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Published on: October 21, 2018
Deterioration of GFR in IgA nephropathy as measured by 51Cr-EDTA clearance
S Rekola1, A Bergstrand, H Bucht
1Department of Renal Medicine, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.
Insights
Repeated glomerular filtration rate (GFR) measurements using 51Cr-EDTA clearance can predict IgA nephropathy progression. Early detection of declining GFR aids in managing kidney disease and preventing end-stage renal failure.
Area of Science:
- Nephrology
- Renal Medicine
- Immunology
Background:
- Mesangial IgA nephropathy is a common cause of chronic kidney disease.
- Subnormal renal function is prevalent in patients with IgA nephropathy.
- Predicting disease progression is crucial for patient management.
Purpose of the Study:
- To assess the progression of GFR in patients with mesangial IgA nephropathy.
- To identify markers associated with progressive renal disease.
- To evaluate the predictive value of repeated GFR measurements.
Main Methods:
- Glomerular filtration rate (GFR) determined by 51Cr-EDTA clearance in 191 patients.
- Longitudinal follow-up of GFR changes in 153 patients.
- Analysis of clinical and histological markers of disease progression.
Main Results:
- 45% of patients had subnormal GFR at follow-up.
- 50.3% experienced a pathological decline in GFR (>1.1 ml/min/year).
- Male sex, proteinuria, severe histology, and hypertension were markers of progression.
Conclusions:
- Repeated 51Cr-EDTA clearance measurements accurately predict IgA nephropathy outcomes.
- Early identification of declining GFR facilitates timely intervention.
- Creatinine clearance is less reliable for detecting mild GFR reductions.
Abstract:
In 191 patients with mesangial IgA nephropathy, GFR was determined as clearance of 51Cr-EDTA. 86 (45%) of them had subnormal renal function 7.3 +/- 4.6 years after renal biopsy. The change in GFR was followed in 153 patients with repeated determinations of 51Cr-EDTA clearance. 50.3% of the patients had a loss of more than 1.1 ml/min/year, which we regard as pathological. The markers of progressive disease were: male sex, high output of urinary protein, severe histological lesions and presence of hypertension. Even patients lacking these markers had a significantly increased incidence of progressive disease. Of 93 patients, with initially normal GFR, 32% will have a subnormal GFR within five years and 25% will develop end-stage renal failure within 20 years. In 38 patients with six or more determinations of 51Cr-EDTA clearance, the predictive value of the first four determinations was calculated. Of 26 with a decrease of more than 1.1 ml/min/year, 13 (50%) developed subnormal GFR during follow-up, while 11 of 12 (91.7%) with a decrease of less than 1.1 ml/min/year (P less than 0.05) remained normal. This shows that repeated determinations of GFR with an accurate method will predict the final outcome early in the disease. We also confirmed that single or repeated determinations of clearance of creatinine are of little value in separating a normal GFR from a slightly decreased one, but more reliable in detecting a markedly reduced GFR.
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