Soluble ST2 Is a Marker for Acute Cardiac Allograft Rejection

被引:38
作者
Pascual-Figal, Domingo A.
Garrido, Iris P.
Blanco, Rosa
Minguela, Alfredo
Lax, Antonio
Ordonez-Llanos, Jordi
Bayes-Genis, Antoni
Valdes, Mariano
Moore, Stephanie A.
Januzzi, James L.
机构
[1] Virgen de la Arrixaca Hosp, Serv Cardiol, Murcia, Spain
[2] Univ Murcia, Dept Med, Murcia, Spain
[3] Virgen de la Arrixaca Hosp, Inmunol Serv, Murcia, Spain
[4] St Pau Hosp, Serv Biochem, Barcelona, Spain
[5] UAB, Dept Biochem & Mol Biol, Barcelona, Spain
[6] Hosp Badalona Germans Trias & Pujol, Serv Cardiol, Barcelona, Spain
[7] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
关键词
RECEPTOR FAMILY-MEMBER; NATRIURETIC PEPTIDE LEVELS; MYOCARDIAL-INFARCTION; HEART-FAILURE; SERUM-LEVELS; EXPRESSION; TRANSPLANTATION; MORTALITY; SURVEILLANCE; RECIPIENTS;
D O I
10.1016/j.athoracsur.2011.07.048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Soluble ST2 (sST2), an interleukin (IL)-1 receptor family member, has a role in immunologic tolerance and has also emerged as a biomarker of cardiac stretch and remodeling. The sST2 role in heart transplantation is still unknown. Methods. From the heart transplantation population at our institution (n = 74), we selected a subset of 26 patients who had an acute rejection episode in the first year after transplantation (35%; 52 +/- 14 years; 76% men). Endomyocardial biopsy (EMB) results obtained at the time of the first rejection episode represented the rejection cohort (n = 26). Each patient served as a control to himself or herself, with EMB without rejection obtained before and after the rejection episode (n = 52). All laboratory measurements and blood samples were obtained at the time of EMB. Results. sST2 concentrations rose significantly in the context of acute rejection (130 [60 to 238] versus 51 ng/mL [28 to 80]; p = 0.002). Tertile analyses of sST2 concentrations revealed a graded association with rejection (p = 0.002) and repeated measurement analyses showed that sST2 concentrations were significantly modulated by the presence of rejection (p = 0.001). In receiver operator characteristic (ROC) analysis, sST2 had an area under the curve (AUC) of 0.72; the optimal cutoff point was 68 ng/mL (positive predictive value of 53%, negative predictive value of 83%), which predicted acute cellular rejection (odds ratio [OR] 4.9; 95% confidence interval [CI], 1.7 to 14.5; p = 0.004). The addition of sST2 values to those for the N-terminal pro B-type natriuretic peptide (NT-proBNP) resulted in a significant improvement on the integrated discrimination index (IDI) for rejection (relative improvement of 24%; p = 0.021). Conclusions. sST2 concentrations are modulated by the presence of acute rejection and provide complementary predictive ability to NT-proBNP for the biochemical identification of rejection. (Ann Thorac Surg 2011;92:2118-24) (C) 2011 by The Society of Thoracic Surgeons
引用
收藏
页码:2118 / 2124
页数:7
相关论文
共 31 条
  • [1] Noninvasive discrimination of rejection in cardiac allograft recipients using gene expression profiling
    Deng, MC
    Eisen, HJ
    Mehra, MR
    Billingham, M
    Marboe, CC
    Berry, G
    Kobashigawa, J
    Johnson, FL
    Starling, RC
    Murali, S
    Pauly, DF
    Baron, H
    Wohlgemuth, JG
    Woodward, RN
    Klingler, TM
    Walther, D
    Lal, PG
    Rosenberg, S
    Hunt, S
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2006, 6 (01) : 150 - 160
  • [2] Analytical and clinical evaluation of a novel high-sensitivity assay for measurement of soluble ST2 in human plasma - The Presage™ ST2 assay
    Dieplinger, Benjamin
    Januzzi, James L., Jr.
    Steinmair, Martin
    Gabriel, Christian
    Poelz, Werner
    Haltmayer, Meinhard
    Mueller, Thomas
    [J]. CLINICA CHIMICA ACTA, 2009, 409 (1-2) : 33 - 40
  • [3] Clinical utilities of peripheral blood gene expression profiling in the management of cardiac transplant patients
    Fang, Kenneth C.
    [J]. JOURNAL OF IMMUNOTOXICOLOGY, 2007, 4 (03) : 209 - 217
  • [4] Usefulness of Serial Monitoring of B-Type Natriuretic Peptide for the Detection of Acute Rejection After Heart Transplantation
    Garrido, Iris P.
    Pascual-Figal, Domingo A.
    Nicolas, Francisco
    Gonzalez-Carrillo, Maria J.
    Manzano-Fernandez, Sergio
    Sanchez-Mas, Jesus
    Valdes-Chavarri, Mariano
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2009, 103 (08) : 1149 - 1153
  • [5] Costimulatory function and expression of CD40 ligand, CD80, and CD86 in vascularized murine cardiac allograft rejection
    Hancock, WW
    Sayegh, MH
    Zheng, XG
    Peach, R
    Linsley, PS
    Turka, LA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) : 13967 - 13972
  • [6] The IL-33/ST2 pathway: therapeutic target and novel biomarker
    Kakkar, Rahul
    Lee, Richard T.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (10) : 827 - 840
  • [7] The Change in B-Type Natriuretic Peptide Levels Over Time Predicts Significant Rejection in Cardiac Transplant Recipients
    Kittleson, Michelle M.
    Skojec, Diane V.
    Wittstein, Ilan S.
    Champion, Hunter C.
    Judge, Daniel P.
    Barouch, Lili A.
    Halushka, Marc
    Hare, Joshua M.
    Kasper, Edward K.
    Russell, Stuart D.
    [J]. JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2009, 28 (07) : 704 - 709
  • [8] Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans
    Masters, RG
    Davies, RA
    Veinot, JP
    Hendry, PJ
    Smith, SJ
    de Bold, AJ
    [J]. CIRCULATION, 1999, 100 (03) : 287 - 291
  • [9] The Molecular Phenotype of Heart Transplant Biopsies: Relationship to Histopathological and Clinical Variables
    Mengel, M.
    Sis, B.
    Kim, D.
    Chang, J.
    Famulski, K. S.
    Hidalgo, L. G.
    Einecke, G.
    de Freitas, D. G.
    Tymchak, W.
    Burton, J.
    Halloran, P. F.
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2010, 10 (09) : 2105 - 2115
  • [10] Increased plasma concentrations of soluble ST2 are predictive for 1-year mortality in patients with acute destabilized heart failure
    Mueller, Thomas
    Dieplinger, Benjamin
    Gegenhuber, Alfons
    Poelz, Werner
    Pacher, Richard
    Haltmayer, Meinhard
    [J]. CLINICAL CHEMISTRY, 2008, 54 (04) : 752 - 756