indexes of the poisoning groups at different degrees 2 and 3 days after poisoning. Receiver operating characteristic curve analysis confirmed the sensitivity and specificity of sST2 and QTcd. The correlation analysis showed that sST2 and QTcd levels were positively correlated with the incidence of severe heart disease at admission. Generally, the combined observation of sST2 and QTcd improved the prediction sensitivity and were early predictor indexes of toxic heart disease.

MeSH terms

  • Action Potentials*
  • Adult
  • Biomarkers / blood
  • Carbon Monoxide Poisoning / complications*
  • Creatine Kinase, MB Form / blood
  • Electrocardiography*
  • Female
  • Heart Conduction System / physiopathology*
  • Heart Diseases / blood
  • Heart Diseases / diagnosis*
  • Heart Diseases / etiology
  • Heart Diseases / physiopathology
  • Heart Rate*
  • Humans
  • Interleukin-1 Receptor-Like 1 Protein / blood*
  • Male
  • Middle Aged
  • Predictive Value of Tests
  • Prognosis
  • Troponin I / blood
  • Up-Regulation

Substances

  • Biomarkers
  • IL1RL1 protein, human
  • Interleukin-1 Receptor-Like 1 Protein
  • Troponin I
  • Creatine Kinase, MB Form