Abstract: FR-PO341
Intraindividual Difference between Creatinine- and Cystatin C-Based GFR and Association with Cardiovascular Events
Session Information
- Hypertension, CVD, and the Kidneys: Epidemiology
October 25, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Hypertension and CVD
- 1602 Hypertension and CVD: Clinical
Authors
- Tydén, Maria, Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- Batra, Gorav, Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- Fellstrom, Bengt C., Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- Held, Claes Olov Gunnar, Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- Lindbäck, Johan, Uppsala Clinical Research Center, Uppsala, Sweden
- Soveri, Inga, Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- Stewart, Ralph A., Green Lane Cardiovascular Service, Auckland City Hospital and Auckland University, Auckland, New Zealand
- Svensson, Maria K., Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
- White, Harvey D., Green Lane Cardiovascular Service, Auckland City Hospital and Auckland University, Auckland, New Zealand
- Wallentin, Lars, Uppsala Universitet Institutionen for Medicinska Vetenskape, Uppsala, Sweden
Background
Association between eGFRratio (eGFRcys/eGFRcr) and outcomes, was studied in patients with chronic coronary syndrome.
Methods
A post-hoc analysis of 14,513 patients from the STABILITY trial investigated the association between baseline eGFRratio and major adverse cardiac events (MACE) and death using Cox-regression. Analyses were adjusted for eGFRcr, eGFRcys, or both. Discriminative ability was assessed using the C-index, and the incremental value was measured using the fraction of new information (FNI). 2021 CKD-EPI eGFR equations were applied.
Results
The mean age was 65 years, 82% were male. Mean eGFRcys was 77 (61-94) and eGFRcr 79 (65-91) mL/min/1.73 m2. During median follow-up of 3.7 years, there were 1449 MACE and 1063 deaths. Table 1 presents a comparison of eGFRratio of 0.7 with 1.0. After adjustment for eGFRcys, the eGFRratio contributed marginally when assessed by FNI. Figure 1 illustrates the adjusted one-year-risk for MACE and death as a function of eGFRratio for different eGFR levels, indicating a weaker association with the ratio when adjusted for eGFRcys.
Conclusion
In patients with chronic coronary syndrome, lower eGFRratio is associated with higher risk of adverse outcomes. After adjustment for eGFRcys the added value of eGFRratio is limited.
eGFRratio and outcomes
Outcome | HR [95% CI] | P | C-index | FNI |
MACE | ||||
Unadjusted | 1.99 [1.80-2.21] | <0.001 | 0.59 | |
Adjusted for eGFRcr | 1.89 [1.70-2.10] | <0.001 | 0.62 | 0.54 |
Adjusted for eGFRcys | 1.29 [1.13-1.46] | 0.002 | 0.61 | 0.05 |
Adjusted for eGFRcr+ eGFRcys | 1.09 [0.58-2.04] | 0.030 | 0.62 | 0.03 |
Death | ||||
Unadjusted | 2.52 [2.25-2.84] | <0.001 | 0.63 | |
Adjusted for eGFRcr | 2.35 [2.08-2.64] | <0.001 | 0.67 | 0.57 |
Adjusted for eGFRcys | 1.39 [1.20-1.61] | <0.001 | 0.67 | 0.05 |
Adjusted for eGFRcr + eGFRcys | 1.52 [0.75-3.10] | 0.090 | 0.67 | 0.01 |
Funding
- Commercial Support – GlaxoSmithKline