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. 2024 Mar 4;25(1):78.
doi: 10.1186/s12882-024-03512-2.

Validation of IgA nephropathy diagnosis in the Swedish Renal Registry

Affiliations

Validation of IgA nephropathy diagnosis in the Swedish Renal Registry

Johanna Rehnberg et al. BMC Nephrol. .

Abstract

Aim: The Swedish Renal Registry (SRR) is a unique national quality registry that monitors the clinical trajectory of patients with chronic kidney disease (CKD). We have validated the biopsy data registered in the SRR for IgA Nephropathy (IgAN) diagnosis.

Methods: In total 25% of all patients (n = 142), registered with IgAN in the SRR after having performed a kidney biopsy during 2015-2019, were randomly selected. We obtained original biopsy and medical records for 139 (98%) patients. We evaluated the IgAN diagnosis using a standardized template, calculated its positive predictive value (PPV) with 95% confidence interval (CI) and reported clinical features at the time of diagnosis.

Results: A histological and clinical diagnosis of IgAN was confirmed in 132 of the 139 patients, yielding a PPV of 95% (95% CI 90-98%). Median age was 46 years (range: 18-85) and the male:female ratio was 2.1:1. The median creatinine level was 123 µmol/L, with a corresponding estimated glomerular filtration rate (eGFR) level of 51 mL/min/1.73m2. Histological features of IgA deposits were seen in all patients, hypercellularity in 102/132 (77.2%), C3 deposits in 98/132 (72.4%) and C1q deposits in 27/132 (20.5%) of the cases.

Conclusion: Validating data is not research per se, but continuous validation of medical registries is an important feature necessary to ensure reliable data and the foundation of good epidemiological data for future research. Our validation showed a high PPV (95%) for IgAN diagnosis registered in the SRR. Clinical characteristics were consistent with previous reports. The biopsy data in the SRR will be a valuable resource in future IgAN research.

Keywords: IgA nephropathy; Kidney biopsy; Swedish Renal Registry; Validation.

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Conflict of interest statement

Dr Rehnberg has obtained reinbursements for lectures from Astra Zeneca and Bayer. Dr Segelmark is a board member of the Swedish Renal Registry, he has received consultancy fees from Hansa Biopharma AB, Vifor Pharma and Astra Zeneca. Dr Ludvigsson coordinates a study on behalf of the Swedish IBD quality register (SWIBERG) and that study has received funding from Janssen Corporation. Dr Ludvigsson has also received finacial support from MSD developing a paper reviewing national healthcare registers in China. Dr Ludvigsson is currently discussing potential research collaboration with Takeda. Dr Emilsson has no conflicts of interests.

Figures

Fig. 1
Fig. 1
IgAN; IgA Nephropathy
Fig. 2
Fig. 2
IgAN; IgA Nephropathy, SRR; Swedish Renal Registry

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