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Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies
BACKGROUND: Previous epidemiologic studies have reported inconsistent results between parity and pancreatic cancer (PC) risk. To our knowledge, a comprehensive and quantitative assessment of this association has not been conducted. METHODS: Relevant published studies of parity and PC were identified...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962437/ https://www.ncbi.nlm.nih.gov/pubmed/24658609 http://dx.doi.org/10.1371/journal.pone.0092738 |
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author | Guan, Hong-Bo Wu, Lang Wu, Qi-Jun Zhu, Jingjing Gong, Tingting |
author_facet | Guan, Hong-Bo Wu, Lang Wu, Qi-Jun Zhu, Jingjing Gong, Tingting |
author_sort | Guan, Hong-Bo |
collection | PubMed |
description | BACKGROUND: Previous epidemiologic studies have reported inconsistent results between parity and pancreatic cancer (PC) risk. To our knowledge, a comprehensive and quantitative assessment of this association has not been conducted. METHODS: Relevant published studies of parity and PC were identified using MEDLINE (PubMed) and Web of Science databases until November 2013. Two authors (H-BG and LW) independently assessed eligibility and extracted data. Eleven prospective and 11 case-control studies reported relative risk (RR) estimates and 95% confidence intervals (CIs) of PC associated with parity. Fixed- and random-effects models were used to estimate the summary RR depending on the heterogeneity of effects. RESULTS: The summary RR for PC comparing the highest versus lowest parity was 0.86 (95% CI: 0.73–1.02; Q = 50.49, P<0.001, I (2) = 58.4%). Significant inverse associations were also observed in the studies that adjusted for cigarette smoking (RR = 0.81; 95% CI: 0.68–0.98), Type 2 diabetes mellitus (RR = 0.83; 95% CI: 0.75–0.93), and those that included all confounders or important risk factors (RR = 0.85; 95% CI: 0.76–0.96). Additionally, in the dose-response analysis, the summary RR for per one live birth was 0.97 (95% CI: 0.94–1.01; Q = 62.83, P<0.001, I (2) = 69.8%), which also indicated a borderline statistically significant inverse effect of parity on PC risk. No evidence of publication bias and significant heterogeneity between subgroups were detected by meta-regression analyses. CONCLUSION: In summary, these findings suggest that higher parity is associated with a decreased risk of PC. Future large consortia or pooled studies are warranted to fully adjust for potential confounders to confirm this association. |
format | Online Article Text |
id | pubmed-3962437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39624372014-03-24 Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies Guan, Hong-Bo Wu, Lang Wu, Qi-Jun Zhu, Jingjing Gong, Tingting PLoS One Research Article BACKGROUND: Previous epidemiologic studies have reported inconsistent results between parity and pancreatic cancer (PC) risk. To our knowledge, a comprehensive and quantitative assessment of this association has not been conducted. METHODS: Relevant published studies of parity and PC were identified using MEDLINE (PubMed) and Web of Science databases until November 2013. Two authors (H-BG and LW) independently assessed eligibility and extracted data. Eleven prospective and 11 case-control studies reported relative risk (RR) estimates and 95% confidence intervals (CIs) of PC associated with parity. Fixed- and random-effects models were used to estimate the summary RR depending on the heterogeneity of effects. RESULTS: The summary RR for PC comparing the highest versus lowest parity was 0.86 (95% CI: 0.73–1.02; Q = 50.49, P<0.001, I (2) = 58.4%). Significant inverse associations were also observed in the studies that adjusted for cigarette smoking (RR = 0.81; 95% CI: 0.68–0.98), Type 2 diabetes mellitus (RR = 0.83; 95% CI: 0.75–0.93), and those that included all confounders or important risk factors (RR = 0.85; 95% CI: 0.76–0.96). Additionally, in the dose-response analysis, the summary RR for per one live birth was 0.97 (95% CI: 0.94–1.01; Q = 62.83, P<0.001, I (2) = 69.8%), which also indicated a borderline statistically significant inverse effect of parity on PC risk. No evidence of publication bias and significant heterogeneity between subgroups were detected by meta-regression analyses. CONCLUSION: In summary, these findings suggest that higher parity is associated with a decreased risk of PC. Future large consortia or pooled studies are warranted to fully adjust for potential confounders to confirm this association. Public Library of Science 2014-03-21 /pmc/articles/PMC3962437/ /pubmed/24658609 http://dx.doi.org/10.1371/journal.pone.0092738 Text en © 2014 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, Lang Wu, Qi-Jun Zhu, Jingjing Gong, Tingting Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title | Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title_full | Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title_fullStr | Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title_full_unstemmed | Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title_short | Parity and Pancreatic Cancer Risk: A Dose-Response Meta-Analysis of Epidemiologic Studies |
title_sort | parity and pancreatic cancer risk: a dose-response meta-analysis of epidemiologic studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962437/ https://www.ncbi.nlm.nih.gov/pubmed/24658609 http://dx.doi.org/10.1371/journal.pone.0092738 |
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