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AKT1 and neurocognition in schizophrenia.

Publication ,  Journal Article
Pinheiro, AP; Keefe, RSE; Skelly, T; Olarte, M; Leviel, K; Lange, LA; Lange, EM; Stroup, TS; Lieberman, J; Sullivan, PF
Published in: Aust N Z J Psychiatry
February 2007

OBJECTIVE: Previous research has shown conflicting results for the significance of five v-akt murine thymoma viral oncogene homolog 1 (AKT1) single-nucleotide polymorphisms (SNPs) to the aetiology of schizophrenia. Neurocognition is a plausible endophenotype for schizophrenia and it was reasoned that the lack of agreement might be due to variability in neurocognition across studies. Therefore, the association of genetic variation in AKT1 with neurocognition was investigated in patients with schizophrenia. METHODS: The same five SNPs used in previous studies of the etiology of schizophrenia (rs2494732, rs2498799, rs3730358, rs1130214, [corrected] and rs3803300) were genotyped in 641 individuals with schizophrenia who had participated in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) project. The primary dependent variable was a neurocognitive composite score and exploratory analyses investigated five domain scores (processing speed, reasoning, verbal memory, working memory, and vigilance). RESULTS: There were no significant asymptotic or empirical associations between any SNP and the neurocognitive composite score. The authors also investigated the association of five-SNP haplotypes with the neurocognitive composite score. A marginally significant association was observed for the neurocognitive composite score with one of the five-SNP haplotypes (global score statistic 19.51, df = 9, permutation p = 0.02). Exploratory analyses of five domain scores (processing speed, reasoning, verbal memory, working memory, and vigilance) were non-significant for all five SNPs. CONCLUSION: Results published to date for an association between genetic variation in AKT1 with schizophrenia are inconsistent. The results suggest that the AKT1 markers studied are not associated with neurocognition in schizophrenia, and do not support unassessed variation in neurocognitive scores as a reason for this discrepancy.

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Published In

Aust N Z J Psychiatry

DOI

ISSN

0004-8674

Publication Date

February 2007

Volume

41

Issue

2

Start / End Page

169 / 177

Location

England

Related Subject Headings

  • Treatment Outcome
  • Schizophrenia
  • Racial Groups
  • Psychiatry
  • Proto-Oncogene Proteins c-akt
  • Neuropsychological Tests
  • Middle Aged
  • Male
  • Linkage Disequilibrium
  • Humans
 

Citation

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Pinheiro, A. P., Keefe, R. S. E., Skelly, T., Olarte, M., Leviel, K., Lange, L. A., … Sullivan, P. F. (2007). AKT1 and neurocognition in schizophrenia. Aust N Z J Psychiatry, 41(2), 169–177. https://doi.org/10.1080/00048670601109956
Pinheiro, Andrea Poyastro, Richard S. E. Keefe, Tara Skelly, Megan Olarte, Keren Leviel, Leslie A. Lange, Ethan M. Lange, T Scott Stroup, Jeffrey Lieberman, and Patrick F. Sullivan. “AKT1 and neurocognition in schizophrenia.Aust N Z J Psychiatry 41, no. 2 (February 2007): 169–77. https://doi.org/10.1080/00048670601109956.
Pinheiro AP, Keefe RSE, Skelly T, Olarte M, Leviel K, Lange LA, et al. AKT1 and neurocognition in schizophrenia. Aust N Z J Psychiatry. 2007 Feb;41(2):169–77.
Pinheiro, Andrea Poyastro, et al. “AKT1 and neurocognition in schizophrenia.Aust N Z J Psychiatry, vol. 41, no. 2, Feb. 2007, pp. 169–77. Pubmed, doi:10.1080/00048670601109956.
Pinheiro AP, Keefe RSE, Skelly T, Olarte M, Leviel K, Lange LA, Lange EM, Stroup TS, Lieberman J, Sullivan PF. AKT1 and neurocognition in schizophrenia. Aust N Z J Psychiatry. 2007 Feb;41(2):169–177.
Journal cover image

Published In

Aust N Z J Psychiatry

DOI

ISSN

0004-8674

Publication Date

February 2007

Volume

41

Issue

2

Start / End Page

169 / 177

Location

England

Related Subject Headings

  • Treatment Outcome
  • Schizophrenia
  • Racial Groups
  • Psychiatry
  • Proto-Oncogene Proteins c-akt
  • Neuropsychological Tests
  • Middle Aged
  • Male
  • Linkage Disequilibrium
  • Humans