AI Article Synopsis

  • The study investigated how glycemic variability (GV) affects heart recovery after a major heart attack (STEMI) using continuous glucose monitoring.
  • It included 201 patients, measuring GV through the mean amplitude of glycemic excursion (MAGE) and assessing heart function via cardiac imaging.
  • Results showed that lower GV predicts better heart recovery (LVRR), with a significantly lower incidence of major heart-related events in those who experienced LVRR compared to those who didn't.

Article Abstract

Background: This study aimed to investigate the effect of glycemic variability (GV), determined using a continuous glucose monitoring system (CGMS), on left ventricular reverse remodeling (LVRR) after ST-segment elevation myocardial infarction (STEMI).

Methods: A total of 201 consecutive patients with STEMI who underwent reperfusion therapy within 12 h of onset were enrolled. GV was measured using a CGMS and determined as the mean amplitude of glycemic excursion (MAGE). Left ventricular volumetric parameters were measured using cardiac magnetic resonance imaging (CMRI). LVRR was defined as an absolute decrease in the LV end-systolic volume index of > 10% from 1 week to 7 months after admission. Associations were also examined between GV and LVRR and between LVRR and the incidence of major adverse cardiovascular events (MACE; cardiovascular death, acute coronary syndrome recurrence, non-fatal stroke, and heart failure hospitalization).

Results: The prevalence of LVRR was 28% (n = 57). The MAGE was independent predictor of LVRR (odds ratio [OR] 0.98, p = 0.002). Twenty patients experienced MACE during the follow-up period (median, 65 months). The incidence of MACE was lower in patients with LVRR than in those without (2% vs. 13%, p = 0.016).

Conclusion: Low GV, determined using a CGMS, was significantly associated with LVRR, which might lead to a good prognosis. Further studies are needed to validate the importance of GV in LVRR in patients with STEMI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403862PMC
http://dx.doi.org/10.1186/s12933-023-01931-3DOI Listing

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