Elevated uric acid is related to the no-/slow-reflow phenomenon in STEMI undergoing primary PCI.

2021 
BACKGROUND No-/slow-reflow phenomenon (NRP) is a severe complication in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI). This study aimed to explore the relationship between elevated serum uric acid (SUA) and NRP in patients with STEMI undergoing pPCI, focusing on inflammation and angiographic findings. METHODS A total of 610 patients who received pPCI for STEMI were retrospectively enrolled. Patients were divided into a hyperuricemia group and a non-hyperuricemia group according to SUA levels. Clinical information and angiographic indicators were compared between the two groups. Thrombolysis in myocardial infarction (TIMI) flow and TIMI myocardial perfusion grade (TMPG) < 3 after stent implantation were defined as TIMI-NRP and TMPG-NRP, respectively. A logistic model was used to analyze the relationship between hyperuricemia and NRP. RESULTS The hyperuricemia group had a higher incidence of TIMI-NRP (24.9% vs 14.0%, P < 0.001) and TMPG-NRP (33.0% vs 24.9%, P = 0.03), higher levels of C-reactive protein (7.2 vs 4.1 mg/L, P < 0.001), and worse left ventricular ejection fraction (51.5% vs 54.0%, P = 0.002) than the non-hyperuricemia group. As for angiographic findings, there was no significant difference between the two groups in terms of lesion characteristics measured by quantitative coronary angiography. After multivariable adjustment, elevated SUA was significantly associated with TIMI-NRP (odds ratio: 1.94, 95% confidence interval: 1.24-3.01, P = 0.003). Subgroup analysis showed that the effect of hyperuricemia in TIMI-NRP was more pronounced in patients with delayed perfusion as well as in patients with diabetes mellitus. CONCLUSIONS Elevated SUA is associated with severe inflammation and has higher incidence of TIMI-NRP in patients with STEMI undergoing pPCI, especially in those with delayed perfusion or diabetes mellitus.
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    33
    References
    0
    Citations
    NaN
    KQI
    []