Applied Physiology and Advanced Imaging Lab, University of Texas at Arlington, 655 West Mitchell St, Arlington, TX, 76010, USA.
Barbra Streisand Women's Heart Center, Smidt Heart Institute, Cedars-Sinai Medical Center, 127 S San Vicente Blvd, AHSP Suite A3206, Los Angeles, CA, 90048, USA.
Curr Heart Fail Rep. 2020 Dec;17(6):409-423. doi: 10.1007/s11897-020-00487-7. Epub 2020 Sep 28.
This review summarizes sex-related changes in the heart and vasculature that occur with aging, both in the presence and absence of cardiovascular disease (CVD).
In the presence of CVD risk factors and/or overt CVD, sex-specific changes in the number of cardiomyocytes, extent of the myocardial extracellular matrix, and myocellular hypertrophy promote unique patterns of LV remodeling in men and women. In addition, age- and sex-specific vascular stiffening is also well established, driven by changes in endothelial dysfunction, elastin-collagen content, microvascular dysfunction, and neurohormonal signaling. Together, these changes in LV chamber geometry and morphology, coupled with heightened vascular stiffness, appear to drive both age-related increases in systolic function and declines in diastolic function, particularly in postmenopausal women. Accordingly, estrogen has been implicated as a key mediator, given its direct vasodilating properties, association with nitric oxide excretion, and involvement in myocellular Ca handling, mitochondrial energy production, and oxidative stress. The culmination of the abovementioned sex-specific cardiac and vascular changes across the lifespan provides important insight into heart failure development, particularly of the preserved ejection fraction variety, while offering promise for future preventive strategies and therapeutic approaches.
本综述总结了存在和不存在心血管疾病(CVD)时,衰老过程中心脏和血管的性别相关变化。
在存在 CVD 风险因素和/或明显 CVD 的情况下,心肌细胞数量、心肌细胞外基质的程度以及心肌细胞肥大的性别特异性变化促进了男性和女性 LV 重构的独特模式。此外,年龄和性别特异性血管僵硬也得到了很好的证实,这是由内皮功能障碍、弹性蛋白-胶原含量、微血管功能障碍和神经激素信号的变化驱动的。这些 LV 腔室几何形状和形态的变化,加上血管僵硬程度的增加,似乎共同导致了收缩功能随年龄的增长而增加和舒张功能随年龄的增长而下降,尤其是在绝经后女性中。因此,鉴于雌激素具有直接的血管扩张特性、与一氧化氮排泄的关联以及参与肌细胞 Ca 处理、线粒体能量产生和氧化应激,雌激素被认为是一个关键的调节因子。上述与性别相关的心脏和血管变化在整个生命周期中的综合作用,为心力衰竭的发展提供了重要的见解,特别是对于射血分数保留型心力衰竭,同时为未来的预防策略和治疗方法提供了希望。