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The APOE4 effect: structural brain differences in Alzheimer's disease according to the age at symptom onset

The APOE4 effect: structural brain differences in Alzheimer's disease according to the age at symptom onset
The APOE4 effect: structural brain differences in Alzheimer's disease according to the age at symptom onset

BACKGROUND AND PURPOSE: How the APOE genotype can differentially affect cortical and subcortical memory structures in biomarker-confirmed early-onset (EOAD) and late-onset (LOAD) Alzheimer's disease (AD) was assessed.

METHOD: Eighty-seven cerebrospinal fluid (CSF) biomarker-confirmed AD patients were classified according to their APOE genotype and age at onset. 28 were EOAD APOE4 carriers (+EOAD), 21 EOAD APOE4 non-carriers (-EOAD), 23 LOAD APOE4 carriers (+LOAD) and 15 LOAD APOE4 non-carriers (-LOAD). Grey matter (GM) volume differences were analyzed using voxel-based morphometry in Papez circuit regions. Multiple regression analyses were performed to determine the relation between GM volume loss and cognition.

RESULTS: Significantly more mammillary body atrophy in +EOAD compared to -EOAD is reported. The medial temporal and posterior cingulate cortex showed less GM in +LOAD compared to -LOAD. Medial temporal GM volume loss was also found in +EOAD compared to -LOAD. With an exception for +EOAD, medial temporal GM was strongly associated with episodic memory in the three groups, whilst posterior cingulate cortex GM volume was more related with visuospatial abilities. Visuospatial abilities and episodic memory were also associated with the anterior thalamic nucleus in -LOAD.

CONCLUSIONS: Our results show that the APOE genotype has a significant effect on GM integrity as a function of age of disease onset. Specifically, whilst LOAD APOE4 genotype is mostly associated with increased medial temporal and parietal atrophy compared to -LOAD, for EOAD APOE4 might have a more specific effect on subcortical (mammillary body) structures. The findings suggest that APOE genotype needs to be taken into account when classifying patients by age at onset.

Humans, Alzheimer Disease/diagnostic imaging, Apolipoprotein E4/genetics, Magnetic Resonance Imaging/methods, Age of Onset, Brain/pathology, Atrophy/pathology, Biomarkers
1351-5101
597-605
Forno, Gonzalo
9119ed81-614d-4d2c-b302-7b69a2a498f7
Contador, Jose
e87b1492-61a2-471e-a20b-74dfb251bc7d
Pérez-Millan, Agnès
9a537795-ace6-4647-85f6-ff1a02beb113
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
al, et
df099e87-31d7-4ccf-a9fa-b92a380537f9
Forno, Gonzalo
9119ed81-614d-4d2c-b302-7b69a2a498f7
Contador, Jose
e87b1492-61a2-471e-a20b-74dfb251bc7d
Pérez-Millan, Agnès
9a537795-ace6-4647-85f6-ff1a02beb113
Hornberger, Michael
a48c1c63-422a-4c11-9a51-c7be0aa3026d
al, et
df099e87-31d7-4ccf-a9fa-b92a380537f9

Forno, Gonzalo, Contador, Jose, Pérez-Millan, Agnès, Hornberger, Michael and al, et (2022) The APOE4 effect: structural brain differences in Alzheimer's disease according to the age at symptom onset. European Journal of Neurology, 30 (3), 597-605. (doi:10.1111/ene.15657).

Record type: Article

Abstract

BACKGROUND AND PURPOSE: How the APOE genotype can differentially affect cortical and subcortical memory structures in biomarker-confirmed early-onset (EOAD) and late-onset (LOAD) Alzheimer's disease (AD) was assessed.

METHOD: Eighty-seven cerebrospinal fluid (CSF) biomarker-confirmed AD patients were classified according to their APOE genotype and age at onset. 28 were EOAD APOE4 carriers (+EOAD), 21 EOAD APOE4 non-carriers (-EOAD), 23 LOAD APOE4 carriers (+LOAD) and 15 LOAD APOE4 non-carriers (-LOAD). Grey matter (GM) volume differences were analyzed using voxel-based morphometry in Papez circuit regions. Multiple regression analyses were performed to determine the relation between GM volume loss and cognition.

RESULTS: Significantly more mammillary body atrophy in +EOAD compared to -EOAD is reported. The medial temporal and posterior cingulate cortex showed less GM in +LOAD compared to -LOAD. Medial temporal GM volume loss was also found in +EOAD compared to -LOAD. With an exception for +EOAD, medial temporal GM was strongly associated with episodic memory in the three groups, whilst posterior cingulate cortex GM volume was more related with visuospatial abilities. Visuospatial abilities and episodic memory were also associated with the anterior thalamic nucleus in -LOAD.

CONCLUSIONS: Our results show that the APOE genotype has a significant effect on GM integrity as a function of age of disease onset. Specifically, whilst LOAD APOE4 genotype is mostly associated with increased medial temporal and parietal atrophy compared to -LOAD, for EOAD APOE4 might have a more specific effect on subcortical (mammillary body) structures. The findings suggest that APOE genotype needs to be taken into account when classifying patients by age at onset.

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More information

e-pub ahead of print date: 4 December 2022
Additional Information: © 2022 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.
Keywords: Humans, Alzheimer Disease/diagnostic imaging, Apolipoprotein E4/genetics, Magnetic Resonance Imaging/methods, Age of Onset, Brain/pathology, Atrophy/pathology, Biomarkers

Identifiers

Local EPrints ID: 505378
URI: http://eprints.soton.ac.uk/id/eprint/505378
ISSN: 1351-5101
PURE UUID: 7a15e3e7-5431-4dd4-9fcf-35c5c5de4b91
ORCID for Michael Hornberger: ORCID iD orcid.org/0000-0002-2214-3788

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Date deposited: 07 Oct 2025 16:52
Last modified: 08 Oct 2025 02:17

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Contributors

Author: Gonzalo Forno
Author: Jose Contador
Author: Agnès Pérez-Millan
Author: Michael Hornberger ORCID iD
Author: et al

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