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Published on: May 2, 2013
De Novo Biopsy-Proven Glomerular Disease Following COVID-19 Vaccination
Cheng-Hsu Chen1,2,3,4, Yu-Wei Chiu1,5, Bo-Ding Chen1,6
1Division of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, 160, Sec. 3, Taiwan Boulevard, Taichung 407, Taiwan.
Insights
COVID-19 vaccine-associated glomerular disease (CVAGD) can manifest as IgA nephropathy or ANCA-related RPGN. While most patients recover, some cases of CVAGD, particularly ANCA-related RPGN, may not fully resolve.
Area of Science:
- Nephrology
- Immunology
- Vaccinology
Background:
- The association between COVID-19 vaccination and glomerular disease (CVAGD) lacks consensus.
- Understanding CVAGD is crucial due to widespread vaccination and varied global presentations.
- This study investigates CVAGD in a Taiwanese cohort.
Purpose of the Study:
- To analyze biopsy-proven cases of CVAGD in Taiwan.
- To describe the clinical and pathological characteristics of CVAGD.
- To identify specific vaccine types associated with CVAGD.
Main Methods:
- Retrospective analysis of renal biopsy data from June 2021 to October 2022.
- Inclusion of 14 patients with suspected CVAGD after expert nephrologist review.
- Assessment of clinical presentation, urinary findings, and renal biopsy results.
Main Results:
- 14 patients presented with proteinuria and hematuria, indicative of CVAGD.
- IgA nephropathy (35.7%) and ANCA-related RPGN (28.6%) were the most frequent diagnoses.
- Oxford-AstraZeneca, Moderna, and BNT162b2 vaccines were implicated; most patients showed renal function improvement, though ANCA-related RPGN cases had poorer outcomes.
Conclusions:
- IgA nephropathy and ANCA-related RPGN are the primary forms of CVAGD observed.
- All COVID-19 vaccine types appear to carry a risk for CVAGD development.
- Further research is needed to establish definitive causality between COVID-19 vaccines and glomerular diseases.
Abstract:
Background: There is still no consensus about the coronavirus disease 2019 (COVID-19) vaccine-associated glomerular disease (CVAGD). Given the large number of vaccinations administered and the variations in glomerulopathy observed across different countries and regional environments, CVAGD remains an important area of concern. Aim of study: We aimed to elucidate the findings of CVAGD within a Taiwanese cohort using biopsy data. Additionally, we endeavored to clarify the presentation of CVAGD. Methods: We collected data from patients who underwent renal biopsy from June 2021 to October 2022 at Taichung Veterans General Hospital. Two independent nephrologists meticulously reviewed the charts to exclude cases unrelated to vaccination. Results: Initially, a total of 286 patients underwent renal biopsy at our institute. Ultimately, we identified 14 patients with highly suspected CVAGD. All 14 patients exhibited proteinuria and hematuria. The urinary protein-to-creatinine ratio was elevated (median of 2012.1 mg/g; interquartile range (IQR) 25%-IQR 75%: 941.85-3884.1 mg/g) with a median serum creatinine level of 1.71 mg/dL (0.79-5.35). The majority of CVAGD cases were diagnosed as immunoglobulin A (IgA) nephropathy (n = 5, 35.7%), followed by antineutrophil cytoplasmic antibody (ANCA)-related rapidly progressive glomerulonephritis (RPGN) (n = 4, 28.6%). There were only three cases of minimal change disease each: one case of focal segmental glomerulosclerosis, one of membranous glomerulonephritis, and one of lupus nephritis. The culprit of COVID-19 vaccinations was 35.7% (n = 5) of Oxford-AstraZeneca (ChAdOx1-S), 42.9% (n = 6) of Moderna, and 21.4% (n = 3) of BNT162b2. Most patients experienced improvements in renal function. Only two cases of P-ANCA RPGN and one case of IgA nephropathy did not recover. Eighty percent of IgA nephropathy cases had favorable outcomes, but none of the patients with P-ANCA RPGN achieved full recovery. Conclusions: IgA nephropathy and ANCA-related RPGN were the most common CVAGD, and all types of COVID-19 vaccines posed a risk for CVAGD. However, further studies are required to confirm causality.
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