超声心动图测量的心脏微观结构变化可确定心力衰竭的性别特异性风险

Alan Kwan, Emmanuella Demosthenes, Gerran Salto, David Ouyang, Trevor Nguyen, Chike C Nwabuo, Eric Luong, Amy Hoang, Ewa Osypiuk, Plamen Stantchev, Elizabeth H Kim, Pranoti Hiremath, Debiao Li, Ramachandran Vasan, Vanessa Xanthakis, Susan Cheng
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引用次数: 0

摘要

目的建立基于心脏宏观结构重构的心衰(HF)风险临床前影像学评估。鉴于微结构改变也可能影响心衰风险,尤其是女性,我们研究了微结构改变与心衰事件之间的关系。方法:我们研究了Framingham后代研究中基线无心血管疾病的N=2511名成年参与者(平均年龄65.7±8.8岁,56%为女性)。基于高频谱信号强度系数(HS-SIC),我们采用超声心动图纹理分析来量化微结构改变。我们在考虑传统HF危险因素和宏观结构改变的性别池和性别特异性Cox模型中检查了其与HF事件的关系。结果在7.4±1.7年的时间内共观察到94例HF新发病例。HS-SIC较高的个体发生HF的风险增加(HS-SIC的HR为1.67 / 1-SD, 95% CI为1.31 ~ 2.13;p < 0.0001)。调整年龄和抗高血压药物使用后,这种关联在女性中显著(p=0.02),而在男性中不显著(p=0.78)。对传统危险因素(包括体重指数、总/高密度脂蛋白胆固醇、血压特征、糖尿病和吸烟)进行调整后,女性的相关性减弱(HR 1.30, p=0.07), HS-SIC对大多数这些危险因素有中介作用。然而,除了这些危险因素外,在调整相对壁厚(代表宏观结构改变)后,HS-SIC与女性HF的关联仍然显著(HR 1.47, p=0.02)。结论:心脏微结构改变与心衰风险升高相关,尤其是女性。显微结构改变可以识别个体从危险因素发展到临床心衰的性别特异性途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac microstructural alterations measured by echocardiography identify sex-specific risk for heart failure.

Objective: Established preclinical imaging assessments of heart failure (HF) risk are based on macrostructural cardiac remodelling. Given that microstructural alterations may also influence HF risk, particularly in women, we examined associations between microstructural alterations and incident HF.

Methods: We studied N=2511 adult participants (mean age 65.7±8.8 years, 56% women) of the Framingham Offspring Study who were free of cardiovascular disease at baseline. We employed texture analysis of echocardiography to quantify microstructural alteration, based on the high spectrum signal intensity coefficient (HS-SIC). We examined its relations to incident HF in sex-pooled and sex-specific Cox models accounting for traditional HF risk factors and macrostructural alterations.

Results: We observed 94 new HF events over 7.4±1.7 years. Individuals with higher HS-SIC had increased risk for incident HF (HR 1.67 per 1-SD in HS-SIC, 95% CI 1.31 to 2.13; p<0.0001). Adjusting for age and antihypertensive medication use, this association was significant in women (p=0.02) but not men (p=0.78). Adjusting for traditional risk factors (including body mass index, total/high-density lipoprotein cholesterol, blood pressure traits, diabetes and smoking) attenuated the association in women (HR 1.30, p=0.07), with mediation of HF risk by the HS-SIC seen for a majority of these risk factors. However, the HS-SIC association with HF in women remained significant after adjusting for relative wall thickness (representing macrostructure alteration) in addition to these risk factors (HR 1.47, p=0.02).

Conclusions: Cardiac microstructural alterations are associated with elevated risk for HF, particularly in women. Microstructural alteration may identify sex-specific pathways by which individuals progress from risk factors to clinical HF.

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