{"id":51035,"date":"2021-09-29T22:38:12","date_gmt":"2021-09-29T21:38:12","guid":{"rendered":"https:\/\/blogs.bmj.com\/bmj\/?p=51035"},"modified":"2021-09-30T08:05:52","modified_gmt":"2021-09-30T07:05:52","slug":"menopausal-hormone-therapy-and-dementia","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/bmj\/2021\/09\/29\/menopausal-hormone-therapy-and-dementia\/","title":{"rendered":"Menopausal hormone therapy and dementia"},"content":{"rendered":"<p><i><span style=\"font-weight: 400\">Evidence is reassuring for women using hormone therapy to treat menopausal symptoms<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400\">The <a href=\"https:\/\/www.bmj.com\/content\/374\/bmj.n2182\">case-control study by Vinogradova and colleagues<\/a><\/span><span style=\"font-weight: 400\">\u00a0<\/span><span style=\"font-weight: 400\">reports reassuring findings on menopausal hormone therapy (commonly known as hormone replacement therapy in the UK) and risk of dementia. [<\/span><span style=\"font-weight: 400\">1,2]<\/span><span style=\"font-weight: 400\"> An improved understanding of the risks and benefits of hormone therapy is needed to promote evidence based management of menopausal symptoms in women. Concern about the risk of dementia with menopausal hormone therapy stemmed from the Women\u2019s Health Initiative Memory Study (WHIMS), which showed that incidence of all cause dementia doubled in women aged 65 years and older after treatment with conjugated equine oestrogens and medroxyprogesterone acetate for an average of four years. [<\/span><span style=\"font-weight: 400\">1]<\/span><span style=\"font-weight: 400\"> A later article from that study found no increased risk of all cause dementia with conjugated equine oestrogens alone, whereas pooled analyses of both formulations showed a 76% increased risk. [<\/span><span style=\"font-weight: 400\">2]<\/span><span style=\"font-weight: 400\"> WHIMS remains the only large scale randomised trial of hormone therapy for the primary prevention of dementia. Trials of hormone therapy and cognitive function among women in early menopause, however, showed neutral results. [<\/span><span style=\"font-weight: 400\">3-5]<\/span><span style=\"font-weight: 400\"> Thus, key questions remain unanswered. Does oestrogen alone have greater cognitive safety than oestrogen and progestogen combined? Does timing or duration of use, or both, matter? Are the WHIMS findings generalisable to women in early menopause or to women using other hormone formulations?<\/span><\/p>\n<p><span style=\"font-weight: 400\">The new large scale study of 615<\/span><span style=\"font-weight: 400\">\u2009<\/span><span style=\"font-weight: 400\">917 women, including 118<\/span><span style=\"font-weight: 400\">\u2009<\/span><span style=\"font-weight: 400\">501 cases of dementia, allowed for examination of key factors that could not be dealt with in WHIMS. A main finding was that the risk of dementia differed depending on the use of progestogens. Oestrogen alone was associated with a 15% decreased odds of dementia overall among women younger than 80 years who received treatment for at least 10 years, with a 1.1% decrease in risk for each year of treatment. Conversely, oestrogen and progestogen combined was associated with a 11% increased risk of Alzheimer\u2019s disease dementia among women who had used hormone therapy for 5-9 years and a 19% increased risk among women treated for 10 years or more. Results were similar to an 18 year follow-up study of causes of mortality in 27<\/span><span style=\"font-weight: 400\">\u2009<\/span><span style=\"font-weight: 400\">347 women enrolled in the Women\u2019s Health Study randomised trial where treatment with conjugated equine oestrogens alone was associated with a 26% decreased risk of death from Alzheimer\u2019s disease or other dementias, but this risk was not altered with use of conjugated equine oestrogens plus medroxyprogesterone acetate. [<\/span><span style=\"font-weight: 400\">6]<\/span><span style=\"font-weight: 400\"> In the current study, risk of dementia with this combined treatment was similar to that with other progestogens. Of all combination formulations, oestrogen-dydrogesterone use for one to 11 years was associated with the lowest risk (adjusted odds ratio 0.88, 95% confidence interval 0.75 to 1.02). Micronised progesterone was not specifically examined. In earlier studies from these investigators, oestrogen-dydrogesterone was associated with the lowest risk for breast cancer and thromboembolic events compared with other formulations. [<\/span><span style=\"font-weight: 400\">7,8]<\/span><\/p>\n<p><span style=\"font-weight: 400\">Some previous cohort studies support the \u201ctiming hypothesis\u201d that earlier initiation of hormone therapy might confer greater protection against Alzheimer\u2019s disease compared with later use. [<\/span><span style=\"font-weight: 400\">9,10]<\/span><span style=\"font-weight: 400\"> The current study could not address this important issue. In the study, the mean age of cases was 83.5 years and mean duration of treatment in the study period was 16 years, for an average age of 67.5 years at first captured prescription. Most women initiate hormone therapy for symptom relief earlier in the postmenopause period. Women classified as hormone therapy users in this study might have received treatment for several years before the study period, and women classified as non-users might have used hormone therapy earlier in their life but had no prescriptions listed. The authors argue that under-calculation of drug use was unlikely because the findings from a subgroup of women with a diagnosis of dementia when younger than 80 years\u2014a group with more complete data on hormone therapy\u2014were similar to findings overall. That subgroup, however, was the only group to show a statistically significantly lower risk of dementia with oestrogen alone. In this context, early initiation and use of progestogen might be important factors in conferring a decreased risk of dementia.<\/span><\/p>\n<p><span style=\"font-weight: 400\">Observational studies of hormone therapy and dementia risk have other limitations. The potential for confounding by indication is a consideration, particularly for the period 1998-2002 when the view that hormone therapy might protect against dementia could have led to bias in prescribing treatment to women with cognitive concerns or frank dementia. Detection bias, particularly after publication of the WHIMS article in 2003, <\/span><span style=\"font-weight: 400\">could have led to more routine or complete ascertainment of dementia in women who had regular medical visits and prescription refills, compared with women not seen regularly. [1]\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400\">Overall, these observations do not change the recommendation that menopausal hormone therapy should not be used to prevent dementia. [<\/span><span style=\"font-weight: 400\">11]<\/span><span style=\"font-weight: 400\"> At the same time, it is helpful for providers to put dementia findings in context for patients. No increase in risk of dementia was observed with oestrogen alone in this case-control study, and, for oestrogen plus progestogen, the increased risk was five to seven extra cases per 10<\/span><span style=\"font-weight: 400\">\u2009<\/span><span style=\"font-weight: 400\">000 woman years. The primary indication for hormone therapy continues to be the treatment of vasomotor symptoms, and the current study should provide reassurance for women and their providers when treatment is prescribed for that reason.<\/span><\/p>\n<p><em><span style=\"font-weight: 400\"><strong>Pauline M Maki<\/strong>, professor, <\/span><span style=\"font-weight: 400\">Department of Psychiatry, Psychology, and Obstetrics &amp; Gynecology, University of Illinois at Chicago, Chicago, IL, USA.<\/span><\/em><\/p>\n<p><em><span style=\"font-weight: 400\"><strong>JoAnn E Manson<\/strong>, professor, <\/span><span style=\"font-weight: 400\">Department of Medicine, Brigham and Women\u2019s Hospital and Harvard Medical School, Boston, MA, USA and <\/span><span style=\"font-weight: 400\">Department of Epidemiology, Harvard T H Chan School of Public Health, Boston, MI, USA.<\/span><\/em><\/p>\n<p><em><span style=\"font-weight: 400\"><strong>Competing interests<\/strong>: PMM has served as a paid consultant for AbbVie, Astellas, Balchem, Bayer, Johnson &amp; Johnson, and Pfizer unrelated to the topic of this opinion.\u00a0 <\/span><\/em><\/p>\n<p><em><span style=\"font-weight: 400\">Provenance and peer review: commissioned; not peer reviewed.<\/span><\/em><\/p>\n<p><strong>References<\/strong>:<\/p>\n<ol>\n<li><span style=\"font-weight: 400\"> Shumaker S, Legault C, Rapp S, et al. Estrogen plus progestin and the incidence of dementia and mild cognitive impairment in postmenopausal women: The Women&#8217;s Health Initiative Memory Study: a randomized controlled trial. <\/span><i><span style=\"font-weight: 400\">JAMA<\/span><\/i><span style=\"font-weight: 400\"> 2003;289:2651-62.<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Shumaker S, Legault C, Kuller L, et al. Conjugated equine estrogens and incidence of probable dementia and mild cognitive impairment in postmenopausal women: Women&#8217;s Health Initiative Memory Study. <\/span><i><span style=\"font-weight: 400\">JAMA<\/span><\/i><span style=\"font-weight: 400\"> 2004;291:2947-58.<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Gleason CE, Dowling NM, Wharton W, et al. Effects of hormone therapy on cognition and mood in recently postmenopausal women: Findings from the randomized, controlled KEEPS-Cognitive and Affective Study. <\/span><i><span style=\"font-weight: 400\">PLoS medicine<\/span><\/i><span style=\"font-weight: 400\"> 2015;12(6):e1001833. doi: 10.1371\/journal.pmed.1001833<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Henderson VW, St John JA, Hodis HN, et al. Cognitive effects of estradiol after menopause: A randomized trial of the timing hypothesis. <\/span><i><span style=\"font-weight: 400\">Neurology<\/span><\/i><span style=\"font-weight: 400\"> 2016;87(7):699-708. doi: 10.1212\/WNL.0000000000002980<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Espeland MA, Shumaker SA, Leng I, et al. Long-term effects on cognitive function of postmenopausal hormone therapy prescribed to women aged 50 to 55 Years. <\/span><i><span style=\"font-weight: 400\">JAMA Intern Med<\/span><\/i><span style=\"font-weight: 400\"> 2013:1-8. doi: 10.1001\/jamainternmed.2013.7727\u00a0<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Manson JE, Aragaki AK, Rossouw JE, et al. Menopausal hormone therapy and long-term all-cause and cause-specific mortality: The Women&#8217;s Health Initiative Randomized Trials. <\/span><i><span style=\"font-weight: 400\">JAMA<\/span><\/i><span style=\"font-weight: 400\"> 2017;318(10):927-38. doi: 10.1001\/jama.2017.11217<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Vinogradova Y, Coupland C, Hippisley-Cox J. Use of hormone replacement therapy and risk of venous thromboembolism: nested case-control studies using the QResearch and CPRD databases. <\/span><i><span style=\"font-weight: 400\">BMJ<\/span><\/i><span style=\"font-weight: 400\"> 2019;364:k4810. doi: 10.1136\/bmj.k4810<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Vinogradova Y, Coupland C, Hippisley-Cox J. Use of hormone replacement therapy and risk of breast cancer: nested case-control studies using the QResearch and CPRD databases. <\/span><i><span style=\"font-weight: 400\">BMJ<\/span><\/i><span style=\"font-weight: 400\"> 2020;371:m3873. doi: 10.1136\/bmj.m3873<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Whitmer RA, Quesenberry CP, Zhou J, et al. Timing of hormone therapy and dementia: the critical window theory revisited. <\/span><i><span style=\"font-weight: 400\">Ann Neurol<\/span><\/i><span style=\"font-weight: 400\"> 2011;69(1):163-9. doi: 10.1002\/ana.22239\u00a0<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Shao H, Breitner JC, Whitmer RA, et al. Hormone therapy and Alzheimer disease dementia: new findings from the Cache County Study. <\/span><i><span style=\"font-weight: 400\">Neurology<\/span><\/i><span style=\"font-weight: 400\"> 2012;79(18):1846-52. doi: 10.1212\/WNL.0b013e318271f823<\/span><\/li>\n<li><span style=\"font-weight: 400\"> The NHTPSAP. The 2017 hormone therapy position statement of The North American Menopause Society. <\/span><i><span style=\"font-weight: 400\">Menopause<\/span><\/i><span style=\"font-weight: 400\"> 2017;24(7):728-53. doi: 10.1097\/GME.0000000000000921<\/span><\/li>\n<li><span style=\"font-weight: 400\"> Vinogradova Y, Dening T, Hippisley-Cox J, Taylor L, Moore M, Coupland C. Use of menopausal hormone therapy and risk of dementia: nested case-control studies using QResearch and CPRD databases. <\/span><i><span style=\"font-weight: 400\">BMJ<\/span><\/i><span style=\"font-weight: 400\"> 2021;374:n2182.<\/span><\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Evidence is reassuring for women using hormone therapy to treat menopausal symptoms The case-control study by Vinogradova and colleagues\u00a0reports reassuring findings on menopausal hormone therapy (commonly known as hormone replacement [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/bmj\/2021\/09\/29\/menopausal-hormone-therapy-and-dementia\/\">More&#8230;<\/a><\/p>\n","protected":false},"author":66,"featured_media":51052,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18894],"tags":[],"class_list":["post-51035","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-authors-perspective"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - 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