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Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis

BACKGROUND: Metabolic syndrome (MetS) has been related to a high incidence of hepatocellular carcinoma (HCC). However, the influence of MetS on survival of patients with HCC is still unclear. We performed a systematic review and meta-analysis to evaluate the association between MetS and survival of...

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Autores principales: Fu, Jia, Jiang, Jinqiong, Liu, Kanghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995822/
https://www.ncbi.nlm.nih.gov/pubmed/36910647
http://dx.doi.org/10.3389/fonc.2023.1117846
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author Fu, Jia
Jiang, Jinqiong
Liu, Kanghan
author_facet Fu, Jia
Jiang, Jinqiong
Liu, Kanghan
author_sort Fu, Jia
collection PubMed
description BACKGROUND: Metabolic syndrome (MetS) has been related to a high incidence of hepatocellular carcinoma (HCC). However, the influence of MetS on survival of patients with HCC is still unclear. We performed a systematic review and meta-analysis to evaluate the association between MetS and survival of HCC patients. METHODS: A search of PubMed, Embase, and Web of Science retrieved relevant cohort studies from the inception of the databases to October 16, 2022. Data collection, literature search, and statistical analysis were carried out independently by two authors. We pooled the results using a random-effects model that incorporates heterogeneity. RESULTS: In the meta-analysis, 8080 patients with HCC were included from ten cohort studies, and 1166 patients (14.4%) had MetS. Eight studies included patients treated primarily with radical hepatectomy, one study with patients receiving sorafenib, and another study included patients who were treated with radical hepatectomy or non-surgical treatments. Pooled results showed that MetS was associated with poor overall survival (OS, risk ratio [RR]: 1.21, 95% confidence interval [CI]:1.08 to 1.37, p = 0.001; I(2) = 32%) and progression-free survival (PFS, RR: 1.33, 95% CI: 1.18 to 1.49, p < 0.001, I(2) = 14%). Influencing analysis by excluding one study at a time showed consistent results (p all < 0.05). Subgroup analyses showed similar results in studies with MetS diagnosed with the National Cholesterol Education Program Adult Treatment Panel III or International Diabetes Federal criteria, and in studies with mean follow-up durations < or ≥ 3.5 years (p for subgroup difference all > 0.05). CONCLUSION: In patients with HCC, MetS may be a risk factor of poor OS and PFS, particularly for those after radical hepatectomy.
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spelling pubmed-99958222023-03-10 Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis Fu, Jia Jiang, Jinqiong Liu, Kanghan Front Oncol Oncology BACKGROUND: Metabolic syndrome (MetS) has been related to a high incidence of hepatocellular carcinoma (HCC). However, the influence of MetS on survival of patients with HCC is still unclear. We performed a systematic review and meta-analysis to evaluate the association between MetS and survival of HCC patients. METHODS: A search of PubMed, Embase, and Web of Science retrieved relevant cohort studies from the inception of the databases to October 16, 2022. Data collection, literature search, and statistical analysis were carried out independently by two authors. We pooled the results using a random-effects model that incorporates heterogeneity. RESULTS: In the meta-analysis, 8080 patients with HCC were included from ten cohort studies, and 1166 patients (14.4%) had MetS. Eight studies included patients treated primarily with radical hepatectomy, one study with patients receiving sorafenib, and another study included patients who were treated with radical hepatectomy or non-surgical treatments. Pooled results showed that MetS was associated with poor overall survival (OS, risk ratio [RR]: 1.21, 95% confidence interval [CI]:1.08 to 1.37, p = 0.001; I(2) = 32%) and progression-free survival (PFS, RR: 1.33, 95% CI: 1.18 to 1.49, p < 0.001, I(2) = 14%). Influencing analysis by excluding one study at a time showed consistent results (p all < 0.05). Subgroup analyses showed similar results in studies with MetS diagnosed with the National Cholesterol Education Program Adult Treatment Panel III or International Diabetes Federal criteria, and in studies with mean follow-up durations < or ≥ 3.5 years (p for subgroup difference all > 0.05). CONCLUSION: In patients with HCC, MetS may be a risk factor of poor OS and PFS, particularly for those after radical hepatectomy. Frontiers Media S.A. 2023-02-23 /pmc/articles/PMC9995822/ /pubmed/36910647 http://dx.doi.org/10.3389/fonc.2023.1117846 Text en Copyright © 2023 Fu, Jiang and Liu 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 Oncology
Fu, Jia
Jiang, Jinqiong
Liu, Kanghan
Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title_full Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title_fullStr Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title_full_unstemmed Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title_short Metabolic syndrome and survival of patients with hepatocellular carcinoma: A meta-analysis
title_sort metabolic syndrome and survival of patients with hepatocellular carcinoma: a meta-analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995822/
https://www.ncbi.nlm.nih.gov/pubmed/36910647
http://dx.doi.org/10.3389/fonc.2023.1117846
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