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Published on: May 28, 2019
The Uremic Toxin p-Cresyl Sulfate Is a New Predictor of Major Adverse Cardiovascular Events in Patients with
Laure-Anne Raillon1,2, Thomas Bochaton1,3, Griet Glorieux4
1CarMeN Lab, INSERM U1060, INRAe U1397, Université Claude Bernard Lyon-1, 69500 Bron, France.
Insights
In ST-elevation myocardial infarction (STEMI) patients, elevated p-cresyl-sulfate (p-CS) independently predicts major adverse cardiovascular events (MACE). P-CS shows greater predictive value than indoxyl sulfate (IS) in this population.
Area of Science:
- Cardiology
- Nephrology
- Toxicology
Background:
- ST-elevation myocardial infarction (STEMI) poses significant cardiovascular risks.
- Gut-derived uremic toxins, indoxyl sulfate (IS) and p-cresyl-sulfate (p-CS), are linked to poor outcomes in chronic kidney disease (CKD).
- IS predicts major adverse cardiovascular events (MACE) post-STEMI, but p-CS data is limited, especially in patients with preserved renal function.
Purpose of the Study:
- To evaluate the predictive value of plasma IS and p-CS for MACE in STEMI patients with normal kidney function.
- To compare the independent predictive power of IS and p-CS for MACE in this cohort.
Main Methods:
- Plasma IS and p-CS levels were measured in 260 STEMI patients undergoing primary coronary angiography.
- Ultra-performance liquid chromatography with fluorescence detection was used for analysis.
- MACE prediction was assessed using Youden index for cut-offs, log-rank tests, and Cox regression.
Main Results:
- Among 234 analyzed patients, 11.5% experienced MACE within one year.
- Higher IS and p-CS levels were observed in patients with MACE.
- Elevated p-CS independently predicted MACE (HR 3.79, p < 0.05), while IS lost significance after adjusting for kidney function.
Conclusions:
- Plasma p-CS is a stronger independent predictor of MACE than IS in STEMI patients with preserved renal function.
- These findings underscore the potential role of p-CS in the gut-heart axis and cardiovascular risk stratification.
Abstract:
ST-elevation myocardial infarction (STEMI) remains a major health concern despite advances in care. Indoxyl sulfate (IS) and p-cresyl-sulfate (p-CS) are gut-derived uremic toxins linked to higher morbidity and mortality in patients with chronic kidney disease (CKD). IS has been identified as an independent predictor of major adverse cardiovascular events (MACE) after STEMI, but data on p-CS are lacking. This study assessed the predictive value of IS and p-CS in STEMI patients with preserved renal function (cohort # NCT03070496). Plasma IS and p-CS were measured in 260 patients with STEMI who underwent primary coronary angiography. Samples collected 4 h after inclusion were analyzed using ultra-performance liquid chromatography with fluorescence detection. Optimal cut-offs were determined by the Youden index, and associations with MACE were evaluated by log-rank tests and Cox regression. Among 234 analyzed patients, 11.5% experienced MACE within one year. IS and p-CS levels were higher in the MACE group (IS: 3.14 vs. 2.19 µmol/L, p < 0.05; p-CS: 6.76 vs. 2.70 µmol/L, p < 0.01). Elevated p-CS independently predicted MACE (HR 3.79, 95% CI 1.29-11.17, p < 0.05), whereas IS lost significance after adjusting for kidney function. In STEMI patients, plasma p-CS is a stronger independent predictor of MACE than IS, highlighting its potential role in the gut-heart axis.
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