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Associations between dietary carotenoid intakes and the risk of depressive symptoms

BACKGROUND: Dietary factors play an important role in the development of depressive symptoms. Carotenoids have effective antioxidant and anti-inflammatory effects, but few studies have explored the associations between dietary carotenoid intake and depressive symptoms. OBJECTIVE: To evaluate the ass...

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Autores principales: Ge, Honghan, Yang, Tingting, Sun, Jing, Zhang, Dongfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Open Academia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778430/
https://www.ncbi.nlm.nih.gov/pubmed/33447180
http://dx.doi.org/10.29219/fnr.v64.3920
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author Ge, Honghan
Yang, Tingting
Sun, Jing
Zhang, Dongfeng
author_facet Ge, Honghan
Yang, Tingting
Sun, Jing
Zhang, Dongfeng
author_sort Ge, Honghan
collection PubMed
description BACKGROUND: Dietary factors play an important role in the development of depressive symptoms. Carotenoids have effective antioxidant and anti-inflammatory effects, but few studies have explored the associations between dietary carotenoid intake and depressive symptoms. OBJECTIVE: To evaluate the association between dietary carotenoid intake and the risk of depressive symptoms in adults from the United States. DESIGN: This cross-sectional study included adult participants from the National Health and Nutrition Examination Survey 2009–2016. Depressive symptoms were assessed using the Patients’ Health Questionnaire-9. Intake of carotenoids was obtained through two 24-h dietary recall interviews. We applied logistic regression models and restricted cubic spline models to evaluate the associations of dietary alpha-carotene, beta-carotene, beta-cryptoxanthin, lycopene, lutein with zeaxanthin, and total carotenoid intake with the risk of depressive symptoms. RESULTS: Overall, a total of 17,401 adults aged 18–80 years were included in this study. After adjustment for potential confounders, the odds ratios (95% confidence intervals) of depressive symptoms in the highest versus lowest quartiles were 0.71 (0.56–0.92) for alpha-carotene, 0.59 (0.47–0.75) for beta-carotene, 0.71 (0.55–0.92) for beta-cryptoxanthin, 0.66 (0.49–0.89) for lycopene, 0.50 (0.39–0.64) for lutein with zeaxanthin, and 0.59 (0.45–0.78) for total carotenoid intake. U-shaped dose–response relationships were found between both beta-carotene and lutein with zeaxanthin intake and the risk of depressive symptoms. CONCLUSION: Results suggest that alpha-carotene, beta-carotene, beta-cryptoxanthin, lycopene, lutein with zeaxanthin, and total carotenoid intake may be inversely associated with the risk of depressive symptoms in the U.S. adults.
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spelling pubmed-77784302021-01-13 Associations between dietary carotenoid intakes and the risk of depressive symptoms Ge, Honghan Yang, Tingting Sun, Jing Zhang, Dongfeng Food Nutr Res Original Article BACKGROUND: Dietary factors play an important role in the development of depressive symptoms. Carotenoids have effective antioxidant and anti-inflammatory effects, but few studies have explored the associations between dietary carotenoid intake and depressive symptoms. OBJECTIVE: To evaluate the association between dietary carotenoid intake and the risk of depressive symptoms in adults from the United States. DESIGN: This cross-sectional study included adult participants from the National Health and Nutrition Examination Survey 2009–2016. Depressive symptoms were assessed using the Patients’ Health Questionnaire-9. Intake of carotenoids was obtained through two 24-h dietary recall interviews. We applied logistic regression models and restricted cubic spline models to evaluate the associations of dietary alpha-carotene, beta-carotene, beta-cryptoxanthin, lycopene, lutein with zeaxanthin, and total carotenoid intake with the risk of depressive symptoms. RESULTS: Overall, a total of 17,401 adults aged 18–80 years were included in this study. After adjustment for potential confounders, the odds ratios (95% confidence intervals) of depressive symptoms in the highest versus lowest quartiles were 0.71 (0.56–0.92) for alpha-carotene, 0.59 (0.47–0.75) for beta-carotene, 0.71 (0.55–0.92) for beta-cryptoxanthin, 0.66 (0.49–0.89) for lycopene, 0.50 (0.39–0.64) for lutein with zeaxanthin, and 0.59 (0.45–0.78) for total carotenoid intake. U-shaped dose–response relationships were found between both beta-carotene and lutein with zeaxanthin intake and the risk of depressive symptoms. CONCLUSION: Results suggest that alpha-carotene, beta-carotene, beta-cryptoxanthin, lycopene, lutein with zeaxanthin, and total carotenoid intake may be inversely associated with the risk of depressive symptoms in the U.S. adults. Open Academia 2020-12-28 /pmc/articles/PMC7778430/ /pubmed/33447180 http://dx.doi.org/10.29219/fnr.v64.3920 Text en © 2020 Honghan Ge et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
Ge, Honghan
Yang, Tingting
Sun, Jing
Zhang, Dongfeng
Associations between dietary carotenoid intakes and the risk of depressive symptoms
title Associations between dietary carotenoid intakes and the risk of depressive symptoms
title_full Associations between dietary carotenoid intakes and the risk of depressive symptoms
title_fullStr Associations between dietary carotenoid intakes and the risk of depressive symptoms
title_full_unstemmed Associations between dietary carotenoid intakes and the risk of depressive symptoms
title_short Associations between dietary carotenoid intakes and the risk of depressive symptoms
title_sort associations between dietary carotenoid intakes and the risk of depressive symptoms
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778430/
https://www.ncbi.nlm.nih.gov/pubmed/33447180
http://dx.doi.org/10.29219/fnr.v64.3920
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