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PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia
The gene of protein interacting with C kinase 1 alpha (PICK1) has been implicated in schizophrenia, nevertheless, conflicting results existed. However, its role in cognitive function remains unclear. Besides, cognitive deficits impair the long-term outcome. We explored whether the polymorphisms of P...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432511/ https://www.ncbi.nlm.nih.gov/pubmed/28507309 http://dx.doi.org/10.1038/s41598-017-01975-y |
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author | Chen, Yi-Ting Lin, Chieh-Hsin Huang, Chiung-Hsien Liang, Wen-Miin Lane, Hsien-Yuan |
author_facet | Chen, Yi-Ting Lin, Chieh-Hsin Huang, Chiung-Hsien Liang, Wen-Miin Lane, Hsien-Yuan |
author_sort | Chen, Yi-Ting |
collection | PubMed |
description | The gene of protein interacting with C kinase 1 alpha (PICK1) has been implicated in schizophrenia, nevertheless, conflicting results existed. However, its role in cognitive function remains unclear. Besides, cognitive deficits impair the long-term outcome. We explored whether the polymorphisms of PICK1 (rs2076369, rs3952) affected cognitive functions in schizophrenic patients. We analyzed 302 patients and tested the differences of cognitive functions, clinical symptoms between genetic groups. We also used general linear model to analyze the effect of PICK1 genetic polymorphisms on cognitive functions. After adjustment for gender, age, education, the patients with rs2076369 G/T genotype showed better performance than T/T homozygotes in the summary score, global composite score, neurocognitive composite score, category fluency subtest, WAIS-III-Digit Symbol Coding subtest, working memory, WMS-III-Spatial Span (backward) subtest, MSCEIT-managing emotions branch (p = 0.038, 0.025, 0.046, 0.036, 0.025, 0.027, 0.035, 0.028, respectively). G/G homozygotes performed better than T/T in category fluency subtest (p = 0.049). A/A homozygotes of rs3952 performed better than G/G in trail making A subtest (p = 0.048). To our knowledge, this is the first study to indicate that PICK1 polymorphisms may associate with cognitive functions in schizophrenic patients. Further replication studies in healthy controls or other ethnic groups are warranted. |
format | Online Article Text |
id | pubmed-5432511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54325112017-05-17 PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia Chen, Yi-Ting Lin, Chieh-Hsin Huang, Chiung-Hsien Liang, Wen-Miin Lane, Hsien-Yuan Sci Rep Article The gene of protein interacting with C kinase 1 alpha (PICK1) has been implicated in schizophrenia, nevertheless, conflicting results existed. However, its role in cognitive function remains unclear. Besides, cognitive deficits impair the long-term outcome. We explored whether the polymorphisms of PICK1 (rs2076369, rs3952) affected cognitive functions in schizophrenic patients. We analyzed 302 patients and tested the differences of cognitive functions, clinical symptoms between genetic groups. We also used general linear model to analyze the effect of PICK1 genetic polymorphisms on cognitive functions. After adjustment for gender, age, education, the patients with rs2076369 G/T genotype showed better performance than T/T homozygotes in the summary score, global composite score, neurocognitive composite score, category fluency subtest, WAIS-III-Digit Symbol Coding subtest, working memory, WMS-III-Spatial Span (backward) subtest, MSCEIT-managing emotions branch (p = 0.038, 0.025, 0.046, 0.036, 0.025, 0.027, 0.035, 0.028, respectively). G/G homozygotes performed better than T/T in category fluency subtest (p = 0.049). A/A homozygotes of rs3952 performed better than G/G in trail making A subtest (p = 0.048). To our knowledge, this is the first study to indicate that PICK1 polymorphisms may associate with cognitive functions in schizophrenic patients. Further replication studies in healthy controls or other ethnic groups are warranted. Nature Publishing Group UK 2017-05-15 /pmc/articles/PMC5432511/ /pubmed/28507309 http://dx.doi.org/10.1038/s41598-017-01975-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Yi-Ting Lin, Chieh-Hsin Huang, Chiung-Hsien Liang, Wen-Miin Lane, Hsien-Yuan PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title | PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title_full | PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title_fullStr | PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title_full_unstemmed | PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title_short | PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia |
title_sort | pick1 genetic variation and cognitive function in patients with schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432511/ https://www.ncbi.nlm.nih.gov/pubmed/28507309 http://dx.doi.org/10.1038/s41598-017-01975-y |
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