Journal Article

A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights

Volovelsky, Oded, Angel-Korman, Avital, Mor, Nofar, Beckerman, Pazit, Ben-Moshe, Yishay, Khavkin, Yulia, Kaidar, Maital, Pessach, Itai M., Pode-Shakked, Ben, Greenberg, Meidad, Barel, Ortal, Leiba, Adi, Dagan, Amit, Vivante, Asaf, Mor, Eytan, Semo Oz, Rotem, Dekel, Benjamin, Katzir, Ze’ev, Regev, Lilach C., Marek-Yagel, Dina, Borovitz, Yael, Issler, Naomi, Becker-Cohen, Rachel, Lotan, Danny, Javasky, Elisheva, Lahav, Einat, Kol, Nitzan, Raas-Rothschild, Annick, Haskin, Orly, Alfandary, Hadas, Levi, Shely, Ben-Shalom, Efrat, Anikster, Yair, Eliyahu, Aviva, Atias-Varon, Danit, Shlomovitz, Omer, Kagan, Maayan, Bar-Joseph, Ifat, Davidovits, Miriam, Rechavi, Gideon, Shashar, Moshe

2022

Overview

Background Genetic kidney diseases contribute a significant portion of kidney diseases in children and young adults. Nephrogenetics is a rapidly evolving subspecialty; however, in the clinical setting, increased use of genetic testing poses implementation challenges. Consequently, we established a national nephrogenetics clinic to apply a multidisciplinary model. Methods Patients were referred from different pediatric or adult nephrology units across the country if their primary nephrologist suspected an undiagnosed genetic kidney disease. We determined the diagnostic rate and observed the effect of diagnosis on medical care. We also discuss the requirements of a nephrogenetics clinic in terms of logistics, recommended indications for referral, and building a multidisciplinary team. Results Over 24 months, genetic evaluation was completed for a total of 74 unrelated probands, with an age range of 10 days to 72 years. The most common phenotypes included congenital anomalies of the kidneys and urinary tract, nephrotic syndrome or unexplained proteinuria, nephrocalcinosis/nephrolithiasis, tubulopathies, and unexplained kidney failure. Over 80% of patients were referred due to clinical suspicion of an undetermined underlying genetic diagnosis. A molecular diagnosis was reached in 42/74 probands, yielding a diagnostic rate of 57%. Of these, over 71% of diagnoses were made via next generation sequencing (gene panel or exome sequencing). Conclusions We identified a substantial fraction of genetic kidney etiologies among previously undiagnosed individuals which influenced subsequent clinical management. Our results support that nephrogenetics, a rapidly evolving field, may benefit from well-defined multidisciplinary co-management administered by a designated team of nephrologist, geneticist, and bioinformatician. Graphical abstract A higher resolution version of the Graphical abstract is available as Supplementary information

• Publisher: Springer Berlin Heidelberg,Springer,Springer Nature B.V
• Subject: Calcinosis / Children / Congenital defects / Diagnosis / Genetic aspects / Genetic screening / Genetic susceptibility / Kidney diseases / Medical diagnosis / Medicine / Medicine & Public Health / Nephrolithiasis / Nephrology / Nephrotic syndrome / Next-generation sequencing / Original Article / Patients / Pediatric research / Pediatrics / Phenotypes / Proteinuria / Renal failure / Risk factors / Urinary tract / Urology / Young adults