A. Orosz, L. Szabó, A. Vagvolgyi, S. Magony, Szabolcs Nyiraty, B. Tóth, F. Pesei, GY Abraham, A. Nemes, C. Lengyel, T. Várkonyi, I. Baczkó
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Recent data strongly suggest that different QT variability parameters characterizing cardiac repolarization instability represent novel markers in proarrhythmic risk assessment.\n \n \n \n In the present study we investigated ECG repolarization parameters, including QT variability parameters in patients with polycystic ovary syndrome.\n \n \n \n Fifty-five PCOS patients (age: 29±6 years) and 55 age-matched healthy volunteers (age: 29±10 years) were enrolled in the study. Five-minute 12-lead resting electrocardiograms were recorded, the ECGs were digitized and evaluated off-line using the Cardiosys-A01 system (Cardiosys-A01). The following parameters were determined: the frequency corrected QT interval (QTc) using Bazett’s, Fridericia, Framingham and the Hodges formulas; QT dispersion (QTd) and T wave peak-to-end distance (Tpeak-Tend). Among QT variability parameters we analyzed the QT variance (QTv), the QT variability index (QTVI), the short-term beat-to-beat QT and RR interval variability (STV-QT, STV-RR) based on constructed Poincaré plots and the variability ratio (VR).\n \n \n \n The RR interval did not differ significantly in PCOS patients compared to controls (821±129 ms vs. 847±99 ms), however the QT interval (373±30 ms vs. 391±27 ms, p<0.01), the QTc calculated with Bazett’s, Framingham, Fridericia and Hodges correction formulas (QTc Bazett’s: 413±18 ms vs. 426±21 ms, p<0.01) and the Tpeak-Tend intervals were significantly shorter (76±10 ms vs. 83±12 ms, p<0.01). The QTd, QTv, and STV-RR did not differ significantly. However, the VR (0.3±0.4 vs. 0.2±0.2, p<0.05), the QTVI (-0,9±0.5 vs. -1,3±0.4, p<0.001), and importantly, the STV-QT were significantly higher in PCOS patients compared to controls (4.0±0.9 ms vs. 3.2±0.9 ms, p<0.0001).\n \n \n \n Some of the alterations in repolarization parameters and the significant increase in the short-term beat-to-beat QT interval variability and the QT variability index may indicate increased repolarization instability in patients with polycystic ovary syndrome compared to age-matched controls, however, further studies are needed to establish the exact relation of this finding to increased arrhythmia propensity in this population.\n","PeriodicalId":11720,"journal":{"name":"EP Europace","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of electrocardiographic repolarization parameters in patients with polycystic ovary syndrome\",\"authors\":\"A. 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引用次数: 0
摘要
资金来源类型:公共拨款-仅限国家预算。多囊卵巢综合征(PCOS)是一种多因素内分泌疾病,与代谢紊乱(如高胰岛素血症、胰岛素抵抗)和心血管风险增加有关。最近的数据强烈表明,不同的QT变异性参数表征心脏复极不稳定是心律失常风险评估的新指标。在本研究中,我们研究了多囊卵巢综合征患者的心电图复极参数,包括QT变异性参数。55名PCOS患者(年龄:29±6岁)和55名年龄匹配的健康志愿者(年龄:29±10岁)入组研究。记录5分钟12导联静息心电图,心电图数字化并使用Cardiosys-A01系统(Cardiosys-A01)离线评估。使用Bazett’s, Fridericia, Framingham和Hodges公式确定以下参数:频率校正QT间期(QTc);QT离散度(QTd)和T波峰端距离(Tpeak-Tend)。在QT变异性参数中,我们分析了QT方差(QTv)、QT变异性指数(QTVI)、短期搏动-搏动QT和RR间隔变异性(STV-QT, STV-RR),基于构建的poincar图和变异性比(VR)。PCOS患者的RR间期与对照组相比差异无统计学意义(821±129 ms比847±99 ms),但QT间期(373±30 ms比391±27 ms, p<0.01),用Bazett、Framingham、Fridericia和Hodges校正公式计算的QTc (QTc: 413±18 ms比426±21 ms, p<0.01)和t峰值-趋势间期(76±10 ms比83±12 ms, p<0.01)显著缩短。QTd、QTv、STV-RR无显著性差异。然而,PCOS患者的VR(0.3±0.4 vs. 0.2±0.2,p<0.05), QTVI(-0,9±0.5 vs. -1,3±0.4,p<0.001),重要的是,STV-QT显著高于对照组(4.0±0.9 ms vs. 3.2±0.9 ms, p<0.0001)。复极参数的一些改变以及短期搏动间期变异性和QT变异性指数的显著增加可能表明多囊卵巢综合征患者的复极不稳定性比年龄匹配的对照组增加,然而,需要进一步的研究来确定这一发现与该人群中心律失常倾向增加的确切关系。
Evaluation of electrocardiographic repolarization parameters in patients with polycystic ovary syndrome
Type of funding sources: Public grant(s) – National budget only. Main funding source(s): National Research, Development and Innovation Office
Polycystic ovary syndrome (PCOS) is a multifactorial, endocrine disease associated with metabolic disturbances (e.g. hyperinsulinemia, insulin resistance) and increased cardiovascular risk. Recent data strongly suggest that different QT variability parameters characterizing cardiac repolarization instability represent novel markers in proarrhythmic risk assessment.
In the present study we investigated ECG repolarization parameters, including QT variability parameters in patients with polycystic ovary syndrome.
Fifty-five PCOS patients (age: 29±6 years) and 55 age-matched healthy volunteers (age: 29±10 years) were enrolled in the study. Five-minute 12-lead resting electrocardiograms were recorded, the ECGs were digitized and evaluated off-line using the Cardiosys-A01 system (Cardiosys-A01). The following parameters were determined: the frequency corrected QT interval (QTc) using Bazett’s, Fridericia, Framingham and the Hodges formulas; QT dispersion (QTd) and T wave peak-to-end distance (Tpeak-Tend). Among QT variability parameters we analyzed the QT variance (QTv), the QT variability index (QTVI), the short-term beat-to-beat QT and RR interval variability (STV-QT, STV-RR) based on constructed Poincaré plots and the variability ratio (VR).
The RR interval did not differ significantly in PCOS patients compared to controls (821±129 ms vs. 847±99 ms), however the QT interval (373±30 ms vs. 391±27 ms, p<0.01), the QTc calculated with Bazett’s, Framingham, Fridericia and Hodges correction formulas (QTc Bazett’s: 413±18 ms vs. 426±21 ms, p<0.01) and the Tpeak-Tend intervals were significantly shorter (76±10 ms vs. 83±12 ms, p<0.01). The QTd, QTv, and STV-RR did not differ significantly. However, the VR (0.3±0.4 vs. 0.2±0.2, p<0.05), the QTVI (-0,9±0.5 vs. -1,3±0.4, p<0.001), and importantly, the STV-QT were significantly higher in PCOS patients compared to controls (4.0±0.9 ms vs. 3.2±0.9 ms, p<0.0001).
Some of the alterations in repolarization parameters and the significant increase in the short-term beat-to-beat QT interval variability and the QT variability index may indicate increased repolarization instability in patients with polycystic ovary syndrome compared to age-matched controls, however, further studies are needed to establish the exact relation of this finding to increased arrhythmia propensity in this population.