Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment

ABSTRACT Background: The pathogenesis of mild cognitive impairment (MCI) is multifactorial and includes the presence of genetic variants such as the ε4 allele of the apolipoprotein E gene (APOE-ε4). Association between the APOE-ε4 carrier status and deleterious structural and functional changes on magnetic resonance imaging (MRI) has been previously described in individuals with Alzheimer's disease. However, the central nervous system changes may possibly develop in earlier stages of cognitive impairment, as reflected in MCI. Objective: The objective of the study was to determine the association between APOE-ε4 carrier status and qualitative changes on MRI (medial temporal and parietal atrophy), as well as the detection of white matter hyperintensities (WMH) in older adults with MCI, in the memory clinic of a tertiary care hospital in Mexico City. Methods: A cross-sectional study of 72 adults aged 60 years or above who underwent an exhaustive clinical, neuroimaging, and neuropsychological evaluation. Multivariate logistic regression models were constructed to determine the association between APOE-ε4 carrier status and qualitative/quantitative changes on MRI. Results: Mean age was 75.2 years (± 7.2) and 64% were female. Twenty-one participants were cognitively normal and 51 had MCI. Almost 56% were APOE-ε4 carriers and were associated with medial-temporal atrophy according to the Scheltens scale (odds ratio [OR]: 20.0, 95% confidence intervals [CI]: 3.03-131.7), parietal atrophy according to the Koedam's score (OR: 6.3; 95% CI 1.03-39.53), and WMH according to the Fazekas scale (OR: 11.7, 95% CI: 1.26-108.2), even after adjusting for age, educational level, and cardiovascular risk factors. Conclusion: The APOE-ε4 carrier status was associated with medial temporal and parietal atrophy, as well as WMH. Our findings support the hypothesis suggesting the contribution of this genotype to neurodegeneration and cerebral vascular pathology.

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Main Authors: Mimenza-Alvarado,Alberto J., Suing-Ortega,María J., Tusie-Luna,Teresa, Juárez-Cedillo,Teresa, Ávila-Funes,José A., Aguilar-Navarro,Sara G.
Format: Digital revista
Language:English
Published: Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán 2022
Online Access:http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S0034-83762022000200113
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spelling oai:scielo:S0034-837620220002001132022-04-29Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive ImpairmentMimenza-Alvarado,Alberto J.Suing-Ortega,María J.Tusie-Luna,TeresaJuárez-Cedillo,TeresaÁvila-Funes,José A.Aguilar-Navarro,Sara G. Mild cognitive impairment APOE-ε4 carrier status Magnetic resonance imaging Mexican mestizo older adults ABSTRACT Background: The pathogenesis of mild cognitive impairment (MCI) is multifactorial and includes the presence of genetic variants such as the ε4 allele of the apolipoprotein E gene (APOE-ε4). Association between the APOE-ε4 carrier status and deleterious structural and functional changes on magnetic resonance imaging (MRI) has been previously described in individuals with Alzheimer's disease. However, the central nervous system changes may possibly develop in earlier stages of cognitive impairment, as reflected in MCI. Objective: The objective of the study was to determine the association between APOE-ε4 carrier status and qualitative changes on MRI (medial temporal and parietal atrophy), as well as the detection of white matter hyperintensities (WMH) in older adults with MCI, in the memory clinic of a tertiary care hospital in Mexico City. Methods: A cross-sectional study of 72 adults aged 60 years or above who underwent an exhaustive clinical, neuroimaging, and neuropsychological evaluation. Multivariate logistic regression models were constructed to determine the association between APOE-ε4 carrier status and qualitative/quantitative changes on MRI. Results: Mean age was 75.2 years (± 7.2) and 64% were female. Twenty-one participants were cognitively normal and 51 had MCI. Almost 56% were APOE-ε4 carriers and were associated with medial-temporal atrophy according to the Scheltens scale (odds ratio [OR]: 20.0, 95% confidence intervals [CI]: 3.03-131.7), parietal atrophy according to the Koedam's score (OR: 6.3; 95% CI 1.03-39.53), and WMH according to the Fazekas scale (OR: 11.7, 95% CI: 1.26-108.2), even after adjusting for age, educational level, and cardiovascular risk factors. Conclusion: The APOE-ε4 carrier status was associated with medial temporal and parietal atrophy, as well as WMH. Our findings support the hypothesis suggesting the contribution of this genotype to neurodegeneration and cerebral vascular pathology.info:eu-repo/semantics/openAccessInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránRevista de investigación clínica v.74 n.2 20222022-04-01info:eu-repo/semantics/articletext/htmlhttp://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S0034-83762022000200113en10.24875/ric.21000550
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country México
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libraryname SciELO
language English
format Digital
author Mimenza-Alvarado,Alberto J.
Suing-Ortega,María J.
Tusie-Luna,Teresa
Juárez-Cedillo,Teresa
Ávila-Funes,José A.
Aguilar-Navarro,Sara G.
spellingShingle Mimenza-Alvarado,Alberto J.
Suing-Ortega,María J.
Tusie-Luna,Teresa
Juárez-Cedillo,Teresa
Ávila-Funes,José A.
Aguilar-Navarro,Sara G.
Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
author_facet Mimenza-Alvarado,Alberto J.
Suing-Ortega,María J.
Tusie-Luna,Teresa
Juárez-Cedillo,Teresa
Ávila-Funes,José A.
Aguilar-Navarro,Sara G.
author_sort Mimenza-Alvarado,Alberto J.
title Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
title_short Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
title_full Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
title_fullStr Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
title_full_unstemmed Association between APOE-ε4 Carrier Status and Qualitative Neuroimaging Characteristics in Older Adults with Mild Cognitive Impairment
title_sort association between apoe-ε4 carrier status and qualitative neuroimaging characteristics in older adults with mild cognitive impairment
description ABSTRACT Background: The pathogenesis of mild cognitive impairment (MCI) is multifactorial and includes the presence of genetic variants such as the ε4 allele of the apolipoprotein E gene (APOE-ε4). Association between the APOE-ε4 carrier status and deleterious structural and functional changes on magnetic resonance imaging (MRI) has been previously described in individuals with Alzheimer's disease. However, the central nervous system changes may possibly develop in earlier stages of cognitive impairment, as reflected in MCI. Objective: The objective of the study was to determine the association between APOE-ε4 carrier status and qualitative changes on MRI (medial temporal and parietal atrophy), as well as the detection of white matter hyperintensities (WMH) in older adults with MCI, in the memory clinic of a tertiary care hospital in Mexico City. Methods: A cross-sectional study of 72 adults aged 60 years or above who underwent an exhaustive clinical, neuroimaging, and neuropsychological evaluation. Multivariate logistic regression models were constructed to determine the association between APOE-ε4 carrier status and qualitative/quantitative changes on MRI. Results: Mean age was 75.2 years (± 7.2) and 64% were female. Twenty-one participants were cognitively normal and 51 had MCI. Almost 56% were APOE-ε4 carriers and were associated with medial-temporal atrophy according to the Scheltens scale (odds ratio [OR]: 20.0, 95% confidence intervals [CI]: 3.03-131.7), parietal atrophy according to the Koedam's score (OR: 6.3; 95% CI 1.03-39.53), and WMH according to the Fazekas scale (OR: 11.7, 95% CI: 1.26-108.2), even after adjusting for age, educational level, and cardiovascular risk factors. Conclusion: The APOE-ε4 carrier status was associated with medial temporal and parietal atrophy, as well as WMH. Our findings support the hypothesis suggesting the contribution of this genotype to neurodegeneration and cerebral vascular pathology.
publisher Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
publishDate 2022
url http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S0034-83762022000200113
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