Key summary points
To compare the diagnostic accuracy of Cr/CysC, SARC-F, SARC-CalF, the combination of Cr/CysC and SARC-CalF, and the Ishii score for sarcopenia and investigate the predictive value of Cr/CysC concerning clinical outcomes in hospitalized older adults.
AbstractSection FindingsCr/CysC could effectively detect sarcopenia and predict poor outcomes in hospitalized older adults. A more precise sarcopenia screening may be offered by combining Cr/CysC with SARC-CalF. In our study, the Ishii score may be the most accurate clinical method for detecting sarcopenia.
AbstractSection MessageCr/CysC could be used to screen for sarcopenia and predict poor outcomes in clinical settings.
Abstract
Purpose
The utilization of the creatinine-to-cystatin C ratio (Cr/CysC) represents an innovative method for predicting sarcopenia. Our objectives encompassed the evaluation of sarcopenia diagnostic accuracy for Cr/CysC, SARC-F, SARC-CalF, the combination of Cr/CysC and SARC-CalF, and the Ishii score, as well as an exploration of the predictive value of Cr/CysC concerning clinical outcomes within hospitalized older individuals.
Methods
We employed receiver operating characteristic (ROC) curves and calculated areas under the curves (AUCs) to assess the diagnostic accuracy. Furthermore, we applied univariate and multivariate Cox proportional-hazard models to calculate the hazard ratio (HR) and 95% confidence interval (CI) of risk factors affecting prognosis.
Results
Our study included 312 participants, comprising 167 men and 145 women, with an average age of 71 years. Among males, the AUCs for Cr/CysC, SARC-F, SARC-CalF, the combination of Cr/CysC and SARC-CalF, and the Ishii score were 0.717 [95% CI 0.642–0.784], 0.669 (95% CI 0.592–0.739), 0.845 (95% CI 0.781–0.896), 0.882 (95% CI 0.823–0.926), and 0.938 (95% CI 0.890–0.969), respectively. In females, the AUCs for Cr/CysC, SARC-F, SARC-CalF, the combination of Cr/CysC and SARC-CalF, and the Ishii score were 0.706 (95% CI 0.625–0.779), 0.631 (95% CI 0.547–0.710), 0.763 (95% CI 0.686–0.830), 0.789 (95% CI 0.714–0.853), and 0.898 (95% CI 0.837–0.942), respectively. After adjusting for age, sex, physical exercise, smoking, drinking, hypertension, coronary heart disease (CHD), chronic obstructive pulmonary disease (COPD), chronic kidney disease (CKD), and cancer, sarcopenia identified by Cr/CysC (adjusted HR = 2.176, 95% CI 1.062–4.460, P = 0.034) was independently associated with poor overall survival in hospitalized older patients.
Conclusions
Cr/CysC has satisfactory diagnostic accuracy for sarcopenia diagnosis and predictive value for poor outcomes in hospitalized older patients. The combination of Cr/CysC and SARC-CalF may provide a more accurate screening for sarcopenia and the Ishii score may be the most accurate clinical method for detecting sarcopenia.
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Data availability
The data are accessible upon reasonable request from the corresponding author.
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Funding
This study was supported by grants from Chinese National Science & Technology Pillar Program (2020YFC2009004); Sichuan Science and Technology Program (2022YFS0295, 2022YFG0205); 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (ZYJC21005); National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University (Z20191012); Health Research of Cadres in Sichuan province (SCR2022-101).
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XT and TL contributed to conceiving this study and wrote the main manuscript text. LH contributed to the data analysis and prepared the tables and figures. TT, DX, LG, and TJ contributed to the data collection. JY assisted with the research design and reviewed the text. All authors read and approved the final manuscript.
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Approval was obtained from the ethics committee of the West China Hospital of Sichuan University (2019(1041)). The procedures used in this study adhere to the tenets of the Declaration of Helsinki.
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Tu, X., Lin, T., Huang, L. et al. The diagnostic performance of Cr/CysC for sarcopenia and its predictive value on clinical outcomes in hospitalized older patients: a prospective cohort study. Eur Geriatr Med 15, 579–588 (2024). https://doi.org/10.1007/s41999-024-00948-5
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DOI: https://doi.org/10.1007/s41999-024-00948-5