Menopausal hormone therapy is associated with worse levels of Alzheimer's disease biomarkers in <i>APOE</i> ε4‐carrying women: An observational study

Significant interactions were found between apolipoprotein E (APOE) ε4 and menopausal hormone therapy (MHT) use for cerebrospinal fluid (CSF) phosphorylated tau (p-tau)/amyloid beta (Aβ)42 and Aβ42/40 ratios. APOE ε4 carriers who were MHT users showed worse levels of CSF biomarkers than non-users and non-carriers, both users and non-users. Younger age at MHT initiation was associated with worse levels of the p-tau/Aβ42 and Aβ42/40 ratios in carriers only. The presence of both APOE ε4 carriage and MHT use may be associated with elevated amyloid deposition and AD pathology. Further studies with larger sample sizes are necessary to confirm the differences observed in the current study.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-01-09
DOI
https://doi.org/10.1002/alz.14456
Citations
11
Primary Topic
Menopause: Health Impacts and Treatments
Type
article
Field-Weighted Citation Impact
14.24

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article

Menopausal hormone therapy is associated with worse levels of Alzheimer's disease biomarkers in APOE ε4‐carrying women: An observational study

Bruce P. Hermann, Carey Elizabeth Gleason, Barbara B. Bendlin, Eef Hogervorst et al.
11 citations
Alzheimer s & Dementia
Menopause: Health Impacts and Treatments
14.24
article

Menopausal hormone therapy is associated with worse levels of Alzheimer's disease biomarkers in APOE ε4‐carrying women: An observational study

Bruce P. Hermann, Carey Elizabeth Gleason, Barbara B. Bendlin, Eef Hogervorst, Davide Bruno, Ainara Jauregi Zinkunegi, Kimberly D. Mueller, Sterling C. Johnson, Rebecca Langhough, Kaj Blennow, Henrik Zetterberg
article en
11 citations

Abstract

Significant interactions were found between apolipoprotein E (APOE) ε4 and menopausal hormone therapy (MHT) use for cerebrospinal fluid (CSF) phosphorylated tau (p-tau)/amyloid beta (Aβ)42 and Aβ42/40 ratios. APOE ε4 carriers who were MHT users showed worse levels of CSF biomarkers than non-users and non-carriers, both users and non-users. Younger age at MHT initiation was associated with worse levels of the p-tau/Aβ42 and Aβ42/40 ratios in carriers only. The presence of both APOE ε4 carriage and MHT use may be associated with elevated amyloid deposition and AD pathology. Further studies with larger sample sizes are necessary to confirm the differences observed in the current study.

Alzheimer s & DementiaVol. 21(2)
University of Wisconsin–Madison (US), Loughborough University (GB), Hong Kong Science and Technology Parks Corporation (HK), Sahlgrenska University Hospital (SE), Geriatric Research Education and Clinical Center (US), UK Dementia Research Institute (GB), William S. Middleton Memorial Veterans Hospital (US), University College London (GB), Liverpool John Moores University (GB), University of Gothenburg (SE)
Alzheimer's Association, Alzheimer's Drug Discovery Foundation, European Commission, Liverpool John Moores University, Vetenskapsrådet, National Institutes of Health, HORIZON EUROPE Framework Programme, National Institute on Aging
Good health and well-being
Openalex Percentile: Top 1%
Menopause: Health Impacts and Treatments
14.24
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