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Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis
BACKGROUND: Insulin is widely used in patients with type 2 diabetes mellitus (T2DM). More attention was focused on its higher risk of colorectal cancer (CRC). This meta-analysis examined the relationship between levels of insulin use and the risk of CRC. METHODS: A meta-analysis using data from 12 p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107999/ https://www.ncbi.nlm.nih.gov/pubmed/24885616 http://dx.doi.org/10.1186/1746-1596-9-91 |
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author | Yin, Shinan Bai, Hua Jing, Danqing |
author_facet | Yin, Shinan Bai, Hua Jing, Danqing |
author_sort | Yin, Shinan |
collection | PubMed |
description | BACKGROUND: Insulin is widely used in patients with type 2 diabetes mellitus (T2DM). More attention was focused on its higher risk of colorectal cancer (CRC). This meta-analysis examined the relationship between levels of insulin use and the risk of CRC. METHODS: A meta-analysis using data from 12 published epidemiologic studies (7 case–control, and 5 cohort studies) published before Jan. 2014 was done to examine the association between insulin use and CRC. Random effects analyses were done to calculate relative risk (RR) and 95% confidence intervals (CI). Heterogeneity among studies was measured by the χ(2) and I(2) statistic. RESULTS: Overall, the risk of CRC was significantly associated with insulin use to a random-effects model (RR, 1.69; 95% CI, 1.25 -2.27). When subgroup analyses were conducted according to the study types, no associations were detected in cohort group (RR, 1.25; 95% CI, 0.95-1.65; I(2), 75.7%); however significant association was detected in case–control group (RR, 2.15; 95% CI, 1.41-3.26; I(2), 89.1%). CONCLUSIONS: A significant harmful effect of insulin, observed mainly among case–control studies, may result from study design differences and amount of included studies. Although these results suggest a harmful effect of insulin use for CRC risk, additional large studies are warranted to support these preliminary evidences. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/2194715731194123. |
format | Online Article Text |
id | pubmed-4107999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41079992014-07-24 Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis Yin, Shinan Bai, Hua Jing, Danqing Diagn Pathol Research BACKGROUND: Insulin is widely used in patients with type 2 diabetes mellitus (T2DM). More attention was focused on its higher risk of colorectal cancer (CRC). This meta-analysis examined the relationship between levels of insulin use and the risk of CRC. METHODS: A meta-analysis using data from 12 published epidemiologic studies (7 case–control, and 5 cohort studies) published before Jan. 2014 was done to examine the association between insulin use and CRC. Random effects analyses were done to calculate relative risk (RR) and 95% confidence intervals (CI). Heterogeneity among studies was measured by the χ(2) and I(2) statistic. RESULTS: Overall, the risk of CRC was significantly associated with insulin use to a random-effects model (RR, 1.69; 95% CI, 1.25 -2.27). When subgroup analyses were conducted according to the study types, no associations were detected in cohort group (RR, 1.25; 95% CI, 0.95-1.65; I(2), 75.7%); however significant association was detected in case–control group (RR, 2.15; 95% CI, 1.41-3.26; I(2), 89.1%). CONCLUSIONS: A significant harmful effect of insulin, observed mainly among case–control studies, may result from study design differences and amount of included studies. Although these results suggest a harmful effect of insulin use for CRC risk, additional large studies are warranted to support these preliminary evidences. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/2194715731194123. BioMed Central 2014-05-12 /pmc/articles/PMC4107999/ /pubmed/24885616 http://dx.doi.org/10.1186/1746-1596-9-91 Text en Copyright © 2014 Yin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yin, Shinan Bai, Hua Jing, Danqing Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title | Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title_full | Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title_fullStr | Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title_full_unstemmed | Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title_short | Insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
title_sort | insulin therapy and colorectal cancer risk among type 2 diabetes mellitus patients: a systemic review and meta-analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107999/ https://www.ncbi.nlm.nih.gov/pubmed/24885616 http://dx.doi.org/10.1186/1746-1596-9-91 |
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