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Pathological and clinical characteristics of late-onset oligomeganephronia based on a histomorphometric study
Ya-Li Ren1, Yang Li2, Jie Gao3
1Laboratory of Electron Microscopy, Pathological Center, Peking University First Hospital, No. 8, Xishiku Street, Beijing, 100034, People's Republic of China.
Background:
Late-onset oligomeganephronia (OMN) is a rare chronic kidney disease and has no quantitative criteria for diagnosis yet. The current study aimed to explore its clinicopathological features by histomorphometric analysis.
Methods:
We retrospectively re-reviewed all patients with enlarged and sparse glomeruli by light microscopy at Peking University First Hospital from 2012 to 2021, excluding those with any factor known to contribute to similar changes. Age- and sex-matched patients with thin basement membrane nephropathy were selected as control to establish the cut-off values for glomerulomegaly and rarity. Late-onset OMN cases were then confirmed and the clinicopathological characteristics were summarized.
Results:
Mean diameter and density of cortical glomeruli in control was 156.53 ± 27.50 μm and 4.07 ± 0.63 /mm2, giving a lower limit of 211.53 μm for glomerulomegaly and an upper of 2.81 /mm2 for rarity. Seven adults of three females and four males were finally diagnosed as late-onset OMN with a mean age of 26.57 years. They showed mild to moderate proteinuria and/or renal dysfunction at biopsy with the mean proteinuria, serum creatinine (Scr) level, and estimated glomerular filtration rate of 0.50 g/d (0.10-0.95 g/d), 140.9 µmol/L (95.1-227.1 µmol/L), and 58.7 mL/min/1.73m2 (21.3-98.0 mL/min/1.73m2), respectively. Four patients (57.1%) had normal Scr at diagnosis. Six patients with available data showed renal tubular injury with increased urinary microalbumin in all, elevated N-acetyl-β-glucosaminidase in two, and elevated α1 microglobulin in five. Kidney size was normal or slightly reduced. The mean density and glomerular diameter of the seven cases was 0.86 mm2 (0.55-1.41 /mm2) and 229.73 μm (211.88-260.66 μm). Segmental glomerular sclerosis was observed in six (85.7%) with four (66.7%) of perihilar type. Proximal tubule dilation was observed in all, focal to diffuse, lining with enlarged epithelial cells. The mean foot process width was 634.02 nm, wider than 472.54 nm of the control (P = 0.0002).
Conclusion:
Late-onset OMN should be considered a special entity with relatively slow clinical progress characterized by hypertrophy of the sparsely distributed nephron.
Insights
Late-onset oligomeganephronia (OMN) is a rare kidney disease. This study defines diagnostic criteria and reveals OMN involves enlarged glomeruli, tubular injury, and slower progression, offering new insights into this condition.
Area of Science:
- Nephrology
- Pathology
- Histomorphometry
Background:
- Late-onset oligomeganephronia (OMN) is a rare chronic kidney disease.
- Current diagnostic criteria for OMN are lacking.
- This study investigates the clinicopathological features of late-onset OMN.
Purpose of the Study:
- To establish quantitative diagnostic criteria for late-onset OMN.
- To explore the clinicopathological characteristics of late-onset OMN.
- To differentiate OMN from other kidney diseases with similar presentations.
Main Methods:
- Retrospective review of patients with enlarged and sparse glomeruli.
- Histomorphometric analysis of glomeruli and kidney tissue.
- Comparison with age- and sex-matched controls with thin basement membrane nephropathy.
Main Results:
- Established cut-off values for glomerulomegaly (>211.53 μm) and rarity (<2.81/mm²).
- Diagnosed seven adult cases of late-onset OMN with characteristic features including glomerular hypertrophy, segmental sclerosis, and proximal tubule dilation.
- Observed wider glomerular foot process width in OMN patients compared to controls (634.02 nm vs. 472.54 nm).
Conclusions:
- Late-onset OMN is a distinct clinicopathological entity.
- Characterized by hypertrophy of sparsely distributed nephrons and relatively slow clinical progression.
- Histomorphometric analysis provides crucial diagnostic criteria for OMN.
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