Key result
Serum SDMA discriminates early from late-stage diabetic kidney disease with an AUC of ~0.84.
Why the study?
Early detection of diabetic kidney disease remains challenging due to limitations of standard markers like GFR and albuminuria, warranting evaluation of symmetric dimethylarginine as an endogenous biomarker.
Does Symmetric Dimethylarginine (SDMA) level correlate with the severity and stages of Diabetic Kidney Disease in diabetic patients?
Cross-Sectional (n=150)
No
Does Symmetric Dimethylarginine (SDMA) level correlate with the severity and stages of Diabetic Kidney Disease in diabetic patients?
Effect estimate: AUC 0.844
p-value: p=<0.001
SDMA is a promising biomarker that correlates well with traditional renal function markers and offers high diagnostic accuracy for assessing the severity and stages of Diabetic Kidney Disease.
Supports SDMA for diabetic kidney disease staging; hypothesis-generating and requires prospective validation before practice change.
Background Diabetic Kidney Disease (DKD) is a major complication of Diabetes Mellitus (DM), contributing to increased morbidity and mortality. Early detection remains challenging, with standard markers like Glomerular Filtration Rate (GFR) and albuminuria showing limitations. Symmetric Dimethylarginine (SDMA) is a potential biomarker of renal function, cleared by the kidneys, that may offer better insights into DKD severity. Objective To evaluate the diagnostic utility of SDMA as an endogenous biomarker of renal impairment and its correlation with the severity and stages of DKD. Methods This cross-sectional study involved 150 diabetic cases (type 1 or type 2) who were stratified into late-stage (III-V) and early-stage (I-II) groups. SDMA levels were assessed using enzyme immunoassay, along with other renal function markers, and correlations with eGFR, proteinuria, and diabetes duration were analyzed. Results SDMA showed significant correlations with creatinine ( r = 0.785, p < 0.001), eGFR ( r = -0.598, p < 0.001), and urea ( r = 0.698, p < 0.001). SDMA levels significantly differed between early and late stages of DKD, with the highest levels observed in stage V (median 15.3 nmol/mL). ROC analysis demonstrated SDMA's ability to discriminate between early and late-stage DKD, with AUC values of 0.813 (Modification of Diet in Renal Disease (MDRD)) and 0.844 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI). Conclusion SDMA is a promising biomarker for assessing the severity and stages of DKD, correlating well with traditional renal function markers and offering high diagnostic accuracy.
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Omran et al. (2025) conducted a cross-sectional in Diabetic Kidney Disease (n=150). Serum Symmetric Dimethylarginine (SDMA) vs. Early-stage (I-II) vs late-stage (III-V) DKD was evaluated on Discrimination between early and late-stage diabetic kidney disease (CKD-EPI formula) (AUC 0.844, p=<0.001). Serum SDMA effectively discriminated between early and late-stage diabetic kidney disease, yielding an AUC of 0.844 and demonstrating significant inverse correlation with estimated glomerular filtration rate.
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