Multilevel modeling in food science: A case study on heat-induced ascorbic acid degradation kinetics
Variation in oxidation of ascorbic acid can be well characterized by multilevel modeling. [Display omitted] •Multilevel modeling allows to characterize variability at various levels.•Averaging of results should be avoided because of loss of information.•Experimental variability is a source of inform...
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| Published in | Food research international Vol. 158; p. 111565 |
|---|---|
| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
Elsevier Ltd
01.08.2022
Elsevier |
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| Online Access | Get full text |
| ISSN | 0963-9969 1873-7145 1873-7145 |
| DOI | 10.1016/j.foodres.2022.111565 |
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| Abstract | Variation in oxidation of ascorbic acid can be well characterized by multilevel modeling.
[Display omitted]
•Multilevel modeling allows to characterize variability at various levels.•Averaging of results should be avoided because of loss of information.•Experimental variability is a source of information, not a nuisance.•Oxidation of ascorbic acid leads to highly variable experimental results.•Bayesian regression allows to estimate the order of reaction.
Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that may not be the best practice because valuable information is then lost. Three other ways to analyze repetitions are: (1) each experiment is analyzed on its own (no pooling of data), (2) all experiments are analyzed together in one go (complete pooling), (3) data are analyzed together while allowing for similarities as well as differences in the result (partial pooling). Multilevel modeling uses partial pooling by partitioning variance over more than one level. Level 1 consists of the measurements themselves; higher levels consist of groups or clusters of measurements (repetitions, experiments at various temperatures, at various pH values, etc.) and parameters are analyzed both at the population and at the group/cluster level.
The approach is applied to a case study in which heat-induced isothermal degradation of ascorbic acid was studied with 15 repetitions in an aqueous solution, making it a two-level study. The data were analyzed using averaging and complete pooling, complete pooling without averaging, no-pooling at all, and partial pooling. The kinetic model was established by letting the data decide about the order of the reaction, while this was compared to a model where the order was fixed at 1 (first-order model). Results show that both averaging with complete pooling, as well as complete pooling without averaging, strongly underestimate variation. The no-pooling technique overestimates variation, while partial pooling partitions variation over the levels and thus gives a better impression of the variation involved. The kinetics of ascorbic acid appear to be subject to strong variation when each experiment is considered separately because it is a compound that is very sensitive to all kinds of experimental conditions. With multilevel modeling it appeared to be possible to characterize the uncertainties involved much better than with single level modeling. A Bayesian analysis was performed, in which parameters are allowed to be variable, which is useful because multilevel modeling leads to characterization of variation of parameters. The Bayesian method allows to visualize the posterior distribution of parameters, thereby giving more insight in their behaviour. Also, a Bayesian analysis focuses more strongly on predictive accuracy of models, including multilevel models. The predictive accuracy of 4 models describing the same ascorbic acid data was compared and the multilevel model with reaction order estimated from the data performed by far the best in this regard. The pros and cons of multilevel modeling are discussed and it is concluded that multilevel modeling is to be preferred whenever the data allow to perform such an analysis. |
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| AbstractList | Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that may not be the best practice because valuable information is then lost. Three other ways to analyze repetitions are: (1) each experiment is analyzed on its own (no pooling of data), (2) all experiments are analyzed together in one go (complete pooling), (3) data are analyzed together while allowing for similarities as well as differences in the result (partial pooling). Multilevel modeling uses partial pooling by partitioning variance over more than one level. Level 1 consists of the measurements themselves; higher levels consist of groups or clusters of measurements (repetitions, experiments at various temperatures, at various pH values, etc.) and parameters are analyzed both at the population and at the group/cluster level. The approach is applied to a case study in which heat-induced isothermal degradation of ascorbic acid was studied with 15 repetitions in an aqueous solution, making it a two-level study. The data were analyzed using averaging and complete pooling, complete pooling without averaging, no-pooling at all, and partial pooling. The kinetic model was established by letting the data decide about the order of the reaction, while this was compared to a model where the order was fixed at 1 (first-order model). Results show that both averaging with complete pooling, as well as complete pooling without averaging, strongly underestimate variation. The no-pooling technique overestimates variation, while partial pooling partitions variation over the levels and thus gives a better impression of the variation involved. The kinetics of ascorbic acid appear to be subject to strong variation when each experiment is considered separately because it is a compound that is very sensitive to all kinds of experimental conditions. With multilevel modeling it appeared to be possible to characterize the uncertainties involved much better than with single level modeling. A Bayesian analysis was performed, in which parameters are allowed to be variable, which is useful because multilevel modeling leads to characterization of variation of parameters. The Bayesian method allows to visualize the posterior distribution of parameters, thereby giving more insight in their behaviour. Also, a Bayesian analysis focuses more strongly on predictive accuracy of models, including multilevel models. The predictive accuracy of 4 models describing the same ascorbic acid data was compared and the multilevel model with reaction order estimated from the data performed by far the best in this regard. The pros and cons of multilevel modeling are discussed and it is concluded that multilevel modeling is to be preferred whenever the data allow to perform such an analysis.Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that may not be the best practice because valuable information is then lost. Three other ways to analyze repetitions are: (1) each experiment is analyzed on its own (no pooling of data), (2) all experiments are analyzed together in one go (complete pooling), (3) data are analyzed together while allowing for similarities as well as differences in the result (partial pooling). Multilevel modeling uses partial pooling by partitioning variance over more than one level. Level 1 consists of the measurements themselves; higher levels consist of groups or clusters of measurements (repetitions, experiments at various temperatures, at various pH values, etc.) and parameters are analyzed both at the population and at the group/cluster level. The approach is applied to a case study in which heat-induced isothermal degradation of ascorbic acid was studied with 15 repetitions in an aqueous solution, making it a two-level study. The data were analyzed using averaging and complete pooling, complete pooling without averaging, no-pooling at all, and partial pooling. The kinetic model was established by letting the data decide about the order of the reaction, while this was compared to a model where the order was fixed at 1 (first-order model). Results show that both averaging with complete pooling, as well as complete pooling without averaging, strongly underestimate variation. The no-pooling technique overestimates variation, while partial pooling partitions variation over the levels and thus gives a better impression of the variation involved. The kinetics of ascorbic acid appear to be subject to strong variation when each experiment is considered separately because it is a compound that is very sensitive to all kinds of experimental conditions. With multilevel modeling it appeared to be possible to characterize the uncertainties involved much better than with single level modeling. A Bayesian analysis was performed, in which parameters are allowed to be variable, which is useful because multilevel modeling leads to characterization of variation of parameters. The Bayesian method allows to visualize the posterior distribution of parameters, thereby giving more insight in their behaviour. Also, a Bayesian analysis focuses more strongly on predictive accuracy of models, including multilevel models. The predictive accuracy of 4 models describing the same ascorbic acid data was compared and the multilevel model with reaction order estimated from the data performed by far the best in this regard. The pros and cons of multilevel modeling are discussed and it is concluded that multilevel modeling is to be preferred whenever the data allow to perform such an analysis. Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that may not be the best practice because valuable information is then lost. Three other ways to analyze repetitions are: (1) each experiment is analyzed on its own (no pooling of data), (2) all experiments are analyzed together in one go (complete pooling), (3) data are analyzed together while allowing for similarities as well as differences in the result (partial pooling). Multilevel modeling uses partial pooling by partitioning variance over more than one level. Level 1 consists of the measurements themselves; higher levels consist of groups or clusters of measurements (repetitions, experiments at various temperatures, at various pH values, etc.) and parameters are analyzed both at the population and at the group/cluster level. The approach is applied to a case study in which heat-induced isothermal degradation of ascorbic acid was studied with 15 repetitions in an aqueous solution, making it a two-level study. The data were analyzed using averaging and complete pooling, complete pooling without averaging, no-pooling at all, and partial pooling. The kinetic model was established by letting the data decide about the order of the reaction, while this was compared to a model where the order was fixed at 1 (first-order model). Results show that both averaging with complete pooling, as well as complete pooling without averaging, strongly underestimate variation. The no-pooling technique overestimates variation, while partial pooling partitions variation over the levels and thus gives a better impression of the variation involved. The kinetics of ascorbic acid appear to be subject to strong variation when each experiment is considered separately because it is a compound that is very sensitive to all kinds of experimental conditions. With multilevel modeling it appeared to be possible to characterize the uncertainties involved much better than with single level modeling. A Bayesian analysis was performed, in which parameters are allowed to be variable, which is useful because multilevel modeling leads to characterization of variation of parameters. The Bayesian method allows to visualize the posterior distribution of parameters, thereby giving more insight in their behaviour. Also, a Bayesian analysis focuses more strongly on predictive accuracy of models, including multilevel models. The predictive accuracy of 4 models describing the same ascorbic acid data was compared and the multilevel model with reaction order estimated from the data performed by far the best in this regard. The pros and cons of multilevel modeling are discussed and it is concluded that multilevel modeling is to be preferred whenever the data allow to perform such an analysis. Variation in oxidation of ascorbic acid can be well characterized by multilevel modeling. [Display omitted] •Multilevel modeling allows to characterize variability at various levels.•Averaging of results should be avoided because of loss of information.•Experimental variability is a source of information, not a nuisance.•Oxidation of ascorbic acid leads to highly variable experimental results.•Bayesian regression allows to estimate the order of reaction. Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that may not be the best practice because valuable information is then lost. Three other ways to analyze repetitions are: (1) each experiment is analyzed on its own (no pooling of data), (2) all experiments are analyzed together in one go (complete pooling), (3) data are analyzed together while allowing for similarities as well as differences in the result (partial pooling). Multilevel modeling uses partial pooling by partitioning variance over more than one level. Level 1 consists of the measurements themselves; higher levels consist of groups or clusters of measurements (repetitions, experiments at various temperatures, at various pH values, etc.) and parameters are analyzed both at the population and at the group/cluster level. The approach is applied to a case study in which heat-induced isothermal degradation of ascorbic acid was studied with 15 repetitions in an aqueous solution, making it a two-level study. The data were analyzed using averaging and complete pooling, complete pooling without averaging, no-pooling at all, and partial pooling. The kinetic model was established by letting the data decide about the order of the reaction, while this was compared to a model where the order was fixed at 1 (first-order model). Results show that both averaging with complete pooling, as well as complete pooling without averaging, strongly underestimate variation. The no-pooling technique overestimates variation, while partial pooling partitions variation over the levels and thus gives a better impression of the variation involved. The kinetics of ascorbic acid appear to be subject to strong variation when each experiment is considered separately because it is a compound that is very sensitive to all kinds of experimental conditions. With multilevel modeling it appeared to be possible to characterize the uncertainties involved much better than with single level modeling. A Bayesian analysis was performed, in which parameters are allowed to be variable, which is useful because multilevel modeling leads to characterization of variation of parameters. The Bayesian method allows to visualize the posterior distribution of parameters, thereby giving more insight in their behaviour. Also, a Bayesian analysis focuses more strongly on predictive accuracy of models, including multilevel models. The predictive accuracy of 4 models describing the same ascorbic acid data was compared and the multilevel model with reaction order estimated from the data performed by far the best in this regard. The pros and cons of multilevel modeling are discussed and it is concluded that multilevel modeling is to be preferred whenever the data allow to perform such an analysis. |
| ArticleNumber | 111565 |
| Author | Roux, S. van Boekel, M.A.J.S. |
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| CitedBy_id | crossref_primary_10_3390_antiox13020222 crossref_primary_10_1016_j_compag_2024_109683 crossref_primary_10_1016_j_scienta_2025_114015 crossref_primary_10_1016_j_jfoodeng_2024_112403 crossref_primary_10_1016_j_lwt_2024_116377 crossref_primary_10_3390_app122010416 |
| Cites_doi | 10.1016/j.lwt.2016.08.043 10.18637/jss.v080.i01 10.1007/s11222-016-9696-4 10.1038/s41598-020-59384-7 10.18637/jss.v067.i01 10.32614/RJ-2018-017 10.1007/s00180-020-01045-4 10.1016/j.tifs.2020.02.027 10.18637/jss.v076.i01 10.3390/e19100555 10.1016/j.foodres.2018.01.051 10.1016/j.cej.2018.08.203 10.1371/journal.pbio.2005282 10.3150/16-BEJ810 10.1201/b16018 10.1016/j.foodres.2020.109374 10.3390/foods10112630 10.1201/9780429029608 10.1111/rssa.12378 |
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| Keywords | Multilevel modeling Ascorbic acid Reaction order Heating Data pooling Prediction Bayesian regression Kinetics multilevel modeling ascorbic acid prediction data pooling kinetics reaction order heating |
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•Multilevel modeling allows to characterize... Characterization of variation of experimental results is achieved by repeating experiments. Frequently, results are averaged before data are analysed but that... |
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| SubjectTerms | aqueous solutions Ascorbic acid Bayesian regression Bayesian theory case studies Data pooling Food engineering food research Heating Kinetics Life Sciences Multilevel modeling Prediction Reaction order variance |
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| Title | Multilevel modeling in food science: A case study on heat-induced ascorbic acid degradation kinetics |
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