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Gene expression alterations in the postmortem hippocampus from older patients with bipolar disorder - A hypothesis generating study.
Nascimento, Camila; Kyunghee Kim, Helena; Villela Nunes, Paula; Paraiso Leite, Renata Elaine; Katia Cristina, De Oliveira; Barbosa, André; Bernardi Bertonha, Fernanda; Moreira-Filho, Carlos Alberto; Jacob-Filho, Wilson; Nitrini, Ricardo; Pasqualucci, Carlos A; Tenenholz Grinberg, Lea; Kimie Suemoto, Claudia; Brentani, Helena Paula; Lafer, Beny.
Afiliação
  • Nascimento C; Bipolar Disorder Program, Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil; Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil. Electronic address: camilanascimentomantelli@gmail.com.
  • Kyunghee Kim H; Department of Psychiatry, University of Toronto, ON, Canada. Electronic address: helenakim0913@gmail.com.
  • Villela Nunes P; Bipolar Disorder Program, Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil; Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil. Electronic address: paulavillelanunes@gmail.com.
  • Paraiso Leite RE; Division of Geriatrics, University of Sao Paulo Medical School, SP, Brazil. Electronic address: renata.leite@hc.fm.usp.br.
  • Katia Cristina O; Federal University of ABC, Sao Bernardo do Campo, SP, Brazil. Electronic address: kcristinaoliveira@gmail.com.
  • Barbosa A; Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil. Electronic address: andrecode20@gmail.com.
  • Bernardi Bertonha F; Department of Pediatrics, Faculdade de Medicina da Universidade de São Paulo, SP, Brazil. Electronic address: fernanda.bernardi@fm.usp.br.
  • Moreira-Filho CA; Department of Pediatrics, Faculdade de Medicina da Universidade de São Paulo, SP, Brazil. Electronic address: cmoreira@usp.br.
  • Jacob-Filho W; Division of Geriatrics, University of Sao Paulo Medical School, SP, Brazil. Electronic address: wiljac@usp.br.
  • Nitrini R; Department of Neurology, University of Sao Paulo Medical School, SP, Brazil. Electronic address: rnitrini@uol.com.br.
  • Pasqualucci CA; Department of Pathology, University of Sao Paulo Medical School, SP, Brazil. Electronic address: cpasqua@usp.br.
  • Tenenholz Grinberg L; Department of Pathology, University of Sao Paulo Medical School, SP, Brazil; Memory and Aging Center University of California, San Francisco, USA. Electronic address: Lea.Grinberg@ucsf.edu.
  • Kimie Suemoto C; Division of Geriatrics, University of Sao Paulo Medical School, SP, Brazil. Electronic address: cksuemoto@usp.br.
  • Brentani HP; Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil. Electronic address: helena.brentani@gmail.com.
  • Lafer B; Bipolar Disorder Program, Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil; Department of Psychiatry, University of Sao Paulo Medical School, SP, Brazil. Electronic address: blafer@usp.br.
J Psychiatr Res ; 164: 329-334, 2023 08.
Article em En | MEDLINE | ID: mdl-37393798
ABSTRACT
Bipolar disorder (BD) presents with a progressive course in a subset of patients. However, our knowledge of molecular changes in older BD is limited. In this study, we examined gene expression changes in the hippocampus of BD from the Biobank of Aging Studies to identify genes of interest that warrant further exploration. RNA was extracted from the hippocampus from 11 subjects with BD and 11 age and sex-matched controls. Gene expression data was generated using the SurePrint G3 Human Gene Expression v3 microarray. Rank feature selection was performed to identify a subset of features that can optimally differentiate BD and controls. Genes ranked in the top 0.1% with log2 fold change >1.2 were identified as genes of interest. Average age of the subjects was 64 years old; duration of disease was 21 years and 82% were female. Twenty-five genes were identified, of which all but one was downregulated in BD. Of these, CNTNAP4, MAP4, SLC4A1, COBL, and NEURL4 had been associated with BD and other psychiatric conditions in previous studies. We believe our findings have identified promising targets to inform future studies aiming to understand the pathophysiology of BD in later life.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Psychiatr Res Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Psychiatr Res Ano de publicação: 2023 Tipo de documento: Article