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促甲状腺激素与校正 QT 间期变异的相关性:2 型糖尿病患者的前瞻性队列研究。

Association of thyroid-stimulating hormone with corrected QT interval variation: A prospective cohort study among patients with type 2 diabetes.

机构信息

Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka 576104, India; Department of Pharmacology and Clinical Investigation Centre (CIC-1901), Pitié-Salpêtrière Hospital, AP-HP, Sorbonne Université, inserm, 75013 Paris, France.

Department of Cardiovascular Sciences, East Carolina University, Greenville; and Vidant Medical Center, Greenville, NC 27834, USA.

出版信息

Arch Cardiovasc Dis. 2021 Oct;114(10):656-666. doi: 10.1016/j.acvd.2021.06.008. Epub 2021 Sep 17.

Abstract

BACKGROUND

Patients with type 2 diabetes mellitus (T2DM) have a prolonged QT interval and are at high risk of sudden cardiac death. A prolonged QT interval, indicative of impaired ventricular repolarization, is a risk factor for lethal ventricular arrhythmias, such as torsades-de-pointes (TdP).

AIMS

To identify key clinical and biochemical covariates associated with Fridericia's corrected QT interval (QTcF) among euthyroid patients with T2DM, and to describe the temporal relationship between these factors and QTcF.

METHODS

We performed prospective, clinical, biochemical and electrocardiographic measurements among patients with T2DM enrolled in the DIACART study at Pitié-Salpêtrière Hospital, at T1 (baseline) and T2 (follow-up), with a median interval of 2.55 years.

RESULTS

Mean age (63.9±8.5 years), sex (22.35% women), drugs with known risk of TdP according to the CredibleMeds website (Cred-drugsTdP) and serum thyroid-stimulating hormone (TSH) concentrations correlated with QTcF in univariate analysis at both T1 and T2. In multivariable analysis, all these covariates except age were significantly associated with QTcF at both T1 (women: standardized β=0.24±0.07, P=0.001; Cred-drugsTdP: β=0.19±0.07, P=0.007; TSH concentration: β=0.18±0.07, P=0.01) and T2 (women: β=0.25±0.08, P=0.002; Cred-drugsTdP: β=0.25±0.08, P=0.001; TSH concentration: β=0.19±0.08, P=0.01). Furthermore, variation in QTcF over the years was associated with variation in TSH concentration (r=0.24, P=0.007) and changes in use of Cred-drugsTdP (r=0.2, P=0.02).

CONCLUSIONS

Serum TSH concentration and its variation were associated with QTcF and its variation, even after correcting for the main determinants of QTcF. Interventional optimization of TSH concentration in T2DM warrants further investigation to establish its impact on the risk of TdP and sudden cardiac death.

摘要

背景

2 型糖尿病(T2DM)患者的 QT 间期延长,发生心源性猝死的风险较高。QT 间期延长提示心室复极受损,是致死性室性心律失常(如尖端扭转型室性心动过速[TdP])的危险因素。

目的

确定甲状腺功能正常的 T2DM 患者中 Fridericia 校正 QT 间期(QTcF)相关的关键临床和生化协变量,并描述这些因素与 QTcF 之间的时间关系。

方法

我们在 Pitié-Salpêtrière 医院的 DIACART 研究中对 T2DM 患者进行了前瞻性的临床、生化和心电图测量,这些患者在 T1(基线)和 T2(随访)时进行了测量,中位间隔为 2.55 年。

结果

在 T1 和 T2 时,平均年龄(63.9±8.5 岁)、性别(22.35%女性)、根据 CredibleMeds 网站(Cred-drugsTdP)确定的已知有 TdP 风险的药物和血清促甲状腺激素(TSH)浓度与 QTcF 相关。在多变量分析中,除年龄外,所有这些协变量在 T1(女性:标准化β=0.24±0.07,P=0.001;Cred-drugsTdP:β=0.19±0.07,P=0.007;TSH 浓度:β=0.18±0.07,P=0.01)和 T2(女性:β=0.25±0.08,P=0.002;Cred-drugsTdP:β=0.25±0.08,P=0.001;TSH 浓度:β=0.19±0.08,P=0.01)时均与 QTcF 显著相关。此外,多年来 QTcF 的变化与 TSH 浓度的变化相关(r=0.24,P=0.007),与 Cred-drugsTdP 使用的变化相关(r=0.2,P=0.02)。

结论

即使在纠正了 QTcF 的主要决定因素后,血清 TSH 浓度及其变化仍与 QTcF 及其变化相关。进一步研究 T2DM 中 TSH 浓度的干预优化是否可以降低 TdP 和心源性猝死的风险。

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