Abstract: FR-PO850
Cardiorenal Outcomes in Patients with IgAN: The FinnGen Study
Session Information
- IgA Nephropathy: Clinical, Outcomes, and Therapeutics
October 25, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Glomerular Diseases
- 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics
Authors
- Visser, Tomas Juhani, Helsingin Yliopisto Laaketieteellinen Tiedekunta, Helsinki, Finland
- Pyle, Laura, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States
- Narongkiatikhun, Phoom, Chiang Mai University, Chiang Mai, Thailand
- Choi, Ye Ji, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States
- Cherney, David, Toronto General Hospital, Toronto, Ontario, Canada
- Rodosthenous, Rodosthenis S., Helsingin Yliopisto Suomen Molekyylilaaketieteen Instituutti, Helsinki, Finland
- Kiryluk, Krzysztof, Columbia University, New York, New York, United States
- Bjornstad, Petter, University of Colorado Anschutz Medical Campus School of Medicine, Aurora, Colorado, United States
- Niiranen, Teemu, Turun Yliopisto Laaketieteellinen Tiedekunta, Turku, Finland
- Finne, Patrik, Helsingin Seudun Yliopistollinen Keskussairaala, Helsinki, Finland
- Gordin, Daniel, Helsingin Seudun Yliopistollinen Keskussairaala, Helsinki, Finland
Group or Team Name
- FinnGen.
Background
Long-term cardiorenal outcomes of Immunoglobulin A Nephropathy (IgAN) are incompletely understood. We assessed kidney function and cardiorenal events in patients with IgAN in the FinnGen study, which covers approximately 10% of the Finnish population (N=520210).
Methods
Patients with IgAN were identified using Finnish ICD10 diagnosis codes. The outcomes of interest were annual estimated glomerular filtration rate (eGFR) decline, start of kidney replacement therapy (KRT), and major adverse cardiovascular events (MACE). Out of 889 patients with IgAN, 265 were selected based on available data for eGFR. We compared outcomes in patients with IgAN (cases) vs. those with diabetes (controls), being the most common group requiring KRT in Finland. Cases (n=265) and controls (n=1060) were matched by eGFR, age, sex, and birth year (ratio 1:4). Multivariable-adjusted Cox regression and mixed-effects models were used to compare the groups.
Results
Annual eGFR decline was more rapid in patients with IgAN (-2.26; 95% Confidence Interval [95% CI] -2.33, -2.18 ml/min/1.73 m2 per year) compared to those with diabetes (-1.28; 95% CI -1.43, -1.12 ml/min/1.73 m2 per year). The cumulative incidence of KRT and MACE in patiens with IgAN and diabetes is shown in Figure 1. The risk for KRT was higher in individuals with IgAN compared to those with diabetes (Hazard Ratio [HR] 4.63; 95% CI 3.49, 6.16). However, the risk for MACE was lower in patients with IgAN (HR 0.61; 95% CI 0.47, 0.88) compared to patients with diabetes.
Conclusion
In this large register study, we demonstrated that patients with IgAN had a faster decline in eGFR and greater risk for KRT compared to patients with diabetes. In contrast, risk for MACE was lower in IgAN compared to diabetes in long-term follow-up.
Figure 1: Cumulative incidence of major adverse cardiovascular events (MACE) and kidney replacement therapy (KRT) from diagnosis in patients with IgA nephropathy and diabetes.
Funding
- Private Foundation Support