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Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort
BACKGROUND: Club cell secretory protein (CC16) has demonstrated utility as a lung-specific biomarker in predicting mortality in acute respiratory distress syndrome (ARDS). These findings have been observed in pre-clinical trials and a re-analysis of a large, randomized controlled trial of ARDS (Flui...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940244/ https://www.ncbi.nlm.nih.gov/pubmed/36814995 http://dx.doi.org/10.1177/11772719231156308 |
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author | Almuntashiri, Sultan Chase, Aaron Sikora, Andrea Zhang, Duo |
author_facet | Almuntashiri, Sultan Chase, Aaron Sikora, Andrea Zhang, Duo |
author_sort | Almuntashiri, Sultan |
collection | PubMed |
description | BACKGROUND: Club cell secretory protein (CC16) has demonstrated utility as a lung-specific biomarker in predicting mortality in acute respiratory distress syndrome (ARDS). These findings have been observed in pre-clinical trials and a re-analysis of a large, randomized controlled trial of ARDS (Fluid and Catheter Treatment Trial (FACTT)). OBJECTIVES: The purpose of this study was to validate previous findings by evaluating CC16 level as a mortality predictor in patients from the albuterol to treat acute lung injury (ALTA) trial. DESIGN AND METHOD: In this secondary biomarker analysis, plasma CC16 level was measured from 100 ALTA subjects using enzyme-linked immunosorbent assay (ELISA). The rate of mortality was assessed in patients with high (⩾45 ng/mL) versus low CC16 (<45 ng/mL) levels. This cut-off level was applied based on our previous analysis from FACTT trial. Significance was assessed using Kaplan-Meier curves and a log-rank test. RESULTS: Subjects were an average of 50 years old and 46% of them were females. Patients with high CC16 levels had higher 90-day mortality compared to those with low CC16 levels, (37.73% vs 8.95%, P < .001). Other clinical outcomes including ICU-free days, ventilator-free days, and organ failure free days were significantly different between the groups (All P < .05). CONCLUSION: In this validation study, we demonstrated that ARDS patients with high plasma CC16 concentration had a higher mortality rate than those with low CC16 levels, confirming previous findings that CC16 levels are associated with ARDS mortality. |
format | Online Article Text |
id | pubmed-9940244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-99402442023-02-21 Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort Almuntashiri, Sultan Chase, Aaron Sikora, Andrea Zhang, Duo Biomark Insights Original Research BACKGROUND: Club cell secretory protein (CC16) has demonstrated utility as a lung-specific biomarker in predicting mortality in acute respiratory distress syndrome (ARDS). These findings have been observed in pre-clinical trials and a re-analysis of a large, randomized controlled trial of ARDS (Fluid and Catheter Treatment Trial (FACTT)). OBJECTIVES: The purpose of this study was to validate previous findings by evaluating CC16 level as a mortality predictor in patients from the albuterol to treat acute lung injury (ALTA) trial. DESIGN AND METHOD: In this secondary biomarker analysis, plasma CC16 level was measured from 100 ALTA subjects using enzyme-linked immunosorbent assay (ELISA). The rate of mortality was assessed in patients with high (⩾45 ng/mL) versus low CC16 (<45 ng/mL) levels. This cut-off level was applied based on our previous analysis from FACTT trial. Significance was assessed using Kaplan-Meier curves and a log-rank test. RESULTS: Subjects were an average of 50 years old and 46% of them were females. Patients with high CC16 levels had higher 90-day mortality compared to those with low CC16 levels, (37.73% vs 8.95%, P < .001). Other clinical outcomes including ICU-free days, ventilator-free days, and organ failure free days were significantly different between the groups (All P < .05). CONCLUSION: In this validation study, we demonstrated that ARDS patients with high plasma CC16 concentration had a higher mortality rate than those with low CC16 levels, confirming previous findings that CC16 levels are associated with ARDS mortality. SAGE Publications 2023-02-17 /pmc/articles/PMC9940244/ /pubmed/36814995 http://dx.doi.org/10.1177/11772719231156308 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Almuntashiri, Sultan Chase, Aaron Sikora, Andrea Zhang, Duo Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title | Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title_full | Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title_fullStr | Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title_full_unstemmed | Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title_short | Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort |
title_sort | validation of prognostic club cell secretory protein (cc16) cut-point in an independent alta cohort |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940244/ https://www.ncbi.nlm.nih.gov/pubmed/36814995 http://dx.doi.org/10.1177/11772719231156308 |
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