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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.
To explore the association of time-averaged serum uric acid (TA-SUA) on the long-term outcomes of type 2 diabetes mellitus (T2DM) with chronic kidney disease (CKD).
Current retrospective study was conducted in a cohort of type 2 DM with CKD from eight centers, with follow-up period spanning from January 2013 to October 2023. The primary outcomes included serum creatinine doubling, initiation of dialysis, kidney transplantation, progression to end-stage kidney disease, and all-cause mortality.
Total of 1,072 patients were enrolled from 1651 patients diagnosed of T2DM with CKD in cohort. The median of follow-up time was 60.4±5.6 months. The overall prevalence of hyperuricemia (HUA) in current cohort was 46.1%, of which in men (50.4%) was significantly higher than that in women (37.9%). After adjusting for confounding factors, both baseline and time-averaged SUA were identified as the independent risk factor for composite endpoints. Patients with baseline SUA and TA-SUA ≥ 420 μmol/L exhibited 1.9-fold (HR 1.92, 95% CI:1.40-2.62, P < 0.001)and 2.6-fold (HR 2.60, 95% CI:1.82-3.70, P < 0.001)higher risk to composite endpoint compared to those with baseline SUA or TA-SUA < 360 μmol/L respectively. Patients with TA-SUA< 360 μmol/L exhibited much improved composite endpoint after adjusted for age, sex, hemoglobin, glycosylated hemoglobin and usage of lipid-lowering, glucose-lowering, blood- pressure lowering, and urate-lowering drugs.
Type 2 DM with CKD benefits from long-term controlled TA-SUA less than 360 μmol/L by significantly improved renal function decline and all-cause mortality.