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Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
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.
Abstract:
Despite changing epidemiology of chronic kidney disease, autosomal dominant polycystic kidney disease (ADPKD) is one of the most prevalent causes of end stage renal disease. The first symptoms of the disease occur usually in the 3rd or 4th decade of life, however, it can often be diagnosed much earlier. Advances in the understanding of the disease may lead, in the near future, to slowing the progression of ADPKD in asymptomatic individuals. ADPKD is diagnosed on the basis of family history (autosomal dominant inheritance) and radiological imaging. Ultrasound examination (US) of the kidneys is the most important imaging diagnostic method. US is highly sensitive and specific in patients >30 years of age. In US, Ravine criteria are applied and their modifications with other imaging techniques (computed tomography [CT], magnetic resonance [MR]). In all cases, however, there are multiple cysts in both kidneys and, importantly, concomitant renal enlargement can be observed, which is typical of ADPKD. High expectations for early ADPKD diagnosis are risen by genetics and proteomics. However, these methods are not used routinely. The most sensitive parameter in the evaluation of the disease progression is total renal volume. This parameter is presently used in clinical studies, but its utility in monitoring an individual patient has not been fully proven. Unfortunately, MR and CT are expensive and in case of significantly enlarged kidneys US does not yield accurate assessment of their size and is not sensitive enough for monitoring the disease progression. The rate of glomerular filtration rate (GFR) decline is usually constant. Therefore, it is important to monitor GFR in individuals who have developed renal insufficiency. Other tests, including markers of kidney injury, e.g. albuminuria, or vascular flow parameters, are used mainly in clinical studies. Thus, before more efficient therapeutic approaches have been developed, an early diagnosis and prevention of the disease complications are most essential.
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