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Processing speed — A potential candidate cognitive endophenotype for bipolar disorder

BACKGROUND: Bipolar disorder (BD) is a chronic multifactorial disorder that presents with cognitive impairment as one of its main features, in patients as well as in their first-degree relatives. However, the profile of cognitive dysfunction in BD patients and their relatives is not yet well defined...

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Autores principales: Dobri, Mirona Letitia, Prince, Taya, Diaz, Alexandre Paim, Zunta-Soares, Giovana B., Selvaraj, Sudhakar, Machado-Vieira, Rodrigo, Meyer, Thomas D., Sanches, Marsal, Soares, Jair C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957101/
https://www.ncbi.nlm.nih.gov/pubmed/36844417
http://dx.doi.org/10.1016/j.jadr.2022.100459
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author Dobri, Mirona Letitia
Prince, Taya
Diaz, Alexandre Paim
Zunta-Soares, Giovana B.
Selvaraj, Sudhakar
Machado-Vieira, Rodrigo
Meyer, Thomas D.
Sanches, Marsal
Soares, Jair C.
author_facet Dobri, Mirona Letitia
Prince, Taya
Diaz, Alexandre Paim
Zunta-Soares, Giovana B.
Selvaraj, Sudhakar
Machado-Vieira, Rodrigo
Meyer, Thomas D.
Sanches, Marsal
Soares, Jair C.
author_sort Dobri, Mirona Letitia
collection PubMed
description BACKGROUND: Bipolar disorder (BD) is a chronic multifactorial disorder that presents with cognitive impairment as one of its main features, in patients as well as in their first-degree relatives. However, the profile of cognitive dysfunction in BD patients and their relatives is not yet well defined. Various neurocognitive deficits have been proposed as endophenotypes for BD. In the present study, we explored the susceptibility to neurocognitive deficits in BD patients and their siblings compared to healthy controls. METHOD: A sample consisting of patients diagnosed with BD (N=37), their unaffected siblings (N=30) and a healthy control group (N=39) was assessed using the Brief Assessment of Cognition for Affective Disorders (BAC-A) battery of tests in various cognitive domains: memory, processing speed, working memory, reasoning and problem solving, and affective processing. RESULTS: Compared to healthy controls, BD patients and their unaffected siblings showed deficits in attention and motor speed, or processing speed as measured by the Symbol coding task (p = 0.008), as well as a similar degree of impairment (p = 1.000). LIMITATIONS: The lack of statistically significant findings in the other cognitive domains could be related to differences in task difficulty. Most patients were taking psychotropic medication with varying effects on cognition and being treated as outpatients, implying a currently higher level of functioning, which may limit extrapolation of the sample to the general population of BD patients. CONCLUSIONS: These results support the view of considering processing speed as an endophenotype for bipolar disorder.
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spelling pubmed-99571012023-02-24 Processing speed — A potential candidate cognitive endophenotype for bipolar disorder Dobri, Mirona Letitia Prince, Taya Diaz, Alexandre Paim Zunta-Soares, Giovana B. Selvaraj, Sudhakar Machado-Vieira, Rodrigo Meyer, Thomas D. Sanches, Marsal Soares, Jair C. J Affect Disord Rep Article BACKGROUND: Bipolar disorder (BD) is a chronic multifactorial disorder that presents with cognitive impairment as one of its main features, in patients as well as in their first-degree relatives. However, the profile of cognitive dysfunction in BD patients and their relatives is not yet well defined. Various neurocognitive deficits have been proposed as endophenotypes for BD. In the present study, we explored the susceptibility to neurocognitive deficits in BD patients and their siblings compared to healthy controls. METHOD: A sample consisting of patients diagnosed with BD (N=37), their unaffected siblings (N=30) and a healthy control group (N=39) was assessed using the Brief Assessment of Cognition for Affective Disorders (BAC-A) battery of tests in various cognitive domains: memory, processing speed, working memory, reasoning and problem solving, and affective processing. RESULTS: Compared to healthy controls, BD patients and their unaffected siblings showed deficits in attention and motor speed, or processing speed as measured by the Symbol coding task (p = 0.008), as well as a similar degree of impairment (p = 1.000). LIMITATIONS: The lack of statistically significant findings in the other cognitive domains could be related to differences in task difficulty. Most patients were taking psychotropic medication with varying effects on cognition and being treated as outpatients, implying a currently higher level of functioning, which may limit extrapolation of the sample to the general population of BD patients. CONCLUSIONS: These results support the view of considering processing speed as an endophenotype for bipolar disorder. 2023-01 2022-12-07 /pmc/articles/PMC9957101/ /pubmed/36844417 http://dx.doi.org/10.1016/j.jadr.2022.100459 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Dobri, Mirona Letitia
Prince, Taya
Diaz, Alexandre Paim
Zunta-Soares, Giovana B.
Selvaraj, Sudhakar
Machado-Vieira, Rodrigo
Meyer, Thomas D.
Sanches, Marsal
Soares, Jair C.
Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title_full Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title_fullStr Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title_full_unstemmed Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title_short Processing speed — A potential candidate cognitive endophenotype for bipolar disorder
title_sort processing speed — a potential candidate cognitive endophenotype for bipolar disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957101/
https://www.ncbi.nlm.nih.gov/pubmed/36844417
http://dx.doi.org/10.1016/j.jadr.2022.100459
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