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Serum Free Triiodothyronine and the Responsiveness to Clopidogrel in Patients Undergoing Elective Percutaneous
Yicong Ye1, Xiliang Zhao1, Yong Zeng2
1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, China.
Insights
Low free triiodothyronine (FT3) levels are linked to reduced clopidogrel responsiveness in patients undergoing percutaneous coronary intervention (PCI). This finding suggests FT3 may impact cardiovascular event risk in these patients.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Thyroid dysfunction and poor clopidogrel response are associated with higher cardiovascular risk.
- Free triiodothyronine (FT3) plays a crucial role in metabolic regulation.
- Clopidogrel responsiveness is vital for preventing thrombotic events post-PCI.
Purpose of the Study:
- To investigate the association between FT3 levels and clopidogrel responsiveness.
- To determine if FT3 levels predict cardiovascular outcomes in patients undergoing elective PCI.
Main Methods:
- 812 patients undergoing elective percutaneous coronary intervention (PCI) were analyzed.
- Platelet function was assessed using thromboelastography after clopidogrel loading.
- Low clopidogrel responsiveness was defined by specific platelet inhibition rates.
Main Results:
- Lower FT3 levels were observed in patients with low clopidogrel responsiveness (p=0.002).
- A higher percentage of low responders had low FT3 levels (56.1% vs 34.5%, p=0.007).
- Low FT3 was an independent predictor of both low clopidogrel responsiveness (OR 0.720, p=0.033) and major adverse cardiovascular events (aHR 3.040, p=0.036).
Conclusions:
- Low FT3 levels are independently associated with reduced clopidogrel responsiveness.
- Low FT3 is also linked to an increased risk of cardiovascular events in patients undergoing PCI.
- FT3 may serve as a biomarker for cardiovascular risk stratification in patients receiving clopidogrel therapy.
Introduction:
Both thyroid dysfunction and low responsiveness to clopidogrel have been reported to be associated with increased cardiovascular risk. Our study aims at determining the relationship between free triiodothyronine (FT3) and low responsiveness to clopidogrel in patients undergoing elective percutaneous coronary intervention (PCI).
Methods:
Consecutive patients undergoing elective PCI were enrolled. All patients received a loading dose of 300 mg clopidogrel, and platelet function was assessed by thromboelastography at least 12 h later. Low responsiveness to clopidogrel was defined by an adenosine diphosphate-induced platelet-fibrin clot strength > 47 mm and adenosine diphosphate-induced platelet inhibition rate < 50%. Major adverse cardiovascular events (MACEs) were defined as a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, and ischemia-driven revascularization.
Results:
Of 812 patients included in the study, 289 showed low responsiveness to clopidogrel. The FT3 level was significantly lower in low responders (4.61 ± 0.60 pmol/l versus 4.94 ± 4.66 pmol/l, p = 0.002). Moreover, the percentage of low responders was greater among patients with low FT3 level than among those without (56.1% versus 34.5%, p = 0.007). Logistic regression analysis showed that a FT3 level was independently associated with the risk of low responsiveness to clopidogrel (odds ratio 0.720, 95% confidence interval [CI] 0.533-0.973, p = 0.033). In patients with low responsiveness to clopidogrel, low FT3 was independently associated with increased risk of MACEs (adjusted hazard ratio 3.040, 95% CI 1.077-8.580, p = 0.036) at a median of 19-month follow-up.
Conclusions:
Low FT3 was independently associated with increased risks of both low responsiveness to clopidogrel and cardiovascular events in patients undergoing elective PCI.
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