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ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients
The objective of this study was to investigate the expression and clinical role of ATP-binding cassette transporter 13 (ABCA13) gene previously shown to be associated with schizophrenia (SZ) through Genome-wide association studies studies. Thirty-two first-episode drug-naive SZ patients and forty-ei...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726143/ https://www.ncbi.nlm.nih.gov/pubmed/33299069 http://dx.doi.org/10.1038/s41598-020-78530-9 |
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author | Qian, Lu Qin, Yu Chen, Xinyu Zhang, Fuquan Yang, Bixiu Dong, Kunlun Wang, Zhiqiang Zhang, Kai |
author_facet | Qian, Lu Qin, Yu Chen, Xinyu Zhang, Fuquan Yang, Bixiu Dong, Kunlun Wang, Zhiqiang Zhang, Kai |
author_sort | Qian, Lu |
collection | PubMed |
description | The objective of this study was to investigate the expression and clinical role of ATP-binding cassette transporter 13 (ABCA13) gene previously shown to be associated with schizophrenia (SZ) through Genome-wide association studies studies. Thirty-two first-episode drug-naive SZ patients and forty-eight age and gender-matched healthy controls were enrolled in this study. We measured ABCA13 mRNA expression levels using quantitative real-time PCR at baseline and 12 weeks after antipsychotic therapy. Moreover, clinical symptoms were measured by the Positive and Negative Syndrome Scale (PANSS) at baseline and 12-week follow-up. We found that ABCA13 mRNA levels were significantly lower in SZ patients compared with healthy controls at baseline. SZ patients’ symptoms were decreased, but ABCA13 mRNA levels were increased after 12 weeks antipsychotic therapy. In addition, there was a significant difference in ABCA13 mRNA levels among SZ patients at baseline and 12-week follow-up. The ABCA13 mRNA levels were not associated with age, BMI, years of education. Of the clinical symptoms measured, the ABCA13 mRNA levels were negatively associated with the PANSS scores at baseline and 12-week follow-up. The results indicated that the ABCA13 mRNA expression level is of interest, and upon further studies, it could be used as a biomarker for SZ treatment outcome. |
format | Online Article Text |
id | pubmed-7726143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77261432020-12-14 ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients Qian, Lu Qin, Yu Chen, Xinyu Zhang, Fuquan Yang, Bixiu Dong, Kunlun Wang, Zhiqiang Zhang, Kai Sci Rep Article The objective of this study was to investigate the expression and clinical role of ATP-binding cassette transporter 13 (ABCA13) gene previously shown to be associated with schizophrenia (SZ) through Genome-wide association studies studies. Thirty-two first-episode drug-naive SZ patients and forty-eight age and gender-matched healthy controls were enrolled in this study. We measured ABCA13 mRNA expression levels using quantitative real-time PCR at baseline and 12 weeks after antipsychotic therapy. Moreover, clinical symptoms were measured by the Positive and Negative Syndrome Scale (PANSS) at baseline and 12-week follow-up. We found that ABCA13 mRNA levels were significantly lower in SZ patients compared with healthy controls at baseline. SZ patients’ symptoms were decreased, but ABCA13 mRNA levels were increased after 12 weeks antipsychotic therapy. In addition, there was a significant difference in ABCA13 mRNA levels among SZ patients at baseline and 12-week follow-up. The ABCA13 mRNA levels were not associated with age, BMI, years of education. Of the clinical symptoms measured, the ABCA13 mRNA levels were negatively associated with the PANSS scores at baseline and 12-week follow-up. The results indicated that the ABCA13 mRNA expression level is of interest, and upon further studies, it could be used as a biomarker for SZ treatment outcome. Nature Publishing Group UK 2020-12-09 /pmc/articles/PMC7726143/ /pubmed/33299069 http://dx.doi.org/10.1038/s41598-020-78530-9 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Qian, Lu Qin, Yu Chen, Xinyu Zhang, Fuquan Yang, Bixiu Dong, Kunlun Wang, Zhiqiang Zhang, Kai ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title | ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title_full | ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title_fullStr | ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title_full_unstemmed | ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title_short | ATP-binding cassette transporter 13 mRNA expression level in schizophrenia patients |
title_sort | atp-binding cassette transporter 13 mrna expression level in schizophrenia patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726143/ https://www.ncbi.nlm.nih.gov/pubmed/33299069 http://dx.doi.org/10.1038/s41598-020-78530-9 |
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