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Non-glomerular Tip Lesion Focal Segmental Glomerulosclerosis as a Negative Predictor in Idiopathic Membranous
Hui Wang1,2, Cheng Wan1, Man Jiang1
1Department of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Objective:
To assess the significance of focal segmental glomerulosclerosis (FSGS) variants on clinicopathological characteristics and short-term outcomes in idiopathic membranous nephropathy (IMN) patients.
Methods:
The clinicopathological data of 146 IMN patients diagnosed between December 2016 and March 2019 in our center were collected and analyzed. These patients were divided into the pure IMN group, IMN with glomerular tip lesion (GTL) group, and IMN with non-GTL FSGS group.
Results:
The IMN with non-GTL FSGS and IMN with GTL groups both had higher proportions of patients with hypertension, lower serum albumin, and severe proteinuria, while the IMN with non-GTL FSGS group additionally showed higher blood pressure and serum cholesterol, and lower serum IgG than the IMN group (all P<0.05). As for pathology, the IMN with non-GTL FSGS group had higher proportions of patients with acute tubular injury and moderate to severe chronic injuries than the IMN group (all P<0.05). In the IMN, IMN with GTL, and IMN with non-GTL FSGS groups, the overall one-year remission rates were 81.6%, 76%, and 58.8%, respectively. Furthermore, the IMN with non-GTL FSGS group showed the lowest cumulative incidence to reach remission within one year. Multivariate Cox logistic analysis demonstrated that higher level of serum anti-M-type phospholipase A2 receptor antibody and the existence of non-GTL FSGS lesion were independent predictors for no remission in IMN patients.
Conclusion:
The non-GTL FSGS lesion was a novel negative predictor in IMN and should be taken into account in the management of IMN.
Insights
Focal segmental glomerulosclerosis (FSGS) variants impact idiopathic membranous nephropathy (IMN) outcomes. Non-glomerular tip lesion (GTL) FSGS is a negative predictor, worsening clinicopathological characteristics and reducing remission rates in IMN patients.
Area of Science:
- Nephrology
- Pathology
- Clinical Medicine
Background:
- Idiopathic membranous nephropathy (IMN) is a leading cause of nephrotic syndrome in adults.
- Focal segmental glomerulosclerosis (FSGS) variants can coexist with IMN, potentially altering disease course.
- Understanding the impact of FSGS variants on IMN is crucial for accurate prognostication and management.
Purpose of the Study:
- To evaluate the influence of different FSGS variants on the clinicopathological features of IMN patients.
- To assess the short-term outcomes, specifically remission rates, in IMN patients with varying FSGS patterns.
- To identify predictors of poor response to treatment in IMN.
Main Methods:
- Retrospective analysis of 146 IMN patients diagnosed between December 2016 and March 2019.
- Classification of patients into pure IMN, IMN with glomerular tip lesion (GTL), and IMN with non-GTL FSGS groups.
- Comparison of clinicopathological data, including hypertension, serum albumin, proteinuria, blood pressure, serum cholesterol, serum IgG, tubular injury, and chronic injury scores.
Main Results:
- Patients with non-GTL FSGS and GTL showed higher rates of hypertension, lower serum albumin, and severe proteinuria compared to pure IMN.
- The non-GTL FSGS group exhibited worse parameters including higher blood pressure, elevated cholesterol, and lower serum IgG.
- One-year remission rates were 81.6% (IMN), 76% (IMN with GTL), and 58.8% (IMN with non-GTL FSGS), with non-GTL FSGS showing the lowest remission incidence.
- Higher anti-PLA2R antibody levels and non-GTL FSGS lesions were independent predictors for non-remission.
Conclusions:
- The presence of non-GTL FSGS lesions is a significant negative predictor in IMN.
- Non-GTL FSGS variants are associated with adverse clinicopathological characteristics and poorer short-term outcomes in IMN.
- Incorporating the assessment of FSGS variants, particularly non-GTL lesions, is essential for optimizing the management strategies for IMN patients.
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