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The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury
BACKGROUND: To investigate the value of serum Cyclophilin A(Cyp A) in evaluating the prognosis of patients with different severity of craniocerebral injury. METHODS: The clinical data of patients with craniocerebral injury treated in the Department of Emergency from July 2014 to August 2017 were col...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742373/ https://www.ncbi.nlm.nih.gov/pubmed/36518190 http://dx.doi.org/10.3389/fneur.2022.968071 |
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author | Li, Peng-Fei Zhang, Jing-Chen He, Xu-Jian Niu, Jian-Hua Wu, Wei-Fang Li, Tong |
author_facet | Li, Peng-Fei Zhang, Jing-Chen He, Xu-Jian Niu, Jian-Hua Wu, Wei-Fang Li, Tong |
author_sort | Li, Peng-Fei |
collection | PubMed |
description | BACKGROUND: To investigate the value of serum Cyclophilin A(Cyp A) in evaluating the prognosis of patients with different severity of craniocerebral injury. METHODS: The clinical data of patients with craniocerebral injury treated in the Department of Emergency from July 2014 to August 2017 were collected. The patients were divided into survival group and death group, good neurological function group and poor neurological function group with 28-day prognosis and were divided into mild (13–15) group, moderate (9–12) group, and severe (3–8) group with Glasgow Coma Scale (GCS) score. Clinical parameters such as Cyp A and mortality in groups and the relationship between Cyp A and GCS score were compared and its predictive value for prognosis was analyzed with Binary Logistics regression, Cox proportional hazards model and kaplan-meier survival curve. RESULTS: In a single-center retrospective study, 503 patients were enrolled, including 365 males and 138 females; serum Cyp A in the survival group was significantly smaller than the death group [18.7 (10.1, 51.5) ng/mL vs. 149.8 (79.5, 194.4) ng/mL, P < 0.005]. There were significant differences in mortality and Cyp A levels between patients with different severity of craniocerebral injury (P < 0.001). Serum Cyp A levels were negatively correlated with GCS scores in all patients with craniocerebral injury, mild, moderate, or severe craniocerebral injury (r = −0.844, r = −0.256, r = −0.540, r = −0.531, P < 0.001). Predictive value of Serum Cyp A level for all patients with craniocerebral injury, mild, moderate, and severe craniocerebral injury is 0.890, 0.789, 0.806, and 0.833, respectively. Logistics regression analysis showed that lactate (OR = 1.260, 95%CI: 1.023–1.551) and Cyp A (OR = 1.021, 95%CI: 1.011–1.031) were positively correlated with death (P < 0.05), Lactic acid (HR 1.115; 95%CI:1.001–1.243; P = 0.048), GCS score (HR 0.888; 95% CI: 0.794–0.993; P = 0.038), Cyp A levels (HR 1.009; 95% CI: 1.004–1.013; P < 0.001) had a significant effect on short-term mortality. Similar results were seen when neurologic function was used as the outcome. Kaplan-meier survival curve analysis found survival rate of patients with Cyp A level below the cut-off value was significantly higher. CONCLUSION: Serum Cyp A has a certain predictive value for the prognosis of patients with different severity of craniocerebral injury. Among them, patients with severe craniocerebral injury have the highest predictive value and mild craniocerebral injury patients have the least. |
format | Online Article Text |
id | pubmed-9742373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97423732022-12-13 The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury Li, Peng-Fei Zhang, Jing-Chen He, Xu-Jian Niu, Jian-Hua Wu, Wei-Fang Li, Tong Front Neurol Neurology BACKGROUND: To investigate the value of serum Cyclophilin A(Cyp A) in evaluating the prognosis of patients with different severity of craniocerebral injury. METHODS: The clinical data of patients with craniocerebral injury treated in the Department of Emergency from July 2014 to August 2017 were collected. The patients were divided into survival group and death group, good neurological function group and poor neurological function group with 28-day prognosis and were divided into mild (13–15) group, moderate (9–12) group, and severe (3–8) group with Glasgow Coma Scale (GCS) score. Clinical parameters such as Cyp A and mortality in groups and the relationship between Cyp A and GCS score were compared and its predictive value for prognosis was analyzed with Binary Logistics regression, Cox proportional hazards model and kaplan-meier survival curve. RESULTS: In a single-center retrospective study, 503 patients were enrolled, including 365 males and 138 females; serum Cyp A in the survival group was significantly smaller than the death group [18.7 (10.1, 51.5) ng/mL vs. 149.8 (79.5, 194.4) ng/mL, P < 0.005]. There were significant differences in mortality and Cyp A levels between patients with different severity of craniocerebral injury (P < 0.001). Serum Cyp A levels were negatively correlated with GCS scores in all patients with craniocerebral injury, mild, moderate, or severe craniocerebral injury (r = −0.844, r = −0.256, r = −0.540, r = −0.531, P < 0.001). Predictive value of Serum Cyp A level for all patients with craniocerebral injury, mild, moderate, and severe craniocerebral injury is 0.890, 0.789, 0.806, and 0.833, respectively. Logistics regression analysis showed that lactate (OR = 1.260, 95%CI: 1.023–1.551) and Cyp A (OR = 1.021, 95%CI: 1.011–1.031) were positively correlated with death (P < 0.05), Lactic acid (HR 1.115; 95%CI:1.001–1.243; P = 0.048), GCS score (HR 0.888; 95% CI: 0.794–0.993; P = 0.038), Cyp A levels (HR 1.009; 95% CI: 1.004–1.013; P < 0.001) had a significant effect on short-term mortality. Similar results were seen when neurologic function was used as the outcome. Kaplan-meier survival curve analysis found survival rate of patients with Cyp A level below the cut-off value was significantly higher. CONCLUSION: Serum Cyp A has a certain predictive value for the prognosis of patients with different severity of craniocerebral injury. Among them, patients with severe craniocerebral injury have the highest predictive value and mild craniocerebral injury patients have the least. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742373/ /pubmed/36518190 http://dx.doi.org/10.3389/fneur.2022.968071 Text en Copyright © 2022 Li, Zhang, He, Niu, Wu and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Li, Peng-Fei Zhang, Jing-Chen He, Xu-Jian Niu, Jian-Hua Wu, Wei-Fang Li, Tong The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title | The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title_full | The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title_fullStr | The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title_full_unstemmed | The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title_short | The correlation between serum Cyclophilin A level and severity, prognosis of craniocerebral injury |
title_sort | correlation between serum cyclophilin a level and severity, prognosis of craniocerebral injury |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742373/ https://www.ncbi.nlm.nih.gov/pubmed/36518190 http://dx.doi.org/10.3389/fneur.2022.968071 |
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