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Serum glucose and risk of cancer: a meta-analysis

BACKGROUND: Raised serum glucose has been linked to increased risk of many solid cancers. We performed a meta-analysis to quantify and summarise the evidence for this link. METHODS: Pubmed and Embase were reviewed, using search terms representing serum glucose and cancer. Inclusion and exclusion cri...

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Autores principales: Crawley, Danielle J, Holmberg, Lars, Melvin, Jennifer C, Loda, Massimo, Chowdhury, Simon, Rudman, Sarah M, Van Hemelrijck, Mieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320469/
https://www.ncbi.nlm.nih.gov/pubmed/25526881
http://dx.doi.org/10.1186/1471-2407-14-985
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author Crawley, Danielle J
Holmberg, Lars
Melvin, Jennifer C
Loda, Massimo
Chowdhury, Simon
Rudman, Sarah M
Van Hemelrijck, Mieke
author_facet Crawley, Danielle J
Holmberg, Lars
Melvin, Jennifer C
Loda, Massimo
Chowdhury, Simon
Rudman, Sarah M
Van Hemelrijck, Mieke
author_sort Crawley, Danielle J
collection PubMed
description BACKGROUND: Raised serum glucose has been linked to increased risk of many solid cancers. We performed a meta-analysis to quantify and summarise the evidence for this link. METHODS: Pubmed and Embase were reviewed, using search terms representing serum glucose and cancer. Inclusion and exclusion criteria focused on epidemiological studies with clear definitions of serum glucose levels, cancer type, as well as well-described statistical methods with sufficient data available. We used 6.1 mmol/L as the cut-off for high glucose, consistent with the WHO definition of metabolic syndrome. Random effects analyses were performed to estimate the pooled relative risk (RR). RESULTS: Nineteen studies were included in the primary analysis, which showed a pooled RR of 1.32 (95% CI: 1.20 – 1.45). Including only those individuals with fasting glucose measurements did not have a large effect on the pooled RR (1.32 (95% CI: 1.11-1.57). A stratified analysis showed a pooled RR of 1.34 (95% CI: 1.02-1.77) for hormonally driven cancer and 1.21 (95% CI: 1.09-1.36) for cancers thought to be driven by Insulin Growth Factor-1. CONCLUSION: A positive association between serum glucose and risk of cancer was found. The underlying biological mechanisms remain to be elucidated but our subgroup analyses suggest that the insulin- IGF-1 axis does not fully explain the association. These findings are of public health importance as measures to reduce serum glucose via lifestyle and dietary changes could be implemented in the context of cancer mortality.
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spelling pubmed-43204692015-02-08 Serum glucose and risk of cancer: a meta-analysis Crawley, Danielle J Holmberg, Lars Melvin, Jennifer C Loda, Massimo Chowdhury, Simon Rudman, Sarah M Van Hemelrijck, Mieke BMC Cancer Research Article BACKGROUND: Raised serum glucose has been linked to increased risk of many solid cancers. We performed a meta-analysis to quantify and summarise the evidence for this link. METHODS: Pubmed and Embase were reviewed, using search terms representing serum glucose and cancer. Inclusion and exclusion criteria focused on epidemiological studies with clear definitions of serum glucose levels, cancer type, as well as well-described statistical methods with sufficient data available. We used 6.1 mmol/L as the cut-off for high glucose, consistent with the WHO definition of metabolic syndrome. Random effects analyses were performed to estimate the pooled relative risk (RR). RESULTS: Nineteen studies were included in the primary analysis, which showed a pooled RR of 1.32 (95% CI: 1.20 – 1.45). Including only those individuals with fasting glucose measurements did not have a large effect on the pooled RR (1.32 (95% CI: 1.11-1.57). A stratified analysis showed a pooled RR of 1.34 (95% CI: 1.02-1.77) for hormonally driven cancer and 1.21 (95% CI: 1.09-1.36) for cancers thought to be driven by Insulin Growth Factor-1. CONCLUSION: A positive association between serum glucose and risk of cancer was found. The underlying biological mechanisms remain to be elucidated but our subgroup analyses suggest that the insulin- IGF-1 axis does not fully explain the association. These findings are of public health importance as measures to reduce serum glucose via lifestyle and dietary changes could be implemented in the context of cancer mortality. BioMed Central 2014-12-19 /pmc/articles/PMC4320469/ /pubmed/25526881 http://dx.doi.org/10.1186/1471-2407-14-985 Text en © Crawley et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Article
Crawley, Danielle J
Holmberg, Lars
Melvin, Jennifer C
Loda, Massimo
Chowdhury, Simon
Rudman, Sarah M
Van Hemelrijck, Mieke
Serum glucose and risk of cancer: a meta-analysis
title Serum glucose and risk of cancer: a meta-analysis
title_full Serum glucose and risk of cancer: a meta-analysis
title_fullStr Serum glucose and risk of cancer: a meta-analysis
title_full_unstemmed Serum glucose and risk of cancer: a meta-analysis
title_short Serum glucose and risk of cancer: a meta-analysis
title_sort serum glucose and risk of cancer: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320469/
https://www.ncbi.nlm.nih.gov/pubmed/25526881
http://dx.doi.org/10.1186/1471-2407-14-985
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