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No association between CTNNBL1 and episodic memory performance
Polymorphisms in the gene encoding catenin-β-like 1 (CTNNBL1) were recently reported to be associated with verbal episodic memory performance—in particular, delayed verbal free recall assessed between 5 and 30 min after encoding—in a genome-wide association study on healthy young adults. To further...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203019/ https://www.ncbi.nlm.nih.gov/pubmed/25268258 http://dx.doi.org/10.1038/tp.2014.93 |
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author | Liu, T Li, S-C Papenberg, G Schröder, J Roehr, J T Nietfeld, W Lindenberger, U Bertram, L |
author_facet | Liu, T Li, S-C Papenberg, G Schröder, J Roehr, J T Nietfeld, W Lindenberger, U Bertram, L |
author_sort | Liu, T |
collection | PubMed |
description | Polymorphisms in the gene encoding catenin-β-like 1 (CTNNBL1) were recently reported to be associated with verbal episodic memory performance—in particular, delayed verbal free recall assessed between 5 and 30 min after encoding—in a genome-wide association study on healthy young adults. To further examine the genetic effects of CTNNBL1, we tested for association between 455 single-nucleotide polymorphisms (SNPs) in or near CTNNBL1 and 14 measures of episodic memory performance from three different tasks in 1743 individuals. Probands were part of a population-based study of mentally healthy adult men and women, who were between 20 and 70 years old and were recruited as participants for the Berlin Aging Study II. Associations were assessed using linear regression analysis. Despite having sufficient power to detect the previously reported effect sizes, we found no evidence for statistically significant associations between the tested CTNNBL1 SNPs and any of the 14 measures of episodic memory. The previously reported effects of genetic polymorphisms in CTNNBL1 on episodic memory performance do not generalize to the broad range of tasks assessed in our cohort. If not altogether spurious, the effects may be limited to a very narrow phenotypic domain (that is, verbal delayed free recall between 5 and 30 min). More studies are needed to further clarify the role of CTNNBL1 in human memory. |
format | Online Article Text |
id | pubmed-4203019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42030192014-11-06 No association between CTNNBL1 and episodic memory performance Liu, T Li, S-C Papenberg, G Schröder, J Roehr, J T Nietfeld, W Lindenberger, U Bertram, L Transl Psychiatry Original Article Polymorphisms in the gene encoding catenin-β-like 1 (CTNNBL1) were recently reported to be associated with verbal episodic memory performance—in particular, delayed verbal free recall assessed between 5 and 30 min after encoding—in a genome-wide association study on healthy young adults. To further examine the genetic effects of CTNNBL1, we tested for association between 455 single-nucleotide polymorphisms (SNPs) in or near CTNNBL1 and 14 measures of episodic memory performance from three different tasks in 1743 individuals. Probands were part of a population-based study of mentally healthy adult men and women, who were between 20 and 70 years old and were recruited as participants for the Berlin Aging Study II. Associations were assessed using linear regression analysis. Despite having sufficient power to detect the previously reported effect sizes, we found no evidence for statistically significant associations between the tested CTNNBL1 SNPs and any of the 14 measures of episodic memory. The previously reported effects of genetic polymorphisms in CTNNBL1 on episodic memory performance do not generalize to the broad range of tasks assessed in our cohort. If not altogether spurious, the effects may be limited to a very narrow phenotypic domain (that is, verbal delayed free recall between 5 and 30 min). More studies are needed to further clarify the role of CTNNBL1 in human memory. Nature Publishing Group 2014-09 2014-09-30 /pmc/articles/PMC4203019/ /pubmed/25268258 http://dx.doi.org/10.1038/tp.2014.93 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Liu, T Li, S-C Papenberg, G Schröder, J Roehr, J T Nietfeld, W Lindenberger, U Bertram, L No association between CTNNBL1 and episodic memory performance |
title | No association between CTNNBL1 and episodic memory performance |
title_full | No association between CTNNBL1 and episodic memory performance |
title_fullStr | No association between CTNNBL1 and episodic memory performance |
title_full_unstemmed | No association between CTNNBL1 and episodic memory performance |
title_short | No association between CTNNBL1 and episodic memory performance |
title_sort | no association between ctnnbl1 and episodic memory performance |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203019/ https://www.ncbi.nlm.nih.gov/pubmed/25268258 http://dx.doi.org/10.1038/tp.2014.93 |
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