The influence of maturation on exercise‐induced cardiac remodelling and haematological adaptation
Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography),...
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Published in | The Journal of physiology Vol. 600; no. 3; pp. 583 - 601 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.02.2022
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Abstract | Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ in endurance‐trained and untrained boys (n = 42, age = 9.0–17.1 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0–17.7 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2–17.0 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0–17.6 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre‐ or post‐peak height velocity (PHV). Pre‐PHV, only a larger LV end‐diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post‐PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre‐PHV, EDV (R2adj = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R2adj = 0.317, P = 0.002) in girls partially accounted for the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$. Post‐PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R2adj = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R2adj = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post‐PHV, with evidence for a greater role of central components for oxygen delivery.
Key points
It has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty.
We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance‐trained versus untrained, pre‐ and post‐peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption.
Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training‐related differences in LV morphology are evident in pre‐PHV children, with haematological differences also observed between pre‐PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post‐PHV.
Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$) in children that are much stronger post‐PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty.
figure legend Schematic diagram depicting cardiac structural and haematological differences between trained and untrained boys and girls, pre‐peak height velocity (PHV) and post‐PHV alongside cardiac and haematological variables contributions to the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$. Cardiac and haematological variables are greater in trained versus untrained pre‐pubertal children, and a greater number and magnitude of differences are observed post‐PHV. These variables provide significant predictive models for maximal oxygen consumption in children and are much stronger post‐PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty. |
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AbstractList | Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption ( V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ ), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ in endurance-trained and untrained boys (n = 42, age = 9.0-17.1 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0-17.7 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2-17.0 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0-17.6 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre- or post-peak height velocity (PHV). Pre-PHV, only a larger LV end-diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post-PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre-PHV, EDV (R2adj = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R2adj = 0.317, P = 0.002) in girls partially accounted for the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ . Post-PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R2adj = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R2adj = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post-PHV, with evidence for a greater role of central components for oxygen delivery. KEY POINTS: It has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty. We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance-trained versus untrained, pre- and post-peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption. Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training-related differences in LV morphology are evident in pre-PHV children, with haematological differences also observed between pre-PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post-PHV. Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption ( V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ ) in children that are much stronger post-PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty.Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption ( V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ ), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ in endurance-trained and untrained boys (n = 42, age = 9.0-17.1 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0-17.7 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2-17.0 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0-17.6 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre- or post-peak height velocity (PHV). Pre-PHV, only a larger LV end-diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post-PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre-PHV, EDV (R2adj = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R2adj = 0.317, P = 0.002) in girls partially accounted for the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ . Post-PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R2adj = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R2adj = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post-PHV, with evidence for a greater role of central components for oxygen delivery. KEY POINTS: It has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty. We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance-trained versus untrained, pre- and post-peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption. Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training-related differences in LV morphology are evident in pre-PHV children, with haematological differences also observed between pre-PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post-PHV. Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption ( V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ ) in children that are much stronger post-PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty. Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption ( ), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and in endurance-trained and untrained boys (n = 42, age = 9.0-17.1 years, = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0-17.7 years, = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2-17.0 years, = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0-17.6 years, = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre- or post-peak height velocity (PHV). Pre-PHV, only a larger LV end-diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post-PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre-PHV, EDV (R = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R = 0.317, P = 0.002) in girls partially accounted for the variance in . Post-PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post-PHV, with evidence for a greater role of central components for oxygen delivery. KEY POINTS: It has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty. We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance-trained versus untrained, pre- and post-peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption. Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training-related differences in LV morphology are evident in pre-PHV children, with haematological differences also observed between pre-PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post-PHV. Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption ( ) in children that are much stronger post-PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in before puberty. Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ in endurance‐trained and untrained boys (n = 42, age = 9.0–17.1 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0–17.7 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2–17.0 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0–17.6 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre‐ or post‐peak height velocity (PHV). Pre‐PHV, only a larger LV end‐diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post‐PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre‐PHV, EDV (R2adj = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R2adj = 0.317, P = 0.002) in girls partially accounted for the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$. Post‐PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R2adj = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R2adj = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post‐PHV, with evidence for a greater role of central components for oxygen delivery.Key pointsIt has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty.We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance‐trained versus untrained, pre‐ and post‐peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption.Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training‐related differences in LV morphology are evident in pre‐PHV children, with haematological differences also observed between pre‐PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post‐PHV.Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$) in children that are much stronger post‐PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty. Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$), and such adaptations may be augmented following puberty. Therefore, we compared left ventricular (LV) morphology (echocardiography), blood volume, haemoglobin (Hb) mass (CO rebreathing) and V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ in endurance‐trained and untrained boys (n = 42, age = 9.0–17.1 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 61.6 ± 7.2 ml/kg/min, and n = 31, age = 8.0–17.7 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 46.5 ± 6.1 ml/kg/min, respectively) and girls (n = 45, age = 8.2–17.0 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 51.4 ± 5.7 ml/kg/min, and n = 36, age = 8.0–17.6 years, V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ = 39.8 ± 5.7 ml/kg/min, respectively). Pubertal stage was estimated via maturity offset, with participants classified as pre‐ or post‐peak height velocity (PHV). Pre‐PHV, only a larger LV end‐diastolic volume/lean body mass (EDV/LBM) for trained boys (+0.28 ml/kg LBM, P = 0.007) and a higher Hb mass/LBM for trained girls (+1.65 g/kg LBM, P = 0.007) were evident compared to untrained controls. Post‐PHV, LV mass/LBM (boys: +0.50 g/kg LBM, P = 0.0003; girls: +0.35 g/kg LBM, P = 0.003), EDV/LBM (boys: +0.35 ml/kg LBM, P < 0.0001; girls: +0.31 ml/kg LBM, P = 0.0004), blood volume/LBM (boys: +12.47 ml/kg LBM, P = 0.004; girls: +13.48 ml/kg LBM, P = 0.0002.) and Hb mass/LBM (boys: +1.29 g/kg LBM, P = 0.015; girls: +1.47 g/kg LBM, P = 0.002) were all greater in trained versus untrained groups. Pre‐PHV, EDV (R2adj = 0.224, P = 0.001) in boys, and Hb mass and interventricular septal thickness (R2adj = 0.317, P = 0.002) in girls partially accounted for the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$. Post‐PHV, stronger predictive models were evident via the inclusion of LV wall thickness and EDV in boys (R2adj = 0.608, P < 0.0001), and posterior wall thickness and Hb mass in girls (R2adj = 0.490, P < 0.0001). In conclusion, cardiovascular adaptation to exercise training is more pronounced post‐PHV, with evidence for a greater role of central components for oxygen delivery. Key points It has long been hypothesised that cardiovascular adaptation to endurance training is augmented following puberty. We investigated whether differences in cardiac and haematological variables exist, and to what extent, between endurance‐trained versus untrained, pre‐ and post‐peak height velocity (PHV) children, and how these central factors relate to maximal oxygen consumption. Using echocardiography to quantify left ventricular (LV) morphology and carbon monoxide rebreathing to determine blood volume and haemoglobin mass, we identified that training‐related differences in LV morphology are evident in pre‐PHV children, with haematological differences also observed between pre‐PHV girls. However, the breadth and magnitude of cardiovascular remodelling was more pronounced post‐PHV. Cardiac and haematological measures provide significant predictive models for maximal oxygen consumption (V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$) in children that are much stronger post‐PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty. figure legend Schematic diagram depicting cardiac structural and haematological differences between trained and untrained boys and girls, pre‐peak height velocity (PHV) and post‐PHV alongside cardiac and haematological variables contributions to the variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$. Cardiac and haematological variables are greater in trained versus untrained pre‐pubertal children, and a greater number and magnitude of differences are observed post‐PHV. These variables provide significant predictive models for maximal oxygen consumption in children and are much stronger post‐PHV, suggesting that other important determinants within the oxygen transport chain could account for the majority of variance in V̇O2max${\dot{V}_{{{\rm{O}}_{\rm{2}}}{\rm{max}}}$ before puberty. |
Author | Talbot, Jack S. Mackintosh, Kelly A. Lloyd, Rhodri S. Oliver, Jon L. Shave, Rob E. Cooper, Stephen‐Mark Dawkins, Tony G. Baggish, Aaron L. Uzun, Orhan Zaidi, Abbas Perkins, Dean R. Lord, Rachel N. Stembridge, Mike McNarry, Melitta A. |
Author_xml | – sequence: 1 givenname: Dean R. orcidid: 0000-0002-9044-8508 surname: Perkins fullname: Perkins, Dean R. organization: Cardiff Metropolitan University – sequence: 2 givenname: Jack S. orcidid: 0000-0003-0234-1426 surname: Talbot fullname: Talbot, Jack S. organization: Cardiff Metropolitan University – sequence: 3 givenname: Rachel N. orcidid: 0000-0002-5385-7548 surname: Lord fullname: Lord, Rachel N. organization: Cardiff Metropolitan University – sequence: 4 givenname: Tony G. orcidid: 0000-0001-5203-135X surname: Dawkins fullname: Dawkins, Tony G. organization: University of British Columbia Okanagan – sequence: 5 givenname: Aaron L. orcidid: 0000-0003-2042-1489 surname: Baggish fullname: Baggish, Aaron L. organization: Massachusetts General Hospital – sequence: 6 givenname: Abbas surname: Zaidi fullname: Zaidi, Abbas organization: University Hospital of Wales – sequence: 7 givenname: Orhan surname: Uzun fullname: Uzun, Orhan organization: University Hospital of Wales – sequence: 8 givenname: Kelly A. surname: Mackintosh fullname: Mackintosh, Kelly A. organization: Swansea University – sequence: 9 givenname: Melitta A. surname: McNarry fullname: McNarry, Melitta A. organization: Swansea University – sequence: 10 givenname: Stephen‐Mark surname: Cooper fullname: Cooper, Stephen‐Mark organization: Cardiff Metropolitan University – sequence: 11 givenname: Rhodri S. surname: Lloyd fullname: Lloyd, Rhodri S. organization: Waikato Institute of Technology – sequence: 12 givenname: Jon L. surname: Oliver fullname: Oliver, Jon L. organization: AUT University – sequence: 13 givenname: Rob E. surname: Shave fullname: Shave, Rob E. organization: University of British Columbia Okanagan – sequence: 14 givenname: Mike orcidid: 0000-0003-0818-6420 surname: Stembridge fullname: Stembridge, Mike email: mstembridge@cardiffmet.ac.uk organization: Cardiff Metropolitan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34935156$$D View this record in MEDLINE/PubMed |
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Snippet | Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption... Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption ( ), and such adaptations may be augmented... Cardiovascular and haematological adaptations to endurance training facilitate greater maximal oxygen consumption (... |
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SubjectTerms | Adaptation Adaptation, Physiological Adolescent Age Blood Body height Body mass Carbon monoxide Child Children Children & youth Echocardiography endurance training Exercise Female haematology Heart Hematology Hemoglobin Humans Lean body mass Male Maturation Morphology Oxygen Consumption paediatric Physical training Prediction models Puberty Velocity Ventricle Ventricular Remodeling |
Title | The influence of maturation on exercise‐induced cardiac remodelling and haematological adaptation |
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