Short-term dapagliflozin administration in autosomal dominant polycystic kidney disease—a retrospective single-arm case series study

F Morioka, S Nakatani, H Uedono, A Tsuda… - Journal of Clinical …, 2023 - mdpi.com
Treatment with sodium-glucose cotransporter-2 (SGLT2) inhibitors may have pleiotropic and
beneficial effects in terms of ameliorating of risk factors for the progression of autosomal …

[HTML][HTML] Performance of [18F]FDG PET/CT in Diagnosing Cyst Infections in Patients with Autosomal Dominant Polycystic Kidney Disease: A Systematic Review and a …

G Treglia, D Albano, A Rizzo, A Bellasi… - Diagnostics, 2024 - mdpi.com
Background: Fluorine-18 fluorodeoxyglucose positron emission tomography/computed
tomography ([18F] FDG PET/CT) has been suggested as a useful imaging method for …

Impact of kidney function and kidney volume on intracranial aneurysms in patients with autosomal dominant polycystic kidney disease

H Kataoka, H Akagawa, R Yoshida, N Iwasa… - Scientific Reports, 2022 - nature.com
Presently, only personal or family history of intracranial aneurysm/subarachnoid
hemorrhage (IA/SAH) has been established as a risk factor for IA in autosomal dominant …

Factors associated with early-onset intracranial aneurysms in patients with autosomal dominant polycystic kidney disease

Y Ushio, H Kataoka, H Akagawa, M Sato… - Journal of …, 2024 - Springer
Background Recently, the importance of attribute-based medicine has been emphasized.
The effects of early-onset intracranial aneurysms on patients can be significant and long …

Discovery of putative inhibitors of human Pkd1 enzyme: Molecular docking, dynamics and simulation, QSAR, and MM/GBSA

MZ Nawaz, HR Khalid, S Shahbaz, KA Al-Ghanim… - Environmental …, 2024 - Elsevier
Polycystic kidney disease is the most prevalent hereditary kidney disease globally and is
mainly linked to the overexpression of a gene called PKD1. To date, there is no effective …

Long-Term Effects of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease: Predictors of Treatment Response and Safety over 6 Years of Continuous Therapy

M Yamazaki, H Kawano, M Miyoshi, T Kimura… - International Journal of …, 2024 - mdpi.com
Tolvaptan, an oral vasopressin V2 receptor antagonist, reduces renal volume expansion
and loss of renal function in patients with autosomal dominant polycystic kidney disease …

Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP)

S Nakatani, H Kawano, M Sato, J Hoshino… - Clinical and …, 2024 - Springer
Background Autosomal dominant polycystic kidney disease (ADPKD) and autosomal
recessive polycystic kidney disease (ARPKD) are major genetic polycystic kidney diseases …

Mutation type and intracranial aneurysm formation in autosomal dominant polycystic kidney disease

H Kataoka, H Akagawa, Y Ushio, M Sato… - Stroke: Vascular and …, 2022 - Am Heart Assoc
Background Screening for intracranial aneurysms (IAs) in patients with risk factors of IA is
recommended. However, genetic risk factors of IA in patients with autosomal dominant …

A Whole Exome Sequencing Study of a small Indian Autosomal Dominant Polycystic Kidney Disease Patient Cohort

C Devi, S Singh, B Mohapatra, A Kumar, S Vikrant… - medRxiv, 2023 - medrxiv.org
Abstract Autosomal Dominant Polycystic Kidney Disease is characterized by renal cyst
development, often leading to kidney enlargement and failure. We conducted whole exome …

Estimating baseline creatinine levels based on the kidney parenchymal volume

T Sasaki, T Tosaki, H Kuno, H Marumoto… - Clinical and …, 2024 - Springer
Background Acute kidney injury (AKI) diagnosis often lacks a baseline serum creatinine (Cr)
value. Our study aimed to create a regression equation linking kidney morphology to …