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MeSsAGe risk score: tool for renal biopsy decision in steroid-dependent nephrotic syndrome.

Authors :
Chan CY
Resontoc LP
Qader MA
Chan YH
Liu ID
Lau PY
Than M
Yeo WS
Loh AH
Tan PH
Wei C
Reiser J
Biswas SK
Ng KH
Yap HK
Source :
Pediatric research [Pediatr Res] 2019 Mar; Vol. 85 (4), pp. 477-483. Date of Electronic Publication: 2019 Jan 15.
Publication Year :
2019

Abstract

Background: A lack of consensus exists as to the timing of kidney biopsy in children with steroid-dependent nephrotic syndrome (SDNS) where minimal change disease (MCD) predominates. This study aimed at examining the applicability of a biomarker-assisted risk score model to select SDNS patients at high risk of focal segmental glomerulosclerosis (FSGS) for biopsy.<br />Methods: Fifty-five patients with SDNS and biopsy-proven MCD (nā€‰=ā€‰40) or FSGS (nā€‰=ā€‰15) were studied. A risk score model was developed with variables consisting of age, sex, eGFR, suPAR levels and percentage of CD8 <superscript>+</superscript> memory T cells. Following multivariate regression analysis, total risk score was calculated as sum of the products of odds ratios and corresponding variables. Predictive cut-off point was determined using receiver operator characteristics (ROC) curve analysis.<br />Results: Plasma suPAR levels in FSGS patients were significantly higher, while percentage of CD45RO <superscript>+</superscript> CD8 <superscript>+</superscript> CD3 <superscript>+</superscript> was significantly lower than in MCD patients and controls. ROC analysis suggests the risk score model with threshold score of 16.7 (AUC 0.84, 95% CI 0.72-0.96) was a good predictor of FSGS on biopsy. The 100% PPV cut-off was >24.0, while the 100% NPV was <13.3.<br />Conclusion: A suPAR and CD8 <superscript>+</superscript> memory T cell percentage-based risk score model was developed to stratify SDNS patients for biopsy and for predicting FSGS.

Details

Language :
English
ISSN :
1530-0447
Volume :
85
Issue :
4
Database :
MEDLINE
Journal :
Pediatric research
Publication Type :
Academic Journal
Accession number :
30659270
Full Text :
https://doi.org/10.1038/s41390-019-0277-z