Evaluation of cystatin C and neutrophil gelatinase-associated lipocalin as predictors of mortality in patients undergoing percutaneous mitral valve repair (MitraClip)

被引:3
|
作者
Doerr, Oliver [1 ,2 ]
Walther, Claudia [3 ]
Liebetrau, Christoph [1 ,2 ,3 ]
Keller, Till [2 ,3 ]
Ortlieb, Regine M. [1 ]
Boeder, Niklas [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 ,3 ]
机构
[1] Univ Giessen, Dept Cardiol, Klin Str 33, D-35392 Frankfurt, Germany
[2] Partner Site RheinMain, DZHK German Ctr Cardiovasc Res, Frankfurt, Germany
[3] Kerckhoff Heart & Thorax Ctr, Dept Cardiol, Bad Nauheim, Germany
[4] St Johannes Hosp, Dept Cardiol, Dortmund, Germany
关键词
biomarker; valvular heart disease; CHRONIC KIDNEY-DISEASE; ACUTE OUTCOMES; REGURGITATION; THERAPY; RISK; EUROSCORE; IMPLANTATION; GUIDELINES; FAILURE; SURGERY;
D O I
10.1002/clc.23089
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Compromised renal function is a major risk factor that is strongly associated with poor outcome in patients with mitral regurgitation (MR) and heart failure. Cystatin C, a cysteine protease inhibitor, has been used as a specific and sensitive biomarker of renal function. Neutrophil gelatinase-associated lipocalin (NGAL) is another sensitive biomarker that specifically indicates functional and structural kidney damage. The aim of the present study was to determine the predictive value of serum cystatin C and urinary NGAL as indicators of mortality in patients undergoing percutaneous mitral valve repair (PMVR). Methods A total of 120 consecutive patients (age: 77.3 years [+/- 11.2]) undergoing PMVR using the MitraClip system were included in this study. Venous blood and urinary samples were collected for biomarker analysis prior to PMVR. Physiological parameters, medication use, safety events, and all-cause mortality were assessed 12 months after the procedure. Results Twelve months after PMVR, there was a significant reduction in the severity of MR (P < 0.001), and an improvement in the New York Heart Association class (P < 0.01) was documented. Baseline levels of serum cystatin C (nonsurvivors: 2.4 mg/L [interquartile, IQR: 1.7;3.1] vs survivors: 1.7 mg/L [IQR: 1,3;2.1], P < 0.001) and urinary NGAL (nonsurvivors: 242.0 ng/mL [IQR: 154.5;281.5] vs survivors: 132.0 ng/mL [IQR:107.0;177.3], P < 0.001) were significantly higher in patients who died during the 12-month follow-up period. Conclusion Cystatin C and urinary NGAL were found to be predictors of long-term mortality in high-risk patients undergoing PMVR. Thus, cystatin C and NGAL assessment may be helpful in risk stratification in patients undergoing PMVR.
引用
收藏
页码:1474 / 1479
页数:6
相关论文
共 50 条
  • [1] Evaluation of cystatin C and NGAL as predictors of mortality in patients undergoing percutaneous mitral valve repair
    Doerr, O.
    Walther, C.
    Liebetrau, C.
    Ortlieb, M.
    Lorenz, J.
    Moellmann, H.
    Gaede, L.
    Boeder, N.
    Weipert, K. F.
    Troidl, C.
    Voss, S.
    Bauer, T.
    Hamm, C.
    Nef, H. M.
    EUROPEAN HEART JOURNAL, 2017, 38 : 267 - 267
  • [2] Diagnostic value of cystatin C and neutrophil gelatinase-associated lipocalin in primary glomerulopathies
    Proletov, Ya. Yu.
    Saganova, E. S.
    Galkina, O. V.
    Zubina, I. M.
    Bogdanova, E. O.
    Sipovsky, V. G.
    Smirnov, A. V.
    TERAPEVTICHESKII ARKHIV, 2013, 85 (06): : 10 - 16
  • [3] Comparative evaluation of cystatin C and neutrophil gelatinase-associated lipocalin in patients with thalassemia major versus thalassemia intermedia
    Mohammed, Marwah
    Mohammad, Jehan
    Fathi, Zainab
    Al-Hamdany, Muzahim
    Alkazzaz, Nasih
    PHARMACIA, 2021, 68 (04) : 741 - 746
  • [4] Evaluation of Serum Neutrophil Gelatinase-Associated Lipocalin, Cystatin C, and Clusterin Concentrations in Neonatal Calf Diarrhea
    Tumer, Kenan Cagri
    Dincer, Pelin Fatos Polat
    LARGE ANIMAL REVIEW, 2024, 30 (01): : 7 - 11
  • [5] The Evaluation of Neutrophil Gelatinase-Associated Lipocalin in Patients with Pulmonary Sarcoidosis
    Kato, S.
    Inui, N.
    Yasui, H.
    Hozumi, H.
    Karayama, M.
    Suzuki, Y.
    Furuhashi, K.
    Enomoto, N.
    Fujisawa, T.
    Nakamura, Y.
    Suda, T.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 197
  • [6] Neutrophil gelatinase-associated lipocalin in patients with sarcoidosis
    Kato, Shinpei
    Inui, Naoki
    Hozumi, Hironao
    Inoue, Yusuke
    Yasui, Hideki
    Karayama, Masato
    Kono, Masato
    Suzuki, Yuzo
    Furuhashi, Kazuki
    Enomoto, Noriyuki
    Fujisawa, Tomoyuki
    Nakamura, Yutaro
    Watanabe, Hiroshi
    Suda, Takafumi
    RESPIRATORY MEDICINE, 2018, 138 : S20 - S23
  • [7] Renal markers cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) in postmortem samples
    Keltanen, Terhi
    Walta, Anna-Mari
    Salonen, Satu
    Sajantila, Antti
    Lindroos, Katarina
    FORENSIC SCIENCE MEDICINE AND PATHOLOGY, 2016, 12 (02) : 189 - 192
  • [8] Implications of the changes in serum neutrophil gelatinase-associated lipocalin and cystatin C in patients with chronic kidney disease
    Shen, Shui-Juan
    Hu, Zuo-Xiang
    Li, Qing-Hua
    Wang, Shi-Min
    Song, Chun-Jiao
    Wu, Dong-Dong
    He, Jian-Ling
    Guan, Ji-Chao
    Shan, Juan-Ping
    NEPHROLOGY, 2014, 19 (03) : 129 - 135
  • [9] Renal markers cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) in postmortem samples
    Terhi Keltanen
    Anna-Mari Walta
    Satu Salonen
    Antti Sajantila
    Katarina Lindroos
    Forensic Science, Medicine, and Pathology, 2016, 12 : 189 - 192
  • [10] Neutrophil Gelatinase-Associated Lipocalin and Cystatin C Are Sensitive Markers of Renal Injury in Patients With Multiple Myeloma
    Paassotiriou, Gerasimos-Petros
    Kastritis, Efstathios
    Gkotzamanidou, Maria
    Christoulas, Dimitrios
    Eleutherakis-Papaiakovou, Evangelos
    Migkou, Magdalini
    Gavriatopoulou, Maria
    Roussou, Maria
    Margeli, Alexandra
    Papassotiriou, Ioannis
    Dimopoulos, Meletios A.
    Terpos, Evangelos
    CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2016, 16 (01): : 29 - 35