Sequential Cystatin C Levels and Renal Impairment in Acute Heart Failure

This is a single-center, prospective, cohort study. The design of this pilot study focuses on the feasibility to complete the project in a short period of time by the applicant. Subjects will be identified in the morning after their hospital admission and informed consent will be obtained for the study. At the time of enrollment blood samples and urine samples will be collected as baseline, together with a brief history and physical examination to document degree of congestion and basic vital signs. In addition their unused (to be discarded) blood samples from previous clinical labs from this admission may be retrieved from the clinical laboratory.

Patients will be followed daily, and each day a blood draw and urine sample will be obtained for research purposes until the day of discharge. Changes in vital signs, available laboratory data for serum creatinine and BUN, and congestion score will be documented. Physicians treating the patient will be blinded from the laboratory results. Because of the small sample size and the low anticipated rate of adverse events, this study uses a combined outcome of either death in hospital, death within 90 days after discharge or readmission to the hospital facility for heart failure within 90 days. Patients will be called after 90 days for follow up if readmission or death information is not available in the Electronic Medical Record.

Specific aims include:

Specific Aim 1 - To examine the natural history of changes in sequential cystatin C levels during diuretic therapy in Acute Decompensated Heart Failure.

Specific Aim 2 - To determine the predictive value of changes in sequential cystatin C levels to subsequent development of worsening renal function (WRF) and WRF in association with aminoterminal pro B-type natriuretic peptide (NT-proBNP) levels.

Inclusion criteria

• Hospital admission within 48 hours for ADHF, with an expected stay over 24 hours.
• Evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy

Exclusion criteria

• Heart failure due to congenital heart disease or critical aortic stenosis (potentially different cardio-renal pathophysiology)
• Acute myocardial infarction or unstable acute coronary syndromes
• End-stage renal insufficiency on renal replacement therapy (already has underlying advanced renal failure).
• Patients with active cancer (cystatin C has been shown to be produced by some tumors)
• Known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment
• Hemoglobin < 9 mg/dL or clinically significant active bleeding.
• Unable to comply with protocol or unable to have informed consent