Viswanathan Girish, Balasubramaniam Karthik, Hardy Richard, Marshall Sally, Zaman Azfar, Razvi Salman
Institutes of Cellular Medicine (G.V., K.B., S.M., A.Z.) and Institute of Genetic Medicine (S.R.), Newcastle University, Newcastle upon Tyne NE1 7RU, United Kingdom; Department of Cardiology (A.Z.), Freeman Hospital, Newcastle upon Tyne NE7 7DN, United Kingdom; and Gateshead Health National Health Service Foundation Trust (R.H., S.R.), Gateshead NE9 6SX, United Kingdom.
J Clin Endocrinol Metab. 2014 Jun;99(6):E1050-4. doi: 10.1210/jc.2013-3062. Epub 2014 Mar 14.
Higher serum TSH levels, both within the reference range and in those with subclinical hypothyroidism (SCH), have been associated with increased risk of atherosclerosis and cardiovascular (CV) events in a number of cross-sectional and longitudinal studies.
Our objective was to evaluate blood thrombogenicity in patients post-non-ST elevation acute coronary syndrome (NSTE-ACS) in relation to their thyroid function. DESIGN, PATIENTS, AND OUTCOME MEASURE: At 1 week after troponin-positive NSTE-ACS, 70 patients who had been treated with optimal antiplatelet and secondary prevention therapy were studied. Patients with known thyroid disease or on medications affecting thyroid function were excluded. Blood thrombogenicity was assessed using the ex vivo Badimon perfusion chamber.
Serum TSH was associated with higher thrombus burden (β = .30; P = .01) independent of other well-established CV risk factors. Patients with SCH (n = 12; 17%) had a higher thrombus burden than euthyroid individuals as evidenced by the area of the thrombus: mean (SD) 23 608 (10 498) vs 16 661 (10 902) μm(2)/mm (P = .02). However, this association was not evident when the analysis was limited to patients with serum TSH within the reference range. In addition, neither serum free T4 nor free T3 had any significant association with thrombus area.
Serum TSH levels, particularly in the SCH range, are associated with higher thrombus burden despite optimal recommended secondary prevention therapy after NSTE-ACS. This may explain the higher CV risk seen in SCH patients. Future trials to assess the effect of individualized antithrombotic as well as thyroid hormone replacement therapy to reduce atherothrombotic risk in this population are needed.
在多项横断面和纵向研究中,无论是在参考范围内还是亚临床甲状腺功能减退(SCH)患者中,较高的血清促甲状腺激素(TSH)水平都与动脉粥样硬化和心血管(CV)事件风险增加相关。
我们的目的是评估非ST段抬高型急性冠状动脉综合征(NSTE-ACS)患者的血液血栓形成倾向与其甲状腺功能的关系。
设计、患者和结局指标:在肌钙蛋白阳性的NSTE-ACS发作1周后,对70例接受了最佳抗血小板和二级预防治疗的患者进行了研究。排除已知患有甲状腺疾病或正在服用影响甲状腺功能药物的患者。使用体外Badimon灌注腔评估血液血栓形成倾向。
血清TSH与较高的血栓负荷相关(β = 0.30;P = 0.01),独立于其他已确定的CV危险因素。SCH患者(n = 12;17%)的血栓负荷高于甲状腺功能正常的个体,血栓面积可证明这一点:平均(标准差)23 608(10 498)与16 661(10 902)μm²/mm(P = 0.02)。然而,当分析仅限于血清TSH在参考范围内的患者时,这种关联并不明显。此外,血清游离T4和游离T3均与血栓面积无显著关联。
尽管在NSTE-ACS后进行了最佳推荐的二级预防治疗,但血清TSH水平,特别是在SCH范围内,与较高的血栓负荷相关。这可能解释了SCH患者中较高的CV风险。未来需要进行试验,以评估个体化抗血栓治疗以及甲状腺激素替代治疗对降低该人群动脉粥样硬化血栓形成风险的效果。