Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.

Mansour, B., Lemberg, K., Schneider, R., Saida, K., Elmubarak, I., Yu, S., Yousef, K., Frank, C. N., Riedhammer, K. M., Zahoor, M. Y., Kolvenbach, C. M., Merz, L. M., Mertens, N. D., Bao, A., Salmanullah, D., Kalkar, G., Hölzel, S., Zion, E., Marchuk, D., … Hildebrandt, F. (2026). Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.. Pediatric Nephrology (Berlin, Germany).

Abstract

BACKGROUND: Steroid-resistant nephrotic syndrome (SRNS) constitutes the second most common cause of chronic kidney disease (CKD) in children. A monogenic cause can be identified in approximately 25% of SRNS cases. In contrast, steroid-sensitive or steroid-dependent nephrotic syndrome (SSNS/SDNS) is typically attributed to multifactorial or immunological causes and rarely linked to monogenic etiology.

METHODS: We performed exome sequencing (ES) in 237 families, including 183 with SRNS and 54 with SSNS/SDNS.

RESULTS: A (likely) pathogenic variant in a known SRNS gene was identified in 29/183 individuals with SRNS (15.8%). Additionally, 6/183 (3.3%) individuals with SRNS carried pathogenic variants in phenocopy genes-genes associated with diseases that clinically mimic SRNS. The diagnostic yield was significantly higher in individuals with ≥ 50 Mb homozygosity-by-descent (HBD) (44.7% vs. 8.5%) and in those with SRNS disease onset before 1 year of age (41.9%). In individuals with SSNS/SDNS, we found a likely causative variant in only 1 of 54 probands.

CONCLUSIONS: A genetic cause was established in 19.1% of SRNS patients (15.8% in known SRNS genes and 3.3% in phenocopy genes), but only 1.9% of non-steroid-resistant cases.

Last updated on 04/01/2026
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