TY - JOUR
T1 - Flow-mediated dilation is modified by exercise training status during childhood and adolescence
T2 - preliminary evidence of the youth athlete's artery
AU - Talbot, Jack S.
AU - Perkins, Dean R.
AU - Dawkins, Tony G.
AU - Lord, Rachel N.
AU - Oliver, Jon L.
AU - Lloyd, Rhodri S.
AU - McManus, Ali M
AU - Stembridge, Mike
AU - Pugh, Christopher J.A.
PY - 2024/7/15
Y1 - 2024/7/15
N2 - Chronic exercise training is associated with an "athlete's artery" phenotype in young adults and an attenuated age-related decline in endothelium-dependent arterial function. Adolescence is associated with an influx of sex-specific hormones that may exert divergent effects on endothelial function, but whether training adaptations interact with biological maturation to produce a "youth athlete's artery" has not been explored. We investigated the influence of exercise-training status on endothelium-dependent arterial function during childhood and adolescence. Brachial artery flow-mediated dilation (FMD) was assessed in
n = 102 exercise-trained (males,
n = 25; females,
n = 29) and untrained (males,
n = 23; females,
n = 25) youths, characterized as pre (males,
n = 25; females,
n = 26)- or post (males,
n = 23; females,
n = 28)-predicted age at peak height velocity (PHV). Baseline brachial artery diameter was larger in post- compared with pre-PHV youths (
P ≤ 0.001), males compared with females (
P ≤ 0.001), and trained compared with untrained youths (3.26 ± 0.51 vs. 3.11 ± 0.42 mm;
P = 0.041). Brachial FMD was similar in pre- and post-PHV youths (
P = 0.298), and males and females (
P = 0.946). However, exercise-trained youths demonstrated higher FMD when compared with untrained counterparts (5.3 ± 3.3 vs. 3.0 ± 2.6%;
P ≤ 0.001). Furthermore, brachial artery diameter (
r
2 = 0.142;
P = 0.007 vs.
r
2 = 0.004;
P = 0.652) and FMD (
r
2 = 0.138;
P = 0.008 vs.
r
2 = 0.003;
P = 0.706) were positively associated with cardiorespiratory fitness in post-, but not pre-PHV youths, respectively. Collectively, our data indicate that exercise training is associated with brachial artery remodeling and enhanced endothelial function during youth. However, arterial remodeling and endothelium-dependent function are only associated with elevated cardiorespiratory fitness during later stages of adolescence.
NEW & NOTEWORTHY We report preliminary evidence of the "youth athlete's artery," characterized by training-related arterial remodeling and elevated endothelium-dependent arterial function in children and adolescents. However, training-related adaptations in brachial artery diameter and flow-mediated dilation (FMD) were associated with cardiorespiratory fitness in adolescents, but not in children. Our findings indicate that endothelium-dependent arterial function is modifiable with chronic exercise training during childhood, but the association between FMD and elevated cardiorespiratory fitness is only apparent during later stages of adolescence.
AB - Chronic exercise training is associated with an "athlete's artery" phenotype in young adults and an attenuated age-related decline in endothelium-dependent arterial function. Adolescence is associated with an influx of sex-specific hormones that may exert divergent effects on endothelial function, but whether training adaptations interact with biological maturation to produce a "youth athlete's artery" has not been explored. We investigated the influence of exercise-training status on endothelium-dependent arterial function during childhood and adolescence. Brachial artery flow-mediated dilation (FMD) was assessed in
n = 102 exercise-trained (males,
n = 25; females,
n = 29) and untrained (males,
n = 23; females,
n = 25) youths, characterized as pre (males,
n = 25; females,
n = 26)- or post (males,
n = 23; females,
n = 28)-predicted age at peak height velocity (PHV). Baseline brachial artery diameter was larger in post- compared with pre-PHV youths (
P ≤ 0.001), males compared with females (
P ≤ 0.001), and trained compared with untrained youths (3.26 ± 0.51 vs. 3.11 ± 0.42 mm;
P = 0.041). Brachial FMD was similar in pre- and post-PHV youths (
P = 0.298), and males and females (
P = 0.946). However, exercise-trained youths demonstrated higher FMD when compared with untrained counterparts (5.3 ± 3.3 vs. 3.0 ± 2.6%;
P ≤ 0.001). Furthermore, brachial artery diameter (
r
2 = 0.142;
P = 0.007 vs.
r
2 = 0.004;
P = 0.652) and FMD (
r
2 = 0.138;
P = 0.008 vs.
r
2 = 0.003;
P = 0.706) were positively associated with cardiorespiratory fitness in post-, but not pre-PHV youths, respectively. Collectively, our data indicate that exercise training is associated with brachial artery remodeling and enhanced endothelial function during youth. However, arterial remodeling and endothelium-dependent function are only associated with elevated cardiorespiratory fitness during later stages of adolescence.
NEW & NOTEWORTHY We report preliminary evidence of the "youth athlete's artery," characterized by training-related arterial remodeling and elevated endothelium-dependent arterial function in children and adolescents. However, training-related adaptations in brachial artery diameter and flow-mediated dilation (FMD) were associated with cardiorespiratory fitness in adolescents, but not in children. Our findings indicate that endothelium-dependent arterial function is modifiable with chronic exercise training during childhood, but the association between FMD and elevated cardiorespiratory fitness is only apparent during later stages of adolescence.
KW - Adaptation, Physiological
KW - Adolescent
KW - Age Factors
KW - Athletes
KW - Brachial Artery/physiology
KW - Child
KW - Endothelium, Vascular/physiology
KW - Exercise/physiology
KW - Female
KW - Humans
KW - Male
KW - Regional Blood Flow
KW - Vasodilation
UR - http://www.scopus.com/inward/record.url?scp=85199124612&partnerID=8YFLogxK
U2 - 10.1152/ajpheart.00287.2024
DO - 10.1152/ajpheart.00287.2024
M3 - Article
C2 - 38847760
SN - 0363-6135
VL - 327
SP - H331-H339
JO - American Journal of Physiology - Heart and Circulatory Physiology
JF - American Journal of Physiology - Heart and Circulatory Physiology
IS - 2
ER -