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

Author:

Tavares-Júnior José Wagner Leonel12,Oliveira Danilo Nunes12,da Silva Jean Breno Silveira3,Queiroz Feitosa Werbety Lucas12ORCID,Sousa Artur Victor Menezes1,Marinho Samuel Cavalcante4,Cunha Letícia Chaves Vieira12,Gaspar Safira de Brito4,Gomes Carmem Meyve Pereira4,de Oliveira Laís Lacerda Brasil3,Moreira-Nunes Caroline Aquino3ORCID,Sobreira Emmanuelle Silva Tavares12,Moraes Maria Elisabete Amaral de3,Sobreira-Neto Manoel Alves12ORCID,Montenegro Raquel Carvalho3,Braga-Neto Pedro124ORCID

Affiliation:

1. Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil

2. Clinical Research Unit, Walter Cantidio University Hospital, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil

3. Medicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil

4. Health Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, Brazil

Abstract

APOE 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 APOE 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. APOE genotypes were determined. The final number of patients included in this study was 219, of which 186 blood samples were collected for APOE 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 APOE ε4 allele than the normal group (30.8% vs. 16.4%, respectively, p = 0.038). Furthermore, the APOE 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.

Funder

Brazilian National Council for Scientific and Technological Development

Coordination for the Improvement of Higher Education Personnel—Brazil

Foundation to Support Scientific and Technological Development

Publisher

MDPI AG

Subject

General Neuroscience

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