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Hormone replacement therapy is associated with improved cognition and larger brain volumes in at-risk APOE4 women: results from the European Prevention of Alzheimer's Disease (EPAD) cohort

Hormone replacement therapy is associated with improved cognition and larger brain volumes in at-risk APOE4 women: results from the European Prevention of Alzheimer's Disease (EPAD) cohort
Hormone replacement therapy is associated with improved cognition and larger brain volumes in at-risk APOE4 women: results from the European Prevention of Alzheimer's Disease (EPAD) cohort

BACKGROUND: The risk of dementia is higher in women than men. The metabolic consequences of estrogen decline during menopause accelerate neuropathology in women. The use of hormone replacement therapy (HRT) in the prevention of cognitive decline has shown conflicting results. Here we investigate the modulating role of APOE genotype and age at HRT initiation on the heterogeneity in cognitive response to HRT.

METHODS: The analysis used baseline data from participants in the European Prevention of Alzheimer's Dementia (EPAD) cohort (total n= 1906, women= 1178, 61.8%). Analysis of covariate (ANCOVA) models were employed to test the independent and interactive impact of APOE genotype and HRT on select cognitive tests, such as MMSE, RBANS, dot counting, Four Mountain Test (FMT), and the supermarket trolley test (SMT), together with volumes of the medial temporal lobe (MTL) regions by MRI. Multiple linear regression models were used to examine the impact of age of HRT initiation according to APOE4 carrier status on these cognitive and MRI outcomes.

RESULTS: APOE4 HRT users had the highest RBANS delayed memory index score (P-APOE*HRT interaction = 0.009) compared to APOE4 non-users and to non-APOE4 carriers, with 6-10% larger entorhinal (left) and amygdala (right and left) volumes (P-interaction= 0.002, 0.003, and 0.005 respectively). Earlier introduction of HRT was associated with larger right (standardized β= -0.555, p=0.035) and left hippocampal volumes (standardized β= -0.577, p=0.028) only in APOE4 carriers.

CONCLUSION: HRT introduction is associated with improved delayed memory and larger entorhinal and amygdala volumes in APOE4 carriers only. This may represent an effective targeted strategy to mitigate the higher life-time risk of AD in this large at-risk population subgroup. Confirmation of findings in a fit for purpose RCT with prospective recruitment based on APOE genotype is needed to establish causality.

Female, Humans, Alzheimer Disease/diagnostic imaging, Apolipoprotein E4/genetics, Cognition/physiology, Genotype, Hormone Replacement Therapy, Prospective Studies, Temporal Lobe/pathology
1758-9193
10
Saleh, Rasha N M
bfa165c4-1900-4236-847f-044c70353a80
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
Ritchie, Craig W
8ecda9e0-c362-46f6-afac-a6dd280d7b27
Minihane, Anne Marie
e948b1ec-a626-45d1-9e4b-3f667825a4d8
Saleh, Rasha N M
bfa165c4-1900-4236-847f-044c70353a80
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
Ritchie, Craig W
8ecda9e0-c362-46f6-afac-a6dd280d7b27
Minihane, Anne Marie
e948b1ec-a626-45d1-9e4b-3f667825a4d8

Saleh, Rasha N M, Hornberger, Michael, Ritchie, Craig W and Minihane, Anne Marie (2023) Hormone replacement therapy is associated with improved cognition and larger brain volumes in at-risk APOE4 women: results from the European Prevention of Alzheimer's Disease (EPAD) cohort. Alzheimer's Research & Therapy, 15 (1), 10. (doi:10.1186/s13195-022-01121-5).

Record type: Article

Abstract

BACKGROUND: The risk of dementia is higher in women than men. The metabolic consequences of estrogen decline during menopause accelerate neuropathology in women. The use of hormone replacement therapy (HRT) in the prevention of cognitive decline has shown conflicting results. Here we investigate the modulating role of APOE genotype and age at HRT initiation on the heterogeneity in cognitive response to HRT.

METHODS: The analysis used baseline data from participants in the European Prevention of Alzheimer's Dementia (EPAD) cohort (total n= 1906, women= 1178, 61.8%). Analysis of covariate (ANCOVA) models were employed to test the independent and interactive impact of APOE genotype and HRT on select cognitive tests, such as MMSE, RBANS, dot counting, Four Mountain Test (FMT), and the supermarket trolley test (SMT), together with volumes of the medial temporal lobe (MTL) regions by MRI. Multiple linear regression models were used to examine the impact of age of HRT initiation according to APOE4 carrier status on these cognitive and MRI outcomes.

RESULTS: APOE4 HRT users had the highest RBANS delayed memory index score (P-APOE*HRT interaction = 0.009) compared to APOE4 non-users and to non-APOE4 carriers, with 6-10% larger entorhinal (left) and amygdala (right and left) volumes (P-interaction= 0.002, 0.003, and 0.005 respectively). Earlier introduction of HRT was associated with larger right (standardized β= -0.555, p=0.035) and left hippocampal volumes (standardized β= -0.577, p=0.028) only in APOE4 carriers.

CONCLUSION: HRT introduction is associated with improved delayed memory and larger entorhinal and amygdala volumes in APOE4 carriers only. This may represent an effective targeted strategy to mitigate the higher life-time risk of AD in this large at-risk population subgroup. Confirmation of findings in a fit for purpose RCT with prospective recruitment based on APOE genotype is needed to establish causality.

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More information

Published date: 9 January 2023
Additional Information: © 2023. The Author(s).
Keywords: Female, Humans, Alzheimer Disease/diagnostic imaging, Apolipoprotein E4/genetics, Cognition/physiology, Genotype, Hormone Replacement Therapy, Prospective Studies, Temporal Lobe/pathology

Identifiers

Local EPrints ID: 505373
URI: http://eprints.soton.ac.uk/id/eprint/505373
ISSN: 1758-9193
PURE UUID: 196f2456-ad4b-4212-81e2-82be772d024c
ORCID for Michael Hornberger: ORCID iD orcid.org/0000-0002-2214-3788

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Date deposited: 07 Oct 2025 16:51
Last modified: 08 Oct 2025 02:17

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Contributors

Author: Rasha N M Saleh
Author: Michael Hornberger ORCID iD
Author: Craig W Ritchie
Author: Anne Marie Minihane

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