<b><i>Background:</i></b> Chronic endurance exercise training elicits desirable physiological adaptations in the cardiovascular system. The volume of exercise training required to generate healthy adaptations is unclear. This study assessed the effects of differing exercise training levels on arterial stiffness, compliance, and autonomic function. <b><i>Methods:</i></b> Eighty healthy adults (38.5 ± 9.7 years; 44% female) defined as endurance-trained (ET, <i>n</i> = 29), normally active (NA, <i>n</i> = 27), or inactive (IN, <i>n</i> = 24) participated. Cardiovascular markers, including hemodynamics, large arterial compliance and small arterial compliance (LAC and SAC), carotid-femoral pulse wave velocity (PWV), and spontaneous baroreceptor sensitivity (BRS) were assessed. <b><i>Results:</i></b> ET showed significantly greater LAC values (21.4 ± 6.5) than NA (16.9 ± 2.5; <i>p</i> = 0.002) and IN (14.7 ± 3.2 mL × mm Hg × 10; <i>p</i> = 0.028). Values for SAC and BRS were significantly higher in ET than IN (<i>p</i> < 0.001 and <i>p</i> = 0.028, respectively), but not NA. Compared to IN, PWV values for ET and NA were significantly lower (<i>p</i> < 0.003). After adjusting for covariates (age, sex, and SBP), significant associations with cardiovascular fitness status were noted for all markers but BRS. <b><i>Conclusion:</i></b> Endurance exercise increases LAC likely due to high-volume training; however, lower volumes of physical activity may be sufficient to positively benefit vascular health overall.
Background: Aerobic capacity as measured by peak oxygen uptake (VO2peak), is related to functional capacity and is a strong independent predictor of all-cause and disease-specific mortality. Lifelong exercise is associated with reduced central arterial and ventricular stiffness, potential mechanisms that may underpin cardiovascular health benefits as a result of endurance training. The purpose of this study was to evaluate sex-specific ventricular-vascular interactions associated with VO2peak in healthy males and females. Methods: Sixty-eight males and females (35 10 years) characterized as recreational exercisers to highly trained endurance athletes, and free of chronic disease underwent a cycle ergometer test to exhaustion to assess aerobic capacity (VO2peak). Resting arterial compliance and echocardiographic evaluation of left ventricular (LV) function were measured. Results: VO2peak was similar between groups (54 6 vs. 50 7). LV mass indexed to body surface area (LVMI) was higher (110 20 vs. 94 18, p=0.001) and longitudinal diastolic strain rate was lower (1.6 0.3 vs. 1.4 0.2, p=0.005) in males. Linear regression analysis revealed LVMI and longitudinal diastolic strain rate were significantly associated with VO2peak (r2=0.32, p=0.001) in males, while in females LVMI and large artery compliance were the key factors influencing VO2peak (r2=0.61, p<0.001). Conclusion: These findings reveal that in females much of the variance in VO2peak can be attributed to ventricular and vascular adaptations, whereas in males, cardiac factors of structure and function accounted for the majority of this variance. The substantive central vascular adaptations to exercise observed in females in this study further validates engagement in endurance training to prevent age-related arterial stiffening in women.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.