AI Article Synopsis

  • MicroRNA-143 and -145 are non-coding RNAs found in heart muscle cells, and their roles in acute myocardial infarction (AMI) patients were studied for the first time.
  • In a study involving 25 AMI patients and 20 controls, researchers measured plasma levels of these microRNAs on admission (Day 0) and again on Day 7 post-admission, finding significant increases in AMI patients.
  • The rise in microRNA-143 levels from Day 0 to Day 7 was linked to better recovery of heart function, suggesting it could serve as a biomarker for recovery in AMI patients.

Article Abstract

Background: MicroRNA (miR)-143 and miR-145 are non-coding RNAs present in smooth muscle cells and the heart. However, their behavior and physiological role in patients with acute myocardial infarction (AMI) have not been clarified.

Methods and results: Plasma miR-143 and miR-145 concentrations were measured on Day 0 (on admission) and on Day 7 in AMI patients who could be followed up for 6 months (n=25). The control group consisted of subjects without significant coronary stenosis (n=20). Blood samples were collected from the antecubital vein, and plasma miR-143 and miR-145 concentrations were measured by quantitative reverse transcription-polymerase chain reaction. In AMI patients (n=25), left ventricular ejection fraction (LVEF) was measured by echocardiography in the acute and chronic (6 months) phases. On Day 7, plasma miR-143 and miR-145 concentrations were significantly higher in AMI patients than in the control group and on Day 0 in AMI patients. Plasma miR-143 and miR-145 concentrations increased significantly from Day 0 to Day 7. The increase in plasma miR-143 concentrations (∆miR-143) in the acute phase was positively correlated with the increase in LVEF in the chronic phase. Among many factors, only ∆miR-143 was favorably correlated with left ventricle (LV) functional recovery in the chronic phase.

Conclusions: An increase in plasma miR-143 concentrations in the acute phase may be a biomarker predicting recovery of LV function in the chronic phase in AMI patients.

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Source
http://dx.doi.org/10.1253/circj.CJ-22-0698DOI Listing

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