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The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity
To explore the values of C-reactive protein (CRP) and procalcitonin (PCT) in identifying infection and disease activity in systemic lupus erythematosus (SLE) patients. Patients with SLE and infection from April 2015 to January 2018 were included in this study. We compared the clinical characteristic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831178/ https://www.ncbi.nlm.nih.gov/pubmed/31415387 http://dx.doi.org/10.1097/MD.0000000000016798 |
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author | Wang, Jing Niu, Rong Jiang, Lijuan Wang, Yuetao Shao, Xiaonan Wu, Min Ma, Yingchun |
author_facet | Wang, Jing Niu, Rong Jiang, Lijuan Wang, Yuetao Shao, Xiaonan Wu, Min Ma, Yingchun |
author_sort | Wang, Jing |
collection | PubMed |
description | To explore the values of C-reactive protein (CRP) and procalcitonin (PCT) in identifying infection and disease activity in systemic lupus erythematosus (SLE) patients. Patients with SLE and infection from April 2015 to January 2018 were included in this study. We compared the clinical characteristics and biomarkers between different groups and calculated the receiver operating characteristic curve, sensitivity, and specificity of the corresponding biomarkers. Logistic regression analysis was performed on the variables exhibiting significant differences in univariate analysis. A total of 177 SLE patients were retrospectively analyzed. The patients were divided into noninfected-inactive group, noninfected-active group, infected-inactive group, and infected-active group. CRP level of infected-inactive group was significantly higher than noninfected-inactive group (P < .05), but not significantly in infected-active group than noninfected-active group (P > .05). Multivariate analysis showed that CRP (>24.0 mg/L) was the only independent risk factor for SLE infection (odds ratio, OR = 2.896, P = .032). PCT level of infected-active group was significantly higher than infected-inactive group (P < .05), but not significantly in noninfected-active group than noninfected-inactive group (P > .05). SLE active group had shorter disease course, lower infection rate, higher PCT level, and lower platelet count (PLT). Multivariate logistic analysis showed that PCT (>0.048 ng/mL) and PLT (<150 × 10(9)/L) were independent risk factors for SLE activity (OR = 3.498 and 4.391, P = .011 and 0.009), and disease course (>96 months) was independent protective factor (OR = 0.169, P < .001). The area under the curve of the logistic model was significantly larger than any single variable (all P < .05). CRP is the only effective marker for diagnosing infection in SLE patients. Moreover, PCT helps predict SLE activity. |
format | Online Article Text |
id | pubmed-6831178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68311782019-11-19 The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity Wang, Jing Niu, Rong Jiang, Lijuan Wang, Yuetao Shao, Xiaonan Wu, Min Ma, Yingchun Medicine (Baltimore) 6900 To explore the values of C-reactive protein (CRP) and procalcitonin (PCT) in identifying infection and disease activity in systemic lupus erythematosus (SLE) patients. Patients with SLE and infection from April 2015 to January 2018 were included in this study. We compared the clinical characteristics and biomarkers between different groups and calculated the receiver operating characteristic curve, sensitivity, and specificity of the corresponding biomarkers. Logistic regression analysis was performed on the variables exhibiting significant differences in univariate analysis. A total of 177 SLE patients were retrospectively analyzed. The patients were divided into noninfected-inactive group, noninfected-active group, infected-inactive group, and infected-active group. CRP level of infected-inactive group was significantly higher than noninfected-inactive group (P < .05), but not significantly in infected-active group than noninfected-active group (P > .05). Multivariate analysis showed that CRP (>24.0 mg/L) was the only independent risk factor for SLE infection (odds ratio, OR = 2.896, P = .032). PCT level of infected-active group was significantly higher than infected-inactive group (P < .05), but not significantly in noninfected-active group than noninfected-inactive group (P > .05). SLE active group had shorter disease course, lower infection rate, higher PCT level, and lower platelet count (PLT). Multivariate logistic analysis showed that PCT (>0.048 ng/mL) and PLT (<150 × 10(9)/L) were independent risk factors for SLE activity (OR = 3.498 and 4.391, P = .011 and 0.009), and disease course (>96 months) was independent protective factor (OR = 0.169, P < .001). The area under the curve of the logistic model was significantly larger than any single variable (all P < .05). CRP is the only effective marker for diagnosing infection in SLE patients. Moreover, PCT helps predict SLE activity. Wolters Kluwer Health 2019-08-16 /pmc/articles/PMC6831178/ /pubmed/31415387 http://dx.doi.org/10.1097/MD.0000000000016798 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 6900 Wang, Jing Niu, Rong Jiang, Lijuan Wang, Yuetao Shao, Xiaonan Wu, Min Ma, Yingchun The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title | The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title_full | The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title_fullStr | The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title_full_unstemmed | The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title_short | The diagnostic values of C-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
title_sort | diagnostic values of c-reactive protein and procalcitonin in identifying systemic lupus erythematosus infection and disease activity |
topic | 6900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831178/ https://www.ncbi.nlm.nih.gov/pubmed/31415387 http://dx.doi.org/10.1097/MD.0000000000016798 |
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