BMC Nephrology (Aug 2012)

Clinical utility of <it>PKD2</it> mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic

  • Robinson Caroline,
  • Hiemstra Thomas F,
  • Spencer Deborah,
  • Waller Sarah,
  • Daboo Laura,
  • Karet Frankl Fiona E,
  • Sandford Richard N

DOI
https://doi.org/10.1186/1471-2369-13-79
Journal volume & issue
Vol. 13, no. 1
p. 79

Abstract

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Abstract Background ADPKD affects approximately 1:1000 of the worldwide population. It is caused by mutations in two genes, PKD1 and PKD2. Although allelic variation has some influence on disease severity, genic effects are strong, with PKD2 mutations predicting later onset of ESRF by up to 20 years. We therefore screened a cohort of ADPKD patients attending a nephrology out-patient clinic for PKD2 mutations, to identify factors that can be used to offer targeted gene testing and to provide patients with improved prognostic information. Methods 142 consecutive individuals presenting to a hospital nephrology out-patient service with a diagnosis of ADPKD and CKD stage 4 or less were screened for mutations in PKD2, following clinical evaluation and provision of a detailed family history (FH). Results PKD2 mutations were identified in one fifth of cases. 12% of non-PKD2 patients progressed to ESRF during this study whilst none with a PKD2 mutation did (median 38.5 months of follow-up, range 16–88 months, p PKD2 vs. PKD2, 54 yrs vs. 65 yrs; p PKD2 mutations were identified in patients with a FH of ESRF occurring before age 50 yrs, whereas a PKD2 mutation was predicted by a positive FH without ESRF. Conclusions PKD2 testing has a clinically significant detection rate in the pre-ESRF population. It did not accurately distinguish those individuals with milder renal disease defined by stage of CKD but did identify a group less likely to progress to ESRF. When used with detailed FH, it offers useful prognostic information for individuals and their families. It can therefore be offered to all but those whose relatives have developed ESRF before age 50.