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Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function

BACKGROUND: Serum levels of C-reactive protein (CRP) were measured in patients with deficit schizophrenia (DS) to confirm the association between CRP level and cognitive performance and to determine whether CRP was a new biological indicator with the potential clinical applications in DS patients. M...

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Autores principales: Pan, Li-Hong, Qian, Ming, Qu, Weihua, Tang, Qin, Yan, Yuzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718984/
https://www.ncbi.nlm.nih.gov/pubmed/33293814
http://dx.doi.org/10.2147/NDT.S284149
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author Pan, Li-Hong
Qian, Ming
Qu, Weihua
Tang, Qin
Yan, Yuzhong
author_facet Pan, Li-Hong
Qian, Ming
Qu, Weihua
Tang, Qin
Yan, Yuzhong
author_sort Pan, Li-Hong
collection PubMed
description BACKGROUND: Serum levels of C-reactive protein (CRP) were measured in patients with deficit schizophrenia (DS) to confirm the association between CRP level and cognitive performance and to determine whether CRP was a new biological indicator with the potential clinical applications in DS patients. METHODS: Three independent samples [41 DS and 50 non-deficit schizophrenia (NDS) and 30 sex- and age-matched healthy controls (HCs)] were recruited in our study. Serum CRP levels were measured by immunofluorescence. The Positive and Negative Syndrome Scale (PANSS) and alternative forms of the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) were also assessed. And the relationships between serum CRP levels and both PANSS and RBANS scores were finally analyzed. RESULTS: The results of serum CRP level were showed significantly different among the three groups and increased from the HCs to NDS patients to DS patients. There were also significant differences in the cognitive subdomain analyses among the three groups. Serum CRP levels were found positively correlated with total and negative PANSS scores, and showed negatively correlated with overall cognitive test scores in the DS samples. CONCLUSION: Serum C-reactive protein levels and their association with cognitive performance were different between deficit schizophrenia and non-deficit schizophrenia samples, and higher serum CRP level was associated with worse cognitive performance in the DS patients. The results indicated that CRP could be a potential biomarker, and DS could be a distinct subset of schizophrenia.
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spelling pubmed-77189842020-12-07 Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function Pan, Li-Hong Qian, Ming Qu, Weihua Tang, Qin Yan, Yuzhong Neuropsychiatr Dis Treat Original Research BACKGROUND: Serum levels of C-reactive protein (CRP) were measured in patients with deficit schizophrenia (DS) to confirm the association between CRP level and cognitive performance and to determine whether CRP was a new biological indicator with the potential clinical applications in DS patients. METHODS: Three independent samples [41 DS and 50 non-deficit schizophrenia (NDS) and 30 sex- and age-matched healthy controls (HCs)] were recruited in our study. Serum CRP levels were measured by immunofluorescence. The Positive and Negative Syndrome Scale (PANSS) and alternative forms of the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) were also assessed. And the relationships between serum CRP levels and both PANSS and RBANS scores were finally analyzed. RESULTS: The results of serum CRP level were showed significantly different among the three groups and increased from the HCs to NDS patients to DS patients. There were also significant differences in the cognitive subdomain analyses among the three groups. Serum CRP levels were found positively correlated with total and negative PANSS scores, and showed negatively correlated with overall cognitive test scores in the DS samples. CONCLUSION: Serum C-reactive protein levels and their association with cognitive performance were different between deficit schizophrenia and non-deficit schizophrenia samples, and higher serum CRP level was associated with worse cognitive performance in the DS patients. The results indicated that CRP could be a potential biomarker, and DS could be a distinct subset of schizophrenia. Dove 2020-12-01 /pmc/articles/PMC7718984/ /pubmed/33293814 http://dx.doi.org/10.2147/NDT.S284149 Text en © 2020 Pan 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
Pan, Li-Hong
Qian, Ming
Qu, Weihua
Tang, Qin
Yan, Yuzhong
Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title_full Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title_fullStr Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title_full_unstemmed Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title_short Serum C-Reactive Protein in Patients with Deficit Schizophrenia and the Relationship with Cognitive Function
title_sort serum c-reactive protein in patients with deficit schizophrenia and the relationship with cognitive function
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718984/
https://www.ncbi.nlm.nih.gov/pubmed/33293814
http://dx.doi.org/10.2147/NDT.S284149
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