Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome

Abstract Guillain-Barre Syndrome (GBS) is an inflammatory disease of the peripheral nervous system. Given that plasma metabolic profiles in GBS patients have never been explored, plasma samples of 38 GBS patients, 22 multiple sclerosis (MS) patients, and 40 healthy controls were analyzed by using un...

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Autores principales: Hsiang-Yu Tang, Daniel Tsun-yee Chiu, Jui-Fen Lin, Cheng-Yu Huang, Kuo-Hsuan Chang, Rong-Kuo Lyu, Long-Sun Ro, Hung-Chou Kuo, Mei-Ling Cheng, Chiung-Mei Chen
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/0e95220375774a9a99ff92ec8703f65d
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spelling oai:doaj.org-article:0e95220375774a9a99ff92ec8703f65d2021-12-02T15:05:36ZDisturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome10.1038/s41598-017-08338-72045-2322https://doaj.org/article/0e95220375774a9a99ff92ec8703f65d2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08338-7https://doaj.org/toc/2045-2322Abstract Guillain-Barre Syndrome (GBS) is an inflammatory disease of the peripheral nervous system. Given that plasma metabolic profiles in GBS patients have never been explored, plasma samples of 38 GBS patients, 22 multiple sclerosis (MS) patients, and 40 healthy controls were analyzed by using untargeted and targeted metabolomics analysis. The untargeted analysis showed that levels of a set of plasma lipid metabolites were significantly decreased in GBS patients compared to the controls. Furthermore, the targeted analysis demonstrated that levels of 41 metabolites in GBS patients were significantly changed compared to either the controls or MS patients. A further metabolic analysis showed that 12 of 41 metabolites were significantly lower in classical GBS patients compared to Miller-Fisher syndrome. Among them, each of PCae C34:0, PCae C42:2, PCae C42:3, and SM C24:0 was inversely correlated with Hughes functional grading scale of GBS patients at both nadir and discharge. Receiver operating characteristic curve analysis of combination of three metabolites (PCaa C42:2, PCae C36:0 and SM C24:0) showed a good discrimination between the GBS and the controls (area under curve = 0.86). This study has demonstrated disruption of lipid metabolites in GBS may be potential biomarkers to indicate disease severity and prognosis of GBS.Hsiang-Yu TangDaniel Tsun-yee ChiuJui-Fen LinCheng-Yu HuangKuo-Hsuan ChangRong-Kuo LyuLong-Sun RoHung-Chou KuoMei-Ling ChengChiung-Mei ChenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hsiang-Yu Tang
Daniel Tsun-yee Chiu
Jui-Fen Lin
Cheng-Yu Huang
Kuo-Hsuan Chang
Rong-Kuo Lyu
Long-Sun Ro
Hung-Chou Kuo
Mei-Ling Cheng
Chiung-Mei Chen
Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
description Abstract Guillain-Barre Syndrome (GBS) is an inflammatory disease of the peripheral nervous system. Given that plasma metabolic profiles in GBS patients have never been explored, plasma samples of 38 GBS patients, 22 multiple sclerosis (MS) patients, and 40 healthy controls were analyzed by using untargeted and targeted metabolomics analysis. The untargeted analysis showed that levels of a set of plasma lipid metabolites were significantly decreased in GBS patients compared to the controls. Furthermore, the targeted analysis demonstrated that levels of 41 metabolites in GBS patients were significantly changed compared to either the controls or MS patients. A further metabolic analysis showed that 12 of 41 metabolites were significantly lower in classical GBS patients compared to Miller-Fisher syndrome. Among them, each of PCae C34:0, PCae C42:2, PCae C42:3, and SM C24:0 was inversely correlated with Hughes functional grading scale of GBS patients at both nadir and discharge. Receiver operating characteristic curve analysis of combination of three metabolites (PCaa C42:2, PCae C36:0 and SM C24:0) showed a good discrimination between the GBS and the controls (area under curve = 0.86). This study has demonstrated disruption of lipid metabolites in GBS may be potential biomarkers to indicate disease severity and prognosis of GBS.
format article
author Hsiang-Yu Tang
Daniel Tsun-yee Chiu
Jui-Fen Lin
Cheng-Yu Huang
Kuo-Hsuan Chang
Rong-Kuo Lyu
Long-Sun Ro
Hung-Chou Kuo
Mei-Ling Cheng
Chiung-Mei Chen
author_facet Hsiang-Yu Tang
Daniel Tsun-yee Chiu
Jui-Fen Lin
Cheng-Yu Huang
Kuo-Hsuan Chang
Rong-Kuo Lyu
Long-Sun Ro
Hung-Chou Kuo
Mei-Ling Cheng
Chiung-Mei Chen
author_sort Hsiang-Yu Tang
title Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
title_short Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
title_full Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
title_fullStr Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
title_full_unstemmed Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome
title_sort disturbance of plasma lipid metabolic profile in guillain-barre syndrome
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/0e95220375774a9a99ff92ec8703f65d
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