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Invasive Hemodynamic Changes Associated With Sodium-Glucose Cotransporter-2 Inhibitors: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. | LitMetric

AI Article Synopsis

  • SGLT2 inhibitors have been linked to reduced incidences of heart failure (HF) and related hospitalizations, but the exact mechanisms behind these benefits in invasive heart measurements are not well understood.
  • A systematic review of randomized trials using PRISMA guidelines examined the impact of SGLT2i on heart function, measuring hemodynamics before and after treatment through right heart catheterization.
  • The analysis of 3 studies involving 145 patients showed that SGLT2i significantly lowered pulmonary capillary wedge pressure at rest and during exercise, indicating potential improvements in heart function, although the effect on mean pulmonary artery pressure was not statistically significant.

Article Abstract

Sodium-glucose cotransporter-2 inhibitors (SGLT2is) have been shown to lower incident heart failure (HF) and HF hospitalizations, but the mechanisms of benefit in relation to invasive hemodynamics remain unclear. Using PRISMA guidelines, we systematically reviewed multiple online databases for randomized trials evaluating the effect of SGLT2i on invasive hemodynamics. Rest and peak exercise invasive hemodynamics were measured via right heart catheterization pre- and postintervention. Random effects model meta-analysis at a 95% confidence interval was done using RevMan 5.0. A total of 3 studies with a total of 145 patients were included in the meta-analysis. SGLT2i was significantly associated with a reduction in pulmonary capillary wedge pressure at rest and peak exercise. Similarly, SGLT2i reduced mean pulmonary artery pressure at rest and peak exercise, respectively; however, this was not statistically significant. This hypothesis-generating study offers mechanistic insights into the central hemodynamic effects of SGLT2i underpinning the HF benefits of SGLT2i.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11208784PMC
http://dx.doi.org/10.1155/2024/2735577DOI Listing

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