Cardiology Unit, Queen Elizabeth Hospital, 28 Woodville Road, Woodville South, SA, 5011, Australia.
University of Adelaide, Basil Hetzel Institute, Woodville, SA, Australia.
Cardiovasc Drugs Ther. 2020 Feb;34(1):95-100. doi: 10.1007/s10557-019-06918-5.
Although Takotsubo syndrome (TS) was once considered to be rare and largely benign, it is now recognized to represent a major cause of cardiac morbidity and mortality, especially in ageing women. The biochemical precipitant of attacks of TS is an increase in catecholamine concentrations within the myocardium, engendering inflammatory activation via biased post-receptor signalling at myocardial β-adrenoceptor level. Cases of TS have been reported in patients treated with catecholamines, and with antidepressants which limit catecholamine re-uptake. In the current investigation, we sought to delineate the extent and potential impact of this "iatrogenic" form of TS.
METHODS/RESULTS: Patients' data from a regional registry of 301 consecutive cases of TS were evaluated after exclusion of patients (n = 20) in whom TS had occurred in association with life threatening extracardiac disease states. A total of 55 (18%) of patients were identified as having antecedent exposure to potentially "iatrogenic" agents (tricyclic antidepressants in 24 cases, β-adrenoceptor agonists in 15). Demographics, including proportion of male patients, did not differ significantly between patients with and without "iatrogenic" TS, but plasma concentrations of the catecholamine metabolite normetanephrine tended to be greater (median 1149 pmol/L vs 938 pmol/L; p = 0.03). Long-term survival (median follow-up 3 years) was marginally (p = 0.13) worse for patients with "iatrogenic" TS.
Potentially iatrogenic precipitation of TS attacks (via iatrogenic elevation of catecholamine levels and β-adrenoceptor stimulation) is common, associated with greater elevation of plasma normetanephrine concentrations, and also with a trend towards increased long-term mortality when compared to the remainder of TS patients.
虽然 Takotsubo 综合征(TS)曾经被认为是罕见且基本良性的,但现在已被认为是导致心脏发病率和死亡率的主要原因,尤其是在老年女性中。TS 发作的生化诱因是心肌内儿茶酚胺浓度的增加,通过心肌 β-肾上腺素能受体水平的偏向性受体后信号传导引发炎症激活。已有报道称,在接受儿茶酚胺治疗的患者和使用限制儿茶酚胺再摄取的抗抑郁药的患者中出现了 TS 病例。在当前的研究中,我们试图描绘这种“医源性”TS 的程度和潜在影响。
方法/结果:对 301 例连续 TS 患者的区域登记处患者的数据进行评估,排除了 20 例与威胁生命的心脏外疾病状态相关的 TS 患者。共有 55 例(18%)患者被确定有潜在的“医源性”药物暴露史(24 例使用三环类抗抑郁药,15 例使用β-肾上腺素能激动剂)。患者的人口统计学特征,包括男性患者的比例,在有无“医源性”TS 的患者之间没有显著差异,但儿茶酚胺代谢产物去甲肾上腺素的血浆浓度倾向于更高(中位数 1149 pmol/L 比 938 pmol/L;p=0.03)。有“医源性”TS 的患者的长期生存率(中位随访 3 年)略有下降(p=0.13)。
潜在的医源性 TS 发作(通过医源性儿茶酚胺水平升高和 β-肾上腺素能受体刺激)很常见,与血浆去甲肾上腺素浓度的升高相关,并且与 TS 患者的其余部分相比,长期死亡率也呈上升趋势。