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Updated: Aug 18, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
[Clinical and pathologic features of nephropathy with C1q deposits]
N V Chebotareva1, A A Vinogradov1, A N Grishina1
1Sechenov First Moscow State Medical University (Sechenov University).
Insights
C1q deposits in the kidneys were found in 4.05% of chronic glomerulonephritis patients. Membranous nephropathy was the most common form, often presenting with nephrotic syndrome and sometimes renal dysfunction.
Area of Science:
- Nephrology
- Immunopathology
- Glomerular Diseases
Context:
- Chronic glomerulonephritis (CGN) encompasses various kidney diseases.
- C1q is a component of the complement system, implicated in immune complex-mediated kidney damage.
- Understanding C1q deposition patterns aids in diagnosing and managing CGN.
Purpose:
- To investigate the prevalence and characteristics of nephropathy associated with C1q deposits in adult CGN patients.
- To identify the specific morphological types and clinical presentations of CGN with C1q deposition.
- To analyze the association between C1q deposits and disease progression in CGN.
Summary:
- A study analyzed 296 kidney biopsy specimens from CGN patients (2014-2018), excluding lupus nephritis and primary membranoproliferative glomerulonephritis.
- C1q deposits were identified in 4.05% (12/296) of CGN cases using immunofluorescence.
- Morphologically, membranous nephropathy (8 cases) was most common, followed by mesangioproliferative glomerulonephritis (2 cases) and nephrosclerosis (2 cases).
- Clinically, 5 patients presented with nephrotic syndrome initially, while others developed it after proteinuria. Renal dysfunction was noted in 7 patients, with 2 progressing to renal failure within a year.
Impact:
- This study highlights C1q deposition as a relevant finding in a subset of CGN patients.
- It underscores the association of C1q deposits with membranous nephropathy and nephrotic syndrome.
- The findings contribute to a better understanding of CGN pathogenesis and clinical outcomes, potentially guiding diagnostic and therapeutic strategies.
Aim:
To determine the frequency, clinical and morphological features of a nephropathy with C1q deposits in chronic glomerulonephritis adult patients.
Materials And Methods:
296 specimens of kidneys of patients with a chronic glomerulonephritis (CGN) from 2014 for 2018 were analyzed. At the first step, specimens with C1q deposits in glomeruli revealed by immunofluorescent method were chosen. Lupus nephritis and primary membranoproliferative glomerulonephritis were exclusion criteria. At the second step, the retrospective analysis of the clinical characteristics was carried out.
Results And Discussion:
Deposits of C1q in kidneys at 12 of 296 (4.05%) CGN were revealed, m:f ratio 2:1. Average age of the beginning of a disease was 32.1±14.7 years. At a morphological research in 8 membranous nephropathy (MN), in 2 mesangioproliferative glomerulonephritis (MesPGN), in 2 - nephrosclerosis was revealed. Among 12 patients in 5 the disease debuted a nephrotic syndrome, at the others - a proteinuria from 0.5 to 4.0 g/days with the subsequent formation of a nephrotic syndrome. In 5 of 12 patients the disease was characterized by a favor course with preserved kidney function. At 7 patients at the time of inspection decrease in function of kidneys [glomerular filtration rate (eGFR) 31 (30-34) ml/min] was noted. 5 had slow progressing of a renal failure. 2 of 12 progressed to renal failure (eGFR to 19 and 24 ml/min) within a year.
Conclusion:
Deposits of C1q in kidney were revealed in 4.05% of biopsy specimens in CGN. The most frequent morphological form was the membranous nephropathy. The clinical course was characterized by a nephrotic syndrome, more than at a half of patients - with renal dysfunction.
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