Integrative biomarker analysis in diabetic foot: lipids, cellular integrity, and hydration balance

糖尿病足的综合生物标志物分析:脂质、细胞完整性和水合作用平衡

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Abstract

BACKGROUND: Diabetic foot ulcers (DFUs) are a severe complication of type 2 diabetes mellitus (T2DM), linked to high morbidity and mortality. This study explores biomarkers related to DFU risk and progression to improve management strategies. This study was conducted to identify early biomarkers that could predict DFU risk before ulceration occurs. METHODS: A case-control study was conducted with 33 T2DM patients and 37 non-diabetic controls. Bioimpedance-derived metrics—phase angle (PA), extracellular water-to-total body water ratio (AEC/ACT), and extracellular mass-to-body cell mass ratio (ECMe/BCMe)—were analyzed alongside lipid profiles (total cholesterol, LDL, HDL), the Controlling Nutritional Status (CONUT) index, and the triglyceride-glucose index. DFU risk was classified using International Working Group on Diabetic Foot criteria. RESULTS: Low LDL levels (< 50th percentile) correlated with reduced PA in cases (p < 0.001), indicating impaired cellular function and tissue repair. PA negatively correlated with DFU risk (p = 0.005), supporting its utility as a health marker. HDL positively correlated with AEC/ACT in cases (p = 0.004), suggesting its role in fluid regulation. The CONUT index correlated negatively with total cholesterol (p = 0.007) and LDL (p = 0.004), highlighting malnutrition’s impact on lipid imbalances. Hydric indices increased across DFU risk groups, with AEC/ACT significantly higher in Risk Group 1 versus controls (p = 0.048). ECMe/BCMe correlated positively with AEC/ACT in low LDL cases (p = 0.013), reflecting metabolic stress. CONCLUSIONS: LDL and PA are critical biomarkers for DFU risk and progression, offering insights into cellular integrity, tissue repair, and fluid balance. Integrating these biomarkers into clinical practice could optimize DFU management, reduce complications, and improve patient outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-025-01806-5.

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