Plasma kallikrein predicts primary graft dysfunction after heart transplant

被引:10
|
作者
Giangreco, Nicholas P. [1 ,2 ,3 ]
Lebreton, Guillaume [4 ]
Restaino, Susan [5 ]
Farr, Mary Jane [5 ]
Zorn, Emmanuel [6 ]
Colombo, Paolo C. [5 ]
Patel, Jignesh [7 ]
Levine, Ryan [7 ]
Truby, Lauren [5 ]
Soni, Rajesh Kumar [8 ]
Leprince, Pascal [4 ]
Kobashigawa, Jon [7 ]
Tatonetti, Nicholas P. [1 ,2 ,3 ,9 ]
Fine, Barry M. [5 ]
机构
[1] Columbia Univ, Dept Syst Biol, New York, NY USA
[2] Columbia Univ, Dept Biomed Informat, New York, NY USA
[3] Columbia Univ, Dept Med, New York, NY USA
[4] Pitiie Salpetriere Univ Hosp, Chirurg Thorac & Cardiovasc, Paris, France
[5] Columbia Univ Irving Med Ctr, Div Cardiol, Dept Med, New York, NY USA
[6] Columbia Univ Irving Med Ctr, Ctr Translat Immunol, New York, NY USA
[7] Cedars Sinai Med Ctr, Cedars Sinai Heart Inst, Los Angeles, CA 90048 USA
[8] Columbia Univ Irving Med Ctr, Herbert Irving Comprehens Canc Ctr, Prote & Macromol Crystallog Shared Resource, New York, NY USA
[9] Columbia Univ, Inst Genom Med, New York, NY USA
来源
关键词
primary graft dysfunction; exosomes; machine learning; KININ SYSTEM; ACTIVATION; MICROVESICLES; BIOMARKERS; BLOOD; SCORE;
D O I
10.1016/j.healun.2021.07.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Primary graft dysfunction (PGD) is the leading cause of early mortality after heart transplant. Pre-transplant predictors of PGD remain elusive and its etiology remains unclear. METHODS: Microvesicles were isolated from 88 pre-transplant serum samples and underwent proteomic evaluation using TMT mass spectrometry. Monte Carlo cross validation (MCCV) was used to predict the occurrence of severe PGD after transplant using recipient pre-transplant clinical characteristics and serum microvesicle proteomic data. Putative biological functions and pathways were assessed using gene set enrichment analysis (GSEA) within the MCCV prediction methodology. RESULTS: Using our MCCV prediction methodology, decreased levels of plasma kallikrein (KLKB1), a critical regulator of the kinin-kallikrein system, was the most predictive factor identified for PGD (AUROC 0.6444 [0.6293, 0.6655]; odds 0.1959 [0.0592, 0.3663]. Furthermore, a predictive panel combining KLKB1 with inotrope therapy achieved peak performance (AUROC 0.7181 [0.7020, 0.7372]) across and within (AUROCs of 0.66-0.78) each cohort. A classifier utilizing KLKB1 and inotrope therapy outperforms existing composite scores by more than 50 percent. The diagnostic utility of the classifier was validated on 65 consecutive transplant patients, resulting in an AUROC of 0.71 and a negative predictive value of 0.92-0.96. Differential expression analysis revealed a enrichment in inflammatory and immune pathways prior to PGD. CONCLUSIONS: Pre-transplant level of KLKB1 is a robust predictor of post-transplant PGD. The combination with pre-transplant inotrope therapy enhances the prediction of PGD compared to pre-transplant KLKB1 levels alone and the resulting classifier equation validates within a prospective validation cohort. Inflammation and immune pathway enrichment characterize the pre-transplant proteomic signature predictive of PGD. (C) 2021 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:1199 / 1211
页数:13
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