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Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies

Findings on the association of sodium with nonalcoholic fatty liver disease (NAFLD) are conflicting. The present systematic review and meta‐analysis study aimed to assess the association between salt or sodium intake or serum sodium levels and NAFLD risk. Relevant articles were identified by searchi...

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Detalles Bibliográficos
Autores principales: Shojaei‐Zarghani, Sara, Safarpour, Ali Reza, Fattahi, Mohammad Reza, Keshtkar, Abbasali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094449/
https://www.ncbi.nlm.nih.gov/pubmed/35592291
http://dx.doi.org/10.1002/fsn3.2781
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author Shojaei‐Zarghani, Sara
Safarpour, Ali Reza
Fattahi, Mohammad Reza
Keshtkar, Abbasali
author_facet Shojaei‐Zarghani, Sara
Safarpour, Ali Reza
Fattahi, Mohammad Reza
Keshtkar, Abbasali
author_sort Shojaei‐Zarghani, Sara
collection PubMed
description Findings on the association of sodium with nonalcoholic fatty liver disease (NAFLD) are conflicting. The present systematic review and meta‐analysis study aimed to assess the association between salt or sodium intake or serum sodium levels and NAFLD risk. Relevant articles were identified by searching PubMed, Web of Knowledge, Scopus, Proquest, and Embase databases through May 1, 2021, without language restriction. The pooled odds ratio (OR) and 95% confidence interval (CI) were estimated using Der‐Simonian and Laird method and random‐effects meta‐analysis. The certainty of the evidence was rated using the GRADE method. Out of 6470 documents, 7 epidemiological/observational (1 cohort, 1 case–control, and 5 cross‐sectional) studies on the relationship between dietary salt/sodium intakes and NAFLD risk met our inclusion criteria. The meta‐analysis of all studies showed a significant positive association between the highest salt/sodium intake and NALFD risk (OR = 1.60, 95% CI: 1.19–2.15) with a meaningful heterogeneity among studies (I(2) = 96.70%, p‐value <.001). The NAFLD risk was greater in the studies with higher quality (OR = 1.81, 95% CI: 1.24–2.65) or using the equation‐based methods for NAFLD ascertainment (OR = 2.02, 95% CI: 1.29–3.17) or urinary sodium collection as a sodium intake assessment (OR = 2.48, 95% CI: 1.52–4.06). The overall certainty of the evidence was very low. In conclusion, high sodium intake seems to be related to increased NAFLD risk. Further well‐designed studies are needed to clarify this association and shed light on the underlying mechanisms.
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spelling pubmed-90944492022-05-18 Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies Shojaei‐Zarghani, Sara Safarpour, Ali Reza Fattahi, Mohammad Reza Keshtkar, Abbasali Food Sci Nutr Review Findings on the association of sodium with nonalcoholic fatty liver disease (NAFLD) are conflicting. The present systematic review and meta‐analysis study aimed to assess the association between salt or sodium intake or serum sodium levels and NAFLD risk. Relevant articles were identified by searching PubMed, Web of Knowledge, Scopus, Proquest, and Embase databases through May 1, 2021, without language restriction. The pooled odds ratio (OR) and 95% confidence interval (CI) were estimated using Der‐Simonian and Laird method and random‐effects meta‐analysis. The certainty of the evidence was rated using the GRADE method. Out of 6470 documents, 7 epidemiological/observational (1 cohort, 1 case–control, and 5 cross‐sectional) studies on the relationship between dietary salt/sodium intakes and NAFLD risk met our inclusion criteria. The meta‐analysis of all studies showed a significant positive association between the highest salt/sodium intake and NALFD risk (OR = 1.60, 95% CI: 1.19–2.15) with a meaningful heterogeneity among studies (I(2) = 96.70%, p‐value <.001). The NAFLD risk was greater in the studies with higher quality (OR = 1.81, 95% CI: 1.24–2.65) or using the equation‐based methods for NAFLD ascertainment (OR = 2.02, 95% CI: 1.29–3.17) or urinary sodium collection as a sodium intake assessment (OR = 2.48, 95% CI: 1.52–4.06). The overall certainty of the evidence was very low. In conclusion, high sodium intake seems to be related to increased NAFLD risk. Further well‐designed studies are needed to clarify this association and shed light on the underlying mechanisms. John Wiley and Sons Inc. 2022-02-15 /pmc/articles/PMC9094449/ /pubmed/35592291 http://dx.doi.org/10.1002/fsn3.2781 Text en © 2022 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Shojaei‐Zarghani, Sara
Safarpour, Ali Reza
Fattahi, Mohammad Reza
Keshtkar, Abbasali
Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title_full Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title_fullStr Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title_full_unstemmed Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title_short Sodium in relation with nonalcoholic fatty liver disease: A systematic review and meta‐analysis of observational studies
title_sort sodium in relation with nonalcoholic fatty liver disease: a systematic review and meta‐analysis of observational studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094449/
https://www.ncbi.nlm.nih.gov/pubmed/35592291
http://dx.doi.org/10.1002/fsn3.2781
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