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Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study
OBJECTIVES: To compare the use of hormone therapy between Finnish postmenopausal women with and without a diagnosis for Alzheimer’s disease. DESIGN: Nationwide case-control study. SETTING: Finnish national population and drug register, between 1999 and 2013. PARTICIPANTS: All postmenopausal women (n...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402043/ https://www.ncbi.nlm.nih.gov/pubmed/30842086 http://dx.doi.org/10.1136/bmj.l665 |
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author | Savolainen-Peltonen, Hanna Rahkola-Soisalo, Päivi Hoti, Fabian Vattulainen, Pia Gissler, Mika Ylikorkala, Olavi Mikkola, Tomi S |
author_facet | Savolainen-Peltonen, Hanna Rahkola-Soisalo, Päivi Hoti, Fabian Vattulainen, Pia Gissler, Mika Ylikorkala, Olavi Mikkola, Tomi S |
author_sort | Savolainen-Peltonen, Hanna |
collection | PubMed |
description | OBJECTIVES: To compare the use of hormone therapy between Finnish postmenopausal women with and without a diagnosis for Alzheimer’s disease. DESIGN: Nationwide case-control study. SETTING: Finnish national population and drug register, between 1999 and 2013. PARTICIPANTS: 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. INTERVENTIONS: Data on hormone therapy use were obtained from the Finnish national drug reimbursement register. MAIN OUTCOME MEASURES: Odds ratios and 95% confidence intervals for Alzheimer’s disease, calculated with conditional logistic regression analysis. RESULTS: 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). CONCLUSIONS: 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. |
format | Online Article Text |
id | pubmed-6402043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64020432019-04-04 Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study Savolainen-Peltonen, Hanna Rahkola-Soisalo, Päivi Hoti, Fabian Vattulainen, Pia Gissler, Mika Ylikorkala, Olavi Mikkola, Tomi S BMJ Research OBJECTIVES: To compare the use of hormone therapy between Finnish postmenopausal women with and without a diagnosis for Alzheimer’s disease. DESIGN: Nationwide case-control study. SETTING: Finnish national population and drug register, between 1999 and 2013. PARTICIPANTS: 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. INTERVENTIONS: Data on hormone therapy use were obtained from the Finnish national drug reimbursement register. MAIN OUTCOME MEASURES: Odds ratios and 95% confidence intervals for Alzheimer’s disease, calculated with conditional logistic regression analysis. RESULTS: 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). CONCLUSIONS: 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. BMJ Publishing Group Ltd. 2019-03-06 /pmc/articles/PMC6402043/ /pubmed/30842086 http://dx.doi.org/10.1136/bmj.l665 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Savolainen-Peltonen, Hanna Rahkola-Soisalo, Päivi Hoti, Fabian Vattulainen, Pia Gissler, Mika Ylikorkala, Olavi Mikkola, Tomi S Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title | Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title_full | Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title_fullStr | Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title_full_unstemmed | Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title_short | Use of postmenopausal hormone therapy and risk of Alzheimer’s disease in Finland: nationwide case-control study |
title_sort | use of postmenopausal hormone therapy and risk of alzheimer’s disease in finland: nationwide case-control study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402043/ https://www.ncbi.nlm.nih.gov/pubmed/30842086 http://dx.doi.org/10.1136/bmj.l665 |
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