Identification and validation of distinct biological phenotypes in patients with acute respiratory distress syndrome by cluster analysis

被引:216
作者
Bos, L. D. [1 ,2 ,3 ]
Schouten, L. R. [1 ,3 ]
van Vught, L. A. [4 ]
Wiewel, M. A. [4 ]
Ong, D. S. Y. [5 ,6 ]
Cremer, O. [6 ]
Artigas, A. [7 ]
Martin-Loeches, I. [8 ]
Hoogendijk, A. J. [4 ]
van der Poll, T. [4 ]
Horn, J. [1 ,3 ]
Juffermans, N. [1 ,3 ]
Calfee, C. S. [9 ,10 ]
Schultz, M. J. [1 ,3 ]
机构
[1] Acad Med Ctr, Dept Intens Care, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Acad Med Ctr, Dept Resp Med, Amsterdam, Netherlands
[3] Acad Med Ctr, Lab Expt Intens Care & Anesthesiol, Amsterdam, Netherlands
[4] Acad Med Ctr, Ctr Expt & Mol Med, Amsterdam, Netherlands
[5] Univ Med Ctr Utrecht, Dept Med Microbiol, Utrecht, Netherlands
[6] Univ Med Ctr Utrecht, Dept Intens Care Med, Utrecht, Netherlands
[7] Univ Autonoma Barcelona, CIBER Enfermedades Resp CIBERES, Crit Care Ctr, Sabadell Hosp,Corp Sanitaria Univ Parc Tauli, Sabadell, Spain
[8] MICRO, Trinity Ctr Hlth Sci, Dept Clin Med, Dublin, Ireland
[9] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Med, San Francisco, CA 94143 USA
[10] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Anesthesia, San Francisco, CA USA
关键词
ACUTE LUNG INJURY; MORTALITY; ARDS; OUTCOMES; SUBPHENOTYPES; EPIDEMIOLOGY; MECHANISMS; STRATEGIES; PRESSURE; NUMBER;
D O I
10.1136/thoraxjnl-2016-209719
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale We hypothesised that patients with acute respiratory distress syndrome (ARDS) can be clustered based on concentrations of plasma biomarkers and that the thereby identified biological phenotypes are associated with mortality. Methods Consecutive patients with ARDS were included in this prospective observational cohort study. Cluster analysis of 20 biomarkers of inflammation, coagulation and endothelial activation provided the phenotypes in a training cohort, not taking any outcome data into account. Logistic regression with backward selection was used to select the most predictive biomarkers, and these predicted phenotypes were validated in a separate cohort. Multivariable logistic regression was used to quantify the independent association with mortality. Results Two phenotypes were identified in 454 patients, which we named 'uninflamed' (N=218) and 'reactive' (N=236). A selection of four biomarkers (interleukin-6, interferon gamma, angiopoietin 1/2 and plasminogen activator inhibitor-1) could be used to accurately predict the phenotype in the training cohort (area under the receiver operating characteristics curve: 0.98, 95% CI 0.97 to 0.99). Mortality rates were 15.6% and 36.4% (p<0.001) in the training cohort and 13.6% and 37.5% (p<0.001) in the validation cohort (N=207). The 'reactive phenotype' was independent from confounders associated with intensive care unit mortality (training cohort: OR 1.13, 95% CI 1.04 to 1.23; validation cohort: OR 1.18, 95% CI 1.06 to 1.31). Conclusions Patients with ARDS can be clustered into two biological phenotypes, with different mortality rates. Four biomarkers can be used to predict the phenotype with high accuracy. The phenotypes were very similar to those found in cohorts derived from randomised controlled trials, and these results may improve patient selection for future clinical trials targeting host response in patients with ARDS.
引用
收藏
页码:876 / 883
页数:8
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