Subclinical hyperthyroidism (SHyper) does not independently correlate with major adverse cardiovascular events (MACE) in patients with coronary artery disease (CAD) undergoing percutaneous coronary intervention (PCI), results of a study have shown.
A group of researchers conducted this study to explore the relationship between SHyper and adverse cardiovascular events in CAD patients who went through drug-eluting stent implantation. They consecutively recruited a total of 8,283 participants and divided them into two groups based on their thyroid functions: euthyroidism group (n=7,942) and SHyper group (n=341).
After propensity score matching, 1,603 patients (332 in the SHyper group and 1,271 in the euthyroidism group) were included in the analysis. MACE, a composite of cardiac mortality, nonfatal myocardial infarction (MI), and target vessel revascularization (TVR), was the primary endpoint.
On Kaplan‒Meier survival analysis, no significant between-group difference was observed in the primary endpoints (MACE: 11.4 percent vs 8.8 percent; log-rank p=0.124; cardiac death: 1.2 percent vs 0.9 percent; log-rank p=0.540; nonfatal MI: 5.7 percent vs 4 percent; log-rank p=0.177; and TVR: 6 percent vs 4.7 percent; log-rank p=0.303).
Cox regression analysis confirmed that SHyper was not independently predictive of MACE (hazard ratio, 1.33, 95 percent confidence interval, 0.92‒1.92; p=127).
“More studies should be implemented in the future to assess the long-term predictive value of SHyper with thyrotropin levels <0.1 mIU/L for CAD patients undergoing PCI,” the researchers said.