Renal replacement therapy in ADPKD patients: A 25-year survey based on the Catalan registry

Víctor Martínez, Jordi Comas, Emma Arcos, Joan Manel Díaz, Salomé Muray, Juan Cabezuelo, José Ballarín, Elisabet Ars, Roser Torra

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24 Citations (Scopus)


Background: Some 7-10% of patients on replacement renal therapy (RRT) are receiving it because of autosomal dominant polycystic kidney disease (ADPKD). The age at initiation of RRT is expected to increase over time. Methods. Clinical data of 1,586 patients (7.9%) with ADPKD and 18,447 (92.1%) patients with other nephropathies were analysed from 1984 through 2009 (1984-1991, 1992-1999 and 2000-2009). Results: The age at initiation of RRT remained stable over the three periods in the ADPKD group (56.7 ± 10.9 (mean ± SD) vs 57.5 ± 12.1 vs 57.8 ± 13.3 years), whereas it increased significantly in the non-ADPKD group (from 54.8 ± 16.8 to 63.9 ± 16.3 years, p < 0.001). The ratio of males to females was higher for non-ADPKD than for ADPKD patients (1.6-1.8 vs 1.1-1.2). The prevalence of diabetes was significantly lower in the ADPKD group (6.76% vs 11.89%, p < 0.001), as were most of the co-morbidities studied, with the exception of hypertension. The survival rate of the ADPKD patients on RRT was higher than that of the non-ADPKD patients (p < 0.001). Conclusions: Over time neither changes in age nor alterations in male to female ratio have occurred among ADPKD patients who have started RRT, probably because of the impact of unmodifiable genetic factors in the absence of a specific treatment. © 2013 Martínez et al.; licensee BioMed Central Ltd.
Original languageEnglish
Article number186
JournalBMC Nephrology
Issue number1
Publication statusPublished - 9 Sept 2013


  • Autosomal dominant polycystic kidney disease
  • Co-morbidities
  • Renal replacement therapy
  • Survival


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