The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease

Sandro Rossetti, Sarah Burton, Lana Strmecki, Gregory R. Pond, Jośe L. San Millán, Klaus Zerres, T. Martin Barratt, Seza Ozen, Vicente E. Torres, Erik J. Bergstralh, Christopher G. Winearls, Peter C. Harris

Research output: Contribution to journalArticlepeer-review

157 Scopus citations


The severity of renal cystic disease in the major form of autosomal dominant polycystic kidney disease (PKD1) is highly variable. Clinical data was analyzed from 324 mutation-characterized PKD1 patients (80 families) to document factors associated with the renal outcome. The mean age to end-stage renal disease (ESRD) was 54 yr, with no significant difference between men and women and no association with the angiotensin-converting enzyme polymorphism. Considerable intrafamilial variability was observed, reflecting the influences of genetic modifiers and environmental factors. However, significant differences in outcome were also found among families, with rare examples of unusually late-onset PKD1. Possible phenotype/genotype correlations were evaluated by estimating the effects of covariants on the time to ESRD using proportional hazards models. In the total population, the location of the mutation (in relation to the median position; nucleotide 7812), but not the type, was associated with the age at onset of ESRD. Patients with mutations in the 5′ region had significantly more severe disease than the 3′ group; median time to ESRD was 53 and 56 yr, respectively (P = 0.025), with less than half the chance of adequate renal function at 60 yr (18.9% and 39.7%, respectively). This study has shown that the position of the PKD1 mutation is significantly associated with earlier ESRD and questions whether PKD1 mutations simply inactivate all products of the gene.

Original languageEnglish (US)
Pages (from-to)1230-1237
Number of pages8
JournalJournal of the American Society of Nephrology
Issue number5
StatePublished - 2002

ASJC Scopus subject areas

  • Nephrology


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