TY - JOUR
T1 - Predicting cardiometabolic markers in children using tri-ponderal mass index
T2 - A cross-sectional study
AU - Ashley-Martin, Jillian
AU - Ensenauer, Regina
AU - Maguire, Bryan
AU - Kuhle, Stefan
N1 - Funding Information:
Acknowledgements The authors thank Dr Tim Cole (University College London Great Ormond Street Institute of Child Health) for his valuable suggestions on the manuscript. The analysis presented in this paper was conducted at the Atlantic Research Data Centre, which is part of the Canadian Research Data Centre Network (CRDCN). The services and activities provided by the Atlantic Research Data Centre are made possible by the financial or in-kind support of the Social Sciences and Humanities Research Council, the Canadian Institutes of Health Research.
Publisher Copyright:
© Author(s) (or their employer(s)) 2019.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Objective To model the development of the tri-ponderal mass index (TMI, kg/m 3) throughout childhood and adolescence and to compare the utility of the TMI with that of the body mass index (BMI, kg/m 2) to predict cardiometabolic risk in a population-based sample of Canadian children and youth. Methods We used data from the Canadian Health Measures Survey to model TMI from 6 to 19 years of age. Percentile curves were developed using the LMS method. Logistic regression was used to predict abnormal levels of cardiometabolic markers; predictive accuracy was assessed using the area under the ROC curve (AUC). Results Mean TMI was relatively stable from ages 6 to 19 years for both sexes, but variability increased with age. There was no notable difference in AUC values for prediction models based on BMI z-score compared with TMI for any of the outcomes. For both BMI z-score and TMI, prediction accuracy was good for homeostasis model assessment insulin resistance and having ≥3 abnormal tests (AUC>0.80), fair for C-reactive protein and poor for the remainder of the outcomes. Conclusions The use of a single sex-specific TMI cut-off for overweight or obesity is hampered by the increasing variability of the measure with age. Weight-for-height indices likely have only limited ability to predict cardiometabolic marker levels, and changing the scaling power of height is unlikely to improve predictive accuracy.
AB - Objective To model the development of the tri-ponderal mass index (TMI, kg/m 3) throughout childhood and adolescence and to compare the utility of the TMI with that of the body mass index (BMI, kg/m 2) to predict cardiometabolic risk in a population-based sample of Canadian children and youth. Methods We used data from the Canadian Health Measures Survey to model TMI from 6 to 19 years of age. Percentile curves were developed using the LMS method. Logistic regression was used to predict abnormal levels of cardiometabolic markers; predictive accuracy was assessed using the area under the ROC curve (AUC). Results Mean TMI was relatively stable from ages 6 to 19 years for both sexes, but variability increased with age. There was no notable difference in AUC values for prediction models based on BMI z-score compared with TMI for any of the outcomes. For both BMI z-score and TMI, prediction accuracy was good for homeostasis model assessment insulin resistance and having ≥3 abnormal tests (AUC>0.80), fair for C-reactive protein and poor for the remainder of the outcomes. Conclusions The use of a single sex-specific TMI cut-off for overweight or obesity is hampered by the increasing variability of the measure with age. Weight-for-height indices likely have only limited ability to predict cardiometabolic marker levels, and changing the scaling power of height is unlikely to improve predictive accuracy.
KW - epidemiology
KW - growth
KW - metabolic
KW - obesity
KW - statistics
UR - http://www.scopus.com/inward/record.url?scp=85060201462&partnerID=8YFLogxK
U2 - 10.1136/archdischild-2018-316028
DO - 10.1136/archdischild-2018-316028
M3 - Article
C2 - 30655268
AN - SCOPUS:85060201462
SN - 0003-9888
VL - 104
SP - 577
EP - 582
JO - Archives of Disease in Childhood
JF - Archives of Disease in Childhood
IS - 6
ER -