Validation of Prognostic Club Cell Secretory Protein (CC16) Cut-point in an Independent ALTA Cohort

被引:2
作者
Almuntashiri, Sultan [1 ,2 ]
Chase, Aaron [3 ,4 ]
Sikora, Andrea [3 ,4 ]
Zhang, Duo [1 ,5 ,6 ]
机构
[1] Univ Georgia, Coll Pharm, Charlie Norwood VA Med Ctr, Clin & Expt Therapeut, Augusta, GA USA
[2] Univ Hail, Coll Pharm, Dept Clin Pharm, Hail, Saudi Arabia
[3] Univ Georgia, Coll Pharm, Dept Clin & Adm Pharm, Augusta, GA USA
[4] Augusta Univ, Med Ctr, Dept Pharm, Augusta, GA USA
[5] Augusta Univ, Dept Med, Augusta, GA USA
[6] Univ Georgia, Coll Pharm,Clin & Expt Therapeut, Charlie Norwood VA Med Ctr, Clin Pharm, 914 New Ballie St,HM Bldg, Rm 117, Augusta, GA 30912 USA
来源
BIOMARKER INSIGHTS | 2023年 / 18卷
基金
美国国家卫生研究院;
关键词
Acute lung injury; ARDS; lung epithelial cell; critical illness; RESPIRATORY-DISTRESS-SYNDROME; PULMONARY-FIBROSIS; FLUID; SUBPHENOTYPES;
D O I
10.1177/11772719231156308
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
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页数:5
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共 27 条
  • [1] Club Cell Secreted Protein CC16: Potential Applications in Prognosis and Therapy for Pulmonary Diseases
    Almuntashiri, Sultan
    Zhu, Yin
    Han, Yohan
    Wang, Xiaoyun
    Somanath, Payaningal R.
    Zhang, Duo
    [J]. JOURNAL OF CLINICAL MEDICINE, 2020, 9 (12) : 1 - 16
  • [2] Missed or delayed diagnosis of ARDS: a common and serious problem
    Bellani, Giacomo
    Pham, Tai
    Laffey, John G.
    [J]. INTENSIVE CARE MEDICINE, 2020, 46 (06) : 1180 - 1183
  • [3] Broeckaert F, 2000, CLIN EXP ALLERGY, V30, P469
  • [4] Acute respiratory distress syndrome subphenotypes and differential response to simvastatin: secondary analysis of a randomised controlled trial
    Calfee, Carolyn S.
    Delucchi, Kevin L.
    Sinha, Pratik
    Matthay, Michael A.
    Hackett, Jonathan
    Shankar-Hari, Manu
    McDowell, Cliona
    Laffey, John G.
    O'Kane, Cecilia M.
    McAuley, Daniel F.
    [J]. LANCET RESPIRATORY MEDICINE, 2018, 6 (09) : 691 - 698
  • [5] Subphenotypes in acute respiratory distress syndrome: latent class analysis of data from two randomised controlled trials
    Calfee, Carolyn S.
    Delucchi, Kevin
    Parsons, Polly E.
    Thompson, B. Taylor
    Ware, Lorraine B.
    Matthay, Michael A.
    [J]. LANCET RESPIRATORY MEDICINE, 2014, 2 (08) : 611 - 620
  • [6] Acute Respiratory Distress Syndrome and Diffuse Alveolar Damage New Insights on a Complex Relationship
    Cardinal-Fernandez, Pablo
    Lorente, Jose A.
    Ballen-Barragan, Aida
    Matute-Bello, Gustavo
    [J]. ANNALS OF THE AMERICAN THORACIC SOCIETY, 2017, 14 (06) : 844 - 850
  • [7] Chase A., 2022, CRIT CARE EXPLOR, V4, DOI [10.1097/CCE.0000000000000711, DOI 10.1097/CCE.0000000000000711]
  • [8] Epithelial repair mechanisms in the lung
    Crosby, Lynn M.
    Waters, Christopher M.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2010, 298 (06) : L715 - L731
  • [9] Acute Respiratory Distress Syndrome Subphenotypes Respond Differently to Randomized Fluid Management Strategy
    Famous, Katie R.
    Delucchi, Kevin
    Ware, Lorraine B.
    Kangelaris, Kirsten N.
    Liu, Kathleen D.
    Thompson, B. Taylor
    Calfee, Carolyn S.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 195 (03) : 331 - 338
  • [10] EVOLUTION OF METAPLASTIC SQUAMOUS CELLS OF ALVEOLAR WALLS IN PULMONARY FIBROSIS PRODUCED BY PARAQUAT - AN ULTRASTRUCTURAL AND IMMUNOHISTOCHEMICAL STUDY
    FUKUDA, Y
    TAKEMURA, T
    FERRANS, VJ
    [J]. VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1989, 58 (01) : 27 - 43