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Minor Glomerular Abnormalities are Associated with Deterioration of Long-Term Kidney Function and Mitochondrial
Byung Chul Yu1, Nam-Jun Cho2, Samel Park2
1Division of Nephrology, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaru-ro, Bucheon 14584, Korea.
Abstract:
Minor glomerular abnormalities (MGAs) are unclassified glomerular lesions indicated by the presence of minor structural abnormalities that are insufficient for a specific pathological diagnosis. The long-term clinical outcomes and pathogenesis have not been examined. We hypothesized that MGAs would be associated with the deterioration of long-term kidney function and increased urinary mitochondrial DNA (mtDNA) copy numbers. We retrospectively enrolled patients with MGAs, age-/sex-/estimated glomerular filtration rate (eGFR)-matched patients with immunoglobulin A nephropathy (IgAN), and similarly matched healthy controls (MHCs; n = 49 each). We analyzed the time × group interaction effects of the eGFR and compared mean annual eGFR decline rates between the groups. We prospectively enrolled patients with MGAs, age- and sex-matched patients with IgAN, and MHCs (n = 15 each) and compared their urinary mtDNA copy numbers. Compared to the MHC group, the MGA and IgAN groups displayed differences in the time × group effects of eGFR, higher mean annual rates of eGFR decline, and higher urinary mtDNA copy numbers; however, these groups did not significantly differ from each other. The results indicate that MGAs are associated with deteriorating long-term kidney function, and mitochondrial injury, despite few additional pathological changes. We suggest that clinicians conduct close long-term follow-up of patients with MGAs.
Insights
Minor glomerular abnormalities (MGAs) indicate kidney damage and are linked to worsening kidney function and increased urinary mitochondrial DNA (mtDNA) copy numbers, similar to IgA nephropathy. Close patient follow-up is recommended.
Area of Science:
- Nephrology
- Pathology
- Genetics
Background:
- Minor glomerular abnormalities (MGAs) are unclassified glomerular lesions lacking defined long-term outcomes or pathogenesis.
- Previous research has not extensively examined the clinical trajectory or underlying mechanisms of MGAs.
Purpose of the Study:
- To investigate the long-term clinical outcomes of MGAs.
- To assess the association between MGAs and kidney function deterioration.
- To evaluate urinary mitochondrial DNA (mtDNA) copy numbers in patients with MGAs.
Main Methods:
- Retrospective analysis of patients with MGAs, IgA nephropathy (IgAN), and matched healthy controls (MHCs) to assess estimated glomerular filtration rate (eGFR) decline.
- Prospective analysis comparing urinary mtDNA copy numbers in patients with MGAs, IgAN, and MHCs.
Main Results:
- Both MGA and IgAN groups showed significant differences in eGFR time-course effects and higher mean annual eGFR decline rates compared to MHCs.
- Urinary mtDNA copy numbers were elevated in both MGA and IgAN groups relative to MHCs.
- No significant differences in eGFR decline or urinary mtDNA copy numbers were observed between the MGA and IgAN groups.
Conclusions:
- MGAs are associated with progressive kidney function decline and evidence of mitochondrial injury.
- Despite minimal pathological changes, MGAs share similar clinical trajectories and biomarkers with IgA nephropathy.
- Long-term monitoring of patients with MGAs is clinically warranted.
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