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Post-COVID-19 Cognitive Decline and Apoe Polymorphism: Towards a Possible Link?
Tavares-Júnior, José Wagner Leonel; Oliveira, Danilo Nunes; da Silva, Jean Breno Silveira; Queiroz Feitosa, Werbety Lucas; Sousa, Artur Victor Menezes; Marinho, Samuel Cavalcante; Cunha, Letícia Chaves Vieira; Gaspar, Safira de Brito; Gomes, Carmem Meyve Pereira; de Oliveira, Laís Lacerda Brasil; Moreira-Nunes, Caroline Aquino; Sobreira, Emmanuelle Silva Tavares; Moraes, Maria Elisabete Amaral de; Sobreira-Neto, Manoel Alves; Montenegro, Raquel Carvalho; Braga-Neto, Pedro.
  • Tavares-Júnior JWL; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Oliveira DN; Clinical Research Unit, Walter Cantidio University Hospital, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • da Silva JBS; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Queiroz Feitosa WL; Clinical Research Unit, Walter Cantidio University Hospital, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Sousa AVM; Medicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Marinho SC; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Cunha LCV; Clinical Research Unit, Walter Cantidio University Hospital, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Gaspar SB; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Gomes CMP; Health Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, Brazil.
  • de Oliveira LLB; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Moreira-Nunes CA; Clinical Research Unit, Walter Cantidio University Hospital, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Sobreira EST; Health Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, Brazil.
  • Moraes MEA; Health Sciences Center, State University of Ceará (UECE), Fortaleza 60714-903, CE, Brazil.
  • Sobreira-Neto MA; Medicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Montenegro RC; Medicine Research and Development Center (NPDM), Pharmacogenetics Laboratory, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
  • Braga-Neto P; Neurology Division, Clinical Medicine Department, Faculty of Medicine, Federal University of Ceará (UFC), Fortaleza 60020-181, CE, Brazil.
Brain Sci ; 13(12)2023 Nov 21.
Article en En | MEDLINE | ID: mdl-38137059
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.
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