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Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation

BACKGROUND: Major depressive disorder (MDD) and suicide are two major health problems, but there are still no objective methods to diagnose MDD or suicidal ideation (SI). This study was conducted to identify potential biomarkers for diagnosing MDD patients with SI. METHODS: First-episode drug-naïve...

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Autores principales: Bai, Shunjie, Fang, Liang, Xie, Jing, Bai, Huili, Wang, Wei, Chen, Jian-jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910095/
https://www.ncbi.nlm.nih.gov/pubmed/33654420
http://dx.doi.org/10.2147/JIR.S297930
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author Bai, Shunjie
Fang, Liang
Xie, Jing
Bai, Huili
Wang, Wei
Chen, Jian-jun
author_facet Bai, Shunjie
Fang, Liang
Xie, Jing
Bai, Huili
Wang, Wei
Chen, Jian-jun
author_sort Bai, Shunjie
collection PubMed
description BACKGROUND: Major depressive disorder (MDD) and suicide are two major health problems, but there are still no objective methods to diagnose MDD or suicidal ideation (SI). This study was conducted to identify potential biomarkers for diagnosing MDD patients with SI. METHODS: First-episode drug-naïve MDD patients with SI and demographics-matched healthy controls (HCs) were recruited. First-episode drug-naïve MDD patients without SI were also included. The serum lipids, C-reactive protein (CRP), transferring (TRSF), homocysteine (HCY) and alpha 1-antitrypsin (AAT) in serum were detected. The univariate and multivariate statistical analyses were used to identify and validate the potential biomarkers. RESULTS: The 86 HCs, 53 MDD patients with SI and 20 MDD patients without SI were included in this study. Four potential biomarkers were identified: AAT, TRSF, high-density lipoprotein cholesterol (HDLC), and apolipoprotein A1 (APOA1). After one month treatment, the levels of AAT and APOA1 were significantly improved. The panel consisting of these potential biomarkers had an excellent diagnostic performance, yielding an area under the ROC curve (AUC) of 0.994 and 0.990 in the training and testing set, respectively. Moreover, this panel could effectively distinguish MDD patients with SI from MDD patients without SI (AUC=0.928). CONCLUSION: These results showed that these potential biomarkers could facilitate the development of an objective method for diagnosing MDD patients with SI, and the decreased AAT levels in MDD patients might lead to the appearance of SI by resulting in the elevated inflammation.
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spelling pubmed-79100952021-03-01 Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation Bai, Shunjie Fang, Liang Xie, Jing Bai, Huili Wang, Wei Chen, Jian-jun J Inflamm Res Original Research BACKGROUND: Major depressive disorder (MDD) and suicide are two major health problems, but there are still no objective methods to diagnose MDD or suicidal ideation (SI). This study was conducted to identify potential biomarkers for diagnosing MDD patients with SI. METHODS: First-episode drug-naïve MDD patients with SI and demographics-matched healthy controls (HCs) were recruited. First-episode drug-naïve MDD patients without SI were also included. The serum lipids, C-reactive protein (CRP), transferring (TRSF), homocysteine (HCY) and alpha 1-antitrypsin (AAT) in serum were detected. The univariate and multivariate statistical analyses were used to identify and validate the potential biomarkers. RESULTS: The 86 HCs, 53 MDD patients with SI and 20 MDD patients without SI were included in this study. Four potential biomarkers were identified: AAT, TRSF, high-density lipoprotein cholesterol (HDLC), and apolipoprotein A1 (APOA1). After one month treatment, the levels of AAT and APOA1 were significantly improved. The panel consisting of these potential biomarkers had an excellent diagnostic performance, yielding an area under the ROC curve (AUC) of 0.994 and 0.990 in the training and testing set, respectively. Moreover, this panel could effectively distinguish MDD patients with SI from MDD patients without SI (AUC=0.928). CONCLUSION: These results showed that these potential biomarkers could facilitate the development of an objective method for diagnosing MDD patients with SI, and the decreased AAT levels in MDD patients might lead to the appearance of SI by resulting in the elevated inflammation. Dove 2021-02-22 /pmc/articles/PMC7910095/ /pubmed/33654420 http://dx.doi.org/10.2147/JIR.S297930 Text en © 2021 Bai et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Bai, Shunjie
Fang, Liang
Xie, Jing
Bai, Huili
Wang, Wei
Chen, Jian-jun
Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title_full Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title_fullStr Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title_full_unstemmed Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title_short Potential Biomarkers for Diagnosing Major Depressive Disorder Patients with Suicidal Ideation
title_sort potential biomarkers for diagnosing major depressive disorder patients with suicidal ideation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910095/
https://www.ncbi.nlm.nih.gov/pubmed/33654420
http://dx.doi.org/10.2147/JIR.S297930
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