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Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer
BACKGROUND: The hepatic microenvironment, which may include chronic inflammation and fibrosis, is considered to contribute to the development of liver metastases. Hepatic steatosis (HS) might cause liver inflammation and fibrosis. However, to date, no studies have investigated the impact of HS on li...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421062/ https://www.ncbi.nlm.nih.gov/pubmed/30886784 http://dx.doi.org/10.7717/peerj.6612 |
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author | Wu, Wenyu Liao, Haiyan Ye, Weilin Li, Xi Zhang, Jian Bu, Junguo |
author_facet | Wu, Wenyu Liao, Haiyan Ye, Weilin Li, Xi Zhang, Jian Bu, Junguo |
author_sort | Wu, Wenyu |
collection | PubMed |
description | BACKGROUND: The hepatic microenvironment, which may include chronic inflammation and fibrosis, is considered to contribute to the development of liver metastases. Hepatic steatosis (HS) might cause liver inflammation and fibrosis. However, to date, no studies have investigated the impact of HS on liver metastasis in patients with non-small cell lung cancer (NSCLC). METHODS: A retrospective cohort study was performed on patients who received NSCLC treatment at two hospitals affiliated with the Southern Medical University from January 2005 to December 2015. The patients were grouped according to the presence of HS. The clinicopathological features of patients between the two groups were compared. The effect of HS on liver metastasis and overall metastasis was evaluated, adjusting for other confounders using Cox regression analyses. RESULTS: In total, 1,873 patients with NSCLC with no distant metastases were included in this study, and 408 (21.8%) patients were diagnosed with HS (at the time of diagnosis or before diagnosis). Liver metastases occurred in 166 (8.9%) patients. Liver metastasis-free survival was significantly worse in the study (HS) group (hazard ratio (HR) 1.42; (95% CI [1.03–1.96]); P = 0.031). Multivariate regression analysis demonstrated that HS was an independent risk factor for liver metastasis (HR 1.43; 95% CI [1.02–2.01]; P = 0.039). However, HS was not associated with overall metastasis of NSCLC (HR 0.99; 95% CI [0.84–1.17]; P = 0.895). CONCLUSION: Hepatic steatosis was an independent predictor of liver metastasis from in patients with NSCLC. |
format | Online Article Text |
id | pubmed-6421062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64210622019-03-18 Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer Wu, Wenyu Liao, Haiyan Ye, Weilin Li, Xi Zhang, Jian Bu, Junguo PeerJ Epidemiology BACKGROUND: The hepatic microenvironment, which may include chronic inflammation and fibrosis, is considered to contribute to the development of liver metastases. Hepatic steatosis (HS) might cause liver inflammation and fibrosis. However, to date, no studies have investigated the impact of HS on liver metastasis in patients with non-small cell lung cancer (NSCLC). METHODS: A retrospective cohort study was performed on patients who received NSCLC treatment at two hospitals affiliated with the Southern Medical University from January 2005 to December 2015. The patients were grouped according to the presence of HS. The clinicopathological features of patients between the two groups were compared. The effect of HS on liver metastasis and overall metastasis was evaluated, adjusting for other confounders using Cox regression analyses. RESULTS: In total, 1,873 patients with NSCLC with no distant metastases were included in this study, and 408 (21.8%) patients were diagnosed with HS (at the time of diagnosis or before diagnosis). Liver metastases occurred in 166 (8.9%) patients. Liver metastasis-free survival was significantly worse in the study (HS) group (hazard ratio (HR) 1.42; (95% CI [1.03–1.96]); P = 0.031). Multivariate regression analysis demonstrated that HS was an independent risk factor for liver metastasis (HR 1.43; 95% CI [1.02–2.01]; P = 0.039). However, HS was not associated with overall metastasis of NSCLC (HR 0.99; 95% CI [0.84–1.17]; P = 0.895). CONCLUSION: Hepatic steatosis was an independent predictor of liver metastasis from in patients with NSCLC. PeerJ Inc. 2019-03-14 /pmc/articles/PMC6421062/ /pubmed/30886784 http://dx.doi.org/10.7717/peerj.6612 Text en © 2019 Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Epidemiology Wu, Wenyu Liao, Haiyan Ye, Weilin Li, Xi Zhang, Jian Bu, Junguo Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title | Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title_full | Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title_fullStr | Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title_full_unstemmed | Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title_short | Fatty liver is a risk factor for liver metastasis in Chinese patients with non-small cell lung cancer |
title_sort | fatty liver is a risk factor for liver metastasis in chinese patients with non-small cell lung cancer |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421062/ https://www.ncbi.nlm.nih.gov/pubmed/30886784 http://dx.doi.org/10.7717/peerj.6612 |
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