Sex-specific urinary biomarkers for diagnosing bipolar disorder.

Sex-based differences are prominent in affective disorders, but there are no biomarkers available to support sex-specific, laboratory-based diagnostics for male and female bipolar disorder (BD) patients. Here, a NMR-based metabonomic approach was used to preliminarily identify sex-specific urinary m...

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Main Authors: Jian-jun Chen, Hua Huang, Li-bo Zhao, De-zhi Zhou, Yong-tao Yang, Peng Zheng, De-yu Yang, Peng He, Jing-jing Zhou, Liang Fang, Peng Xie
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4274077?pdf=render
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spelling doaj-a04e02b73c9e4467a4ab45f696cb6a452020-11-24T21:42:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11522110.1371/journal.pone.0115221Sex-specific urinary biomarkers for diagnosing bipolar disorder.Jian-jun ChenHua HuangLi-bo ZhaoDe-zhi ZhouYong-tao YangPeng ZhengDe-yu YangPeng HeJing-jing ZhouLiang FangPeng XieSex-based differences are prominent in affective disorders, but there are no biomarkers available to support sex-specific, laboratory-based diagnostics for male and female bipolar disorder (BD) patients. Here, a NMR-based metabonomic approach was used to preliminarily identify sex-specific urinary metabolite biomarkers for diagnosing male and female BD patients. A male-specific biomarker panel consisting of four metabolites (α-hydroxybutyrate, choline, formate, and N-methylnicotinamide) effectively discriminated between male BD and healthy controls (HC) subjects, achieving an area under the receiver operating characteristic curve (AUC) of 0.942. A female-specific biomarkers panel consisting of four metabolites (α-hydroxybutyrate, oxalacetate, acetone, and N-methylnicotinamide) effectively discriminated between female BD and HC subjects, achieving an AUC of 0.909. The male-specific biomarker panel displayed low discriminatory power in the female group, and the female-specific biomarker panel displayed low discriminatory power in the male group. Moreover, several other metabolites showed different trends between male and female BD subjects. These findings suggest that male and female BD patients have distinct biomarker fingerprints and that these two sex-specific biomarker panels may serve as effective diagnostic tools in distinguishing male and female BD patients from their healthy counterparts. Our work may provide a window into the mechanisms underlying the pathoetiology of BD in both men and women.http://europepmc.org/articles/PMC4274077?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jian-jun Chen
Hua Huang
Li-bo Zhao
De-zhi Zhou
Yong-tao Yang
Peng Zheng
De-yu Yang
Peng He
Jing-jing Zhou
Liang Fang
Peng Xie
spellingShingle Jian-jun Chen
Hua Huang
Li-bo Zhao
De-zhi Zhou
Yong-tao Yang
Peng Zheng
De-yu Yang
Peng He
Jing-jing Zhou
Liang Fang
Peng Xie
Sex-specific urinary biomarkers for diagnosing bipolar disorder.
PLoS ONE
author_facet Jian-jun Chen
Hua Huang
Li-bo Zhao
De-zhi Zhou
Yong-tao Yang
Peng Zheng
De-yu Yang
Peng He
Jing-jing Zhou
Liang Fang
Peng Xie
author_sort Jian-jun Chen
title Sex-specific urinary biomarkers for diagnosing bipolar disorder.
title_short Sex-specific urinary biomarkers for diagnosing bipolar disorder.
title_full Sex-specific urinary biomarkers for diagnosing bipolar disorder.
title_fullStr Sex-specific urinary biomarkers for diagnosing bipolar disorder.
title_full_unstemmed Sex-specific urinary biomarkers for diagnosing bipolar disorder.
title_sort sex-specific urinary biomarkers for diagnosing bipolar disorder.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Sex-based differences are prominent in affective disorders, but there are no biomarkers available to support sex-specific, laboratory-based diagnostics for male and female bipolar disorder (BD) patients. Here, a NMR-based metabonomic approach was used to preliminarily identify sex-specific urinary metabolite biomarkers for diagnosing male and female BD patients. A male-specific biomarker panel consisting of four metabolites (α-hydroxybutyrate, choline, formate, and N-methylnicotinamide) effectively discriminated between male BD and healthy controls (HC) subjects, achieving an area under the receiver operating characteristic curve (AUC) of 0.942. A female-specific biomarkers panel consisting of four metabolites (α-hydroxybutyrate, oxalacetate, acetone, and N-methylnicotinamide) effectively discriminated between female BD and HC subjects, achieving an AUC of 0.909. The male-specific biomarker panel displayed low discriminatory power in the female group, and the female-specific biomarker panel displayed low discriminatory power in the male group. Moreover, several other metabolites showed different trends between male and female BD subjects. These findings suggest that male and female BD patients have distinct biomarker fingerprints and that these two sex-specific biomarker panels may serve as effective diagnostic tools in distinguishing male and female BD patients from their healthy counterparts. Our work may provide a window into the mechanisms underlying the pathoetiology of BD in both men and women.
url http://europepmc.org/articles/PMC4274077?pdf=render
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