Galectin-3 and ST2 as predictors of therapeutic success in high-risk patients undergoing percutaneous mitral valve repair (MitraClip)

被引:8
作者
Doerr, Oliver [1 ,2 ]
Walther, Claudia [3 ]
Liebetrau, Christoph [2 ,3 ]
Keller, Till [2 ,3 ]
Sommer, Thomas [1 ]
Boeder, Niklas [1 ]
Bayer, Matthias [1 ]
Bauer, Pascal [1 ]
Moellmann, Helge [4 ]
Gaede, Luise [4 ]
Troidl, Christian [2 ,3 ]
Voss, Sandra [2 ,3 ]
Bauer, Timm [1 ]
Hamm, Christian W. [1 ,2 ,3 ]
Nef, Holger [1 ,2 ]
机构
[1] Univ Giessen, Dept Cardiol, Klin Str 33, D-35392 Giessen, Germany
[2] DZHK German Ctr Cardiovasc Res, Partner Site RheinMain, Frankfurt, Germany
[3] Kerckhoff Heart & Thorax Ctr, Dept Cardiol, Bad Nauheim, Germany
[4] St Johannes Hosp, Dept Cardiol, Dortmund, Germany
关键词
Biomarker; Cardiac Fibrosis; Heart Failure; MitraClip; Mitral Regurgitation; Percutaneous Mitral Valve Repair; HEART-FAILURE; SOLUBLE ST2; REGURGITATION; ASSOCIATION; BIOMARKERS; MORTALITY; DIAGNOSIS; DISEASE; DEATH; SERUM;
D O I
10.1002/clc.22996
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Percutaneous mitral valve repair (PMVR) is an interventional treatment option in patients with severe mitral regurgitation (MR) and at high risk for open-heart surgery. Currently, limited information exists about predictors of procedural success after PMVR. Galectin-3 (Gal-3) and suppression of tumorigenicity 2 (ST2) induce fibrotic alterations in severe MR and heart failure. We sought to examine the predictive value of Gal-3 and ST2 as specific indicators of therapeutic success in high-risk patients undergoing PMVR. Hypothesis: We hypothesize that extended cardiac fibrotic alterations might have impact on successful MR reduction after the MitraClip procedure. Methods: A total of 210 consecutive patients undergoing PMVR using the MitraClip system were included in this study. Procedural success was defined as an immediate reduction of MR by >= 2 grades, assessed by echocardiography. Venous blood samples were collected prior to PMVR and at 6 months follow-up for biomarker analysis. Results: After PMVR there was a significant reduction in the severity of MR (MR grade: 3 +/- 0.3 vs 1.6 +/- 0.6, P <0.001). Low baseline Gal-3 levels (PMVRsuccess: 22.0 ng/mL [IQR, 17.3-30.9] vs PMVRfailure: 30.6 ng/mL [IQR, 24.8-42.3], P <0.001) and ST2 levels (PMVRsuccess: 900.0 pg/mL [IQR, 619.5-1114.5] vs PMVRfailure: 1728.0 pg/mL [IQR, 1051.March 1, 1930], P < 0.001) were associated with successful MR reduction after PMVR. Also, ROC analysis identified low baseline Gal-3 and ST2 levels as predictors of therapeutic success after PMVR (AUC(Gal-3):0.721 [IQR, 0.64-0.803], P < 0.001; AUC(ST2): 0.807 [IQR, 0.741-0.872], P < 0.001). Conclusions: There was an association between low Gal-3 and ST2 plasma levels and successful MR reduction in patients with severe MR undergoing PMVR using the MitraClip system.
引用
收藏
页码:1164 / 1169
页数:6
相关论文
共 30 条
[11]   Increased soluble ST2 is a stronger predictor of long-term cardiovascular death than natriuretic peptides in heart failure patients with reduced ejection fraction [J].
Gruson, Damien ;
Lepoutre, Thibault ;
Ahn, Sylvie A. ;
Rousseau, Michel F. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2014, 172 (01) :E250-E252
[12]   A prospective survey of patients with valvular heart disease in Europe:: The Euro Heart Survey on Valvular Heart Disease [J].
Iung, B ;
Baron, G ;
Butchart, EG ;
Delahaye, F ;
Gohlke-Bärwolf, C ;
Levang, OW ;
Tornos, P ;
Vanoverschelde, JL ;
Vermeer, F ;
Boersma, E ;
Ravaud, P ;
Vahanian, A .
EUROPEAN HEART JOURNAL, 2003, 24 (13) :1231-1243
[13]   ST2 Testing for Chronic Heart Failure Therapy Monitoring: The International ST2 Consensus Panel [J].
Januzzi, James L. ;
Pascual-Figal, Domingo ;
Daniels, Lori B. .
AMERICAN JOURNAL OF CARDIOLOGY, 2015, 115 (07) :70B-75B
[14]   The IL-33/ST2 pathway: therapeutic target and novel biomarker [J].
Kakkar, Rahul ;
Lee, Richard T. .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (10) :827-840
[15]   MEASURING EXTRACELLULAR-MATRIX TURNOVER IN THE SERUM OF PATIENTS WITH IDIOPATHIC OR ISCHEMIC DILATED CARDIOMYOPATHY AND IMPACT ON DIAGNOSIS AND PROGNOSIS [J].
KLAPPACHER, G ;
FRANZEN, P ;
HAAB, D ;
MEHRABI, M ;
BINDER, M ;
PLESCH, K ;
PACHER, R ;
GRIMM, M ;
PRIBILL, I ;
EICHLER, HG ;
GLOGAR, HD .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (14) :913-918
[16]   High-Sensitivity ST2 for Prediction of Adverse Outcomes in Chronic Heart Failure [J].
Ky, Bonnie ;
French, Benjamin ;
McCloskey, Kristin ;
Rame, J. Eduardo ;
McIntosh, Erin ;
Shahi, Puja ;
Dries, Daniel L. ;
Tang, W. H. Wilson ;
Wu, Alan H. B. ;
Fang, James C. ;
Boxer, Rebecca ;
Sweitzer, Nancy K. ;
Levy, Wayne C. ;
Goldberg, Lee R. ;
Jessup, Mariell ;
Cappola, Thomas P. .
CIRCULATION-HEART FAILURE, 2011, 4 (02) :180-U107
[17]  
Maisano F, 2011, MINERVA CARDIOANGIOL, V59, P455
[18]   Percutaneous Mitral Valve Interventions in the Real World [J].
Maisano, Francesco ;
Franzen, Olaf ;
Baldus, Stephan ;
Schaefer, Ulrich ;
Hausleiter, Jrg ;
Butter, Christian ;
Ussia, Gian Paolo ;
Sievert, Horst ;
Richardt, Gert ;
Widder, Julian D. ;
Moccetti, Tiziano ;
Schillinger, Wolfgang .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 62 (12) :1052-1061
[19]   The ARCHITECT galectin-3 assay: comparison with other automated and manual assays for the measurement of circulating galectin-3 levels in heart failure [J].
Meijers, Wouter C. ;
van der Velde, A. Rogier ;
de Boer, Rudolf A. .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2014, 14 (03) :257-266
[20]   Association between matrix metalloproteinase-9 and worsening heart failure events in patients with chronic heart failure [J].
Morishita, Tetsuji ;
Uzui, Hiroyasu ;
Mitsuke, Yasuhiko ;
Amaya, Naoki ;
Kaseno, Kenichi ;
Ishida, Kentaro ;
Fukuoka, Yoshitomo ;
Ikeda, Hiroyuki ;
Tama, Naoki ;
Yamazaki, Taketoshi ;
Lee, Jong-Dae ;
Tada, Hiroshi .
ESC HEART FAILURE, 2017, 4 (03) :321-330