Current diagnostic evaluation of autosomal dominant polycystic kidney disease

Wojciech Wołyniec1, Magdalena Maria Jankowska, Ewa Król

  • 1Department of Nephrology, Transplantology and Internal Medicine, Medical University, Gdańsk, Poland. wwolyniec@wp.pl

Insights

Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of kidney failure. Early diagnosis through imaging and monitoring kidney function are crucial for managing this genetic disorder before effective treatments are widely available.

Area of Science:

  • Nephrology
  • Medical Imaging
  • Genetics

Background:

  • Autosomal dominant polycystic kidney disease (ADPKD) is a leading cause of end-stage renal disease.
  • Symptoms typically appear in the 3rd or 4th decade, but early diagnosis is possible.
  • Advances in understanding ADPKD may enable slowing disease progression in asymptomatic individuals.

Purpose of the Study:

  • To review current diagnostic methods for ADPKD.
  • To highlight the importance of early diagnosis and prevention of complications.
  • To discuss the role of imaging and emerging biomarkers in disease management.

Main Methods:

  • Diagnosis relies on family history and radiological imaging, primarily ultrasound (US).
  • Ravine criteria and modifications with CT and MR are used.
  • Genetic and proteomic methods show promise for early diagnosis but are not routine.

Main Results:

  • Ultrasound is sensitive and specific for ADPKD diagnosis in patients over 30.
  • Typical findings include bilateral renal cysts and enlargement.
  • Total renal volume is a sensitive marker for progression, but its individual monitoring utility is unproven.

Conclusions:

  • Early ADPKD diagnosis and complication prevention are essential pending more efficient therapies.
  • Glomerular filtration rate (GFR) monitoring is important for individuals with renal insufficiency.
  • Current imaging methods have limitations for monitoring disease progression in advanced stages.

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