Key result
Elevated post-CABG urinary thromboxane linked to ~2.8-fold higher risk of 1-year MACCE.
Why the study?
Does elevated perioperative urinary thromboxane metabolite generation increase the risk of major adverse cardiac and cerebrovascular events in patients undergoing CABG?
Case-Control (n=224)
No
Does elevated perioperative urinary thromboxane metabolite generation increase the risk of major adverse cardiac and cerebrovascular events in patients undergoing CABG?
Elevated post-CABG 24-hour urinary thromboxane metabolites predict a significantly higher risk of 1-year MACCE, highlighting a potential prognostic biomarker.
Answers are grounded in this paper and cite their sources.
May identify higher-risk CABG patients; leaves open whether thromboxane-targeted therapy improves outcomes.
OBJECTIVE: As a marker of in vivo thromboxane generation, high-level urinary thromboxane metabolites (TXA-M) increase the occurrence of cardiovascular events in high-risk patients. To investigate whether perioperative urinary TXA-M level is associated with major adverse cardiac and cerebrovascular events (MACCE) after coronary artery bypass graft (CABG) surgery, we designed a nested case-control study. DESIGN: Observational, nested case-control study. SETTING: Single-centre outcomes research in Fuwai Hospital, Beijing, China. PARTICIPANTS: One thousand six hundred and seventy Chinese patients undergoing CABG surgery from September 2011 to October 2013. METHODS: We obtained urinary samples from 1670 Chinese patients undergoing CABG 1 hour before surgery (pre-CABG), and 6 hours (post-CABG 6 hours) and 24 hours after surgery (post-CABG 24 hours). Patients were followed up for 1 year, and we observed 56 patients had MACCE. For each patient with MACCE, we matched three control subjects. Perioperative urinary TXA-M of the three time spots was detected in these 224 patients. RESULTS: Post-CABG 24 hours TXA-M is significantly higher than that of patients without MACCE (11 101vs8849 pg/mg creatine, P=0.007). In addition, patients in the intermediate tertile and upper tertile of post-CABG 24 hours urinary TXA-M have a 2.2 times higher (HR 2.22, 95% CI 1.04 to 4.71, P=0.038) and a 2.8 times higher (HR 2.81, 95% CI 1.35 to 5.85, P=0.006) risk of 1 year MACCE than those in the lower tertile, respectively. CONCLUSIONS: In conclusion, post-CABG 24 hours urinary TXA-M elevation is associated with an increase of 1 year adverse events after CABG, indicating that the induction of cyclo-oxygenase-2 by surgery-related inflammatory stimuli or platelet turnover may be responsible for the high levels of post-CABG urinary TXA-M. TRIAL REGISTRATION NUMBER: NCT01573143.
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Liu et al. (2018) conducted a case-control in Coronary artery disease undergoing CABG surgery (n=224). High post-CABG 24 hours urinary thromboxane metabolites (upper tertile) vs. Low post-CABG 24 hours urinary thromboxane metabolites (lower tertile) was evaluated on 1-year major adverse cardiac and cerebrovascular events (MACCE) (HR 2.81, 95% CI 1.35-5.85, p=0.006). Patients in the upper tertile of post-CABG 24 hours urinary thromboxane metabolites had a 2.8-times higher risk of 1-year major adverse cardiac and cerebrovascular events compared to those in the lower tertile.
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