Guan Hong-Bo, Wu Lang, Wu Qi-Jun, Zhu Jingjing, Gong Tingting
Department of Obstetrics and Gynecology, Shengjing Hospital, China Medical University, Shenyang, China.
Center for Clinical and Translational Science, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One. 2014 Mar 21;9(3):e92738. doi: 10.1371/journal.pone.0092738. eCollection 2014.
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.
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.
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.
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.
以往的流行病学研究报告了生育次数与胰腺癌(PC)风险之间的不一致结果。据我们所知,尚未对这种关联进行全面和定量的评估。
使用MEDLINE(PubMed)和Web of Science数据库检索截至2013年11月发表的有关生育次数与PC的相关研究。两位作者(H-BG和LW)独立评估研究的合格性并提取数据。11项前瞻性研究和11项病例对照研究报告了与生育次数相关的PC的相对风险(RR)估计值和95%置信区间(CI)。根据效应的异质性,使用固定效应模型和随机效应模型来估计汇总RR。
比较最高生育次数与最低生育次数时,PC的汇总RR为0.86(95%CI:0.73 - 1.02;Q = 50.49,P < 0.001,I² = 58.4%)。在对吸烟进行调整的研究中(RR = 0.81;95%CI:0.68 - 0.98)、对2型糖尿病进行调整的研究中(RR = 0.83;95%CI:0.75 - 0.93)以及纳入所有混杂因素或重要风险因素的研究中(RR = 0.85;95%CI:0.76 - 0.96)也观察到了显著的负相关。此外,在剂量反应分析中,每一次活产的汇总RR为0.97(95%CI:0.94 - 1.01;Q = 62.83,P < 0.001,I² = 69.8%),这也表明生育次数对PC风险有边缘统计学显著的负向影响。Meta回归分析未发现发表偏倚的证据以及亚组之间存在显著异质性。
总之,这些发现表明较高的生育次数与PC风险降低相关。未来有必要开展大型联合研究或汇总研究,以充分调整潜在的混杂因素来证实这种关联。