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Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis
BACKGROUND: Existing data evaluating the impact of metformin on the colorectal adenoma (CRA) risk in patients suffering from type 2 diabetes (T2D) are limited and controversial. We therefore summarized the studies currently available and assessed the relationship between metformin treatment and risk...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352447/ https://www.ncbi.nlm.nih.gov/pubmed/27903961 http://dx.doi.org/10.18632/oncotarget.13633 |
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author | Hou, Yi-Chao Hu, Qiang Huang, Jiao Fang, Jing-Yuan Xiong, Hua |
author_facet | Hou, Yi-Chao Hu, Qiang Huang, Jiao Fang, Jing-Yuan Xiong, Hua |
author_sort | Hou, Yi-Chao |
collection | PubMed |
description | BACKGROUND: Existing data evaluating the impact of metformin on the colorectal adenoma (CRA) risk in patients suffering from type 2 diabetes (T2D) are limited and controversial. We therefore summarized the studies currently available and assessed the relationship between metformin treatment and risk of CRA in T2D patients. METHODS: We systematically searched databases for eligible studies that explored the impact of metformin treatment on the occurrence of CRA in T2D patients from inception to June 2016. The summary odds ratio (OR) estimates with their 95% confidence interval (CI) were derived using random-effect, generic inverse variance methods. Sensitivity analysis and subgroup analysis were performed. RESULTS: Seven studies involving 7178 participants met the inclusion criteria. The pooling showed that metformin therapy has a 27% decrease in the CRA risk (OR, 0.73; 95% CI, 0.58 - 0.90). In subgroup analysis, we detected that metformin exhibits significant chemoprevention effects in Asia region (OR, 0.68; 95% CI, 0.48 - 0.96). Similar results were identified in both studies with adjusted ORs and high-quality studies (OR, 0.66; 95% CI, 0.50 - 0.86 and OR, 0.70; 95% CI, 0.58 - 0.84, respectively). Of note, an inverse relationship was noted that metformin therapy may result in a significant decrease in the advanced adenoma risk (OR, 0.52; 95% CI, 0.38 - 0.72). Low heterogeneity was observed, however, the results remained robust in multiplesensitivity analyses. CONCLUSIONS: This meta-analysis indicates that metformin therapy is correlated with a significant decrease in the risk of CRA and advanced adenoma in T2D patients. Further confirmatory studies are warranted. |
format | Online Article Text |
id | pubmed-5352447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53524472017-04-14 Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis Hou, Yi-Chao Hu, Qiang Huang, Jiao Fang, Jing-Yuan Xiong, Hua Oncotarget Review BACKGROUND: Existing data evaluating the impact of metformin on the colorectal adenoma (CRA) risk in patients suffering from type 2 diabetes (T2D) are limited and controversial. We therefore summarized the studies currently available and assessed the relationship between metformin treatment and risk of CRA in T2D patients. METHODS: We systematically searched databases for eligible studies that explored the impact of metformin treatment on the occurrence of CRA in T2D patients from inception to June 2016. The summary odds ratio (OR) estimates with their 95% confidence interval (CI) were derived using random-effect, generic inverse variance methods. Sensitivity analysis and subgroup analysis were performed. RESULTS: Seven studies involving 7178 participants met the inclusion criteria. The pooling showed that metformin therapy has a 27% decrease in the CRA risk (OR, 0.73; 95% CI, 0.58 - 0.90). In subgroup analysis, we detected that metformin exhibits significant chemoprevention effects in Asia region (OR, 0.68; 95% CI, 0.48 - 0.96). Similar results were identified in both studies with adjusted ORs and high-quality studies (OR, 0.66; 95% CI, 0.50 - 0.86 and OR, 0.70; 95% CI, 0.58 - 0.84, respectively). Of note, an inverse relationship was noted that metformin therapy may result in a significant decrease in the advanced adenoma risk (OR, 0.52; 95% CI, 0.38 - 0.72). Low heterogeneity was observed, however, the results remained robust in multiplesensitivity analyses. CONCLUSIONS: This meta-analysis indicates that metformin therapy is correlated with a significant decrease in the risk of CRA and advanced adenoma in T2D patients. Further confirmatory studies are warranted. Impact Journals LLC 2016-11-26 /pmc/articles/PMC5352447/ /pubmed/27903961 http://dx.doi.org/10.18632/oncotarget.13633 Text en Copyright: © 2017 Hou et al. http://creativecommons.org/licenses/by/3.0/ 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 | Review Hou, Yi-Chao Hu, Qiang Huang, Jiao Fang, Jing-Yuan Xiong, Hua Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title | Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title_full | Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title_fullStr | Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title_full_unstemmed | Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title_short | Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis |
title_sort | metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: a meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352447/ https://www.ncbi.nlm.nih.gov/pubmed/27903961 http://dx.doi.org/10.18632/oncotarget.13633 |
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