Key result
In patients with normal troponin I levels prior to percutaneous coronary intervention, serum RIPK3 levels after the procedure significantly differentiated patients with impaired left ventricular function (AUC 0.780).
Why the study?
Can serum levels of RIPK3 and troponin I predict impaired left ventricular function in STEMI patients with normal troponin I levels prior to PCI?
Observational (n=123)
No
Can serum levels of RIPK3 and troponin I predict impaired left ventricular function in STEMI patients with normal troponin I levels prior to PCI?
Serum levels of RIPK3 and troponin I after PCI may serve as potential biomarkers to identify STEMI patients at risk for decreased LVEF, particularly when pre-PCI troponin I levels are normal.
Answers are grounded in this paper and cite their sources.
May support post-PCI RIPK3 evaluation for impaired LVEF despite normal pre-PCI troponin; hypothesis-generating for STEMI biomarker strategies.
The current study examined the serum levels of receptor-interacting protein kinase 3 (RIPK3) in 51 patients with New York Heart Association (NYHA) class III-IV heart failure, 53 patients with myocardial infarction with ST elevation (STEMI), and 19 healthy subjects serving as a control group. An enzyme-linked immunoadsorbent assay (ELISA) was used to measure the levels of RIPK3 expression in serum. The area under the receiver operating characteristic curve (AUC) was then used to evaluate the predictive performance of RIPK3 and troponin I in patients with STEMI. In patients with normal levels of troponin I prior to percutaneous coronary intervention (PCI), serum levels of RIPK3 and troponin I after PCI were sufficient to differentiate patients with a preserved left ventricular ejection fraction (LVEF) from those with impaired left ventricular function after PCI (AUC = 0.780 (95% CI: 0.565-0.995, p = 0.043) with a sensitivity of 76.9% and a specificity of 71.4% vs. AUC = 0.735 (95% CI: 0.530-0.941, p = 0.038) with a sensitivity of 88.2% and a specificity of 63.6% at the optimal cutoff values, respectively). Moreover, elevated levels of troponin I after PCI were associated with an increased risk of an LVEF < 50% prior to discharge (odds ratio, 1.014; 95 % CI, 1.001 to 1.027; p = 0.03), while elevated levels of RIPK3 were not associated with such a risk. The current findings suggest that in patients with normal levels of troponin I prior to PCI, serum levels of RIPK3 and troponin I can serve as a potential marker to identify patients with a decreased LVEF, thus possibly allowing an early shift to more intensive therapy.
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Kashlov et al. (2016) conducted an observational in Myocardial infarction with ST elevation (STEMI) and Heart Failure (n=123). Serum levels of RIPK3 and troponin I vs. Normal levels / Preserved LVEF was evaluated on Differentiation of impaired left ventricular function (LVEF < 50%) after PCI (AUC 0.780, 95% CI 0.565-0.995, p=0.043). In patients with normal troponin I levels prior to percutaneous coronary intervention, serum RIPK3 levels after the procedure significantly differentiated patients with impaired left ventricular function (AUC 0.780).
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