Procalcitonin, MR-Proadrenomedullin, and Cytokines Measurement in Sepsis Diagnosis: Advantages from Test Combination

被引:42
作者
Angeletti, Silvia [1 ]
Dicuonzo, Giordano [1 ]
Fioravanti, Marta [1 ]
De Cesaris, Marina [1 ]
Fogolari, Marta [1 ]
Lo Presti, Alessandra [2 ]
Ciccozzi, Massimo [2 ]
De Florio, Lucia [1 ]
机构
[1] Univ Hosp Campus Biomed Rome, Clin Pathol & Microbiol Lab, I-00128 Rome, Italy
[2] Natl Inst Hlth, Dept Infect Parasit & Immune Mediated Dis, Reference Ctr Phylogeny Mol Epidemiol & Microbial, Epidemiol Unit, I-00161 Rome, Italy
关键词
UNITED-STATES; APACHE-II; ADRENOMEDULLIN; SEVERITY; PROADM; SCORE; PREDICTION; MANAGEMENT; PROTEIN-1; MORTALITY;
D O I
10.1155/2015/951532
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Background. Elevated cytokines levels correlate with sepsis severity and mortality but their role in the diagnosis is controversial, whereas Procalcitonin (PCT) has been largely used. Recently, the mid-regional proadrenomedullin (MR-proADM) has been combined with PCT for diagnosis optimization. In this study the combined measurement of PCT, MR-proADM, and cytokines in patients with sepsis was evaluated. Methods. One hundred and four septic patients and 101 controls were enrolled. Receiver operating characteristic (ROC) analysis and multiple logistic regression were used to evaluate applicant markers for sepsis diagnosis. Markers with best Odds Ratio (OR) were combined, and the posttest probability and a composite score were computed. Results. Based upon ROC curves analysis, PCT, MR-proADM, IL-6, IL-10, TNF-alpha, and MCP-1 were considered applicant for sepsis diagnosis. Among these PCT, MR-proADM, IL-6, and TNF-alpha showed the best OR. A better posttest probability was found with the combination of PCT with MR-proADM and PCT with IL-6 or TNF-alpha compared to the single marker. A composite score of PCT, MR-proADM, and TNF-alpha showed the best ROC curve in the early diagnosis of sepsis. Conclusion. The combination of PCT with other markers should expedite diagnosis and treatment of sepsis optimizing clinical management.
引用
收藏
页数:14
相关论文
共 39 条
[1]
ALBERT A, 1982, CLIN CHEM, V28, P1113
[2]
Use of the sequential organ failure assessment score as a severity score [J].
Amaral, ACKB ;
Andrade, FM ;
Moreno, R ;
Artigas, A ;
Cantraine, F ;
Vincent, JL .
INTENSIVE CARE MEDICINE, 2005, 31 (02) :243-249
[3]
Angeletti S, 2015, NEW MICROBIOL, V38, P379
[4]
Diagnostic and prognostic role of procalcitonin (PCT) and MR-pro-Adrenomedullin (MR-proADM) in bacterial infections [J].
Angeletti, Silvia ;
Spoto, Silvia ;
Fogolari, Marta ;
Cortigiani, Marco ;
Fioravanti, Marta ;
de Florio, Lucia ;
Curcio, Brunella ;
Cavalieri, Danilo ;
Costantino, Sebastiano ;
Dicuonzo, Giordano .
APMIS, 2015, 123 (09) :740-748
[5]
Procalcitonin and mid-regional pro-adrenomedullin test combination in sepsis diagnosis [J].
Angeletti, Silvia ;
Battistoni, Fabrizio ;
Fioravanti, Marta ;
Bernardini, Sergio ;
Dicuonzo, Giordano .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2013, 51 (05) :1059-1067
[6]
Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[7]
HIGH SERUM PROCALCITONIN CONCENTRATIONS IN PATIENTS WITH SEPSIS AND INFECTION [J].
ASSICOT, M ;
GENDREL, D ;
CARSIN, H ;
RAYMOND, J ;
GUILBAUD, J ;
BOHUON, C .
LANCET, 1993, 341 (8844) :515-518
[8]
Biological determinants of and reference values for plasma interleukin-8, monocyte chemoattractant protein-1, epidermal growth factor, and vascular endothelial growth factor: Results from the STANISLAS cohort [J].
Berrahmoune, H ;
Lamont, JV ;
Herbeth, B ;
FitzGerald, P ;
Visvikis-Siest, S .
CLINICAL CHEMISTRY, 2006, 52 (03) :504-510
[9]
Homogeneous time-resolved fluoroimmunoassay for the measurement of midregional proadrenomedullin in plasma on the fully automated system BRAHMS KRYPTOR® [J].
Caruhel, Pascaline ;
Mazier, Christian ;
Kunde, Jan ;
Morgenthaler, Nils G. ;
Darbouret, Bruno .
CLINICAL BIOCHEMISTRY, 2009, 42 (7-8) :725-728
[10]
Conlon P J, 1989, Biotechnol Ther, V1, P31