# Clinical and Epidemiological Study of IgA Nephropathy in the Bulgarian Population: Insights into Disease Presentation and Potential Biomarkers

**Authors:** Iva Kostadinova, Mila Lyubomirova, Boris Bogov, Ekaterina Kurteva, Dobroslav Kyurkchiev, Todor Todorov

PMC · DOI: 10.3390/jpm14030269 · Journal of Personalized Medicine · 2024-02-29

## TL;DR

This study explores IgA nephropathy in Bulgaria, identifying potential biomarkers and providing insights into disease characteristics.

## Contribution

The study identifies Gd-IgA1 as a potential diagnostic biomarker for IgA nephropathy in the Bulgarian population.

## Key findings

- Serum concentrations of Gd-IgA1, IgA, Gd-IgA1/IgA, and IgA/C3 were significantly different between IgAN patients and healthy controls.
- No correlation was found between biomarkers and chronic kidney disease progression.
- The study contributes to understanding IgAN in the Bulgarian population and suggests potential diagnostic biomarkers.

## Abstract

IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide and a leading cause of chronic kidney disease and renal failure. However, the Bulgarian population has limited epidemiological data and biomarkers for IgAN. In this retrospective monocentric analysis, we investigated all the patients with biopsy-proven IgAN over 10 years in a tertiary Bulgarian institution. From the analysis of 762 kidney biopsies, the diagnosis of primary IgAN was established in 125, with an average age of 35.94 ± 11.91 years. Our study aimed to assess the clinical characteristics, histological features, and potential biomarkers of IgAN in the Bulgarian population. We evaluated parameters such as proteinuria, hematuria, serum creatinine, and glomerular filtration rate (GFR). In fifty IgAN patients and 30 healthy controls, serum levels of Gd-IgA1, IgA, C3, BAFF, and APRIL using ELISA were examined. The results revealed significant differences in serum concentrations of Gd-IgA1 (p < 0.001), Gd-IgA1/IgA (p = 0.022), IgA (p = 0.014), and IgA/C3 (p = 0.047) between patients and controls. However, no correlation was found between Gd-IgA1, IgA, Gd-IgA1/IgA, and IgA/C3 and chronic kidney disease progression. Our study reports evidence of the diagnostic value of Gd-IgA1 and contributes to the understanding of IgAN in the Bulgarian population and suggests potential biomarkers for disease diagnosis and prognosis.

## Linked entities

- **Proteins:** CD79A (CD79a molecule), C3 (complement C3), TNFSF13B (TNF superfamily member 13b), TNFSF13 (TNF superfamily member 13)
- **Diseases:** IgA nephropathy (MONDO:0005342), chronic kidney disease (MONDO:0005300), renal failure (MONDO:0001106)

## Full-text entities

- **Genes:** CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}
- **Diseases:** hematuria (MESH:D006417), IgA Nephropathy (MESH:D005922), proteinuria (MESH:D011507), chronic kidney disease (MESH:D051436), renal failure (MESH:D051437), glomerulonephritis (MESH:D005921)
- **Chemicals:** creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10970904/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC10970904/full.md

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Source: https://tomesphere.com/paper/PMC10970904