Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?

<i>APOE</i> ε4 polymorphism has been recently described as a possible association with cognitive deficits in COVID-19 patients. This research aimed to establish the correlation between COVID-19 and cognitive impairment, and the <i>APOE</i> gene polymorphism among outpatients....

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Main Authors: José Wagner Leonel Tavares-Júnior, Danilo Nunes Oliveira, Jean Breno Silveira da Silva, Werbety Lucas Queiroz Feitosa, Artur Victor Menezes Sousa, Samuel Cavalcante Marinho, Letícia Chaves Vieira Cunha, Safira de Brito Gaspar, Carmem Meyve Pereira Gomes, Laís Lacerda Brasil de Oliveira, Caroline Aquino Moreira-Nunes, Emmanuelle Silva Tavares Sobreira, Maria Elisabete Amaral de Moraes, Manoel Alves Sobreira-Neto, Raquel Carvalho Montenegro, Pedro Braga-Neto
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Brain Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3425/13/12/1611
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author José Wagner Leonel Tavares-Júnior
Danilo Nunes Oliveira
Jean Breno Silveira da Silva
Werbety Lucas Queiroz Feitosa
Artur Victor Menezes Sousa
Samuel Cavalcante Marinho
Letícia Chaves Vieira Cunha
Safira de Brito Gaspar
Carmem Meyve Pereira Gomes
Laís Lacerda Brasil de Oliveira
Caroline Aquino Moreira-Nunes
Emmanuelle Silva Tavares Sobreira
Maria Elisabete Amaral de Moraes
Manoel Alves Sobreira-Neto
Raquel Carvalho Montenegro
Pedro Braga-Neto
author_facet José Wagner Leonel Tavares-Júnior
Danilo Nunes Oliveira
Jean Breno Silveira da Silva
Werbety Lucas Queiroz Feitosa
Artur Victor Menezes Sousa
Samuel Cavalcante Marinho
Letícia Chaves Vieira Cunha
Safira de Brito Gaspar
Carmem Meyve Pereira Gomes
Laís Lacerda Brasil de Oliveira
Caroline Aquino Moreira-Nunes
Emmanuelle Silva Tavares Sobreira
Maria Elisabete Amaral de Moraes
Manoel Alves Sobreira-Neto
Raquel Carvalho Montenegro
Pedro Braga-Neto
author_sort José Wagner Leonel Tavares-Júnior
collection DOAJ
description <i>APOE</i> ε4 polymorphism has been recently described as a possible association with cognitive deficits in COVID-19 patients. This research aimed to establish the correlation between COVID-19 and cognitive impairment, and the <i>APOE</i> gene polymorphism among outpatients. We performed a cross-sectional study with confirmed COVID-19 patients and neurological symptoms that persisted for more than three months from onset. <i>APOE</i> genotypes were determined. The final number of patients included in this study was 219, of which 186 blood samples were collected for <i>APOE</i> genotyping, evaluated 4.5 months after COVID-19. Among the participants, 143 patients (65.3%) reported memory impairment symptoms as their primary concern. However, this complaint was objectively verified through screening tests (Addenbrooke Cognitive Examination-Revised and Mini-Mental State Examination) in only 36 patients (16.4%). The group experiencing cognitive decline exhibited a higher prevalence of the <i>APOE</i> ε4 allele than the normal group (30.8% vs. 16.4%, respectively, <i>p</i> = 0.038). Furthermore, <i>the APOE</i> ε4 allele and anxiety symptoms remained significant after multivariate analysis. This study assessed an outpatient population where cognitive changes were the primary complaint, even in mild cases. Moreover, the ε4 allele, sleep disorders, and anxiety symptoms were more frequent in the cognitive decline group.
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spelling doaj.art-64376b1467234826b92cb381fa2553782023-12-22T13:56:46ZengMDPI AGBrain Sciences2076-34252023-11-011312161110.3390/brainsci13121611Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?José Wagner Leonel Tavares-Júnior0Danilo Nunes Oliveira1Jean Breno Silveira da Silva2Werbety Lucas Queiroz Feitosa3Artur Victor Menezes Sousa4Samuel Cavalcante Marinho5Letícia Chaves Vieira Cunha6Safira de Brito Gaspar7Carmem Meyve Pereira Gomes8Laís Lacerda Brasil de Oliveira9Caroline Aquino Moreira-Nunes10Emmanuelle Silva Tavares Sobreira11Maria Elisabete Amaral de Moraes12Manoel Alves Sobreira-Neto13Raquel Carvalho Montenegro14Pedro Braga-Neto15Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilMedicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilHealth Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilHealth Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, BrazilHealth Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, BrazilMedicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilMedicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilMedicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilMedicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, BrazilNeurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil<i>APOE</i> ε4 polymorphism has been recently described as a possible association with cognitive deficits in COVID-19 patients. This research aimed to establish the correlation between COVID-19 and cognitive impairment, and the <i>APOE</i> gene polymorphism among outpatients. We performed a cross-sectional study with confirmed COVID-19 patients and neurological symptoms that persisted for more than three months from onset. <i>APOE</i> genotypes were determined. The final number of patients included in this study was 219, of which 186 blood samples were collected for <i>APOE</i> genotyping, evaluated 4.5 months after COVID-19. Among the participants, 143 patients (65.3%) reported memory impairment symptoms as their primary concern. However, this complaint was objectively verified through screening tests (Addenbrooke Cognitive Examination-Revised and Mini-Mental State Examination) in only 36 patients (16.4%). The group experiencing cognitive decline exhibited a higher prevalence of the <i>APOE</i> ε4 allele than the normal group (30.8% vs. 16.4%, respectively, <i>p</i> = 0.038). Furthermore, <i>the APOE</i> ε4 allele and anxiety symptoms remained significant after multivariate analysis. This study assessed an outpatient population where cognitive changes were the primary complaint, even in mild cases. Moreover, the ε4 allele, sleep disorders, and anxiety symptoms were more frequent in the cognitive decline group.https://www.mdpi.com/2076-3425/13/12/1611COVID-19cognitive impairmentlong-COVIDdementia<i>APOE</i>
spellingShingle José Wagner Leonel Tavares-Júnior
Danilo Nunes Oliveira
Jean Breno Silveira da Silva
Werbety Lucas Queiroz Feitosa
Artur Victor Menezes Sousa
Samuel Cavalcante Marinho
Letícia Chaves Vieira Cunha
Safira de Brito Gaspar
Carmem Meyve Pereira Gomes
Laís Lacerda Brasil de Oliveira
Caroline Aquino Moreira-Nunes
Emmanuelle Silva Tavares Sobreira
Maria Elisabete Amaral de Moraes
Manoel Alves Sobreira-Neto
Raquel Carvalho Montenegro
Pedro Braga-Neto
Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
Brain Sciences
COVID-19
cognitive impairment
long-COVID
dementia
<i>APOE</i>
title Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
title_full Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
title_fullStr Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
title_full_unstemmed Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
title_short Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
title_sort post covid 19 cognitive decline and apoe polymorphism towards a possible link
topic COVID-19
cognitive impairment
long-COVID
dementia
<i>APOE</i>
url https://www.mdpi.com/2076-3425/13/12/1611
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