Primary hyperoxaluria type 1—current practice in the siRNA era: an ERA Genes & Kidney Working Group survey

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Authors: Malte P. Bartram, Giovambattista Capasso, Émilie Cornec-Le Gall, Lisa J. Deesker, Albertien M. van Eerde, Lucile Figueres, María Vanessa Pérez-Gómez, Jaap Groothoff, Laila Oubram, Jan Halbritter, Ewout Jasper Hoorn, Tom Nijenhuis
+88 more John Andrew Sayer, Bodo B Beck, Roman-Ulrich Müller, the PH1 Survey Study Group, Olivier Bonny, Stella Stabouli, Matja� Kopa?, Diletta Domenica Torres, Dana Kigitoviča, Ingrid Prkačin, Paul Snelling, Thomas Forbes, Lilian Johnstone, Jasna Trbojevic-Stankovic, Jaap Groothoff, Irene Capelli, Kathy Nicholls, Malte P. Bartram, Bodo Beck, Tom Nijenhuis, Jan Halbritter, Gerlineke Hawkins-van der Cingel, Lucile Figueres, Emilie CORNEC-LE GALL, J L Sayer, Margareta Fištrek, Lovro Lamot, Maria Vanessa Perez Gomez, Giovanna Capolongo, Melissa Pilco Teran, Saulo Fern�ndez, Rebeca Garc�a Agudo, Cristina Castro-Alonso, R Echarri Carrillo, Fernanda Arrojo Alonso, Pedro Arango-Sancho, Gema Ariceta, Laura Mu�iz, Armando Torres, Mario P�rez, Izabela Zakrocka, Jovana Putnik, M�nica Furlano, Beatriz Redondo Navarro, Ivana Vuković Brinar, Sibylle Tschumi, Alexander Ritter, Ann Christin Gjerstad, Merita Rroji, Nereida Spahia, Elda CULE, Marsida Kasa, Shuji Isotani, Shuzo Hamamoto, Katsuhito Miyazawa, Osasuyi Iyasere, Christoph Wanner, Hristos Karakizlis, Leire Madariaga Domínguez, Nicola Hošek, Sergio Camilo Lopez-Garcia, Nikoleta Printza, Georgie Mathew, Mugahid Elamin, Dan Delean, Guerd Baya, R W G van Rooij, Klaus Arbeiter, Germana Longo, Eugene Yu Hin Chan, Mariana Costin, Javier P?narba?? Ay?e Seda Lumbreras, İSMAİL DURSUN, Doaa Alqaoud, Martin Bald, Joanna Sladowska, Aleksandra Paripović, Jovana Putnik, Maria Michela D’Alessandro, Michiel Schreuder, Licia Peruzzi, Brankica Spasojević, Laure Collard, Katja Doerry, No�mie Jourde-Chiche, Thomas Robert, Thomas Stehl�, Bertrand Knebelmann
Cited by: 1
References: 31

Abstract

Background: Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder leading to the formation of kidney stones, nephrocalcinosis, and kidney failure. Besides, PH1 poses the risk of developing systemic oxalosis, a life-threatening condition with oxalate deposits in multiple organ systems. The rarity of the disorder combined with recent major additions to therapeutic options based on small interfering RNA (siRNA) therapeutics make a formal assessment of current practice and implementation of treatment recommendations an important asset. Methods: An international questionnaire survey was conducted among medical doctors involved in the treatment of patients with chronic kidney disease. The survey included 32 questions addressing demographics, diagnostics and therapeutics, and educational needs related to the care for PH1 patients. Results: 176 participants from 43 countries completed the survey, the majority of them were from Europe. The results indicate clear shortcomings in the availability of recommended diagnostics, especially with regards to plasma oxalate. Genetic testing strategies often do not include patients who may have PH1, e.g. when the underlying cause of kidney failure is unknown or in patients with nephrolithiasis or nephrocalcinosis. Treatment modalities are only partly harmonized and intensified dialysis is not fully implemented across centers. Strategies toward combination of conventional therapeutics such as hyperhydration and pyridoxine with new siRNA therapeutics depend on the treating physician's expertise. The survey identifies clear needs regarding implementation of current treatment recommendations as well as important educational gaps. Conclusion: The advent of targeted treatment opportunities for PH1 comes with an increased need to provide guidance to the field. Filling the existing gaps will ensure that a growing number of patients get access to optimal care and novel life-changing therapies.

Fields of Study & Subjects

Kidney Stones and Urolithiasis Treatments Biomedical Research and Pathophysiology Chemotherapy-induced organ toxicity mitigation

Publication details

Journal / source
Clinical Kidney Journal
Publisher
Oxford University Press (OUP)
Volume
19
Issue
7
Pages
sfag162–sfag162
Publication date
23 May 2026
Language
EN