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Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study
STUDY DESIGN: A multicentre retrospective study. OBJECTIVE: A multicentre retrospective study was performed to observe the changes in serum cystatin C (CysC) levels in patients with acute spinal cord injury (SCI). SETTING: Four hospitals in China. METHODS: Over a 5-year study period, the CysC, creat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062626/ https://www.ncbi.nlm.nih.gov/pubmed/31586154 http://dx.doi.org/10.1038/s41393-019-0360-7 |
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author | Zhang, JinYuan Ding, RuoTing Xian, QingZhang Wang, ZhiKun Liu, ZhongYuan Yang, JinCheng Chen, JianTing |
author_facet | Zhang, JinYuan Ding, RuoTing Xian, QingZhang Wang, ZhiKun Liu, ZhongYuan Yang, JinCheng Chen, JianTing |
author_sort | Zhang, JinYuan |
collection | PubMed |
description | STUDY DESIGN: A multicentre retrospective study. OBJECTIVE: A multicentre retrospective study was performed to observe the changes in serum cystatin C (CysC) levels in patients with acute spinal cord injury (SCI). SETTING: Four hospitals in China. METHODS: Over a 5-year study period, the CysC, creatinine (Cr), and blood urea nitrogen (BUN) levels of people who had incurred SCI in the preceding 7 days were collected and compared with those of people with limb fracture (LF) who were matched for injury time and gender. People with SCI also were grouped by injury duration, ASIA Impairment Scale (AIS) grade and the presence or absence of steroid therapy and compared each day. RESULTS: Three hundred and twenty-three samples from people with SCI were retrospectively collected; their mean serum CysC levels were significantly higher than those of people with LF (p < 0.001); No significant difference was observed in Cr or BUN levels between the two groups (p > 0.14). CysC levels increased on the second day, peaked on day 3, and returned to normal on day 5. The more severely injured individuals had higher CysC levels. Steroid therapy or not had no influence for CysC levels. CONCLUSION: CysC levels are increased in patients with acute SCI, possibly as a direct result of injury. Serum CysC is a potential biomarker of SCI. |
format | Online Article Text |
id | pubmed-7062626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70626262020-03-19 Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study Zhang, JinYuan Ding, RuoTing Xian, QingZhang Wang, ZhiKun Liu, ZhongYuan Yang, JinCheng Chen, JianTing Spinal Cord Article STUDY DESIGN: A multicentre retrospective study. OBJECTIVE: A multicentre retrospective study was performed to observe the changes in serum cystatin C (CysC) levels in patients with acute spinal cord injury (SCI). SETTING: Four hospitals in China. METHODS: Over a 5-year study period, the CysC, creatinine (Cr), and blood urea nitrogen (BUN) levels of people who had incurred SCI in the preceding 7 days were collected and compared with those of people with limb fracture (LF) who were matched for injury time and gender. People with SCI also were grouped by injury duration, ASIA Impairment Scale (AIS) grade and the presence or absence of steroid therapy and compared each day. RESULTS: Three hundred and twenty-three samples from people with SCI were retrospectively collected; their mean serum CysC levels were significantly higher than those of people with LF (p < 0.001); No significant difference was observed in Cr or BUN levels between the two groups (p > 0.14). CysC levels increased on the second day, peaked on day 3, and returned to normal on day 5. The more severely injured individuals had higher CysC levels. Steroid therapy or not had no influence for CysC levels. CONCLUSION: CysC levels are increased in patients with acute SCI, possibly as a direct result of injury. Serum CysC is a potential biomarker of SCI. Nature Publishing Group UK 2019-10-04 2020 /pmc/articles/PMC7062626/ /pubmed/31586154 http://dx.doi.org/10.1038/s41393-019-0360-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, JinYuan Ding, RuoTing Xian, QingZhang Wang, ZhiKun Liu, ZhongYuan Yang, JinCheng Chen, JianTing Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title | Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title_full | Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title_fullStr | Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title_full_unstemmed | Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title_short | Serum cystatin C is increased in acute spinal cord injury: a multicentre retrospective study |
title_sort | serum cystatin c is increased in acute spinal cord injury: a multicentre retrospective study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062626/ https://www.ncbi.nlm.nih.gov/pubmed/31586154 http://dx.doi.org/10.1038/s41393-019-0360-7 |
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