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Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014

INTRODUCTION: Large prospective cohort studies show a lower risk of developing type 2 diabetes among adults with higher whole grain consumption. Less is known about the relationship between whole grain consumption and precursors for diabetes risk in adolescents. We examined whether intake of whole g...

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Autores principales: Tester, June M., Stiers, Katharine B., Garber, Andrea, Leung, Cindy W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587298/
https://www.ncbi.nlm.nih.gov/pubmed/33092687
http://dx.doi.org/10.5888/pcd17.190439
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author Tester, June M.
Stiers, Katharine B.
Garber, Andrea
Leung, Cindy W.
author_facet Tester, June M.
Stiers, Katharine B.
Garber, Andrea
Leung, Cindy W.
author_sort Tester, June M.
collection PubMed
description INTRODUCTION: Large prospective cohort studies show a lower risk of developing type 2 diabetes among adults with higher whole grain consumption. Less is known about the relationship between whole grain consumption and precursors for diabetes risk in adolescents. We examined whether intake of whole grains was associated with impaired fasting glucose (IFG) in adolescents. METHODS: We analyzed data on dietary intake from an average of two 24-hour diet recalls from fasting, nondiabetic adolescents aged 12–18 years (N = 2,286) across 5 cycles of the National Health and Nutrition Examination Survey (NHANES 2005–2014). We used logistic regression to calculate the odds of having IFG (100–125 mg/dL) with respect to servings of whole and refined grains, as well as percentage of whole grains, adjusting for sex, age, race/ethnicity, annual household income, obesity, total energy, and diet quality. RESULTS: IFG was present in 17% of participants. After adjusting for covariates, number of servings per day of whole grains was significantly associated with lower odds of IFG, but there was no relationship between IFG and servings of refined grains or percentage of whole grains. Consuming at least 1 ounce-equivalent serving (16 g) of whole grains daily, compared with consuming no whole grains, was associated with a 40% reduction in the adjusted odds of having IFG (adjusted odds ratio = 0.60; 95% CI, 0.38–0.93). CONCLUSION: Analysis of 10 years of national cross-sectional data suggests that US adolescents whose daily diets consist of a minimum threshold amount of whole grains may be less likely to have IFG, a finding that has implications for diabetes prevention in adolescents.
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spelling pubmed-75872982020-10-28 Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014 Tester, June M. Stiers, Katharine B. Garber, Andrea Leung, Cindy W. Prev Chronic Dis Original Research INTRODUCTION: Large prospective cohort studies show a lower risk of developing type 2 diabetes among adults with higher whole grain consumption. Less is known about the relationship between whole grain consumption and precursors for diabetes risk in adolescents. We examined whether intake of whole grains was associated with impaired fasting glucose (IFG) in adolescents. METHODS: We analyzed data on dietary intake from an average of two 24-hour diet recalls from fasting, nondiabetic adolescents aged 12–18 years (N = 2,286) across 5 cycles of the National Health and Nutrition Examination Survey (NHANES 2005–2014). We used logistic regression to calculate the odds of having IFG (100–125 mg/dL) with respect to servings of whole and refined grains, as well as percentage of whole grains, adjusting for sex, age, race/ethnicity, annual household income, obesity, total energy, and diet quality. RESULTS: IFG was present in 17% of participants. After adjusting for covariates, number of servings per day of whole grains was significantly associated with lower odds of IFG, but there was no relationship between IFG and servings of refined grains or percentage of whole grains. Consuming at least 1 ounce-equivalent serving (16 g) of whole grains daily, compared with consuming no whole grains, was associated with a 40% reduction in the adjusted odds of having IFG (adjusted odds ratio = 0.60; 95% CI, 0.38–0.93). CONCLUSION: Analysis of 10 years of national cross-sectional data suggests that US adolescents whose daily diets consist of a minimum threshold amount of whole grains may be less likely to have IFG, a finding that has implications for diabetes prevention in adolescents. Centers for Disease Control and Prevention 2020-10-22 /pmc/articles/PMC7587298/ /pubmed/33092687 http://dx.doi.org/10.5888/pcd17.190439 Text en https://creativecommons.org/licenses/by/4.0/Preventing Chronic Disease is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Original Research
Tester, June M.
Stiers, Katharine B.
Garber, Andrea
Leung, Cindy W.
Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title_full Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title_fullStr Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title_full_unstemmed Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title_short Whole Grain Intake and Impaired Fasting Glucose in Adolescents, National Health and Nutrition Examination Survey, 2005–2014
title_sort whole grain intake and impaired fasting glucose in adolescents, national health and nutrition examination survey, 2005–2014
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587298/
https://www.ncbi.nlm.nih.gov/pubmed/33092687
http://dx.doi.org/10.5888/pcd17.190439
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