Key result
Baseline serum cystatin C (2.4 vs 1.7 mg/L) and urinary NGAL (242.0 vs 132.0 ng/mL) were significantly higher in patients who died during 12-month follow-up after PMVR (both P<0.001).
Why the study?
Do baseline serum cystatin C and urinary NGAL predict 12-month mortality in patients undergoing percutaneous mitral valve repair?
Cohort (n=120)
Do baseline serum cystatin C and urinary NGAL predict 12-month mortality in patients undergoing percutaneous mitral valve repair?
p-value: p=<0.001
Elevated baseline serum cystatin C and urinary NGAL are significant predictors of 12-month mortality in high-risk patients undergoing percutaneous mitral valve repair.
Cystatin C and NGAL may refine mortality risk stratification before PMVR; leaves open whether they guide therapy or improve outcomes.
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.
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Dörr et al. (2018) conducted a cohort in Mitral regurgitation and heart failure (n=120). Serum cystatin C and urinary NGAL was evaluated on All-cause mortality at 12 months (p=<0.001). Baseline serum cystatin C (2.4 vs 1.7 mg/L) and urinary NGAL (242.0 vs 132.0 ng/mL) were significantly higher in patients who died during 12-month follow-up after PMVR (both P<0.001).
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