GLP-1 in patients with myocardial infarction complicated by cardiogenic shock-an IABP-SHOCK II-substudy
- PMID: 38170249
- DOI: 10.1007/s00392-023-02366-2
GLP-1 in patients with myocardial infarction complicated by cardiogenic shock-an IABP-SHOCK II-substudy
Abstract
Background: Glucagon-like peptide-1 (GLP-1) is a gut-derived peptide secreted in response to nutritional and inflammatory stimuli. Elevated GLP-1 levels predict adverse outcome in patients with acute myocardial infarction or sepsis. GLP-1 holds cardioprotective effects and GLP-1 receptor agonists reduce cardiovascular events in high-risk patients with diabetes. In this study, we aimed to investigate the capacity of GLP-1 to predict outcome in patients with cardiogenic shock (CS) complicating myocardial infarction.
Methods: Circulating GLP-1 levels were serially assessed in 172 individuals during index PCI and day 2 in a prospectively planned biomarker substudy of the IABP-SHOCK II trial. All-cause mortality at short- (30 days), intermediate- (1 year), and long-term (6 years) follow-up was used for outcome assessment.
Results: Patients with fatal short-term outcome (n = 70) exhibited higher GLP-1 levels [86 (interquartile range 45-130) pM] at ICU admission in comparison to patients with 30-day survival [48 (interquartile range 33-78) pM; p < 0.001] (n = 102). Repeated measures ANOVA revealed a significant interaction of GLP-1 dynamics from baseline to day 2 between survivors and non-survivors (p = 0.04). GLP-1 levels above vs. below the median proved to be predictive for short- [hazard ratio (HR) 2.43; 95% confidence interval (CI) 1.50-3.94; p < 0.001], intermediate- [HR 2.46; 95% CI 1.62-3.76; p < 0.001] and long-term [HR 2.12; 95% CI 1.44-3.11; p < 0.001] outcome by multivariate Cox-regression analysis.
Conclusion: Elevated plasma levels of GLP-1 are an independent predictor for impaired prognosis in patients with myocardial infarction complicated by CS. The functional relevance of GLP-1 in this context is currently unknown and needs further investigations.
Trial registration: www.
Clinicaltrials: gov Identifier: NCT00491036.
Keywords: Cardiogenic shock; Critical illness; GLP-1; Inflammation; Mortality.
© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.
References
-
- Thiele H, Ohman EM, de Waha-Thiele S et al (2019) Management of cardiogenic shock complicating myocardial infarction: an update 2019. Eur Heart J 40:2671–2683. https://doi.org/10.1093/eurheartj/ehz363 - DOI - PubMed
-
- Shimizu K, Ogura H, Goto M et al (2006) Altered gut flora and environment in patients with severe SIRS. J Trauma 60:126–133. https://doi.org/10.1097/01.ta.0000197374.99755.fe - DOI - PubMed
-
- Baggio LL, Drucker DJ (2007) Biology of incretins: GLP-1 and GIP. Gastroenterology 132:2131–2157. https://doi.org/10.1053/j.gastro.2007.03.054 - DOI - PubMed
-
- Drucker DJ (2016) The Cardiovascular Biology of Glucagon-like Peptide-1. Cell Metab 24:15–30. https://doi.org/10.1016/j.cmet.2016.06.009 - DOI - PubMed
-
- Diebold S, Moellmann J, Kahles F et al (2018) Myocardial infarction is sufficient to increase GLP-1 secretion, leading to improved left ventricular contractility and mitochondrial respiratory capacity. Diabetes Obes Metab 20:2911–2918. https://doi.org/10.1111/dom.13472 - DOI - PubMed
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