Parity and pancreatic cancer risk: a dose-response meta-analysis of epidemiologic studies.

PLoS One

Department of Obstetrics and Gynecology, Shengjing Hospital, China Medical University, Shenyang, China.

Published: November 2014

AI Article Synopsis

  • Previous studies on the relationship between having children (parity) and pancreatic cancer risk have shown mixed results, leading researchers to conduct a more thorough assessment.
  • A review of existing literature identified a total of 22 studies that reported on the relative risk of pancreatic cancer in relation to parity, finding a summary relative risk of 0.86 for those with the highest parity compared to the lowest.
  • The results indicate that higher parity may be linked to a reduced risk of pancreatic cancer, suggesting the need for further large-scale studies to better understand this relationship and adjust for other influencing factors.

Article Abstract

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, I2 = 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, I2 = 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962437PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0092738PLOS

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