Zhuohui Gan, Christian J M I Klein, Jaap Keijer, Evert M van Schothorst
{"title":"Quantitative interpretation and modeling of continuous nonprotein respiratory quotients.","authors":"Zhuohui Gan, Christian J M I Klein, Jaap Keijer, Evert M van Schothorst","doi":"10.1152/ajpendo.00459.2024","DOIUrl":null,"url":null,"abstract":"<p><p>The respiratory exchange ratio (RER), which is the ratio of total carbon dioxide produced over total oxygen consumed, serves as a qualitative measure to determine the substrate usage of a particular organism on the whole body level. Quantification of RER by its direct conversion into %glucose- (%G<sub>ox</sub>) and %lipid oxidation (%L<sub>ox</sub>) at a given timepoint can be done by utilizing nonprotein respiratory quotient tables. These tables, however, are limited to specific increments, and intermediate RER values are not covered by these tables. RER data are mostly continuous, which requires faithful interpolation, which we aimed for here. We first determined, statistically and schematically, that linear interpolation would lead to incorrect values. Therefore, we constructed a new mathematical model as an interpolating strategy to translate continuous RER values into correct values of %G<sub>ox</sub> and %L<sub>ox</sub>. We validated our new mathematical model against the original table by Péronnet and Massicotte (<i>Can J Sport Sci</i> 16: 23-29, 1991), against a linear interpolation of these data, as well as against a model based on an exponential approach using a dataset of a nutritional intervention study in mice. This showed that our model outperforms the other methods, providing more accurate data. We conclude that applying our mathematical model will lead to an increase in data quality and offer a very simple, straightforward approach to obtain the best %G<sub>ox</sub> and %L<sub>ox</sub> levels from continuous RER values.<b>NEW & NOTEWORTHY</b> With the here proposed mathematical model, we provide a new tool to convert continuous RER data into more accurate estimations of %G<sub>ox</sub> and %L<sub>ox</sub>. It circumvents the use of nonprotein respiratory quotient tables and thereby aids and simplifies by automating the conversions. The model can further be implemented into software commonly used for indirect calorimetry measurements and thereby provides %G<sub>ox</sub> and %L<sub>ox</sub> data in real-time during a running experiment.</p>","PeriodicalId":7594,"journal":{"name":"American journal of physiology. Endocrinology and metabolism","volume":" ","pages":"E289-E296"},"PeriodicalIF":4.2000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Endocrinology and metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpendo.00459.2024","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/24 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
The respiratory exchange ratio (RER), which is the ratio of total carbon dioxide produced over total oxygen consumed, serves as a qualitative measure to determine the substrate usage of a particular organism on the whole body level. Quantification of RER by its direct conversion into %glucose- (%Gox) and %lipid oxidation (%Lox) at a given timepoint can be done by utilizing nonprotein respiratory quotient tables. These tables, however, are limited to specific increments, and intermediate RER values are not covered by these tables. RER data are mostly continuous, which requires faithful interpolation, which we aimed for here. We first determined, statistically and schematically, that linear interpolation would lead to incorrect values. Therefore, we constructed a new mathematical model as an interpolating strategy to translate continuous RER values into correct values of %Gox and %Lox. We validated our new mathematical model against the original table by Péronnet and Massicotte (Can J Sport Sci 16: 23-29, 1991), against a linear interpolation of these data, as well as against a model based on an exponential approach using a dataset of a nutritional intervention study in mice. This showed that our model outperforms the other methods, providing more accurate data. We conclude that applying our mathematical model will lead to an increase in data quality and offer a very simple, straightforward approach to obtain the best %Gox and %Lox levels from continuous RER values.NEW & NOTEWORTHY With the here proposed mathematical model, we provide a new tool to convert continuous RER data into more accurate estimations of %Gox and %Lox. It circumvents the use of nonprotein respiratory quotient tables and thereby aids and simplifies by automating the conversions. The model can further be implemented into software commonly used for indirect calorimetry measurements and thereby provides %Gox and %Lox data in real-time during a running experiment.
期刊介绍:
The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.