Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry

Lisa J. Deesker, Sander F. Garrelfs, Giorgia Mandrile, Michiel J. S. Oosterveld, Pierre Cochat, Georges Deschênes, J. rôme Harambat, Sally-Anne Hulton, Asheeta Gupta, Bernd Hoppe, Bodo B. Beck, Laure Collard, Rezan Topaloglu, Larisa Prikhodina, Eduardo Salido, Thomas Neuhaus, Jaap W. Groothoff, Justine Bacchetta

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Introduction: Infantile oxalosis is the most severe form of primary hyperoxaluria type 1 (PH1), with onset of end-stage kidney disease (ESKD) during infancy. We aimed to analyze the outcome of these patients as our current understanding is limited owing to a paucity of reports. Methods: A retrospective registry study was conducted using data from the OxalEurope registry. All PH1 patients with ESKD onset at age <1 year were analyzed. Results: We identified 95 patients born between 1980 and 2018 with infantile oxalosis. Median (interquartile range [IQR]) age at ESKD was 0.4 (0.3–0.5) year. There were 4 patients diagnosed by family screening who developed ESKD despite early diagnosis. There were 11 patients who had biallelic missense mutations associated with vitamin B6 responsiveness. Of 89 patients, 27 (30%) died at a median age of 1.4 (0.6–2.0) years (5-year patient survival of 69%). Systemic oxalosis was described in 54 of 56 screened patients (96%). First transplantation was performed at a median age of 1.7 (1.3–2.9) years. In 42 cases, this procedure was a combined liver-kidney transplantation (LKTx), and in 23 cases, liver transplantations (LTx) was part of a sequential procedure. Survival rates of both strategies were similar. Patient survival was significantly higher in patients born after 2000. Intrafamilial phenotypic variability was present in 14 families of patients with infantile oxalosis. Conclusion: Nearly all screened patients with infantile oxalosis developed systemic disease. Mortality is still high but has significantly improved over time and might further improve under new therapies. The intrafamilial phenotypic variability warrants further investigation.

Original languageEnglish
Pages (from-to)1608-1618
Number of pages11
JournalKidney International Reports
Volume7
Issue number7
Early online date2022
DOIs
Publication statusPublished - Jul 2022

Keywords

  • children
  • end-stage kidney disease
  • infant
  • infantile oxalosis
  • primary hyperoxaluria

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