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Circulating resistin levels and obesity-related cancer risk: A meta-analysis

Resistin levels have been reported to be abnormal in obesity-related cancer patients with epidemiological studies yielding inconsistent results. Therefore, a meta-analysis was performed to assess the association between blood resistin levels and obesity-related cancer risk. A total of 13 studies wer...

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Autores principales: Gong, Wei-Jing, Zheng, Wei, Xiao, Ling, Tan, Li-Ming, Song, Jian, Li, Xiang-Ping, Xiao, Di, Cui, Jia-Jia, Li, Xi, Zhou, Hong-Hao, Yin, Ji-Ye, Liu, Zhao-Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295382/
https://www.ncbi.nlm.nih.gov/pubmed/27509174
http://dx.doi.org/10.18632/oncotarget.11034
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author Gong, Wei-Jing
Zheng, Wei
Xiao, Ling
Tan, Li-Ming
Song, Jian
Li, Xiang-Ping
Xiao, Di
Cui, Jia-Jia
Li, Xi
Zhou, Hong-Hao
Yin, Ji-Ye
Liu, Zhao-Qian
author_facet Gong, Wei-Jing
Zheng, Wei
Xiao, Ling
Tan, Li-Ming
Song, Jian
Li, Xiang-Ping
Xiao, Di
Cui, Jia-Jia
Li, Xi
Zhou, Hong-Hao
Yin, Ji-Ye
Liu, Zhao-Qian
author_sort Gong, Wei-Jing
collection PubMed
description Resistin levels have been reported to be abnormal in obesity-related cancer patients with epidemiological studies yielding inconsistent results. Therefore, a meta-analysis was performed to assess the association between blood resistin levels and obesity-related cancer risk. A total of 13 studies were included for pooling ORs analysis. High resistin levels were found in cancer patients (OR= 1.20, 95% CI= 1.10-1.30). After excluding one study primarily contributing to between-study heterogeneity, the association between resistin levels and cancer risk was still significant (OR=1.18, 95% CI = 1.09-1.28). Stratification analysis found resistin levels were not associated with cancer risk in prospective studies. Meta-regression analysis identified factors such as geographic area, detection assay, or study design as confounders to between-study variance. The result of 18 studies of pooling measures on SMD analysis was that high resistin levels were associated with increased cancer risk (SMD = 0.94, 95% CI = 0.63-1.25), but not in the pooling SMD analysis of prospective studies. Except for the studies identified as major contributors to heterogeneity by Galbraith plot, resistin levels were still higher in cancer patients (SMD = 0.75, 95% CI = 0.63-0.87) in retrospective studies. Meta-regression analysis found factors, such as geographic area, BMI-match, size, and quality score, could account for 66.7% between-study variance in pooling SMD analysis of retrospective studies. Publication bias was not found in pooling ORs analysis. Our findings indicated high resistin levels were associated with increased obesity-related cancer risk. However, it may not be a predictor.
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spelling pubmed-52953822017-02-08 Circulating resistin levels and obesity-related cancer risk: A meta-analysis Gong, Wei-Jing Zheng, Wei Xiao, Ling Tan, Li-Ming Song, Jian Li, Xiang-Ping Xiao, Di Cui, Jia-Jia Li, Xi Zhou, Hong-Hao Yin, Ji-Ye Liu, Zhao-Qian Oncotarget Research Paper Resistin levels have been reported to be abnormal in obesity-related cancer patients with epidemiological studies yielding inconsistent results. Therefore, a meta-analysis was performed to assess the association between blood resistin levels and obesity-related cancer risk. A total of 13 studies were included for pooling ORs analysis. High resistin levels were found in cancer patients (OR= 1.20, 95% CI= 1.10-1.30). After excluding one study primarily contributing to between-study heterogeneity, the association between resistin levels and cancer risk was still significant (OR=1.18, 95% CI = 1.09-1.28). Stratification analysis found resistin levels were not associated with cancer risk in prospective studies. Meta-regression analysis identified factors such as geographic area, detection assay, or study design as confounders to between-study variance. The result of 18 studies of pooling measures on SMD analysis was that high resistin levels were associated with increased cancer risk (SMD = 0.94, 95% CI = 0.63-1.25), but not in the pooling SMD analysis of prospective studies. Except for the studies identified as major contributors to heterogeneity by Galbraith plot, resistin levels were still higher in cancer patients (SMD = 0.75, 95% CI = 0.63-0.87) in retrospective studies. Meta-regression analysis found factors, such as geographic area, BMI-match, size, and quality score, could account for 66.7% between-study variance in pooling SMD analysis of retrospective studies. Publication bias was not found in pooling ORs analysis. Our findings indicated high resistin levels were associated with increased obesity-related cancer risk. However, it may not be a predictor. Impact Journals LLC 2016-08-04 /pmc/articles/PMC5295382/ /pubmed/27509174 http://dx.doi.org/10.18632/oncotarget.11034 Text en Copyright: © 2016 Gong et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Gong, Wei-Jing
Zheng, Wei
Xiao, Ling
Tan, Li-Ming
Song, Jian
Li, Xiang-Ping
Xiao, Di
Cui, Jia-Jia
Li, Xi
Zhou, Hong-Hao
Yin, Ji-Ye
Liu, Zhao-Qian
Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title_full Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title_fullStr Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title_full_unstemmed Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title_short Circulating resistin levels and obesity-related cancer risk: A meta-analysis
title_sort circulating resistin levels and obesity-related cancer risk: a meta-analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295382/
https://www.ncbi.nlm.nih.gov/pubmed/27509174
http://dx.doi.org/10.18632/oncotarget.11034
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