Key result
12-month decline in eGFRcr-cys linked to ~31% higher risk of major CV events.
Why the study?
Cystatin C-based eGFR measures are more predictive of worse outcomes than creatinine-based measures in HFrEF, but whether they yield more accurate prognoses in HFpEF is unknown.
Do cystatin C-based measures of eGFR yield more accurate prognoses than creatinine-based measures in patients with heart failure with preserved ejection fraction (HFpEF)?
Cohort (n=214)
Do cystatin C-based measures of eGFR yield more accurate prognoses than creatinine-based measures in patients with heart failure with preserved ejection fraction (HFpEF)?
Hazard Ratio: 1.31 (95% CI 1.02–1.67)
In patients with HFpEF, a decline in combined creatinine-cystatin C eGFR over 12 months predicts adverse cardiovascular outcomes, but cystatin C alone does not offer superior prognostic value over creatinine-based measures.
Relative eGFRcr-cys decline may flag higher CV risk in HFpEF; leaves open whether cystatin C improves prognostication over creatinine.
Rationale and Objective Cystatin C- vs. creatinine-based measures of estimated glomerular filtration rate (eGFR) are more predictive of worse outcomes in people with heart failure with reduced ejection fraction (HFrEF). It is unknown if cystatin C-based measures may also yield more accurate prognoses in heart failure with preserved ejection fraction (HFpEF). Study Design Longitudinal analysis of people with HFpEF Setting & Participants 214 participants from the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist trial with available serum at baseline and 12 months in the National Heart, Lung, and Blood Institute's Biologic Specimen and Data Repository Information Coordinating Center. Exposures Baseline, time-varying, or change over 12 months in eGFRcr, eGFRcys, and eGFRcr-cys Outcomes Composite of aborted cardiac arrest, heart failure hospitalization, or CV death. Analytical Approach Fine-Gray and joint models. Results Median follow-up was (IQR) 3.09 (2.07, 4.44) years. All 3 baseline eGFR measures were independently associated with the risk of the composite endpoint, after adjustment for race, diabetes mellitus, and BMI: HR (95% CI) per 5ml/min/1.73m 2 lower eGFR: eGFRcr, 1.16 (1.04-1.28); eGFRcys, 1.20 (1.08-1.34); eGFRcr-cys, 1.19 (1.08-1.32). After adjusting for NT-proBNP and age, no baseline eGFR measure was statistically significantly associated with the composite endpoint. Only a relative decline in eGFRcr-cys from baseline to 12 months was associated with the composite endpoint in fully-adjusted models: eGFRcr-cys, HR 1.31 (1.02-1.67); per 10% eGFR decrease). Lower eGFR at any timepoint, using all 3 measures, was associated with the composite endpoint in fully-adjusted models. Limitations small number of events, possible survival bias Conclusions A decline in eGFRcr-cys from baseline to 12 months is associated with adverse cardiovascular outcomes in people with HFrEF. Measures of eGFR that incorporate only cystatin C may not be of greater prognostic value in people with HFpEF than measures that also incorporate serum creatinine. Plain-Language Summary Cystatin C-based measures of kidney function have been more predictive of adverse outcomes in people with heart failure with reduced ejection fraction (HFrEF), but their prognostic utility in heart failure with preserved ejection fraction (HFpEF) is unclear. In a longitudinal analysis of 214 participants from the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist trial, a HFpEF population, we found that a relative decline in eGFRcr-cys from baseline to 12 months was associated with adverse cardiovascular outcomes. However, cystatin C based measures on their own were not associated with adverse cardiovascular outcomes. This suggests that cystatin C based measures may not be more prognostic that creatinine based measures in HFpEF.
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Roehm et al. (2026) conducted a cohort in Heart failure with preserved ejection fraction (HFpEF) (n=214). Decline in eGFRcr-cys was evaluated on Composite of aborted cardiac arrest, heart failure hospitalization, or CV death (HR 1.31, 95% CI 1.02-1.67). A relative decline in eGFRcr-cys from baseline to 12 months was associated with an increased risk of aborted cardiac arrest, heart failure hospitalization, or CV death (HR 1.31; 95% CI 1.02-1.67).
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