University of Helsinki and Helsinki University Hospital, Obstetrics and Gynecology, Haartmaninkatu 2, PO Box 140, FIN-00029 HUS, 00029 Helsinki, Finland.
Folkhälsan Research Center, Biomedicum, Helsinki, Finland.
BMJ. 2019 Mar 6;364:l665. doi: 10.1136/bmj.l665.
To compare the use of hormone therapy between Finnish postmenopausal women with and without a diagnosis for Alzheimer's disease.
Nationwide case-control study.
Finnish national population and drug register, between 1999 and 2013.
All postmenopausal women (n=84 739) in Finland who, between 1999 and 2013, received a diagnosis of Alzheimer's disease from a neurologist or geriatrician, and who were identified from a national drug register. Control women without a diagnosis (n=84 739), matched by age and hospital district, were traced from the Finnish national population register.
Data on hormone therapy use were obtained from the Finnish national drug reimbursement register.
Odds ratios and 95% confidence intervals for Alzheimer's disease, calculated with conditional logistic regression analysis.
In 83 688 (98.8%) women, a diagnosis for Alzheimer's disease was made at the age of 60 years or older, and 47 239 (55.7%) women had been over 80 years of age at diagnosis. Use of systemic hormone therapy was associated with a 9-17% increased risk of Alzheimer's disease. The risk of the disease did not differ significantly between users of estradiol only (odds ratio 1.09, 95% confidence interval 1.05 to 1.14) and those of oestrogen-progestogen (1.17, 1.13 to 1.21). The risk increases in users of oestrogen-progestogen therapy were not related to different progestogens (norethisterone acetate, medroxyprogesterone acetate, or other progestogens); but in women younger than 60 at hormone therapy initiation, these risk increases were associated with hormone therapy exposure over 10 years. Furthermore, the age at initiation of systemic hormone therapy was not a decisive determinant for the increase in risk of Alzheimer's disease. The exclusive use of vaginal estradiol did not affect the risk of the disease (0.99, 0.96 to 1.01).
Long term use of systemic hormone therapy might be accompanied with an overall increased risk of Alzheimer's disease, which is not related to the type of progestogen or the age at initiation of systemic hormone therapy. By contrast, use of vaginal estradiol shows no such risk. Even though the absolute risk increase for Alzheimer's disease is small, our data should be implemented into information for present and future users of hormone therapy.
比较芬兰绝经后女性中患有和未患有阿尔茨海默病的人群使用激素疗法的情况。
全国范围内的病例对照研究。
芬兰全国人口和药物登记处,时间为 1999 年至 2013 年。
所有在芬兰的绝经后女性(n=84739),她们在 1999 年至 2013 年间,被神经科医生或老年病学家诊断为阿尔茨海默病,并从全国药物登记处确认。未诊断为阿尔茨海默病的对照组女性(n=84739),按年龄和医院区域匹配,从芬兰全国人口登记处追踪。
激素治疗使用的数据从芬兰国家药物报销登记处获得。
使用条件逻辑回归分析计算的阿尔茨海默病的比值比和 95%置信区间。
在 83688 名(98.8%)女性中,60 岁或以上时被诊断为阿尔茨海默病,47239 名(55.7%)女性在诊断时年龄在 80 岁以上。全身激素治疗与阿尔茨海默病风险增加 9-17%相关。雌激素仅使用者(比值比 1.09,95%置信区间 1.05 至 1.14)和雌激素-孕激素使用者(1.17,1.13 至 1.21)之间的疾病风险差异无统计学意义。雌激素-孕激素治疗使用者的风险增加与不同孕激素(醋酸甲地孕酮、醋酸甲羟孕酮或其他孕激素)无关;但在激素治疗开始时年龄小于 60 岁的女性中,这些风险增加与激素治疗暴露时间超过 10 年有关。此外,全身激素治疗开始的年龄并不是增加阿尔茨海默病风险的决定性因素。单独使用阴道雌二醇不会影响疾病风险(0.99,0.96 至 1.01)。
长期使用全身激素疗法可能会增加整体患阿尔茨海默病的风险,与孕激素类型或全身激素疗法开始的年龄无关。相比之下,使用阴道雌二醇不会有这种风险。尽管阿尔茨海默病的绝对风险增加很小,但我们的数据应该纳入目前和未来激素治疗使用者的信息中。