CSF metabolic and proteomic profiles in patients prodromal for psychosis.
BACKGROUND: The initial prodromal state of psychosis (IPS) is defined as an early disease stage prior to the onset of overt psychosis characterized by sub-threshold or more unspecific psychiatric symptoms. Little is known regarding the biochemical changes during this period. METHODOLOGY/PRINCIPAL FI...
Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
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Public Library of Science (PLoS)
2007-01-01
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Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC1942084?pdf=render |
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author | Jeffrey T-J Huang F Markus Leweke Tsz M Tsang Dagmar Koethe Laura Kranaster Christoph W Gerth Sonja Gross Daniela Schreiber Stephan Ruhrmann Frauke Schultze-Lutter Joachim Klosterkötter Elaine Holmes Sabine Bahn |
author_facet | Jeffrey T-J Huang F Markus Leweke Tsz M Tsang Dagmar Koethe Laura Kranaster Christoph W Gerth Sonja Gross Daniela Schreiber Stephan Ruhrmann Frauke Schultze-Lutter Joachim Klosterkötter Elaine Holmes Sabine Bahn |
author_sort | Jeffrey T-J Huang |
collection | DOAJ |
description | BACKGROUND: The initial prodromal state of psychosis (IPS) is defined as an early disease stage prior to the onset of overt psychosis characterized by sub-threshold or more unspecific psychiatric symptoms. Little is known regarding the biochemical changes during this period. METHODOLOGY/PRINCIPAL FINDINGS: We investigated the metabolic/proteomic profiles of cerebrospinal fluid (CSF) of first-onset drug naïve paranoid schizophrenia patients (n = 54) and individuals presenting with initial prodromal symptoms (n = 24), alongside healthy volunteers (n = 70) using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy and surface enhanced laser desorption ionization (SELDI) mass spectrometry, respectively. Partial least square discriminant analysis (PLS-DA) showed that 36%/29% of IPS patients displayed proteomic/metabolic profiles characteristic of first-onset, drug naïve schizophrenia, i.e., changes in levels of glucose and lactate as well as changes in a VGF-derived peptide (VGF23-62) and transthyretin protein concentrations. However, only 29% (n = 7) of the investigated IPS patients (who to date have been followed up for up to three years) have so far received a diagnosis of schizophrenia. The presence of biochemical alterations in the IPS group did not correlate with the risk to develop schizophrenia. CONCLUSIONS/SIGNIFICANCE: Our results imply that schizophrenia-related biochemical disease processes can be traced in CSF of prodromal patients. However, the biochemical disturbances identified in IPS patients, at least when measured at a single time point, may not be sufficient to predict clinical outcome. |
first_indexed | 2024-12-11T14:01:55Z |
format | Article |
id | doaj.art-f6a9aae8d688456fb433348f6c376a7d |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-11T14:01:55Z |
publishDate | 2007-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-f6a9aae8d688456fb433348f6c376a7d2022-12-22T01:03:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032007-01-0128e75610.1371/journal.pone.0000756CSF metabolic and proteomic profiles in patients prodromal for psychosis.Jeffrey T-J HuangF Markus LewekeTsz M TsangDagmar KoetheLaura KranasterChristoph W GerthSonja GrossDaniela SchreiberStephan RuhrmannFrauke Schultze-LutterJoachim KlosterkötterElaine HolmesSabine BahnBACKGROUND: The initial prodromal state of psychosis (IPS) is defined as an early disease stage prior to the onset of overt psychosis characterized by sub-threshold or more unspecific psychiatric symptoms. Little is known regarding the biochemical changes during this period. METHODOLOGY/PRINCIPAL FINDINGS: We investigated the metabolic/proteomic profiles of cerebrospinal fluid (CSF) of first-onset drug naïve paranoid schizophrenia patients (n = 54) and individuals presenting with initial prodromal symptoms (n = 24), alongside healthy volunteers (n = 70) using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy and surface enhanced laser desorption ionization (SELDI) mass spectrometry, respectively. Partial least square discriminant analysis (PLS-DA) showed that 36%/29% of IPS patients displayed proteomic/metabolic profiles characteristic of first-onset, drug naïve schizophrenia, i.e., changes in levels of glucose and lactate as well as changes in a VGF-derived peptide (VGF23-62) and transthyretin protein concentrations. However, only 29% (n = 7) of the investigated IPS patients (who to date have been followed up for up to three years) have so far received a diagnosis of schizophrenia. The presence of biochemical alterations in the IPS group did not correlate with the risk to develop schizophrenia. CONCLUSIONS/SIGNIFICANCE: Our results imply that schizophrenia-related biochemical disease processes can be traced in CSF of prodromal patients. However, the biochemical disturbances identified in IPS patients, at least when measured at a single time point, may not be sufficient to predict clinical outcome.http://europepmc.org/articles/PMC1942084?pdf=render |
spellingShingle | Jeffrey T-J Huang F Markus Leweke Tsz M Tsang Dagmar Koethe Laura Kranaster Christoph W Gerth Sonja Gross Daniela Schreiber Stephan Ruhrmann Frauke Schultze-Lutter Joachim Klosterkötter Elaine Holmes Sabine Bahn CSF metabolic and proteomic profiles in patients prodromal for psychosis. PLoS ONE |
title | CSF metabolic and proteomic profiles in patients prodromal for psychosis. |
title_full | CSF metabolic and proteomic profiles in patients prodromal for psychosis. |
title_fullStr | CSF metabolic and proteomic profiles in patients prodromal for psychosis. |
title_full_unstemmed | CSF metabolic and proteomic profiles in patients prodromal for psychosis. |
title_short | CSF metabolic and proteomic profiles in patients prodromal for psychosis. |
title_sort | csf metabolic and proteomic profiles in patients prodromal for psychosis |
url | http://europepmc.org/articles/PMC1942084?pdf=render |
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