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The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study

CONTEXT: We describe here the contributions of the Tehran lipid and glucose study (TLGS) to understanding different aspects of the nitrate (NO(3))-nitrite (NO(2))-nitric oxide (NO) pathway in health and disease. EVIDENCE ACQUISITION: All English-language documents from the TLGS, focused on NO pathwa...

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Autores principales: Bahadoran, Zahra, Mirmiran, Parvin, Jeddi, Sajad, Momenan, Amir Abbas, Azizi, Fereidoun, Ghasemi, Asghar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289293/
https://www.ncbi.nlm.nih.gov/pubmed/30584441
http://dx.doi.org/10.5812/ijem.84775
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author Bahadoran, Zahra
Mirmiran, Parvin
Jeddi, Sajad
Momenan, Amir Abbas
Azizi, Fereidoun
Ghasemi, Asghar
author_facet Bahadoran, Zahra
Mirmiran, Parvin
Jeddi, Sajad
Momenan, Amir Abbas
Azizi, Fereidoun
Ghasemi, Asghar
author_sort Bahadoran, Zahra
collection PubMed
description CONTEXT: We describe here the contributions of the Tehran lipid and glucose study (TLGS) to understanding different aspects of the nitrate (NO(3))-nitrite (NO(2))-nitric oxide (NO) pathway in health and disease. EVIDENCE ACQUISITION: All English-language documents from the TLGS, focused on NO pathway were searched using the PubMed, Scopus, and Embase databases. RESULTS: Reference values of serum concentrations of NO metabolites (nitrate+nitrite or NOx) were 11.5 - 76.4, 10.1 - 65.6, and 10.3 - 66.8 μmol/L in men, women, and the total population, respectively. Circulating NOx was affected by age, smoking habits, menopause status, thyroid hormones, and various pathologic conditions. Elevated serum NOx was related to increased incidence of metabolic syndrome (odds ratio (OR) = 1.75, 95% confidence interval (CI) = 1.19 - 2.59), hypertriglyceridemic-waist phenotype (OR = 1.39, 95% CI = 1.05 - 1.93), chronic kidney disease (OR = 1.86, 95% CI = 1.10 - 3.14) in women, and cardiovascular disease (hazard ratio (HR) = 1.35, 95% CI = 1.01 - 1.80] in the total population. In participants with low vitamin C intake, higher intakes of NO(2) (≥ 8.77 mg/d) were accompanied with increased risk of diabetes (HR = 2.43, 95% CI = 1.45 - 4.05). A decreased risk of hypertension (OR = 0.58, 95% CI = 0.33 - 0.98) and chronic kidney disease (OR = 0.50, 95% CI = 0.24 - 0.89) was observed in response to higher intakes of NO(2). CONCLUSIONS: Circulating NOx is associated with and could predict the risk of metabolic disorders in a general population. Moreover, dietary NO(3)/NO(2) exposure from usual diets seems to contribute to development of noncommunicable diseases.
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spelling pubmed-62892932018-12-24 The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study Bahadoran, Zahra Mirmiran, Parvin Jeddi, Sajad Momenan, Amir Abbas Azizi, Fereidoun Ghasemi, Asghar Int J Endocrinol Metab Review Article CONTEXT: We describe here the contributions of the Tehran lipid and glucose study (TLGS) to understanding different aspects of the nitrate (NO(3))-nitrite (NO(2))-nitric oxide (NO) pathway in health and disease. EVIDENCE ACQUISITION: All English-language documents from the TLGS, focused on NO pathway were searched using the PubMed, Scopus, and Embase databases. RESULTS: Reference values of serum concentrations of NO metabolites (nitrate+nitrite or NOx) were 11.5 - 76.4, 10.1 - 65.6, and 10.3 - 66.8 μmol/L in men, women, and the total population, respectively. Circulating NOx was affected by age, smoking habits, menopause status, thyroid hormones, and various pathologic conditions. Elevated serum NOx was related to increased incidence of metabolic syndrome (odds ratio (OR) = 1.75, 95% confidence interval (CI) = 1.19 - 2.59), hypertriglyceridemic-waist phenotype (OR = 1.39, 95% CI = 1.05 - 1.93), chronic kidney disease (OR = 1.86, 95% CI = 1.10 - 3.14) in women, and cardiovascular disease (hazard ratio (HR) = 1.35, 95% CI = 1.01 - 1.80] in the total population. In participants with low vitamin C intake, higher intakes of NO(2) (≥ 8.77 mg/d) were accompanied with increased risk of diabetes (HR = 2.43, 95% CI = 1.45 - 4.05). A decreased risk of hypertension (OR = 0.58, 95% CI = 0.33 - 0.98) and chronic kidney disease (OR = 0.50, 95% CI = 0.24 - 0.89) was observed in response to higher intakes of NO(2). CONCLUSIONS: Circulating NOx is associated with and could predict the risk of metabolic disorders in a general population. Moreover, dietary NO(3)/NO(2) exposure from usual diets seems to contribute to development of noncommunicable diseases. Kowsar 2018-10-14 /pmc/articles/PMC6289293/ /pubmed/30584441 http://dx.doi.org/10.5812/ijem.84775 Text en Copyright © 2018, International Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Review Article
Bahadoran, Zahra
Mirmiran, Parvin
Jeddi, Sajad
Momenan, Amir Abbas
Azizi, Fereidoun
Ghasemi, Asghar
The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title_full The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title_fullStr The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title_full_unstemmed The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title_short The Nitrate-Nitrite-Nitric Oxide Pathway: Findings from 20 Years of the Tehran Lipid and Glucose Study
title_sort nitrate-nitrite-nitric oxide pathway: findings from 20 years of the tehran lipid and glucose study
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289293/
https://www.ncbi.nlm.nih.gov/pubmed/30584441
http://dx.doi.org/10.5812/ijem.84775
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