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High‐mobility group box‐1 and biomarkers of inflammation in the vitreous from patients with proliferative diabetic retinopathy
Author(s) -
ABU EL ASRAR A,
NAWAZ MI,
KANGAVE D,
GEBOES K,
OLA MS,
AHMAD S,
ALSHABRAWEY M
Publication year - 2011
Publication title -
acta ophthalmologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.534
H-Index - 87
eISSN - 1755-3768
pISSN - 1755-375X
DOI - 10.1111/j.1755-3768.2011.2211.x
Subject(s) - hmgb1 , diabetic retinopathy , inflammation , medicine , glycation , diabetes mellitus , monocyte , retinopathy , endocrinology , interleukin , immunology , gastroenterology , cytokine
Purpose To measure levels of high‐mobility group box‐1 (HMGB1), and soluble receptor for advanced glycation end products (sRAGE) in the vitreous fluid from patients with proliferative diabetic retinopathy (PDR) and to correlate their levels with clinical disease activity and the levels of the inflammatory biomarkers monocyte chemoattractant protein‐1 (MCP‐1), soluble intercellular adhesion molecule‐1 (sICAM‐1), interleukin‐1 (IL‐1) and granulocyte macrophage colony‐stimulating factor (GM‐CSF). In addition, we examined the expression of HMGB1 in the retinas of diabetic mice. Methods Vitreous samples from 29 PDR and 17 nondiabetic patients were studied by enzyme‐linked immunosorbent assay. Retinas of mice were examined by immunofluorescence analysis and Western blotting. Results HMGB1 was detected in all vitreous samples and sRAGE was detected in 5 PDR samples. IL‐1 was detected in 3PDR samples and GM‐CSF was not detected. Mean HMGB1 levels in PDR with active neovascularization were 2‐fold and 3‐fold higher than that in inactive PDR and nondiabetic patients, respectively. Mean HMGB1 levels in PDR patients with hemorrhage were significantly higher than those in PDR patients without hemorrhage and nondiabetic patients (p=0.0111). There were significant correlations between levels of HMGB1 and levels of MCP‐1 (r=0.333, p=0.025) and sICAM‐1 (r=0.548, p<0.001). HMGB1 expression was also upregulated in the retinas of diabetic mice. Conclusion Subclinical, chronic inflammation might contribute to the progression of PDR.