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Novel urinary metabolite signature for diagnosing postpartum depression
BACKGROUND: Postpartum depression (PPD) could affect ~10% of women and impair the quality of mother–infant interactions. Currently, there are no objective methods to diagnose PPD. Therefore, this study was conducted to identify potential biomarkers for diagnosing PPD. MATERIALS AND METHODS: Morning...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436788/ https://www.ncbi.nlm.nih.gov/pubmed/28546751 http://dx.doi.org/10.2147/NDT.S135190 |
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author | Lin, Lin Chen, Xiao-mei Liu, Rong-hua |
author_facet | Lin, Lin Chen, Xiao-mei Liu, Rong-hua |
author_sort | Lin, Lin |
collection | PubMed |
description | BACKGROUND: Postpartum depression (PPD) could affect ~10% of women and impair the quality of mother–infant interactions. Currently, there are no objective methods to diagnose PPD. Therefore, this study was conducted to identify potential biomarkers for diagnosing PPD. MATERIALS AND METHODS: Morning urine samples of PPD subjects, postpartum women without depression (PPWD) and healthy controls (HCs) were collected. The gas chromatography-mass spectroscopy (GC-MS)-based urinary metabolomic approach was performed to characterize the urinary metabolic profiling. The orthogonal partial least-squares-discriminant analysis (OPLS-DA) was used to identify the differential metabolites. The logistic regression analysis and Bayesian information criterion rule were further used to identify the potential biomarker panel. The receiver operating characteristic curve analysis was conducted to evaluate the diagnostic performance of the identified potential biomarker panel. RESULTS: Totally, 73 PPD subjects, 73 PPWD and 74 HCs were included, and 68 metabolites were identified using GC-MS. The OPLS-DA model showed that there were 22 differential metabolites (14 upregulated and 8 downregulated) responsible for separating PPD subjects from HCs and PPWD. Meanwhile, a panel of five potential biomarkers – formate, succinate, 1-methylhistidine, α-glucose and dimethylamine – was identified. This panel could effectively distinguish PPD subjects from HCs and PPWD with an area under the curve (AUC) curve of 0.948 in the training set and 0.944 in the testing set. CONCLUSION: These results demonstrated that the potential biomarker panel could aid in the future development of an objective diagnostic method for PPD. |
format | Online Article Text |
id | pubmed-5436788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54367882017-05-25 Novel urinary metabolite signature for diagnosing postpartum depression Lin, Lin Chen, Xiao-mei Liu, Rong-hua Neuropsychiatr Dis Treat Original Research BACKGROUND: Postpartum depression (PPD) could affect ~10% of women and impair the quality of mother–infant interactions. Currently, there are no objective methods to diagnose PPD. Therefore, this study was conducted to identify potential biomarkers for diagnosing PPD. MATERIALS AND METHODS: Morning urine samples of PPD subjects, postpartum women without depression (PPWD) and healthy controls (HCs) were collected. The gas chromatography-mass spectroscopy (GC-MS)-based urinary metabolomic approach was performed to characterize the urinary metabolic profiling. The orthogonal partial least-squares-discriminant analysis (OPLS-DA) was used to identify the differential metabolites. The logistic regression analysis and Bayesian information criterion rule were further used to identify the potential biomarker panel. The receiver operating characteristic curve analysis was conducted to evaluate the diagnostic performance of the identified potential biomarker panel. RESULTS: Totally, 73 PPD subjects, 73 PPWD and 74 HCs were included, and 68 metabolites were identified using GC-MS. The OPLS-DA model showed that there were 22 differential metabolites (14 upregulated and 8 downregulated) responsible for separating PPD subjects from HCs and PPWD. Meanwhile, a panel of five potential biomarkers – formate, succinate, 1-methylhistidine, α-glucose and dimethylamine – was identified. This panel could effectively distinguish PPD subjects from HCs and PPWD with an area under the curve (AUC) curve of 0.948 in the training set and 0.944 in the testing set. CONCLUSION: These results demonstrated that the potential biomarker panel could aid in the future development of an objective diagnostic method for PPD. Dove Medical Press 2017-05-10 /pmc/articles/PMC5436788/ /pubmed/28546751 http://dx.doi.org/10.2147/NDT.S135190 Text en © 2017 Lin et al. 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. |
spellingShingle | Original Research Lin, Lin Chen, Xiao-mei Liu, Rong-hua Novel urinary metabolite signature for diagnosing postpartum depression |
title | Novel urinary metabolite signature for diagnosing postpartum depression |
title_full | Novel urinary metabolite signature for diagnosing postpartum depression |
title_fullStr | Novel urinary metabolite signature for diagnosing postpartum depression |
title_full_unstemmed | Novel urinary metabolite signature for diagnosing postpartum depression |
title_short | Novel urinary metabolite signature for diagnosing postpartum depression |
title_sort | novel urinary metabolite signature for diagnosing postpartum depression |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436788/ https://www.ncbi.nlm.nih.gov/pubmed/28546751 http://dx.doi.org/10.2147/NDT.S135190 |
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