Proteomic Associations of NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) in Heart Failure With Preserved Ejection Fraction

被引:8
作者
Azzo, Joe David [1 ]
Dib, Marie-Joe [2 ]
Zagkos, Loukas [3 ]
Zhao, Lei [4 ]
Wang, Zhaoqing [4 ]
Chang, Ching-Pin [4 ]
Ebert, Christina [4 ]
Salman, Oday [1 ]
Gan, Sushrima [2 ]
Zamani, Payman [1 ,2 ]
Cohen, Jordana B. [4 ,5 ]
van Empel, Vanessa [6 ]
Richards, A. Mark [7 ,8 ]
Javaheri, Ali [9 ,10 ]
Mann, Douglas L. [9 ]
Rietzschel, Ernst R. [11 ]
Schafer, Peter H. [4 ]
Seiffert, Dietmar A. [4 ]
Gill, Dipender [3 ]
Burgess, Stephen [12 ]
Ramirez-Valle, Francisco [4 ]
Gordon, David A. [4 ]
Cappola, Thomas P. [1 ,2 ]
Chirinos, Julio A. [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Hosp Univ Penn, Div Cardiovasc Med, Philadelphia, PA 19104 USA
[3] Imperial Coll London, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England
[4] Bristol Myers Squibb Co, Lawrenceville, PQ, Canada
[5] Univ Penn, Perelman Sch Med, Renal Electrolyte & Hypertens Div, Philadelphia, PA 19104 USA
[6] Maastricht Univ, Med Ctr, Dept Cardiol, Maastricht, Netherlands
[7] Natl Univ Singapore, Cardiovasc Res Inst, Singapore, Singapore
[8] Univ Otago, Christchurch Heart Inst, Christchurch 8140, New Zealand
[9] Washington Univ, Sch Med, St Louis, MO USA
[10] John J Cochran Vet Hosp, St Louis, MO USA
[11] Ghent Univ Hosp, Dept Cardiovasc Dis, Ghent, Belgium
[12] Univ Cambridge, Dept Publ Hlth & Primary Care, Cambridge, England
基金
美国国家卫生研究院;
关键词
biomarkers; fibrosis; heart failure; inflammation; proteomics; NEPRILYSIN INHIBITION; ENDOTHELIAL-CELLS; ANGIOPOIETIN-2; RISK;
D O I
10.1161/CIRCHEARTFAILURE.123.011146
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels are variably elevated in heart failure with preserved ejection fraction (HFpEF), even in the presence of increased left ventricular filling pressures. NT-proBNP levels are prognostic in HFpEF and have been used as an inclusion criterion for several recent randomized clinical trials. However, the underlying biologic differences between HFpEF participants with high and low NT-proBNP levels remain to be fully understood. Methods: We measured 4928 proteins using an aptamer-based proteomic assay (SOMAScan) in available plasma samples from 2 cohorts: (1) Participants with HFpEF enrolled in the PHFS (Penn Heart Failure Study; n=253); (2) TOPCAT (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist Trial) participants in the Americas (n=218). We assessed the relationship between SOMAScan-derived plasma NT-proBNP and levels of other proteins available in the SOMAScan assay version 4 using robust linear regression, with correction for multiple comparisons, followed by pathway analysis. Results: NT-proBNP levels exhibited prominent proteome-wide associations in PHFS and TOPCAT cohorts. Proteins most strongly associated with NT-proBNP in both cohorts included SVEP1 (sushi, von Willebrand factor type-A, epidermal growth factor, and pentraxin domain containing 1; beta(TOPCAT)=0.539; P<0.0001; beta(PHFS)=0.516; P<0.0001) and ANGPT2 (angiopoietin 2; beta(TOPCAT)=0.571; P<0.0001; beta(PHFS)=0.459; P<0.0001). Canonical pathway analysis demonstrated consistent associations with multiple pathways related to fibrosis and inflammation. These included hepatic fibrosis and inhibition of matrix metalloproteases. Analyses using cut points corresponding to estimated quantitative concentrations of 360 pg/mL (and 480 pg/mL in atrial fibrillation) revealed similar proteomic associations. Conclusions: Circulating NT-proBNP levels exhibit prominent proteomic associations in HFpEF. Our findings suggest that higher NT-proBNP levels in HFpEF are a marker of fibrosis and inflammation. These findings will aid the interpretation of NT-proBNP levels in HFpEF and may guide the selection of participants in future HFpEF clinical trials.
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页数:14
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