Key result
Serum cystatin C levels significantly increased from admission to 6 weeks (7.1 to 7.8 mg/dL, p <0.0001) after NSTE-ACS, indicating it is not an acute-phase reactant.
Cohort (n=222)
Yes
Absolute Event Rate: 7.8% vs 7.1%
p-value: p=<0.0001
Cystatin C is a reliable marker of renal function during ACS that is not affected by acute-phase inflammation or myocardial necrosis.
Cystatin C may aid dual renal-CV risk assessment after NSTE-ACS; leaves open its independent prognostic value beyond eGFR.
Serum cystatin C (Cys-C) levels perform better than other markers of renal function as indicator of cardiovascular outcome both in population-based studies and in patients with non-ST-elevation acute coronary syndrome (NSTE-ACS). Whether the relation between elevated serum Cys-C levels and risk of a worse cardiovascular prognosis reflects a more precise measurement of renal function or an association with non-renal factors such as inflammation is a matter still poorly defined. In a prospective, multicenter study our group evaluated the time course of serum Cys-C levels in 222 patients over the first 6 weeks after an episode of NSTE-ACS and a successful percutaneous revascularization. We observed that Cys-C levels slightly but significantly increased from the admission to 6-week samples (7.1 to 7.8 mg/dL, p <0.0001), contrary to high sensitivity C Reactive Protein (hsCRP), N-terminal portion of the proBNP peptide (NT-proBNP), and Interleukin 6 (IL-6) levels which significantly decreased in the same period. Cys-C levels were not different in patients with or without elevated troponin (c-TnT), whereas the other inflammatory and biomechanical markers showed higher values in patients with versus those without elevated c-TnT. Cys-C was highly correlated with estimated glomerular filtration rate both in ACS and 6-week samples. In conclusion, our data seem to contradict the hypothesis that inflammation is a determinant of the Cys-C levels because they did not show the typical pattern of an acute-phase reactant and secondly they were independent from myocardial necrosis diagnosed by c-TnT levels. Moreover, our results indicate that Cys-C remains a reliable marker of renal function also during ACS because is not affected by myocardial necrosis or by acute left ventricular impairment, as detected by increased NT-proBNP values
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A 2014 study conducted a cohort in Non-ST-elevation acute coronary syndrome (NSTE-ACS) (n=222). Serum cystatin C (Cys-C) levels vs. Admission levels was evaluated on Time course of serum Cys-C levels from admission to 6 weeks (p=<0.0001). Serum cystatin C levels significantly increased from admission to 6 weeks (7.1 to 7.8 mg/dL, p <0.0001) after NSTE-ACS, indicating it is not an acute-phase reactant.
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