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Non-steroidal anti-inflammatory drug use and ovarian cancer risk: Findings from the NIH-AARP Diet and Health Study and systematic review

机译:非甾体类抗炎药的使用和卵巢癌的风险:NIH-AARP饮食与健康研究和系统评价的结果

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Background Chronic inflammation has been proposed as a risk factor for ovarian cancer. Some data suggest that anti-inflammatory medications may be protective against ovarian cancer; however, results have been inconsistent. Methods We evaluated the risk of epithelial ovarian cancer with regular use of NSAIDs prospectively in the NIH-AARP Diet and Health Study, using Cox proportional hazard models. We also examined the risk of common subtypes of epithelial ovarian cancer (serous, mucinous, endometrioid, clear cell, and other epithelial) with regular use of NSAIDs. In addition, we performed meta-analyses summarizing the risk of ovarian cancer with "regular use" of NSAIDs in previously published studies. Results We did not observe a significant association between regular use of NSAIDs with ovarian cancer risk in the AARP cohort (aspirin: RR 1.06, 95 % CI 0.87-1.29; non-aspirin NSAIDs: RR 0.93, 95 % CI 0.74-1.15); however, summary estimates from prospective cohort studies demonstrated that use of non-aspirin NSAIDs may reduce the risk of ovarian cancer (RR 0.88, 95 % CI 0.77-1.01). Although not significant, we found that mucinous tumors were inversely associated with non-aspirin NSAID use (RR 0.69, 95 % CI 0.23-2.10) in the AARP cohort, which was supported by the meta-analysis (RR 0.69, CI 0.50-0.94.) Conclusion Although results from the NIH-AARP cohort study were not statistically significant, our meta-analysis suggests that non-aspirin NSAIDs may be protective against ovarian cancer. Additional analyses, focusing on dose, duration, and frequency of NSAID use and accounting for ovarian cancer heterogeneity are necessary to further elucidate the association between NSAID use and ovarian cancer risk.
机译:背景技术已提出将慢性炎症作为卵巢癌的危险因素。一些数据表明抗炎药可能对卵巢癌有保护作用。但是,结果不一致。方法我们使用Cox比例风险模型在NIH-AARP饮食与健康研究中评估了定期使用NSAIDs上皮性卵巢癌的风险。我们还检查了经常使用NSAID的上皮性卵巢癌常见亚型(浆液性,粘液性,子宫内膜样,透明细胞和其他上皮性)的风险。此外,我们在先前发表的研究中进行了荟萃分析,总结了“常规使用” NSAIDs对卵巢癌的风险。结果在AARP队列中,我们并未观察到正常使用NSAIDs与卵巢癌风险之间存在显着相关性(阿司匹林:RR 1.06,95%CI 0.87-1.29;非阿司匹林NSAID:RR 0.93,95%CI 0.74-1.15);但是,前瞻性队列研究的汇总估计表明,使用非阿司匹林NSAID可以降低卵巢癌的风险(RR 0.88,95%CI 0.77-1.01)。尽管不显着,但我们发现粘液性肿瘤与AARP人群中非阿司匹林NSAID的使用呈负相关(RR 0.69,95%CI 0.23-2.10),这受到荟萃分析(RR 0.69,CI 0.50-0.94)的支持。结论尽管NIH-AARP队列研究的结果没有统计学意义,但我们的荟萃分析表明,非阿司匹林NSAIDs可能对卵巢癌具有保护作用。为了进一步阐明NSAID使用与卵巢癌风险之间的关系,还需要进行其他分析,重点是NSAID使用的剂量,持续时间和频率以及卵巢癌异质性的说明。

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