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Updated: Jun 12, 2026

Microfluidic Assay for the Assessment of Leukocyte Adhesion to Human Induced Pluripotent Stem Cell-derived Endothelial Cells hiPSC-ECs
Published on: November 26, 2018
Reliable discrimination of type 1 and type 2 diabetes by flow-through leukocyte-endothelium interactions exploiting
Jonathan Hermenejildo1, Sandra López-Doménech1, María Pelechá-Salvador1
1Department of Endocrinology and Nutrition, University Hospital Doctor Peset, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, 46017, Spain.
Abstract:
Type 1 (T1D) and type 2 diabetes (T2D) are both associated with chronic inflammation and endothelial dysfunction, yet their discrimination based on conventional inflammatory biomarkers remains challenging. In this context, a proof-of-concept study exploring whether advanced hydrodynamic descriptors of leukocyte-endothelium interactions under flow conditions might disclose invaluable information to differentiate between diabetic phenotypes is presented. Neutrophil dynamics were investigated using a parallel-plate flow chamber and quantitative video tracking, from which an expanded set of novel hydrodynamic variables encompassing velocity-, acceleration-, rolling-, interaction-, and count-based hydrodynamic parameters was extracted. Supervised machine learning models based on linear discriminant analysis (LDA) were developed and validated using cross-validation strategies. While classical flow parameters and circulating inflammatory biomarkers showed limited discriminatory power, a parsimonious subset of novel hydrodynamic descriptors enabled robust separation between healthy, T1D, and T2D individuals, despite the moderate cohort size (n = 10 per group). Weak to moderate correlations with biomarkers indicate that leukocyte dynamics capture complementary functional information beyond static molecular markers. Overall, this approach highlights the potential of flow-based leukocyte dynamics and interpretable machine learning models as a promising functional platform for phenotyping inflammatory microvascular alterations in diabetes.
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