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Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis

BACKGROUND: Metabolic syndrome (MetS) has been related to increased risks of a variety of cancers. However, the association between MetS and the risk of renal cell cancer (RCC) remains not fully determined. This meta-analysis was conducted to investigate whether MetS is independently associated with...

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Autores principales: Du, Wurong, Guo, Kaibo, Jin, Huimin, Sun, Leitao, Ruan, Shanming, Song, Qiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271793/
https://www.ncbi.nlm.nih.gov/pubmed/35832547
http://dx.doi.org/10.3389/fonc.2022.928619
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author Du, Wurong
Guo, Kaibo
Jin, Huimin
Sun, Leitao
Ruan, Shanming
Song, Qiaoling
author_facet Du, Wurong
Guo, Kaibo
Jin, Huimin
Sun, Leitao
Ruan, Shanming
Song, Qiaoling
author_sort Du, Wurong
collection PubMed
description BACKGROUND: Metabolic syndrome (MetS) has been related to increased risks of a variety of cancers. However, the association between MetS and the risk of renal cell cancer (RCC) remains not fully determined. This meta-analysis was conducted to investigate whether MetS is independently associated with the risk of RCC in adults. METHODS: Relevant observational studies were obtained by searching PubMed, Embase, Cochrane’s Library, and Web of Science databases. Study characteristics and outcome data were extracted independently by two authors. The random-effect model was used for meta-analysis considering the possible influence of between-study heterogeneity. Predefined subgroup analyses were used to evaluate the possible influences of study characteristics on the outcome. RESULTS: Eight studies involving 10,601,006 participants contributed to the meta-analysis. Results showed that MetS was independently associated with a higher risk of RCC in adult population (risk ratio [RR]: 1.62, 95% confidence interval [CI]: 1.41 to 1.87, p<0.001; I(2 )= 85%). Subgroup analyses showed consistent association in men (RR: 1.52, 95% CI: 1.23 to 1.89, p<0.001) and in women (RR: 1.71, 95% CI: 1.28 to 2.27, p<0.001), in Asians (RR: 1.51, 95% CI: 1.25 to 1.83, p<0.001) and in Caucasians (RR: 1.76, 95% CI: 1.46 to 2.12, p<0.001), and in community derived (RR: 1.56, 95% CI: 1.34 to 1.82, p<0.001) and non-community derived population (RR: 1.87, 95% CI: 1.71 to 2.04, p<0.001). Differences in study design or quality score also did not significantly affect the association (p for subgroup difference both >0.05). CONCLUSIONS: MetS may be independently associated with RCC in adult population.
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spelling pubmed-92717932022-07-12 Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis Du, Wurong Guo, Kaibo Jin, Huimin Sun, Leitao Ruan, Shanming Song, Qiaoling Front Oncol Oncology BACKGROUND: Metabolic syndrome (MetS) has been related to increased risks of a variety of cancers. However, the association between MetS and the risk of renal cell cancer (RCC) remains not fully determined. This meta-analysis was conducted to investigate whether MetS is independently associated with the risk of RCC in adults. METHODS: Relevant observational studies were obtained by searching PubMed, Embase, Cochrane’s Library, and Web of Science databases. Study characteristics and outcome data were extracted independently by two authors. The random-effect model was used for meta-analysis considering the possible influence of between-study heterogeneity. Predefined subgroup analyses were used to evaluate the possible influences of study characteristics on the outcome. RESULTS: Eight studies involving 10,601,006 participants contributed to the meta-analysis. Results showed that MetS was independently associated with a higher risk of RCC in adult population (risk ratio [RR]: 1.62, 95% confidence interval [CI]: 1.41 to 1.87, p<0.001; I(2 )= 85%). Subgroup analyses showed consistent association in men (RR: 1.52, 95% CI: 1.23 to 1.89, p<0.001) and in women (RR: 1.71, 95% CI: 1.28 to 2.27, p<0.001), in Asians (RR: 1.51, 95% CI: 1.25 to 1.83, p<0.001) and in Caucasians (RR: 1.76, 95% CI: 1.46 to 2.12, p<0.001), and in community derived (RR: 1.56, 95% CI: 1.34 to 1.82, p<0.001) and non-community derived population (RR: 1.87, 95% CI: 1.71 to 2.04, p<0.001). Differences in study design or quality score also did not significantly affect the association (p for subgroup difference both >0.05). CONCLUSIONS: MetS may be independently associated with RCC in adult population. Frontiers Media S.A. 2022-06-27 /pmc/articles/PMC9271793/ /pubmed/35832547 http://dx.doi.org/10.3389/fonc.2022.928619 Text en Copyright © 2022 Du, Guo, Jin, Sun, Ruan and Song 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
Du, Wurong
Guo, Kaibo
Jin, Huimin
Sun, Leitao
Ruan, Shanming
Song, Qiaoling
Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title_full Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title_fullStr Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title_full_unstemmed Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title_short Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis
title_sort association between metabolic syndrome and risk of renal cell cancer: a meta-analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271793/
https://www.ncbi.nlm.nih.gov/pubmed/35832547
http://dx.doi.org/10.3389/fonc.2022.928619
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