Primary hyperoxaluria: Long‐term outcomes of isolated kidney versus simultaneous liver/kidney transplant

Author:

Habash Nawras W.1,Jaoudeh Rasha A. R. A.12,Hentz Roland C.3,Sas David J.4,Ibrahim Samar H.1,Hassan Sara1ORCID

Affiliation:

1. Division of Pediatric Gastroenterology and Hepatology Mayo Clinic Rochester Minnesota USA

2. Mayo Clinic School of Graduate Medical Education, Mayo Clinic College of Medicine and Science Rochester Minnesota USA

3. Division of Clinical Trials and Biostatistics Mayo Clinic Rochester Minnesota USA

4. Division of Pediatric Nephrology Mayo Clinic Rochester Minnesota USA

Abstract

AbstractObjectivesTo compare long‐term transplant outcomes (organ rejection and retransplant) of simultaneous liver/kidney transplant (SLK) versus isolated kidney transplant (IK) for patients with primary hyperoxaluria (PH).MethodsThe Rare Kidney Stone Consortium PH registry was queried to identify patients with PH who underwent SLK or IK from 1999 to 2021. Patient characteristics and long‐term transplant outcomes were abstracted and analyzed. Statistical comparisons were performed with Kaplan–Meier plots and Cox proportional hazards models.ResultsWe identified 250 patients with PH, of whom 35 received care at Mayo Clinic and underwent SLK or IK. Patients who underwent SLK as their index transplant had lower odds of kidney rejection than did those who underwent IK (hazard ratio [HR], 0.29; 95% confidence interval [CI], 0.08–0.99; p = .048). The immunoprotective effect of concomitant liver and kidney transplant appeared to enhance outcomes for patients with PH. Additionally, the odds of retransplant were significantly lower for patients who underwent SLK as their index transplant than for those who underwent IK (HR, 0.08; 95% CI, 0.02–0.42; p = .003). Of five patients who underwent IK and had maintained graft function for at least 5 years after transplant, three (60%) had documented vitamin B6 responsiveness.ConclusionsPatients with PH who underwent SLK had a lower risk of kidney rejection and retransplant than those who underwent IK. Accurate genetic assessment for vitamin B6 responsiveness may optimize IK allocation. Novel therapeutics, such as lumasiran, have been introduced as promising agents for the management of PH.

Publisher

Wiley

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