Excellent long-term outcome of renal transplantation in cystinosis patients

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Abstract

Background: Cystinosis is a rare lysosomal disorder leading to end stage renal disease in more than 90 % of patients before 20 years of age. Data about safety and efficiency of renal transplantation in patients with cystinosis is scarce. We evaluated long-term outcomes of renal transplantation in adult patients with cystinosis. Methods: Data of renal transplantation (n∈=∈31) in 30 adult patients with cystinosis in 5 French university transplant centers between 1980 and 2013 were retrospectively analyzed. A control cohort of 93 patients was matched for age, graft date, living/deceased donor status and transplant center. Results: Median age at transplantation was 20.4 years (7-36.5). At transplantation, all patients with cystinosis had corneal cystine deposits, 3 had diabetes and 7 had hypothyroidism. Graft survival was better in patients with cystinosis than in control patients (p∈=∈0.013). Multivariate analysis confirmed that cystinosis was an independent protective factor for graft survival (Hazard Ratio (HR) 0.11; CI95 [0.02-0.61]). Specific complications of cystinosis occurred during follow up: diabetes mellitus (n∈=∈4), hypothyroidism (n∈=∈1), liver involvement (n∈=∈1), neurologic involvement (n∈=∈2). Proportion of post-transplant diabetes mellitus (PTDM) was not statistically different in cystinosis group compared to control group: 4 (13.0 %) compared to 5 (5.0 %), respectively (p∈=∈0.25), with no differences regarding calcineurin inhibitors and steroids treatments during follow-up. Conclusions: Renal transplantation appears to be safe with excellent long-term outcomes in patients with cystinosis. These patients may receive standard immunosuppressive regimens with steroids and calcineurin inhibitors.

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Cohen, C., Charbit, M., Chadefaux-Vekemans, B., Giral, M., Garrigue, V., Kessler, M., … Servais, A. (2015). Excellent long-term outcome of renal transplantation in cystinosis patients. Orphanet Journal of Rare Diseases, 10(1). https://doi.org/10.1186/s13023-015-0307-9

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