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. 2008 Mar-Apr;14(3-4):109-15.
doi: 10.2119/2007-00107.Bruchfeld.

High Mobility Group Box Protein-1 correlates with renal function in chronic kidney disease (CKD)

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High Mobility Group Box Protein-1 correlates with renal function in chronic kidney disease (CKD)

Annette Bruchfeld et al. Mol Med. 2008 Mar-Apr.

Abstract

Chronic kidney disease (CKD) is associated with inflammation and malnutrition and carries a markedly increased risk of cardiovascular disease (CVD). High Mobility Group Box Protein-1 (HMGB-1) is a 30-kDa nuclear and cytosolic protein known as a transcription and growth factor, recently identified as a proinflammatory mediator of tissue injury. Recent data implicates HMGB-1 in endotoxin lethality, rheumatoid arthritis, and atherosclerosis. The aim of this post-hoc, cross-sectional study was to determine whether HMGB-1 serum levels are elevated in CKD patients. The study groups were categorized as follows: 110 patients starting dialysis defined as CKD 5; 67 patients with moderately to severely reduced renal function or CKD 3-4; and 48 healthy controls. High-sensitivity C-reactive-protein (hs-CRP), interleukin-6 (IL-6), tumor necrosis factor (TNF), serum-albumin (S-albumin), hemoglobin A(1c) (HbA(1c)), hemoglobin, subjective global nutritional assessment (SGA), and glomerular filtration rate (GFR) were analyzed. Kruskal-Wallis test was used to compare groups and Spearman's rank correlation test was used for continuous variables. HMGB-1, measured by Western blot, was significantly (P < 0.001) elevated in CKD 5 (146.7 +/- 58.6 ng/mL) and CKD 3-4 (85.6 +/- 31.8) compared with controls (10.9 +/- 10.5). HMGB-1 levels were correlated positively with TNF (Rho = 0.52; P < 0.001), hs-CRP (Rho = 0.38; P < 0.001), IL-6 (Rho = 0.30; P < 0.001), HbA(1c) (Rho = 0.14; P = 0.02) and SGA (Rho = 0.21; P = 0.002) and negatively correlated with GFR (Rho = -0.69; P = 0.0001), Hb (Rho = -0.60; P < 0.001), S-albumin (Rho = -0.31; P < 0.001). The current study has revealed that HMGB-1 is elevated significantly in CKD patients and correlates with GFR as well as markers of inflammation and malnutrition. Future studies may delineate whether HMGB-1 is also a marker of disease activity and severity as well as a predictor of outcome in CKD.

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Figures

Figure 1
Figure 1
(A). Representative HMGB1 Western Blot results in 37/110 CKD five patients versus 10/48 controls. (B) HMGB-1 significantly (P < 0.001) elevated in CKD 5 and CKD 3–4 compared with controls.
Figure 2
Figure 2
(A) Spearman rank correlations: HMGB-1 negative correlation with GFR (Rho = –0.69; P = 0.0001). (B) Spearman rank correlations: positive correlation with IL-6 (Rho = 0.31 P < 0.001). (C) Spearman rank correlations: TNF (Rho = 0.52 P < 0.001). (D) Spearman rank correlations: hs-CRP (Rho = 0.35 P < 0.001). CKD 5 (filled circles), CKD 3–4 (empty triangles) and controls (crosses).

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