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Unopposed estrogen and estrogen plus progestin menopausal hormone therapy and lung cancer risk in the NIH-AARP Diet and Health Study Cohort.

机译:NIH-AARP饮食与健康研究队列中的雌激素和雌激素联合孕激素更年期激素治疗和肺癌风险。

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Previous studies have reported that lung cancer risk may be decreased, increased, or unaffected by prior use of menopausal hormone therapy (MHT).To assess this issue further, we examined relationships among 118,008 women, ages 50-71?years who were recruited during 1995-1996 for the NIH-AARP Diet and Health Study and in whom 2,097 incident lung carcinomas were identified during follow-up through 2006. Multivariable Cox proportional hazards models estimated relative risks (RR) and 95% confidence intervals (CIs) associated with various measures of self-reported MHT use.We found no evidence that either estrogen therapy (ET)-only or estrogen plus progestin therapy (EPT) use was substantially related to subsequent lung cancer risk (respective RRs and 95% CIs for ever use?=?0.97, 0.86-1.09 and 1.03, 0.90-1.17). There were no significant variations according to currency or duration of use of either formulation, nor was there evidence that risks varied within subgroups defined by cigarette smoking or body size. The absence of effect was seen for nearly all lung cancer subtypes, with the exception of an increased risk of undifferentiated/large cell cancers associated with long-term ET-only use (p (trend)?=?0.02), a relationship not observed among EPT users.Our results failed to support any substantial alterations in lung cancer risk associated with use of either unopposed estrogen or estrogen plus progestin MHT, even when detailed exposure measures and other risk predictors were considered.
机译:先前的研究报告称,更年期激素治疗(MHT)的使用可能降低,增加或不影响肺癌的风险。为了进一步评估此问题,我们研究了118,008名年龄在50-71岁之间的女性之间的关系。 1995-1996年用于NIH-AARP饮食与健康研究,在直到2006年的随访期间共发现了2,097例肺癌。多变量Cox比例风险模型估计了与各种风险相关的相对风险(RR)和95%置信区间(CIs)我们发现没有证据表明仅使用雌激素疗法(ET)或使用雌激素加孕激素疗法(EPT)与随后的肺癌风险有很大关系(分别使用过的RR和95%CI?= 0.97,0.86-1.09和1.03,0.90-1.17)。没有根据货币或使用任一种配方的持续时间发生显着变化,也没有证据表明在吸烟或体型定义的亚组中风险有所不同。几乎所有肺癌亚型均未见疗效,但长期仅使用ET相关的未分化/大细胞癌风险增加(p(趋势)≤0.02),未观察到这种关系即使考虑到详细的接触措施和其他风险预测因素,我们的结果也未能支持与使用未对抗雌激素或雌激素加孕激素MHT相关的肺癌风险的任何实质性变化。

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