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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.
Sarcopenia, defined as a decrease in muscle mass and strength, is prevalent among patients with chronic kidney disease (CKD) and is associated with adverse clinical outcomes. The ratio of creatinine- to cystatin C-based eGFR (eGFRcre/eGFRcys) and the serum creatinine-to-cystatin C ratio (sCre/sCys), which account for the influence of muscle mass, have been reported to be associated with sarcopenia. However, data concerning advanced CKD are limited, and no study has specifically examined this association in Japanese patients with CKD. We aimed to investigate the relationship between these indices and sarcopenia in Japanese patients with CKD.
This was a cross-sectional study of 119 outpatients with CKD treated at our department. Sarcopenia was defined according to the Asian Working Group for Sarcopenia (AWGS) 2019 criteria. Physical performance was assessed using the Short Physical Performance Battery (SPPB), and skeletal muscle mass was measured by bioelectrical impedance analysis (InBody). Receiver operating characteristic (ROC) curves were constructed to calculate the area under the curve (AUC) for eGFRcre/eGFRcys and sCre/sCys in predicting sarcopenia.
The mean age of participants was 70 years, and the mean eGFR was 30 ml/min/1.73m². Sarcopenia was identified in 19 patients. The AUC for sarcopenia prediction was 0.71 for eGFRcre/eGFRcys and 0.70 for sCre/sCys. Among patients aged ≥65 years, the predictive performance of eGFRcre/eGFRcys improved, with an AUC of 0.77. Using a cutoff value of 1.0 for eGFRcre/eGFRcys, sensitivity was 86%, specificity was 68%, and the negative predictive value was 96%. These findings indicate that values ≤1 reliably exclude sarcopenia.
The eGFRcre/eGFRcys ratio is a simple and practical predictor of sarcopenia in patients with CKD, particularly among those aged ≥65 years. This index may serve as a useful screening tool to rule out sarcopenia in clinical practice.