Evidence map›Paper›PMID 40266336›Full record

ArticlePediatric nephrology (Berlin, Germany)2025

The clinical characteristics of patients with congenital nephrotic syndrome secondary to NPHS1 mutation: Is nephrectomy still a therapeutic option for selected cases?

Yüksel Uğurlu, Bora Gülhan, İsmail Dursun, Hülya Nalçacıoğlu, Gülşah Kaya Aksoy, Nur Canpolat, Aysun Bayazıt, Zeynep Birsin Özçakar, Selcuk Yüksel, Gönül Parmaksız and 5 more

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Article in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Yüksel Uğurlu *Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Türkiye.
Bora Gülhan *Department of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Türkiye.
İsmail DursunDepartment of Pediatric Nephrology, Faculty of Medicine, Erciyes University, Kayseri, Türkiye.
Hülya NalçacıoğluDepartment of Pediatric Nephrology, Faculty of Medicine, Ondokuz Mayıs University, Samsun, Türkiye.
Gülşah Kaya AksoyDepartment of Pediatric Nephrology, Faculty of Medicine, Akdeniz University, Antalya, Türkiye.
Nur CanpolatDepartment of Pediatric Nephrology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
Aysun BayazıtDepartment of Pediatric Nephrology, Faculty of Medicine, Çukurova University, Adana, Türkiye.
Zeynep Birsin ÖzçakarDepartment of Pediatric Nephrology, Faculty of Medicine, Ankara University, Ankara, Türkiye.
Selcuk YükselDepartment of Pediatric Nephrology, Faculty of Medicine, ÇAnakkale Onsekiz Mart University, Çanakkale, Türkiye.
Gönül ParmaksızDepartment of Pediatric Nephrology, Başkent University Adana Dr. Turgut Noyan Training and Research Center, Adana, Türkiye.
Gülşah ÖzdemirDepartment of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Türkiye.
Eda Didem Kurt-ŞükürDepartment of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Türkiye.
Ali DüzovaDepartment of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Türkiye.
Mutlu HayranDepartment of Preventive Oncology, Hacettepe University Cancer Institute, Ankara, Türkiye.
Fatih OzaltinDepartment of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Türkiye. fozaltin@hacettepe.edu.tr.ORCID 0000-0003-1194-0164

Funding

Scientific and Technological Research Council of Türkiye (TÜBİTAK)
6 · The paper itself

Abstract

backgroundManaging congenital nephrotic syndrome (CNS) remains a clinical challenge. While albumin infusions and nephrectomy have been long-standing treatments, a conservative approach is increasingly favored. This study aimed to compare clinical outcomes between nephrectomy (Nx) and non-Nx in patients with bi-allelic NPHS1 mutations.

methodsThis retrospective cohort study included 29 pediatric CNS patients (15 female, 14 male) with confirmed NPHS1 mutations. Clinical parameters including albumin infusion requirements, infections, hospitalizations, growth, and survival rates were analyzed in the Nx and non-Nx groups.

resultsThe median age at the time CNS was diagnosed was 29 days (IQR: 11-62 days). In all, 24 patients (82.8%) had homozygous NPHS1 mutations and 5 (17.2%) had compound heterozygous NPHS1 mutations. None of the patients had Fin-major mutation (i.e., p. Leu41 Aspfs*50). Unilateral/bilateral nephrectomy was performed in 16 patients. At 12 months post-nephrectomy the number of albumin infusions required, infections, and hospitalizations decreased significantly in the Nx group, as compared to the pre-nephrectomy period (p = 0.001, p = 0.027, and p = 0.004, respectively). Among the 13 (44.8%) patients in the non-Nx group, at 12 months after CNS was diagnosed the number of serum albumin infusions required significantly decreased (p = 0.007); however, the number of infections and hospitalization did not differ significantly (p = 0.589 and p = 0.5, respectively). Receiver operating characteristic (ROC) analysis showed that requiring albumin infusions ≥ 14 days/month predicted the decision to perform nephrectomy with 68% accuracy (73% sensitivity and 62% specificity).

conclusionsNephrectomy reduces albumin infusions, infections, and hospitalizations, suggesting it may be a beneficial treatment for selected CNS patients with NPHS1 mutations.

Indexed as

Membrane ProteinsNephrectomyNephrotic SyndromeChild, PreschoolFemaleHospitalizationHumansInfantInfant, NewbornMaleMutationRetrospective StudiesTreatment OutcomeMembrane ProteinsnephrinCongenital nephrotic syndromeNephrectomyNephrinNPHS1 mutation

Identifiers

PMID40266336
PMCPMC12187890

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.