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Metformin therapy and the risk of colorectal adenoma in patients with type 2 diabetes: A meta-analysis

Yi-Chao Hou, Qiang Hu, Jiao Huang, Jing-Yuan Fang and Hua Xiong _

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Oncotarget. 2017; 8:8843-8853. https://doi.org/10.18632/oncotarget.13633

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Abstract

Yi-Chao Hou1, Qiang Hu1, Jiao Huang1, Jing-Yuan Fang1, Hua Xiong1

1Division of Gastroenterology and Hepatology, Key Laboratory Gastroenterology and Hepatology, Ministry of Health, State Key Laboratory for Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Institute of Digestive Disease, Shanghai 200001, China

Correspondence to:

Hua Xiong, email: [email protected]

Jing-Yuan Fang, email: [email protected]

Keywords: metformin, colorectal adenoma, advanced adenoma, diabetes, meta-analysis

Received: September 16, 2016    Accepted: November 08, 2016    Published: November 26, 2016

ABSTRACT

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 multiple sensitivity 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.


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