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Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia
BACKGROUND: Based on genome-wide association studies, a single-nucleotide polymorphism in the NRGN gene (rs12807809) is considered associated with schizophrenia (SZ). Moreover, hippocampal dysfunction is associated with rs12807809. In addition, converging evidence suggests that hippocampal dysfuncti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451258/ https://www.ncbi.nlm.nih.gov/pubmed/30953482 http://dx.doi.org/10.1186/s12888-019-2088-5 |
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author | Zhang, Yifan Gong, Xiaohong Yin, Zhiyang Cui, Lingling Yang, Jian Wang, Pengshuo Zhou, Yifang Jiang, Xiaowei Wei, Shengnan Wang, Fei Tang, Yanqing |
author_facet | Zhang, Yifan Gong, Xiaohong Yin, Zhiyang Cui, Lingling Yang, Jian Wang, Pengshuo Zhou, Yifang Jiang, Xiaowei Wei, Shengnan Wang, Fei Tang, Yanqing |
author_sort | Zhang, Yifan |
collection | PubMed |
description | BACKGROUND: Based on genome-wide association studies, a single-nucleotide polymorphism in the NRGN gene (rs12807809) is considered associated with schizophrenia (SZ). Moreover, hippocampal dysfunction is associated with rs12807809. In addition, converging evidence suggests that hippocampal dysfunction is involved in SZ pathophysiology. However, the association among rs12807809, hippocampal dysfunction and SZ pathophysiology is unknown. Therefore, this study investigated the association between rs12807809 and hippocampal functional connectivity at rest in SZ. METHODS: In total, 158 participants were studied, including a C-carrier group carrying the non-risk C allele (29 SZ patients and 46 healthy controls) and a TT homozygous group carrying the risk T allele (30 SZ patients and 53 healthy controls). All participants were scanned using resting-state functional magnetic resonance imaging. Hippocampal functional connectivity was computed and compared among the 4 groups. RESULTS: Significant main effects of diagnosis were observed in the functional connectivity between the hippocampus and bilateral fusiform gyrus, bilateral lingual gyrus, left inferior temporal gyrus, left caudate nucleus, bilateral thalamus and bilateral anterior cingulate gyri. In contrast, no significant main effect of genotype was found. In addition, a significant genotype by diagnosis interaction in the functional connectivity between the hippocampus and left anterior cingulate gyrus, as well as bilateral middle cingulate gyri, was observed, with TT homozygotes with SZ showing less functional connectivity than C-carriers with SZ and healthy control TT homozygotes. CONCLUSIONS: These findings are the first to suggest an association between rs12807809 and abnormal Papez circuit function in patients with SZ. This study also implicates NRGN variation and abnormal Papez circuit function in SZ pathophysiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-019-2088-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6451258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64512582019-04-16 Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia Zhang, Yifan Gong, Xiaohong Yin, Zhiyang Cui, Lingling Yang, Jian Wang, Pengshuo Zhou, Yifang Jiang, Xiaowei Wei, Shengnan Wang, Fei Tang, Yanqing BMC Psychiatry Research Article BACKGROUND: Based on genome-wide association studies, a single-nucleotide polymorphism in the NRGN gene (rs12807809) is considered associated with schizophrenia (SZ). Moreover, hippocampal dysfunction is associated with rs12807809. In addition, converging evidence suggests that hippocampal dysfunction is involved in SZ pathophysiology. However, the association among rs12807809, hippocampal dysfunction and SZ pathophysiology is unknown. Therefore, this study investigated the association between rs12807809 and hippocampal functional connectivity at rest in SZ. METHODS: In total, 158 participants were studied, including a C-carrier group carrying the non-risk C allele (29 SZ patients and 46 healthy controls) and a TT homozygous group carrying the risk T allele (30 SZ patients and 53 healthy controls). All participants were scanned using resting-state functional magnetic resonance imaging. Hippocampal functional connectivity was computed and compared among the 4 groups. RESULTS: Significant main effects of diagnosis were observed in the functional connectivity between the hippocampus and bilateral fusiform gyrus, bilateral lingual gyrus, left inferior temporal gyrus, left caudate nucleus, bilateral thalamus and bilateral anterior cingulate gyri. In contrast, no significant main effect of genotype was found. In addition, a significant genotype by diagnosis interaction in the functional connectivity between the hippocampus and left anterior cingulate gyrus, as well as bilateral middle cingulate gyri, was observed, with TT homozygotes with SZ showing less functional connectivity than C-carriers with SZ and healthy control TT homozygotes. CONCLUSIONS: These findings are the first to suggest an association between rs12807809 and abnormal Papez circuit function in patients with SZ. This study also implicates NRGN variation and abnormal Papez circuit function in SZ pathophysiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-019-2088-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-05 /pmc/articles/PMC6451258/ /pubmed/30953482 http://dx.doi.org/10.1186/s12888-019-2088-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhang, Yifan Gong, Xiaohong Yin, Zhiyang Cui, Lingling Yang, Jian Wang, Pengshuo Zhou, Yifang Jiang, Xiaowei Wei, Shengnan Wang, Fei Tang, Yanqing Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title | Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title_full | Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title_fullStr | Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title_full_unstemmed | Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title_short | Association between NRGN gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
title_sort | association between nrgn gene polymorphism and resting-state hippocampal functional connectivity in schizophrenia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451258/ https://www.ncbi.nlm.nih.gov/pubmed/30953482 http://dx.doi.org/10.1186/s12888-019-2088-5 |
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