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Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort

BACKGROUND: The aim of this study was to determine whether physical activity volume and intensity in mid-childhood and early adolescence were associated with cardiometabolic risk factors at 13.5 years. METHODS: Participants were recruited from the Mysore Parthenon observational birth cohort. At ages...

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Autores principales: Kehoe, Sarah H., Krishnaveni, Ghattu V., Veena, Sargoor, Kiran, Krishnarajasagara N., Karat, Samuel C., Dhubey, Asha, Coakley, Patsy, Fall, Caroline H. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918651/
https://www.ncbi.nlm.nih.gov/pubmed/31849318
http://dx.doi.org/10.1186/s12887-019-1855-2
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author Kehoe, Sarah H.
Krishnaveni, Ghattu V.
Veena, Sargoor
Kiran, Krishnarajasagara N.
Karat, Samuel C.
Dhubey, Asha
Coakley, Patsy
Fall, Caroline H. D.
author_facet Kehoe, Sarah H.
Krishnaveni, Ghattu V.
Veena, Sargoor
Kiran, Krishnarajasagara N.
Karat, Samuel C.
Dhubey, Asha
Coakley, Patsy
Fall, Caroline H. D.
author_sort Kehoe, Sarah H.
collection PubMed
description BACKGROUND: The aim of this study was to determine whether physical activity volume and intensity in mid-childhood and early adolescence were associated with cardiometabolic risk factors at 13.5 years. METHODS: Participants were recruited from the Mysore Parthenon observational birth cohort. At ages 6–10 and 11–13 years, volume and intensity of physical activity were assessed using AM7164 or GT1M actigraph accelerometers worn for ≥4 days, and expressed as mean counts per day and percentage time spent in light, moderate and vigorous physical activity according to criteria defined by Evenson et al. At 13.5 years, fasting blood samples were collected; lipids, glucose and insulin concentrations were measured and insulin resistance (HOMA) was calculated. Systolic and diastolic blood pressure were measured at the left arm using a Dinamap (Criticon). Anthropometry and bio-impedance analysis were used to assess body size and composition. Metabolic and anthropometric measures were combined to produce a metabolic syndrome risk score. RESULTS: At 6–10 years, boys and girls respectively spent a median (IQR) of 1.1 (0.5, 2.0) % and 0.8 (0.4, 1.3) % of recorded time vigorously active. At 11–13 years, boys and girls respectively spent a median (IQR) of 0.8 (0.4, 1.7) % and 0.3 (0.1, 0.6) % of time vigorously active. All of the physical activity parameters were positively correlated between the 6–10 year and the 11–13 year measurements indicating that physical activity tracked from childhood to early adolescence. There were no associations between physical activity at 6–10 years and individual 13.5 year risk factors but % time vigorously active was inversely associated with metabolic syndrome score (B = −0.40, 95% CI −0.75, 0.05). Volume of physical activity at 11–13 years was inversely associated with 13.5 year HOMA and fat percentage and vigorous physical activity was associated with HOMA, fat percentage, sum of skinfolds, waist circumference and total: HDL cholesterol ratio. Vigorous physical activity was inversely associated with metabolic syndrome score (B = −0.51, 95% CI −0.94, −0.08). CONCLUSIONS: Volume and intensity of physical activity in early adolescence were negatively associated with metabolic and anthropometric risk factors. Interventions that aim to increase adolescent physical activity, especially vigorous, may prevent cardiometabolic disease in later life.
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spelling pubmed-69186512019-12-20 Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort Kehoe, Sarah H. Krishnaveni, Ghattu V. Veena, Sargoor Kiran, Krishnarajasagara N. Karat, Samuel C. Dhubey, Asha Coakley, Patsy Fall, Caroline H. D. BMC Pediatr Research Article BACKGROUND: The aim of this study was to determine whether physical activity volume and intensity in mid-childhood and early adolescence were associated with cardiometabolic risk factors at 13.5 years. METHODS: Participants were recruited from the Mysore Parthenon observational birth cohort. At ages 6–10 and 11–13 years, volume and intensity of physical activity were assessed using AM7164 or GT1M actigraph accelerometers worn for ≥4 days, and expressed as mean counts per day and percentage time spent in light, moderate and vigorous physical activity according to criteria defined by Evenson et al. At 13.5 years, fasting blood samples were collected; lipids, glucose and insulin concentrations were measured and insulin resistance (HOMA) was calculated. Systolic and diastolic blood pressure were measured at the left arm using a Dinamap (Criticon). Anthropometry and bio-impedance analysis were used to assess body size and composition. Metabolic and anthropometric measures were combined to produce a metabolic syndrome risk score. RESULTS: At 6–10 years, boys and girls respectively spent a median (IQR) of 1.1 (0.5, 2.0) % and 0.8 (0.4, 1.3) % of recorded time vigorously active. At 11–13 years, boys and girls respectively spent a median (IQR) of 0.8 (0.4, 1.7) % and 0.3 (0.1, 0.6) % of time vigorously active. All of the physical activity parameters were positively correlated between the 6–10 year and the 11–13 year measurements indicating that physical activity tracked from childhood to early adolescence. There were no associations between physical activity at 6–10 years and individual 13.5 year risk factors but % time vigorously active was inversely associated with metabolic syndrome score (B = −0.40, 95% CI −0.75, 0.05). Volume of physical activity at 11–13 years was inversely associated with 13.5 year HOMA and fat percentage and vigorous physical activity was associated with HOMA, fat percentage, sum of skinfolds, waist circumference and total: HDL cholesterol ratio. Vigorous physical activity was inversely associated with metabolic syndrome score (B = −0.51, 95% CI −0.94, −0.08). CONCLUSIONS: Volume and intensity of physical activity in early adolescence were negatively associated with metabolic and anthropometric risk factors. Interventions that aim to increase adolescent physical activity, especially vigorous, may prevent cardiometabolic disease in later life. BioMed Central 2019-12-18 /pmc/articles/PMC6918651/ /pubmed/31849318 http://dx.doi.org/10.1186/s12887-019-1855-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kehoe, Sarah H.
Krishnaveni, Ghattu V.
Veena, Sargoor
Kiran, Krishnarajasagara N.
Karat, Samuel C.
Dhubey, Asha
Coakley, Patsy
Fall, Caroline H. D.
Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title_full Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title_fullStr Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title_full_unstemmed Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title_short Active children are less adipose and insulin resistant in early adolescence; evidence from the Mysore Parthenon Cohort
title_sort active children are less adipose and insulin resistant in early adolescence; evidence from the mysore parthenon cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918651/
https://www.ncbi.nlm.nih.gov/pubmed/31849318
http://dx.doi.org/10.1186/s12887-019-1855-2
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