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Association between SII and hepatic steatosis and liver fibrosis: A population-based study

BACKGROUND: The systemic immune-inflammation index (SII) is a novel marker of inflammation, and hepatic steatosis and fibrosis are associated with inflammation. This study aimed to investigate the possible relationship between SII and hepatic steatosis and fibrosis. METHODS: The datasets from the Na...

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Autores principales: Xie, Ruijie, Xiao, Mengde, Li, Lihong, Ma, Nengqian, Liu, Mingjiang, Huang, Xiongjie, Liu, Qianlong, Zhang, Ya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520084/
https://www.ncbi.nlm.nih.gov/pubmed/36189280
http://dx.doi.org/10.3389/fimmu.2022.925690
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author Xie, Ruijie
Xiao, Mengde
Li, Lihong
Ma, Nengqian
Liu, Mingjiang
Huang, Xiongjie
Liu, Qianlong
Zhang, Ya
author_facet Xie, Ruijie
Xiao, Mengde
Li, Lihong
Ma, Nengqian
Liu, Mingjiang
Huang, Xiongjie
Liu, Qianlong
Zhang, Ya
author_sort Xie, Ruijie
collection PubMed
description BACKGROUND: The systemic immune-inflammation index (SII) is a novel marker of inflammation, and hepatic steatosis and fibrosis are associated with inflammation. This study aimed to investigate the possible relationship between SII and hepatic steatosis and fibrosis. METHODS: The datasets from the National Health and Nutrition Examination Survey (NHANES) 2017–2020 were used in a cross-sectional investigation. Multivariate linear regression models were used to examine the linear connection between SII and controlled attenuation parameter (CAP) and liver stiffness measurement (LSM). Fitted smoothing curves and threshold effect analysis were used to describe the nonlinear relationship. RESULTS: This population-based study included a total of 6,792 adults aged 18–80 years. In a multivariate linear regression analysis, a significant positive association between SII and CAP was shown [0.006 (0.001, 0.010)]. This positive association in a subgroup analysis was maintained in men [0.011 (0.004, 0.018)] but not in women. Furthermore, the association between SII and CAP was nonlinear; using a two-segment linear regression model, we found an inverted U-shaped relationship between SII and CAP with an inflection point of 687.059 (1,000 cells/µl). The results of the multiple regression analysis showed that the relationship between SII and LSM was not significant (P = 0.263). CONCLUSIONS: Our findings imply that increased SII levels are linked to hepatic steatosis, but SII is not linked to liver fibrosis. To confirm our findings, more large-scale prospective investigations are needed.
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spelling pubmed-95200842022-09-30 Association between SII and hepatic steatosis and liver fibrosis: A population-based study Xie, Ruijie Xiao, Mengde Li, Lihong Ma, Nengqian Liu, Mingjiang Huang, Xiongjie Liu, Qianlong Zhang, Ya Front Immunol Immunology BACKGROUND: The systemic immune-inflammation index (SII) is a novel marker of inflammation, and hepatic steatosis and fibrosis are associated with inflammation. This study aimed to investigate the possible relationship between SII and hepatic steatosis and fibrosis. METHODS: The datasets from the National Health and Nutrition Examination Survey (NHANES) 2017–2020 were used in a cross-sectional investigation. Multivariate linear regression models were used to examine the linear connection between SII and controlled attenuation parameter (CAP) and liver stiffness measurement (LSM). Fitted smoothing curves and threshold effect analysis were used to describe the nonlinear relationship. RESULTS: This population-based study included a total of 6,792 adults aged 18–80 years. In a multivariate linear regression analysis, a significant positive association between SII and CAP was shown [0.006 (0.001, 0.010)]. This positive association in a subgroup analysis was maintained in men [0.011 (0.004, 0.018)] but not in women. Furthermore, the association between SII and CAP was nonlinear; using a two-segment linear regression model, we found an inverted U-shaped relationship between SII and CAP with an inflection point of 687.059 (1,000 cells/µl). The results of the multiple regression analysis showed that the relationship between SII and LSM was not significant (P = 0.263). CONCLUSIONS: Our findings imply that increased SII levels are linked to hepatic steatosis, but SII is not linked to liver fibrosis. To confirm our findings, more large-scale prospective investigations are needed. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520084/ /pubmed/36189280 http://dx.doi.org/10.3389/fimmu.2022.925690 Text en Copyright © 2022 Xie, Xiao, Li, Ma, Liu, Huang, Liu and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Xie, Ruijie
Xiao, Mengde
Li, Lihong
Ma, Nengqian
Liu, Mingjiang
Huang, Xiongjie
Liu, Qianlong
Zhang, Ya
Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title_full Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title_fullStr Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title_full_unstemmed Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title_short Association between SII and hepatic steatosis and liver fibrosis: A population-based study
title_sort association between sii and hepatic steatosis and liver fibrosis: a population-based study
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520084/
https://www.ncbi.nlm.nih.gov/pubmed/36189280
http://dx.doi.org/10.3389/fimmu.2022.925690
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