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Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression
Subsyndromal symptomatic depression (SSD) and major depressive disorder (MDD) have been classified as distinct diseases, due to their dissimilar gene expression profiles and responses to venlafaxine. To identify specific biomarkers of these two diseases, we conducted a secondary analysis of the gene...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148500/ https://www.ncbi.nlm.nih.gov/pubmed/33971621 http://dx.doi.org/10.18632/aging.202995 |
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author | Hu, Guoqin Yu, Shunying Yuan, Chengmei Hong, Wu Wang, Zuowei Zhang, Ran Wang, Dongxiang Li, Zezhi Yi, Zhenghui Fang, Yiru |
author_facet | Hu, Guoqin Yu, Shunying Yuan, Chengmei Hong, Wu Wang, Zuowei Zhang, Ran Wang, Dongxiang Li, Zezhi Yi, Zhenghui Fang, Yiru |
author_sort | Hu, Guoqin |
collection | PubMed |
description | Subsyndromal symptomatic depression (SSD) and major depressive disorder (MDD) have been classified as distinct diseases, due to their dissimilar gene expression profiles and responses to venlafaxine. To identify specific biomarkers of these two diseases, we conducted a secondary analysis of the gene expression signatures of SSD patients, MDD patients and healthy controls (n=8/group) from the study of Yi et al. Global, individual, specific, enrichment and co-expression analyses were used to compare the transcriptomic profiles of peripheral blood lymphocytes from the three groups. The global and individual analyses revealed that different genes were up- and downregulated in the SSD and MDD groups. Through our specific analysis, we identified 1719 and 3278 differentially expressed genes specifically associated with MDD and SSD, respectively. Enrichment and co-expression analyses demonstrated that the genes specific to MDD were enriched in pathways associated with hormone levels and immune responses, while those specific to SSD were associated with immune function. The specific hub gene for the MDD co-expression network was transmembrane protein 132B (TMEM132B), while the hub genes for SSD were actin-related protein 2/3 complex (ARPC2) and solute carrier family 5 member 5 (SLC5A5). This bioinformatic analysis has provided potential biomarkers that can distinguish SSD from MDD. |
format | Online Article Text |
id | pubmed-8148500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-81485002021-05-26 Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression Hu, Guoqin Yu, Shunying Yuan, Chengmei Hong, Wu Wang, Zuowei Zhang, Ran Wang, Dongxiang Li, Zezhi Yi, Zhenghui Fang, Yiru Aging (Albany NY) Research Paper Subsyndromal symptomatic depression (SSD) and major depressive disorder (MDD) have been classified as distinct diseases, due to their dissimilar gene expression profiles and responses to venlafaxine. To identify specific biomarkers of these two diseases, we conducted a secondary analysis of the gene expression signatures of SSD patients, MDD patients and healthy controls (n=8/group) from the study of Yi et al. Global, individual, specific, enrichment and co-expression analyses were used to compare the transcriptomic profiles of peripheral blood lymphocytes from the three groups. The global and individual analyses revealed that different genes were up- and downregulated in the SSD and MDD groups. Through our specific analysis, we identified 1719 and 3278 differentially expressed genes specifically associated with MDD and SSD, respectively. Enrichment and co-expression analyses demonstrated that the genes specific to MDD were enriched in pathways associated with hormone levels and immune responses, while those specific to SSD were associated with immune function. The specific hub gene for the MDD co-expression network was transmembrane protein 132B (TMEM132B), while the hub genes for SSD were actin-related protein 2/3 complex (ARPC2) and solute carrier family 5 member 5 (SLC5A5). This bioinformatic analysis has provided potential biomarkers that can distinguish SSD from MDD. Impact Journals 2021-05-08 /pmc/articles/PMC8148500/ /pubmed/33971621 http://dx.doi.org/10.18632/aging.202995 Text en Copyright: © 2021 Hu et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Hu, Guoqin Yu, Shunying Yuan, Chengmei Hong, Wu Wang, Zuowei Zhang, Ran Wang, Dongxiang Li, Zezhi Yi, Zhenghui Fang, Yiru Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title | Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title_full | Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title_fullStr | Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title_full_unstemmed | Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title_short | Gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
title_sort | gene expression signatures differentiating major depressive disorder from subsyndromal symptomatic depression |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148500/ https://www.ncbi.nlm.nih.gov/pubmed/33971621 http://dx.doi.org/10.18632/aging.202995 |
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