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Circulatory neutrophil chemokines in statin-treated diabetic patients
Saudi Medical Journal. 2008; 29 (4): 584-588
in English | IMEMR | ID: emr-100323
ABSTRACT
To assess the effect of statins on the circulatory levels of neutrophil chemokines, namely, granulocyte chemotactic protein-2 [GCP-2], growth regulated oncogene-alpha [GRO-alpha] and epithelial-cell-derived neutrophil-activating peptide-78 [ENA-78] in patients with diabetes. We studied 91 diabetic patients [46 were statin-treated and 45 were not] and 28 healthy subjects. We measured the levels of GCP-2, GRO-alpha, and ENA-78 in the serum for the 3 groups using an enzyme linked immunosorbent assay. This cross-sectional study was conducted at King Khalid University Hospital [KKUH], Riyadh, Kingdom of Saudi Arabia, from January 2006 to July 2007. Circulating levels of GCP-2, ENA-78, and not GRO-alpha, were significantly higher in diabetic patients as compared to healthy subjects [p<0.05]. Statins dropped the levels of both GCP-2 and GRO-alpha. The ENA-78 levels were not affected by statin therapy. There was no correlation between the levels of these chemokines with the body mass index and glycemia in the population studied. Diabetes is associated with an elevation of GCP-2 and ENA-78, and not GRO-alpha. Statins have a significant role in reducing the level of GCP-2
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Index: IMEMR (Eastern Mediterranean) Main subject: Enzyme-Linked Immunosorbent Assay / Cross-Sectional Studies / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Diabetes Mellitus / Chemokine CXCL1 / Chemokine CXCL5 / Microtubule-Associated Proteins Type of study: Prevalence study Limits: Female / Humans / Male Language: English Journal: Saudi Med. J. Year: 2008

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Index: IMEMR (Eastern Mediterranean) Main subject: Enzyme-Linked Immunosorbent Assay / Cross-Sectional Studies / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Diabetes Mellitus / Chemokine CXCL1 / Chemokine CXCL5 / Microtubule-Associated Proteins Type of study: Prevalence study Limits: Female / Humans / Male Language: English Journal: Saudi Med. J. Year: 2008