Calibration of citrus intake assessed by food frequency questionnaires using urinary proline betaine in an observational study setting

Whether observational study can be employed to establish calibration equations for self-reported dietary intake using food biomarkers is unknown. This study aims to demonstrate the feasibility of obtaining calibration equations based on food biomarkers and 7-d diet records (7DDRs) to correct measure...

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Veröffentlicht in:The American journal of clinical nutrition 2024-07, Vol.120 (1), p.178-186
Hauptverfasser: Hu, Yang, Wang, Molin, Willett, Walter C, Stampfer, Meir, Liang, Liming, Hu, Frank B, Rimm, Eric, Brennan, Lorraine, Sun, Qi
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container_issue 1
container_start_page 178
container_title The American journal of clinical nutrition
container_volume 120
creator Hu, Yang
Wang, Molin
Willett, Walter C
Stampfer, Meir
Liang, Liming
Hu, Frank B
Rimm, Eric
Brennan, Lorraine
Sun, Qi
description Whether observational study can be employed to establish calibration equations for self-reported dietary intake using food biomarkers is unknown. This study aims to demonstrate the feasibility of obtaining calibration equations based on food biomarkers and 7-d diet records (7DDRs) to correct measurement errors of food frequency questionnaires (FFQs) in an observational study setting. The study population consisted of 669 males and 749 females from the Women’s and Men’s Lifestyle Validation Studies. In the training set, the biomarker-predicted intake derived by regressing 7DDR-assessed intake on urinary proline betaine concentration was regressed on the FFQ-assessed intake to obtain the calibration equations. The regression coefficients were applied to the test set to calculate the calibrated FFQ intake. We examined total citrus as well as individual citrus fruits/beverages. Urinary proline betaine was moderately correlated with orange juice intake (Pearson correlation [r] = 0.53 for 7DDR and 0.48 for FFQ) but only weakly correlated with intakes of orange (r = 0.12 for 7DDR and 0.15 for FFQ) and grapefruit (r = 0.14 for 7DDR and 0.09 for FFQ). The FFQ-assessed citrus intake was systematically higher than the 7DDR-assessed intake, and after calibrations, the mean calibrated FFQ measurements were almost identical to 7DDR assessments. In the test set, the mean intake levels from 7DDRs, FFQs, and calibrated FFQs were 62.5, 75.3, and 63.2 g/d for total citrus; 41.6, 42.5, and 41.9 g/d for orange juice; 11.8, 24.3, and 12.3 g/d for oranges; and 8.3, 9.3, and 8.6 g/d for grapefruit, respectively. We observed larger differences between calibrated FFQ and 7DDR assessments at the extreme ends of intake, although, on average, good agreements were observed for all citrus except grapefruit. Our 2-step calibration approach has the potential to be adapted to correct systematic measurement error for other foods/nutrients with established food biomarkers in a cost effective way.
doi_str_mv 10.1016/j.ajcnut.2024.05.011
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This study aims to demonstrate the feasibility of obtaining calibration equations based on food biomarkers and 7-d diet records (7DDRs) to correct measurement errors of food frequency questionnaires (FFQs) in an observational study setting. The study population consisted of 669 males and 749 females from the Women’s and Men’s Lifestyle Validation Studies. In the training set, the biomarker-predicted intake derived by regressing 7DDR-assessed intake on urinary proline betaine concentration was regressed on the FFQ-assessed intake to obtain the calibration equations. The regression coefficients were applied to the test set to calculate the calibrated FFQ intake. We examined total citrus as well as individual citrus fruits/beverages. Urinary proline betaine was moderately correlated with orange juice intake (Pearson correlation [r] = 0.53 for 7DDR and 0.48 for FFQ) but only weakly correlated with intakes of orange (r = 0.12 for 7DDR and 0.15 for FFQ) and grapefruit (r = 0.14 for 7DDR and 0.09 for FFQ). The FFQ-assessed citrus intake was systematically higher than the 7DDR-assessed intake, and after calibrations, the mean calibrated FFQ measurements were almost identical to 7DDR assessments. In the test set, the mean intake levels from 7DDRs, FFQs, and calibrated FFQs were 62.5, 75.3, and 63.2 g/d for total citrus; 41.6, 42.5, and 41.9 g/d for orange juice; 11.8, 24.3, and 12.3 g/d for oranges; and 8.3, 9.3, and 8.6 g/d for grapefruit, respectively. We observed larger differences between calibrated FFQ and 7DDR assessments at the extreme ends of intake, although, on average, good agreements were observed for all citrus except grapefruit. 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This study aims to demonstrate the feasibility of obtaining calibration equations based on food biomarkers and 7-d diet records (7DDRs) to correct measurement errors of food frequency questionnaires (FFQs) in an observational study setting. The study population consisted of 669 males and 749 females from the Women’s and Men’s Lifestyle Validation Studies. In the training set, the biomarker-predicted intake derived by regressing 7DDR-assessed intake on urinary proline betaine concentration was regressed on the FFQ-assessed intake to obtain the calibration equations. The regression coefficients were applied to the test set to calculate the calibrated FFQ intake. We examined total citrus as well as individual citrus fruits/beverages. 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This study aims to demonstrate the feasibility of obtaining calibration equations based on food biomarkers and 7-d diet records (7DDRs) to correct measurement errors of food frequency questionnaires (FFQs) in an observational study setting. The study population consisted of 669 males and 749 females from the Women’s and Men’s Lifestyle Validation Studies. In the training set, the biomarker-predicted intake derived by regressing 7DDR-assessed intake on urinary proline betaine concentration was regressed on the FFQ-assessed intake to obtain the calibration equations. The regression coefficients were applied to the test set to calculate the calibrated FFQ intake. We examined total citrus as well as individual citrus fruits/beverages. Urinary proline betaine was moderately correlated with orange juice intake (Pearson correlation [r] = 0.53 for 7DDR and 0.48 for FFQ) but only weakly correlated with intakes of orange (r = 0.12 for 7DDR and 0.15 for FFQ) and grapefruit (r = 0.14 for 7DDR and 0.09 for FFQ). The FFQ-assessed citrus intake was systematically higher than the 7DDR-assessed intake, and after calibrations, the mean calibrated FFQ measurements were almost identical to 7DDR assessments. In the test set, the mean intake levels from 7DDRs, FFQs, and calibrated FFQs were 62.5, 75.3, and 63.2 g/d for total citrus; 41.6, 42.5, and 41.9 g/d for orange juice; 11.8, 24.3, and 12.3 g/d for oranges; and 8.3, 9.3, and 8.6 g/d for grapefruit, respectively. We observed larger differences between calibrated FFQ and 7DDR assessments at the extreme ends of intake, although, on average, good agreements were observed for all citrus except grapefruit. Our 2-step calibration approach has the potential to be adapted to correct systematic measurement error for other foods/nutrients with established food biomarkers in a cost effective way.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38762186</pmid><doi>10.1016/j.ajcnut.2024.05.011</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0200-5951</orcidid><orcidid>https://orcid.org/0000-0002-8480-1563</orcidid></addata></record>
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ispartof The American journal of clinical nutrition, 2024-07, Vol.120 (1), p.178-186
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subjects Assessments
Betaine
Beverages
Biomarkers
Calibration
calibration analysis
Citrus
Citrus fruits
clinical nutrition
Correlation
cost effectiveness
Diet
diet records
Dietary intake
Error analysis
Error correction
Feasibility studies
Food
Food intake
Fruit juices
Fruits
Grapefruit
grapefruits
lifestyle
measurement error
NMR-spectroscopy
Nutrients
Observational studies
orange juice
Oranges
Population studies
Proline
Questionnaires
Regression coefficients
Test sets
urinary food biomarker
title Calibration of citrus intake assessed by food frequency questionnaires using urinary proline betaine in an observational study setting
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