Department of Microbiology, Tumour and Cell Biology, Centre for Translational Microbiome Research (CTMR), Karolinska Institutet, Stockholm, Sweden.
Science for Life Laboratory (SciLifeLab), Stockholm, Sweden.
Acta Oncol. 2022 May;61(5):632-640. doi: 10.1080/0284186X.2022.2033316. Epub 2022 Feb 7.
The net effect of menopausal hormone therapy on the risk of death is understudied, and current evidence is conflicting. Our aim was to investigate the association between menopausal hormones and risk of all-cause, cardiovascular, and cancer-specific mortality, based on the Swedish Prescribed Drug Registry and National Patient Registry.
This Swedish population-based matched cohort study included all women, 40 years or older, who had received at least one prescription of systemic menopausal hormone therapy between 2005-2014 ( = 290,186), group level matched 1:3 to non-users ( = 870,165). Multivariable conditional logistic regression models estimated the relative risk of all-cause and cause-specific mortality, adjusting for several clinical factors and comorbidities.
Ever-use of menopausal hormones was associated with a slightly lower overall odds of all-cause (OR = 0.97, 95%CI 0.95-0.98) and cardiovascular (OR = 0.97, 95%CI 0.95-0.99) mortality, whilst 30% lower overall odds of cancer-related mortality (OR = 0.70, 95%CI 0.68-0.72) was shown. The odds of all-cause and cancer-related mortality were consistently reduced among women who began menopausal hormone therapy ≤60 years, whereas the association with cardiovascular mortality was inconsistent. In contrast, oestrogen-only therapy was associated with elevated odds of all-cause (OR = 1.14, 95%CI 1.11-1.16) and cardiovascular mortality (OR = 1.04, 95%CI 1.01-1.06) among women who began treatment at ≥70 years. Among current users, oestrogen-only therapy was associated with higher odds of all-cause (OR = 1.48, 95%CI 1.44-1.52) and cardiovascular mortality (OR = 1.24, 95%CI 1.20-1.28), whereas past use of oestrogen-only therapy suggested lower odds of mortality.
Our generalisable data suggest that early menopausal hormone treatment initiation does not increase the odds of mortality. However, the role of oestrogens in particularly cardiovascular mortality remains to be investigated.
绝经激素治疗对死亡风险的净效应研究较少,目前的证据相互矛盾。我们的目的是基于瑞典处方药物登记处和国家患者登记处,研究绝经激素与全因、心血管和癌症特异性死亡率之间的关联。
这项瑞典基于人群的匹配队列研究纳入了 2005-2014 年期间至少接受过一次系统绝经激素治疗的所有 40 岁及以上的女性(n=290186),按组水平以 1:3 比例与非使用者匹配(n=870165)。多变量条件逻辑回归模型调整了多种临床因素和合并症后,估计了全因和病因特异性死亡率的相对风险。
绝经激素的使用与全因(OR=0.97,95%CI 0.95-0.98)和心血管(OR=0.97,95%CI 0.95-0.99)死亡率的总体降低几率略有相关,而癌症相关死亡率的总体降低几率为 30%(OR=0.70,95%CI 0.68-0.72)。对于 60 岁及以下开始绝经激素治疗的女性,全因和癌症相关死亡率的几率持续降低,而与心血管死亡率的关联则不一致。相比之下,雌激素单药治疗与 70 岁及以上开始治疗的女性全因(OR=1.14,95%CI 1.11-1.16)和心血管(OR=1.04,95%CI 1.01-1.06)死亡率的升高几率相关。在当前使用者中,雌激素单药治疗与全因(OR=1.48,95%CI 1.44-1.52)和心血管(OR=1.24,95%CI 1.20-1.28)死亡率的升高几率相关,而过去使用雌激素单药治疗则表明死亡率降低的几率较低。
我们的可推广数据表明,早期开始绝经激素治疗不会增加死亡率的几率。然而,雌激素在心血管死亡率中的作用仍需进一步研究。