Autosomal dominant polycystic kidney disease (ADPKD) is characterized by cysts originating from different nephron segments. Researchers developed a non-invasive 23Na MRI method at 7 Tesla that classifies cysts based on their sodium concentration. Two distinct cyst types were identified: high-sodium cysts similar to blood serum and low-sodium cysts. High-sodium cysts originate from proximal tubules, while low-sodium cysts originate from distal tubules and collecting ducts. The V2R receptor, which is the target of tolvaptan therapy, is found exclusively in low-sodium cysts. Analysis of 2,299 cysts in 20 ADPKD patients showed that high-sodium cysts were 1.8-fold more frequent. Patients exhibited significant variability in cyst composition, with low-sodium cysts comprising 4.6% to 83.9% of all cysts. This heterogeneity may influence disease progression and therapeutic response.