Lower estimates of myocardial perfusion are associated with greater aortic perivascular adipose tissue density in humans independent of aortic stiffness.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Nicholas A Carlini, Matthew P Harber, Bradley S Fleenor
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引用次数: 0

Abstract

Aortic perivascular adipose tissue (aPVAT) density is associated with age-related aortic stiffness in humans and therefore, may contribute to cardiovascular dysfunction. A lower subendocardial viability ratio (SEVR), an estimate of myocardial perfusion, indicates greater cardiovascular disease (CVD) risk and is associated with aortic stiffness in clinical populations. However, the influence of aortic stiffness on the relation between aPVAT density and SEVR/cardiovascular (CV) hemodynamics in apparently healthy adults is unknown. We hypothesize that greater aPVAT density will be associated with lower SEVR and higher CV hemodynamics independent of aortic stiffness. Fourteen (6 males/8 females; mean age, 55.4 ± 5.6 yr; body mass index, 25.5 ± 0.6 kg/m2) adults completed resting measures of myocardial perfusion (SEVR), CV hemodynamics (pulse wave analysis), aortic stiffness [carotid-femoral pulse wave velocity (cfPWV)], and a computed tomography scan to acquire aPVAT and visceral adipose tissue (VAT) density. Greater aPVAT density (i.e., higher density) was associated with lower SEVR (r = -0.78, P < 0.001) and a higher systolic pressure time integral (r = 0.49, P = 0.03), forward pulse height (r = 0.49, P = 0.03), reflected pulse height (r = 0.55, P = 0.02), ejection duration (r = 0.56, P = 0.02), and augmentation pressure (r = 0.69, P = 0.003), but not with the diastolic pressure time integral (r = -0.22, P = 0.22). VAT density was not associated with SEVR or any CV hemodynamic endpoints (all, P > 0.05). Furthermore, the relation between aPVAT density and SEVR remained after adjusting for aortic stiffness (r = -0.66, P = 0.01) but not age (r = -0.24, P > 0.05). These data provide initial evidence for aPVAT as a novel yet understudied local fat depot contributing to lower myocardial perfusion in apparently healthy adults with aging.NEW & NOTEWORTHY Aortic perivascular adipose tissue (aPVAT) density is associated with aging and aortic stiffness in humans and, therefore, may contribute to lower myocardial perfusion. We demonstrate that greater aPVAT, but not visceral adipose tissue density is associated with lower myocardial perfusion and augmentation pressure independent of aortic stiffness, but not independent of age. These data provide novel evidence for aPVAT as a potential therapeutic target to improve myocardial perfusion and cardiovascular function in humans with aging.

较低的心肌灌注估计值与人体主动脉血管周围脂肪组织密度较高有关,而与主动脉僵硬度无关。
人体主动脉血管周围脂肪组织(aPVAT)密度与年龄相关的主动脉僵化有关,因此可能导致心血管功能障碍。心内膜下心肌活力比(SEVR)是对心肌灌注的估计,心内膜下心肌活力比越低,表明心血管疾病(CVD)风险越大,在临床人群中与主动脉僵化有关。然而,在表面健康的成年人中,主动脉僵硬度对 aPVAT 密度和 SEVR/心血管(CV)血液动力学之间关系的影响尚不清楚。我们假设更大的 aPVAT 密度将与更低的 SEVR 和更高的 CV 血流动力学相关,而与主动脉僵硬度无关。14名(6男/8女,平均年龄(55.4 ± 5.6)岁,体重指数(25.5 ± 0.6 kg/m2)成年人完成了心肌灌注(SEVR)、心血管血液动力学(脉搏波分析)、主动脉僵化(颈动脉-股动脉脉搏波速度[cfPWV])的静息测量,并通过计算机断层扫描获得了aPVAT和内脏脂肪组织(VAT)密度。aPVAT密度越大(即密度越高),SEVR越低(r=-0.78,P0.05)。此外,在调整了主动脉僵硬度(r=-0.66,p=0.01)而非年龄(r=-0.24,p>0.05)后,aPVAT 密度与 SEVR 之间的关系依然存在。这些数据为 aPVAT 提供了初步证据,证明它是一个新的但未被充分研究的局部脂肪库,会导致表面上健康的成年人心肌灌注降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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