Cargando…
Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies
BACKGROUND: Patients with metabolic syndrome (MetS) were suggested to have a higher risk of hepatocellular carcinoma (HCC), although the results of previous cohort studies are not consistent. AIM: To perform an updated meta-analysis to evaluate the association between MetS and subsequent incidence o...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166758/ https://www.ncbi.nlm.nih.gov/pubmed/30310291 http://dx.doi.org/10.2147/OTT.S154848 |
_version_ | 1783360091589705728 |
---|---|
author | Chen, Yongxin Li, Xiaofei Wu, Shuang Ye, Weiwei Lou, Lianqing |
author_facet | Chen, Yongxin Li, Xiaofei Wu, Shuang Ye, Weiwei Lou, Lianqing |
author_sort | Chen, Yongxin |
collection | PubMed |
description | BACKGROUND: Patients with metabolic syndrome (MetS) were suggested to have a higher risk of hepatocellular carcinoma (HCC), although the results of previous cohort studies are not consistent. AIM: To perform an updated meta-analysis to evaluate the association between MetS and subsequent incidence of HCC. METHODS: Relevant cohort studies were identified by searching PubMed and Embase databases. Cochrane’s Q-test and I(2) statistic were used to analyze the heterogeneity. Random effects model was used for the meta-analysis. RESULTS: Six cohort studies with 127,198 participants and 1,293 HCC cases during follow-up were included. Patients with MetS had a significantly higher incidence of HCC in studies with MetS defined by the revised National Cholesterol Education Program’s Adults Treatment Panel III (risk ratio [RR]: 1.43, 95% CI: 1.19–1.72, p<0.001; I(2)=29%) or International Diabetes Federation criteria (RR: 1.59, 95% CI: 1.13–2.23, p=0.008; I2=0%). Results of subgroup analysis showed that the presence of MetS was associated with a higher incidence of HCC in males (RR: 1.75, 95% CI: 1.28–2.38, p<0.001) but not in females (RR: 1.18, 95% CI: 0.76–1.84, p=0.46), and the association between MetS and higher risk of HCC was consistent regardless whether alcohol intake was adjusted. Although both were significant, MetS conferred higher risk of HCC in carriers of hepatitis B virus when compared with general population (p=0.06). CONCLUSION: The presence of MetS is associated with significantly increased incidence of HCC in male participants. |
format | Online Article Text |
id | pubmed-6166758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61667582018-10-11 Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies Chen, Yongxin Li, Xiaofei Wu, Shuang Ye, Weiwei Lou, Lianqing Onco Targets Ther Original Research BACKGROUND: Patients with metabolic syndrome (MetS) were suggested to have a higher risk of hepatocellular carcinoma (HCC), although the results of previous cohort studies are not consistent. AIM: To perform an updated meta-analysis to evaluate the association between MetS and subsequent incidence of HCC. METHODS: Relevant cohort studies were identified by searching PubMed and Embase databases. Cochrane’s Q-test and I(2) statistic were used to analyze the heterogeneity. Random effects model was used for the meta-analysis. RESULTS: Six cohort studies with 127,198 participants and 1,293 HCC cases during follow-up were included. Patients with MetS had a significantly higher incidence of HCC in studies with MetS defined by the revised National Cholesterol Education Program’s Adults Treatment Panel III (risk ratio [RR]: 1.43, 95% CI: 1.19–1.72, p<0.001; I(2)=29%) or International Diabetes Federation criteria (RR: 1.59, 95% CI: 1.13–2.23, p=0.008; I2=0%). Results of subgroup analysis showed that the presence of MetS was associated with a higher incidence of HCC in males (RR: 1.75, 95% CI: 1.28–2.38, p<0.001) but not in females (RR: 1.18, 95% CI: 0.76–1.84, p=0.46), and the association between MetS and higher risk of HCC was consistent regardless whether alcohol intake was adjusted. Although both were significant, MetS conferred higher risk of HCC in carriers of hepatitis B virus when compared with general population (p=0.06). CONCLUSION: The presence of MetS is associated with significantly increased incidence of HCC in male participants. Dove Medical Press 2018-09-27 /pmc/articles/PMC6166758/ /pubmed/30310291 http://dx.doi.org/10.2147/OTT.S154848 Text en © 2018 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Yongxin Li, Xiaofei Wu, Shuang Ye, Weiwei Lou, Lianqing Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title | Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title_full | Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title_fullStr | Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title_full_unstemmed | Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title_short | Metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
title_sort | metabolic syndrome and the incidence of hepatocellular carcinoma: a meta-analysis of cohort studies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166758/ https://www.ncbi.nlm.nih.gov/pubmed/30310291 http://dx.doi.org/10.2147/OTT.S154848 |
work_keys_str_mv | AT chenyongxin metabolicsyndromeandtheincidenceofhepatocellularcarcinomaametaanalysisofcohortstudies AT lixiaofei metabolicsyndromeandtheincidenceofhepatocellularcarcinomaametaanalysisofcohortstudies AT wushuang metabolicsyndromeandtheincidenceofhepatocellularcarcinomaametaanalysisofcohortstudies AT yeweiwei metabolicsyndromeandtheincidenceofhepatocellularcarcinomaametaanalysisofcohortstudies AT loulianqing metabolicsyndromeandtheincidenceofhepatocellularcarcinomaametaanalysisofcohortstudies |