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Updated: Mar 13, 2026

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
Diagnostic Imaging of Autosomal Dominant Polycystic Kidney Disease
Monika Gradzik1, Mariusz Niemczyk2, Marek Gołębiowski1
1Department of Clinical Radiology, Medical University of Warsaw, Warsaw, Poland.
Insights
Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic disorder causing kidney cysts and enlargement. Advanced imaging is crucial for diagnosing ADPKD, monitoring its progression, and detecting complications like aneurysms.
Area of Science:
- Nephrology
- Medical Genetics
- Radiology
Background:
- Autosomal dominant polycystic kidney disease (ADPKD) is a prevalent single-gene genetic disorder.
- ADPKD typically manifests between ages 30-40, leading to kidney cyst formation, enlargement, and eventual renal insufficiency.
- Extrarenal manifestations, including intracranial aneurysms and liver cysts, are significant complications.
Approach:
- Diagnostic imaging modalities such as sonography, computed tomography (CT), and magnetic resonance imaging (MRI) are essential.
- These imaging techniques aid in the early diagnosis of ADPKD.
- Imaging facilitates the monitoring of disease progression and the identification of potential complications.
Key Points:
- Imaging plays a critical role in ADPKD diagnostics and management.
- Sonography, CT, and MRI are vital for assessing renal cyst development and kidney function decline.
- Extrarenal findings, particularly intracranial aneurysms and hepatic cysts, can be detected via imaging.
Conclusions:
- Advanced imaging is indispensable for the comprehensive management of ADPKD.
- Utilizing imaging allows for timely intervention and improved patient outcomes.
- Radiological assessment is key to understanding the full spectrum of ADPKD, including its systemic effects.
Abstract:
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic disorders caused by a single gene mutation. The disease usually manifests itself at the age of 30-40 years and is characterized by formation of renal cysts along with the enlargement of kidneys and deterioration of their function, eventually leading to renal insufficiency. Imaging studies (sonography, computed tomography, magnetic resonance imaging) play an important role in the diagnostics of the disease, the monitoring of its progression, and the detection of complications. Imaging is also helpful in detecting extrarenal manifestations of ADPKD, most significant of which include intracranial aneurysms and cystic liver diseases.
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