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Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies
BACKGROUND: Association between parity and colorectal cancer (CRC) risk has been investigated by several epidemiological studies but results are controversial, yet a comprehensive and quantitative assessment of this association has not been reported so far. METHODS: Relevant published studies of par...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787107/ https://www.ncbi.nlm.nih.gov/pubmed/24098689 http://dx.doi.org/10.1371/journal.pone.0075279 |
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author | Guan, Hong-Bo Wu, Qi-Jun Gong, Ting-Ting Lin, Bei Wang, Yong-Lai Liu, Cai-Xia |
author_facet | Guan, Hong-Bo Wu, Qi-Jun Gong, Ting-Ting Lin, Bei Wang, Yong-Lai Liu, Cai-Xia |
author_sort | Guan, Hong-Bo |
collection | PubMed |
description | BACKGROUND: Association between parity and colorectal cancer (CRC) risk has been investigated by several epidemiological studies but results are controversial, yet a comprehensive and quantitative assessment of this association has not been reported so far. METHODS: Relevant published studies of parity and CRC were identified using MEDLINE, EMBASE and Web of Science databases through end of April 2013. Two authors independently assessed eligibility and extracted data. Eleven prospective studies reported relative risk (RR) estimates and 95% confidence intervals (CIs) of CRC risk associated with parity. We pooled the RR from individual studies using fixed- or random-effects models and carried out heterogeneity and publication bias analyses. RESULTS: The summary RR for the ever parity vs. nulliparous was 0.95 (95% CI: 0.88–1.02), with no heterogeneity (Q = 9.04, P = 0.443, I (2) = 0.5%). Likewise, no significant association was yielded for the highest vs. lowest parity number (RR = 1.02, 95% CI: 0.89–1.17), with moderate heterogeneity (Q = 17.48, P = 0.094, I (2) = 37.1%). Dose-response analysis still indicated no effect of parity on CRC risk and the summary RR of per one livebirth was 0.99 (95% CI: 0.96–1.02), with moderate of heterogeneity (Q = 16.50, P<0.021, I (2) = 57.6%). Similar results were observed among all the subgroup analyses. No evidence of publication bias and significant heterogeneity between subgroups were detected by meta-regression analyses. CONCLUSION: Results of this dose-response meta-analysis of prospective studies found that there was little evidence of an association between parity and CRC risk. |
format | Online Article Text |
id | pubmed-3787107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37871072013-10-04 Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies Guan, Hong-Bo Wu, Qi-Jun Gong, Ting-Ting Lin, Bei Wang, Yong-Lai Liu, Cai-Xia PLoS One Research Article BACKGROUND: Association between parity and colorectal cancer (CRC) risk has been investigated by several epidemiological studies but results are controversial, yet a comprehensive and quantitative assessment of this association has not been reported so far. METHODS: Relevant published studies of parity and CRC were identified using MEDLINE, EMBASE and Web of Science databases through end of April 2013. Two authors independently assessed eligibility and extracted data. Eleven prospective studies reported relative risk (RR) estimates and 95% confidence intervals (CIs) of CRC risk associated with parity. We pooled the RR from individual studies using fixed- or random-effects models and carried out heterogeneity and publication bias analyses. RESULTS: The summary RR for the ever parity vs. nulliparous was 0.95 (95% CI: 0.88–1.02), with no heterogeneity (Q = 9.04, P = 0.443, I (2) = 0.5%). Likewise, no significant association was yielded for the highest vs. lowest parity number (RR = 1.02, 95% CI: 0.89–1.17), with moderate heterogeneity (Q = 17.48, P = 0.094, I (2) = 37.1%). Dose-response analysis still indicated no effect of parity on CRC risk and the summary RR of per one livebirth was 0.99 (95% CI: 0.96–1.02), with moderate of heterogeneity (Q = 16.50, P<0.021, I (2) = 57.6%). Similar results were observed among all the subgroup analyses. No evidence of publication bias and significant heterogeneity between subgroups were detected by meta-regression analyses. CONCLUSION: Results of this dose-response meta-analysis of prospective studies found that there was little evidence of an association between parity and CRC risk. Public Library of Science 2013-09-30 /pmc/articles/PMC3787107/ /pubmed/24098689 http://dx.doi.org/10.1371/journal.pone.0075279 Text en © 2013 Guan et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Guan, Hong-Bo Wu, Qi-Jun Gong, Ting-Ting Lin, Bei Wang, Yong-Lai Liu, Cai-Xia Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title | Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title_full | Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title_fullStr | Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title_full_unstemmed | Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title_short | Parity and Risk of Colorectal Cancer: A Dose-Response Meta-Analysis of Prospective Studies |
title_sort | parity and risk of colorectal cancer: a dose-response meta-analysis of prospective studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787107/ https://www.ncbi.nlm.nih.gov/pubmed/24098689 http://dx.doi.org/10.1371/journal.pone.0075279 |
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