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Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis

The functional significance of extracellular Niemann–Pick disease type C2 protein (NPC2) is poorly defined. It is not known whether there is an association between plasma NPC2 and sepsis. Our exploratory, quantitative proteomic analysis showed a significant increase in the level of plasma NPC2 in mo...

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Autores principales: Bai, Yu, Yin, Shuangyi, Gbordzor, Vivian, Guo, Yu, Bai, Qing, Wang, Shuaiwei, Wei, Xiangyan, Chen, Na, Zhang, Yijie, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961030/
https://www.ncbi.nlm.nih.gov/pubmed/33723331
http://dx.doi.org/10.1038/s41598-021-85478-x
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author Bai, Yu
Yin, Shuangyi
Gbordzor, Vivian
Guo, Yu
Bai, Qing
Wang, Shuaiwei
Wei, Xiangyan
Chen, Na
Zhang, Yijie
Li, Wei
author_facet Bai, Yu
Yin, Shuangyi
Gbordzor, Vivian
Guo, Yu
Bai, Qing
Wang, Shuaiwei
Wei, Xiangyan
Chen, Na
Zhang, Yijie
Li, Wei
author_sort Bai, Yu
collection PubMed
description The functional significance of extracellular Niemann–Pick disease type C2 protein (NPC2) is poorly defined. It is not known whether there is an association between plasma NPC2 and sepsis. Our exploratory, quantitative proteomic analysis showed a significant increase in the level of plasma NPC2 in moribund sepsis patients. Thus, we subsequently determined NPC2 concentration in plasma from healthy subjects, pneumonia patients and sepsis patients with comorbid pneumonia; and analyzed the association of plasma NPC2 with organ dysfunction and prognosis of sepsis patients. Our data shows that plasma NPC2 concentration was significantly higher in pneumonia and sepsis patients than healthy subjects, and was further increased in sepsis patients when the SOFA score reached 14. In addition, NPC2 concentration was significantly higher in patients that subsequently developed septic shock or died within 30 days. Moreover, NPC2 level showed the strongest association with the degree of renal dysfunction in sepsis patients. In moribund sepsis patients, however, NPC2 had highest correlation coefficient with indicators of coagulation anomaly. Based on these results, we conclude that the increase in plasma NPC2 in sepsis patients is associated with multiple organ failure, possibly results from a deficiency in renal clearance, and may serve as a prognostic marker for sepsis.
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spelling pubmed-79610302021-03-19 Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis Bai, Yu Yin, Shuangyi Gbordzor, Vivian Guo, Yu Bai, Qing Wang, Shuaiwei Wei, Xiangyan Chen, Na Zhang, Yijie Li, Wei Sci Rep Article The functional significance of extracellular Niemann–Pick disease type C2 protein (NPC2) is poorly defined. It is not known whether there is an association between plasma NPC2 and sepsis. Our exploratory, quantitative proteomic analysis showed a significant increase in the level of plasma NPC2 in moribund sepsis patients. Thus, we subsequently determined NPC2 concentration in plasma from healthy subjects, pneumonia patients and sepsis patients with comorbid pneumonia; and analyzed the association of plasma NPC2 with organ dysfunction and prognosis of sepsis patients. Our data shows that plasma NPC2 concentration was significantly higher in pneumonia and sepsis patients than healthy subjects, and was further increased in sepsis patients when the SOFA score reached 14. In addition, NPC2 concentration was significantly higher in patients that subsequently developed septic shock or died within 30 days. Moreover, NPC2 level showed the strongest association with the degree of renal dysfunction in sepsis patients. In moribund sepsis patients, however, NPC2 had highest correlation coefficient with indicators of coagulation anomaly. Based on these results, we conclude that the increase in plasma NPC2 in sepsis patients is associated with multiple organ failure, possibly results from a deficiency in renal clearance, and may serve as a prognostic marker for sepsis. Nature Publishing Group UK 2021-03-15 /pmc/articles/PMC7961030/ /pubmed/33723331 http://dx.doi.org/10.1038/s41598-021-85478-x Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bai, Yu
Yin, Shuangyi
Gbordzor, Vivian
Guo, Yu
Bai, Qing
Wang, Shuaiwei
Wei, Xiangyan
Chen, Na
Zhang, Yijie
Li, Wei
Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title_full Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title_fullStr Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title_full_unstemmed Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title_short Increase in plasma Niemann–Pick disease type C2 protein is associated with poor prognosis of sepsis
title_sort increase in plasma niemann–pick disease type c2 protein is associated with poor prognosis of sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961030/
https://www.ncbi.nlm.nih.gov/pubmed/33723331
http://dx.doi.org/10.1038/s41598-021-85478-x
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