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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Chronic kidney disease (CKD) is recognized as a major health problem, causing more than a million deaths each year worldwide. For most CKD, peripheral kidney microvascular damage can be correlated with disease progression. Ultrasound localization microscopy (ULM) is a novel non-invasive method for quantitatively assessing renal microcirculation. This study evaluates the use of ULM in CKD and its correlation with renal biopsy in IgA nephropathy.
The study comprised 33 CKD patients and 20 control subjects between June 2025 and September 2025 in the department of ultrasound of the first affiliated hospital of Chongqing medical university. All participants underwent renal biopsy. ULM was performed to measure microvascular flow quantitative characteristics the cortex area. ULM parameters were compared with eGFR. Subsequently, 21 patients with pathologically confirmed IgA nephropathy were divided into M0 and M1 groups based on the Oxford classification. ULM parameters of these two groups were compared.
ULM analysis revealed that, compared to controls, CKD patients exhibited significantly lower vessel ratio, blood velocity, and vessel count (p < 0.05). These parameters were negatively correlated with eGFR (r=-0.346). In IgA nephropathy patients, vessel ratio and blood velocity in the M1 group were significantly lower than in the M0 group (p < 0.05). Vessel ratio and blood velocity were negatively correlated with mesangial cell proliferation (r=-0.427), proteinuria (r=-0.485), and endocapillary hypercellularity (r=-0.373).
ULM provides detailed insight into the microvascular structure and hemodynamic changes in CKD, presenting a promising tool for early diagnosis and monitoring of disease progression.