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Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis

BACKGROUND/AIMS: A growing body of evidence has suggested that thiazolidinediones (TZDs) potentially reduce the risk of colorectal cancer (CRC). This study aimed to evaluate the effect of TZDs on CRC risk in patients with diabetes mellitus (DM). PATIENTS AND METHODS: A systematic search of electroni...

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Autores principales: Liu, Yang, Jin, Piao-Piao, Sun, Xue-Cheng, Hu, Ting-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900477/
https://www.ncbi.nlm.nih.gov/pubmed/29637913
http://dx.doi.org/10.4103/sjg.SJG_295_17
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author Liu, Yang
Jin, Piao-Piao
Sun, Xue-Cheng
Hu, Ting-Ting
author_facet Liu, Yang
Jin, Piao-Piao
Sun, Xue-Cheng
Hu, Ting-Ting
author_sort Liu, Yang
collection PubMed
description BACKGROUND/AIMS: A growing body of evidence has suggested that thiazolidinediones (TZDs) potentially reduce the risk of colorectal cancer (CRC). This study aimed to evaluate the effect of TZDs on CRC risk in patients with diabetes mellitus (DM). PATIENTS AND METHODS: A systematic search of electronic databases was performed for studies evaluating the exposure to TZDs and reporting CRC risk in diabetic patients. Pooled estimates with 95% confidence intervals (CIs) were estimated using fixed or random effects models. RESULTS: A total of 10 observational studies reporting more than 18,972 CRC cases in 2,470,768 DM patients were included. Meta-analysis showed a 9% reduction in CRC risk associated with TZDs use in all studies [relative risk (RR) =0.91, 95% CI = 0.84–0.99, P = 0.03] and cohort studies (RR = 0.89, 95% CI = 0.80–0.99, P = 0.04), respectively. However, such effect was not shown in case–control studies. In subgroup analyses, lower CRC risk was found in Asian population (RR = 0.40, 95% CI = 0.29–0.53, P = 0.00), and a trend toward lower CRC risk was observed in US population (RR = 0.94, 95% CI = 0.88–1.01, P = 0.08). CRC risk was significantly modified with non-pioglitazone TZD use (RR = 0.88, 95% CI = 0.82–0.95, P = 0.00), but not with pioglitazone use (RR = 0.95, 95% CI = 0.89–1.01, P = 0.11). No significant difference was observed with cancer site (colon or rectum). There was considerable inherent heterogeneity across studies, partly explained by study location. CONCLUSIONS: This meta-analysis supports a protective association between TZDs use and CRC risk in patients with DM. Future well-designed prospective studies with larger cohorts would be needed to understand this association better.
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spelling pubmed-59004772018-04-24 Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis Liu, Yang Jin, Piao-Piao Sun, Xue-Cheng Hu, Ting-Ting Saudi J Gastroenterol Systematic Review and Meta-Analysis BACKGROUND/AIMS: A growing body of evidence has suggested that thiazolidinediones (TZDs) potentially reduce the risk of colorectal cancer (CRC). This study aimed to evaluate the effect of TZDs on CRC risk in patients with diabetes mellitus (DM). PATIENTS AND METHODS: A systematic search of electronic databases was performed for studies evaluating the exposure to TZDs and reporting CRC risk in diabetic patients. Pooled estimates with 95% confidence intervals (CIs) were estimated using fixed or random effects models. RESULTS: A total of 10 observational studies reporting more than 18,972 CRC cases in 2,470,768 DM patients were included. Meta-analysis showed a 9% reduction in CRC risk associated with TZDs use in all studies [relative risk (RR) =0.91, 95% CI = 0.84–0.99, P = 0.03] and cohort studies (RR = 0.89, 95% CI = 0.80–0.99, P = 0.04), respectively. However, such effect was not shown in case–control studies. In subgroup analyses, lower CRC risk was found in Asian population (RR = 0.40, 95% CI = 0.29–0.53, P = 0.00), and a trend toward lower CRC risk was observed in US population (RR = 0.94, 95% CI = 0.88–1.01, P = 0.08). CRC risk was significantly modified with non-pioglitazone TZD use (RR = 0.88, 95% CI = 0.82–0.95, P = 0.00), but not with pioglitazone use (RR = 0.95, 95% CI = 0.89–1.01, P = 0.11). No significant difference was observed with cancer site (colon or rectum). There was considerable inherent heterogeneity across studies, partly explained by study location. CONCLUSIONS: This meta-analysis supports a protective association between TZDs use and CRC risk in patients with DM. Future well-designed prospective studies with larger cohorts would be needed to understand this association better. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5900477/ /pubmed/29637913 http://dx.doi.org/10.4103/sjg.SJG_295_17 Text en Copyright: © 2018 Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Systematic Review and Meta-Analysis
Liu, Yang
Jin, Piao-Piao
Sun, Xue-Cheng
Hu, Ting-Ting
Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title_full Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title_fullStr Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title_full_unstemmed Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title_short Thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: A meta-analysis
title_sort thiazolidinediones and risk of colorectal cancer in patients with diabetes mellitus: a meta-analysis
topic Systematic Review and Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900477/
https://www.ncbi.nlm.nih.gov/pubmed/29637913
http://dx.doi.org/10.4103/sjg.SJG_295_17
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