Submitted
Abstract Submission
Survey of plasma creatinine/cystatin c ratio and its association with glycemic control and renal impairment in patients with diabetes mellitus
Oral Presentation
Scientific Research Abstract
Diabetes
Author's Information
2
No more than 15 authors can be listed (as per the Good Publication Practice (GPP) Guidelines).
Please ensure the authors are listed in the right order.
Tan Duc Nguyen Tanduc300896@gmail.com Military Hospital 175 Department of Biochemistry Ho Chi Minh city Vietnam *
Quoc Tuan Le dr.lequoctuan@ump.edu.vn University of Medicine and Pharmacy at Ho Chi Minh City Department of Physiology – Pathophysiology, Immunology, and Pharmacology, School of Medicine Ho Chi Minh city Vietnam -
-
-
-
-
-
-
-
-
-
-
-
-
-
Abstract Content
The Creatinine-to-Cystatin C (Cre/CysC) ratio has recently emerged as a composite biomarker integrating information on muscle mass, metabolic homeostasis, and renal hemodynamics. In type 2 diabetes mellitus (T2DM), subtle muscle decline, deteriorating glycemic control, and early renal alterations frequently coexist but remain challenging to detect using conventional indices. This study aimed to determine the median Cre/CysC ratio and examine its independent associations with glycemic control and renal injury markers in Vietnamese patients with T2DM
A cross-sectional descriptive study was conducted on 124 T2DM outpatients at Military Hospital 175 from January 2025 to May 2025. Data collection included anthropometric parameters (BMI), fasting plasma glucose, HbA1c, plasma Creatinine, Cystatin C, and urinary Albumin-to-Creatinine Ratio (ACR). The estimated Glomerular Filtration Rate (eGFR) was calculated using the CKD-EPI 2021 equation (combining Creatinine and Cystatin C). Statistical analysis employed Pearson/Spearman correlation tests and multivariate linear regression to identify independent predictors
The median Cre/CysC ratio was 11.8 (IQR: 11.1–12.8), with no statistically significant difference observed between males and females (p > 0.05). Analysis revealed a strong negative correlation between the Cre/CysC ratio and both BMI (r = -0.78; p < 0.05) and HbA1c (r = -0.5; p < 0.05). In multivariable analysis, Cre/CysC remained an independent negative predictor of HbA1c (β = –0.4; p < 0.05), indicating a robust association between lower ratios and poorer long-term glycemic control. A strong positive correlation was observed between Cre/CysC and ACR (r = 0.8; p < 0.05). Multivariable regression confirmed Cre/CysC (β = 0.4; p < 0.05) and diastolic blood pressure as independent predictors of ACR. This profile is consistent with early diabetic kidney disease physiology, where glomerular hyperfiltration enhances cystatin C clearance while microalbuminuria begins to manifest, reflecting early hemodynamic stress before overt eGFR decline
The Cre/CysC ratio serves as a valuable biomarker in clinical practice for patients with T2DM. This index not only reflects muscle mass status but is also independently and closely associated with long-term glycemic control. In the early stages of the disease, an elevated Cre/CysC ratio accompanied by increased ACR suggests glomerular hyperfiltration, serving as an early warning of hemodynamic alterations prior to overt decline in renal function
Creatinine/Cystatin C, Diabetes, Sarcopenia
 
 
366
Tan Duc
Nguyen
Tanduc300896@gmail.com
 
Presentation Details