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Published on: August 19, 2020
Risk profiles of progression in primary focal segmental glomerulosclerosis
Lori L Travis1, James C M Chan
1Center for Outcome Research and Evaluation, Maine Medical Center, Portland, Maine, USA.
Insights
Children with focal segmental glomerulosclerosis (FSGS) younger than 10 years and elevated baseline diastolic blood pressure (DBP) face a higher risk of kidney failure (KF). These factors are key indicators for progression in pediatric FSGS patients.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
- Kidney Failure Progression
Background:
- Focal segmental glomerulosclerosis (FSGS) affects 10%-20% of childhood nephrotic syndrome cases.
- 25%-50% of children with FSGS progress to kidney failure (KF).
- Understanding risk factors for KF progression in pediatric FSGS is crucial.
Purpose of the Study:
- To identify risk profiles for kidney failure (KF) progression in a cohort of pediatric FSGS patients.
- To delineate baseline characteristics associated with KF development.
Main Methods:
- Retrospective analysis of patient data (1977-2002) from a regional nephrology center.
- KF defined by serum creatinine doubling, dialysis, or kidney transplant.
- Comparison of baseline characteristics between KF and non-kidney failure (NKF) groups using hazard ratios and regression analysis.
Main Results:
- Approximately 60% of 34 FSGS patients developed KF.
- KF patients were younger at diagnosis (9 vs. 12 years, P=0.05) and had higher baseline diastolic blood pressure (DBP) (P<0.0001).
- Baseline DBP was a significant risk factor for KF progression (HR: 1.03; 95%CI: 1.01-1.06).
Conclusions:
- Younger age at diagnosis (<10 years) and elevated baseline DBP are significant risk factors for KF in children with FSGS.
- Baseline DBP is a critical predictor of kidney failure progression.
- These findings aid in understanding and managing FSGS progression in pediatric populations.
Background:
Focal segmental glomerulosclerosis (FSGS) is a component of childhood nephrotic syndrome occurring in 10%-20% of all cases. Over time, 25%-50% of children with FSGS develop kidney failure disease. We followed a cohort of children with FSGS in order to delineate the risk profile of progression to kidney failure (KF).
Methods:
We evaluated patient data collected from 1977 to 2002 at a regional mid-Atlantic nephrology center in the United States. KF was defined primarily for those patients whose serum creatinine (SCr) value doubled compared with the SCr value from a previous visit. Patients who received dialysis or a kidney transplant were also defined as having KF. We analyzed patient data for those who had at least two visits with SCr values recorded. Various baseline characteristics of patients who had developed KF and those with no kidney failure (NKF) were compared. Hazard ratios and correlation were used to further investigate potential risk factors of the kidney failure. We also compared the inverse SCr trend for KF and NKF patients using weighted linear regression.
Results:
Thirty-four of 43 FSGS patients had adequate follow-up data. About 60% of the patients developed KF over the study period. The average age of the KF patients at diagnosis of FSGS was 9 years, and that of NKF patients 12 years (P=0.05). FSGS patients with KF had a significantly higher mean diastolic blood pressure (DBP) at baseline, compared to those with NKF (P<0.0001). Other baseline characteristics including race, body mass index (BMI), systolic blood pressure, total cholesterol, urinary protein/creatinine ratio and calculated glomerular filtration rate (cGFR) were not significantly different. Baseline DBP was a significant risk factor in progression to KF (HR: 1.03; 95%CI: 1.01-1.06). Inverse SCr values were significantly decreased over time in KF patients (P=0.01).
Conclusions:
The data of this study indicate that children diagnosed with FSGS who are younger than 10 years and have elevated baseline DBP are more likely to develop kidney failure. The non-significant hazard ratios for other baseline characteristics including gender, race, and BMI are not instrumental risk factors. These results may help understand what may affect progression towards kidney failure in children with FSGS.
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