The Impact of Subclinical Hyperthyroidism on Cardiovascular Prognosis in Patients Undergoing Percutaneous Coronary Intervention

Context: Limited studies have focused on the impact of subclinical hyperthyroidism (SHyper) on poor prognosis in patients with known coronary artery disease (CAD). Objective: We implemented the present study to explore the association between SHyper and adverse cardiovascular events in CAD patients...

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Main Authors: Gao, J. (Author), Li, C. (Author), Liu, Y. (Author), Meng, X. (Author), Shao, C. (Author), Tang, Y.-D (Author), Wang, W. (Author), Yang, J. (Author), Zhang, K. (Author), Zheng, Y. (Author), Zhou, Q. (Author)
Format: Article
Language:English
Published: Endocrine Society 2022
Subjects:
CAD
Online Access:View Fulltext in Publisher
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020 |a 0021972X (ISSN) 
245 1 0 |a The Impact of Subclinical Hyperthyroidism on Cardiovascular Prognosis in Patients Undergoing Percutaneous Coronary Intervention 
260 0 |b Endocrine Society  |c 2022 
300 |a 12 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1210/clinem/dgab855 
520 3 |a Context: Limited studies have focused on the impact of subclinical hyperthyroidism (SHyper) on poor prognosis in patients with known coronary artery disease (CAD). Objective: We implemented the present study to explore the association between SHyper and adverse cardiovascular events in CAD patients who underwent drug-eluting stent implantation. Methods: We consecutively recruited 8283 CAD patients undergoing percutaneous coronary intervention (PCI). All subjects were divided into 2 groups according to their thyroid function: group 1 (euthyroidism group, n = 7942) and group 2 (SHyper group, n = 341). After 1:4 propensity score (PS) matching, 1603 patients (332 SHyper group and 1271 euthyroidism group) were selected. The primary endpoint was major adverse cardiovascular events (MACEs), a composite of cardiac mortality, nonfatal myocardial infarction (MI), and target vessel revascularization (TVR). Results: Kaplan-Meier (K-M) survival analyses suggested that there was no significant difference in the primary endpoint and secondary endpoints (MACE: 11.4% vs 8.8%, log-rank P =. 124; cardiac death: 1.2% vs 0.9%, log-rank P =. 540; nonfatal MI: 5.7% vs 4%, log-rank P =. 177; and TVR: 6% vs 4.7%, log-rank P =. 303) in the PS-matched population. Cox regression analysis indicated that SHyper was not an independent risk factor for MACEs (HR 1.33, 95% CI 0.92-1.92, P =. 127). Conclusion: SHyper is not independently associated with adverse cardiovascular events in CAD patients undergoing PCI. 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. © 2021 The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 
650 0 4 |a CAD 
650 0 4 |a PCI MACE 
650 0 4 |a SHyper 
650 0 4 |a thyroid 
700 1 |a Gao, J.  |e author 
700 1 |a Li, C.  |e author 
700 1 |a Liu, Y.  |e author 
700 1 |a Meng, X.  |e author 
700 1 |a Shao, C.  |e author 
700 1 |a Tang, Y.-D.  |e author 
700 1 |a Wang, W.  |e author 
700 1 |a Yang, J.  |e author 
700 1 |a Zhang, K.  |e author 
700 1 |a Zheng, Y.  |e author 
700 1 |a Zhou, Q.  |e author 
773 |t Journal of Clinical Endocrinology and Metabolism