Cargando…

Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk

OBJECTIVE: To evaluate and compare ratio and allometric scaling models of maximal oxygen consumption (VO(2)max) for different body size measurements in relation to cardiovascular disease (CVD) incidence and all-cause mortality. METHODS: 316 116 individuals participating in occupational health screen...

Descripción completa

Detalles Bibliográficos
Autores principales: Salier Eriksson, Jane, Ekblom, Björn, Andersson, Gunnar, Wallin, Peter, Ekblom-Bak, Elin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849897/
https://www.ncbi.nlm.nih.gov/pubmed/33537151
http://dx.doi.org/10.1136/bmjsem-2020-000854
_version_ 1783645376317751296
author Salier Eriksson, Jane
Ekblom, Björn
Andersson, Gunnar
Wallin, Peter
Ekblom-Bak, Elin
author_facet Salier Eriksson, Jane
Ekblom, Björn
Andersson, Gunnar
Wallin, Peter
Ekblom-Bak, Elin
author_sort Salier Eriksson, Jane
collection PubMed
description OBJECTIVE: To evaluate and compare ratio and allometric scaling models of maximal oxygen consumption (VO(2)max) for different body size measurements in relation to cardiovascular disease (CVD) incidence and all-cause mortality. METHODS: 316 116 individuals participating in occupational health screenings, initially free from CVD, were included. VO(2)max was estimated using submaximal cycle test. Height, body mass and waist circumference (WC) were assessed, and eight different scaling models (two evaluated in a restricted sample with WC data) were derived. Participants were followed in national registers for first-time CVD event or all-cause mortality from their health screening to first CVD event, death or 31 December 2015. RESULTS: Increasing deciles of VO(2)max showed lower CVD risk and all-cause mortality for all six models in the full sample (p<0.001) as well as with increasing quintiles in the restricted sample (eight models) (p<0.001). For CVD risk and all-cause mortality, significantly weaker associations with increasing deciles for models 1 (L·min(−1)) and 5 (mL·min(−1)·height(−2)) were seen compared with model 2 (mL·min(−1)·kg(−1)), (CVD, p<0.00001; p<0.00001: all-cause mortality, p=0.008; p=0.001) and in some subgroups. For CVD, model 6 (mL·min(−1)·(kg(1)·height(−1))(−1)) had a stronger association compared with model 2 (p<0.00001) and in some subgroups. In the restricted sample, trends for significantly stronger associations for models including WC compared with model 2 were seen in women for both CVD and all-cause mortality, and those under 50 for CVD. CONCLUSION: In association to CVD and all-cause mortality, only small differences were found between ratio scaling and allometric scaling models where body dimensions were added, with some stronger associations when adding WC in the models.
format Online
Article
Text
id pubmed-7849897
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-78498972021-02-02 Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk Salier Eriksson, Jane Ekblom, Björn Andersson, Gunnar Wallin, Peter Ekblom-Bak, Elin BMJ Open Sport Exerc Med Original Research OBJECTIVE: To evaluate and compare ratio and allometric scaling models of maximal oxygen consumption (VO(2)max) for different body size measurements in relation to cardiovascular disease (CVD) incidence and all-cause mortality. METHODS: 316 116 individuals participating in occupational health screenings, initially free from CVD, were included. VO(2)max was estimated using submaximal cycle test. Height, body mass and waist circumference (WC) were assessed, and eight different scaling models (two evaluated in a restricted sample with WC data) were derived. Participants were followed in national registers for first-time CVD event or all-cause mortality from their health screening to first CVD event, death or 31 December 2015. RESULTS: Increasing deciles of VO(2)max showed lower CVD risk and all-cause mortality for all six models in the full sample (p<0.001) as well as with increasing quintiles in the restricted sample (eight models) (p<0.001). For CVD risk and all-cause mortality, significantly weaker associations with increasing deciles for models 1 (L·min(−1)) and 5 (mL·min(−1)·height(−2)) were seen compared with model 2 (mL·min(−1)·kg(−1)), (CVD, p<0.00001; p<0.00001: all-cause mortality, p=0.008; p=0.001) and in some subgroups. For CVD, model 6 (mL·min(−1)·(kg(1)·height(−1))(−1)) had a stronger association compared with model 2 (p<0.00001) and in some subgroups. In the restricted sample, trends for significantly stronger associations for models including WC compared with model 2 were seen in women for both CVD and all-cause mortality, and those under 50 for CVD. CONCLUSION: In association to CVD and all-cause mortality, only small differences were found between ratio scaling and allometric scaling models where body dimensions were added, with some stronger associations when adding WC in the models. BMJ Publishing Group 2021-01-29 /pmc/articles/PMC7849897/ /pubmed/33537151 http://dx.doi.org/10.1136/bmjsem-2020-000854 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Research
Salier Eriksson, Jane
Ekblom, Björn
Andersson, Gunnar
Wallin, Peter
Ekblom-Bak, Elin
Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title_full Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title_fullStr Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title_full_unstemmed Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title_short Scaling VO(2)max to body size differences to evaluate associations to CVD incidence and all-cause mortality risk
title_sort scaling vo(2)max to body size differences to evaluate associations to cvd incidence and all-cause mortality risk
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849897/
https://www.ncbi.nlm.nih.gov/pubmed/33537151
http://dx.doi.org/10.1136/bmjsem-2020-000854
work_keys_str_mv AT saliererikssonjane scalingvo2maxtobodysizedifferencestoevaluateassociationstocvdincidenceandallcausemortalityrisk
AT ekblombjorn scalingvo2maxtobodysizedifferencestoevaluateassociationstocvdincidenceandallcausemortalityrisk
AT anderssongunnar scalingvo2maxtobodysizedifferencestoevaluateassociationstocvdincidenceandallcausemortalityrisk
AT wallinpeter scalingvo2maxtobodysizedifferencestoevaluateassociationstocvdincidenceandallcausemortalityrisk
AT ekblombakelin scalingvo2maxtobodysizedifferencestoevaluateassociationstocvdincidenceandallcausemortalityrisk