左心房应变对肥厚性心肌病无房颤患者血栓事件的预测价值。

IF 3.8 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Lutong Pu, Jie Wang, Jialin Li, Weitang Qi, Yuanwei Xu, Ke Wan, Yu Kang, Qing Zhang, Yuchi Han, Yucheng Chen
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The predictive value of LA strain was determined with Cox analysis. Results Overall, 714 participants with HCM (mean age ± SD, 50.1 years ± 14.3; 441 men, 273 women; obstructive HCM, <i>n</i> = 289; apical HCM, <i>n</i> = 144) were included (median follow-up: 51 months). Twenty-eight (3.9%) participants with HCM experienced TEs, 60% (17 of 28) of whom had no new-onset AF. Those who experienced TEs had lower LA reservoir and conduit strains (16.2% ± 7.3 vs 21.8% ± 8.3, <i>P</i> = .001; 5.9% ± 3.5 vs 9.7% ± 5.5, <i>P</i> = .01, respectively), with no evidence of a difference in LA booster strain between groups. LA reservoir and conduit strain were independent predictors of TEs in different multivariable models, even after adjusting for age, diabetes, and left ventricular ejection fraction (adjusted hazard ratios: reservoir strain [per 5% decrease], 1.29-1.34 [95% CI: 1.05, 1.50]; conduit strain [per 5% decrease], 1.42-1.47 [95% CI: 1.04, 1.67]). 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引用次数: 0

摘要

目的评估心脏MRI左房(LA)快速长轴应变对肥厚性心肌病(HCM)患者血栓事件(TEs)的预测价值。本研究对一项正在进行的前瞻性试验(中国临床试验注册号:ChiCTR1900024094)进行了二次分析,纳入了2012年1月至2020年12月接受心脏MRI检查的HCM无房颤(AF)患者。通过半自动跟踪房室交界与左室中后壁之间的距离,获得左室快速长轴应变。主要终点是TEs的发生,包括缺血性卒中、短暂性缺血性发作和全身性血栓栓塞。采用Cox分析确定LA菌株的预测价值。结果共有714名HCM患者(平均年龄±SD, 50.1岁±14.3岁;男性441人,女性273人;梗阻性HCM, n = 289;根尖型HCM患者144例(中位随访51个月)。28例(3.9%)HCM患者发生TEs,其中60%(17 / 28)没有新发房颤。发生TEs的患者LA储层和导管张力较低(16.2%±7.3 vs 21.8%±8.3,P = .001;(5.9%±3.5 vs 9.7%±5.5,P = 0.01),各组间LA增强菌株无差异。在不同的多变量模型中,即使在调整了年龄、糖尿病和左心室射血分数后,LA储液池和导管应变仍是TEs的独立预测因子(调整后的风险比:储液池应变[每降低5%],1.29-1.34 [95% CI: 1.05, 1.50];导管应变[每降低5%],1.42-1.47 [95% CI: 1.04, 1.67])。结论心脏mri来源的LA储层和导管应变是HCM无房颤患者TEs发生的独立预测因素。关键词:磁共振成像,左心房,心肌病,肥厚性心肌病,血栓栓塞,心脏磁共振ChiCTR1900024094本文有补充材料。©rsna, 2025。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive Value of Left Atrial Strain for Thrombotic Events in Hypertrophic Cardiomyopathy without Atrial Fibrillation.

Purpose To assess the predictive value of left atrial (LA) fast long-axis strain derived from cardiac MRI for thrombotic events (TEs) in individuals with hypertrophic cardiomyopathy (HCM). Materials and Methods This secondary analysis of an ongoing prospective trial (Chinese Clinical Trial Registry: ChiCTR1900024094) included consecutive participants with HCM without atrial fibrillation (AF) who underwent cardiac MRI from January 2012 to December 2020. The LA fast long-axis strain was obtained by semiautomatically tracking the distance between the atrioventricular junction and the midposterior LA wall. The primary end point was the occurrence of TEs, including ischemic stroke, transient ischemic attack, and systemic thromboembolism. The predictive value of LA strain was determined with Cox analysis. Results Overall, 714 participants with HCM (mean age ± SD, 50.1 years ± 14.3; 441 men, 273 women; obstructive HCM, n = 289; apical HCM, n = 144) were included (median follow-up: 51 months). Twenty-eight (3.9%) participants with HCM experienced TEs, 60% (17 of 28) of whom had no new-onset AF. Those who experienced TEs had lower LA reservoir and conduit strains (16.2% ± 7.3 vs 21.8% ± 8.3, P = .001; 5.9% ± 3.5 vs 9.7% ± 5.5, P = .01, respectively), with no evidence of a difference in LA booster strain between groups. LA reservoir and conduit strain were independent predictors of TEs in different multivariable models, even after adjusting for age, diabetes, and left ventricular ejection fraction (adjusted hazard ratios: reservoir strain [per 5% decrease], 1.29-1.34 [95% CI: 1.05, 1.50]; conduit strain [per 5% decrease], 1.42-1.47 [95% CI: 1.04, 1.67]). Conclusion Cardiac MRI-derived LA reservoir and conduit strain were independent predictors for the occurrence of TEs in individuals with HCM without AF. Keywords: MR-Imaging, Left Atrium, Cardiomyopathies, Hypertrophic Cardiomyopathy, Thromboembolism, Cardiac Magnetic Resonance Chinese Clinical Trial Registry no. ChiCTR1900024094 Supplemental material is available for this article. © RSNA, 2025.

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