In addition, the #Nec-1s molecular weight randurls[1|1|,|CHEM1|]# chemokine monocyte chemoattractant protein (MCP)-1 is a key mediator of the arteriosclerosis-related diabetic complications via monocyte/macrophage trafficking to the vascular endothelium in diabetic conditions [6]. It has been reported in cell studies that hyperglycemia induces expression of ICAM-1, VCAM-1,

E-selectin, and MCP-1 in vascular endothelial cells [7–9]. Previous longitudinal and cross-sectional studies including Japanese populations have demonstrated that serum concentrations of soluble (s) sE-selectin in particular, as well as sICAM-1 and sVCAM-1, are positively associated with arteriosclerosis-related clinical parameters and the subsequent incidence of CVD in type 2

diabetic patients [10–13]. Moreover, many longitudinal and cross-sectional studies have demonstrated that circulating MCP-1 concentrations are strongly and positively associated with atherosclerosis-associated clinical parameters in healthy subjects, subjects with obesity, or subjects with type 2 diabetes [14–16]. Our previous study demonstrated that switching α-GI from acarbose or voglibose to miglitol, which has a greater effect on reducing 1 h postprandial glucose levels than other α-GIs [17], in type 2 diabetic patients reduced glucose fluctuations and messenger selleck chemicals RNA (mRNA) levels of inflammatory cytokines such as interleukin (IL)-1β and tumor necrosis factor (TNF)-α, which are known to induce attachment of Astemizole activated leukocytes to blood vessels [18], in peripheral leukocytes and circulating TNF-α

protein levels [19]. However, whether circulating levels of soluble adhesion molecules and MCP-1 are suppressed by miglitol treatment in type 2 diabetic patients has not been determined. In this study, we examined whether switching from acarbose or voglibose to miglitol in type 2 diabetic patients reduced glucose fluctuations and circulating levels of soluble adhesion molecules such as sE-selectin, sICAM-1, sVCAM-1, and MCP-1. 2 Methods 2.1 Study Population This study was a prospective exploratory trial conducted in a hospital setting (Naka Kinen Clinic, Ibaraki) in Japan. We first reviewed the clinical records of potential subjects and identified those that met the criteria of inclusion and exclusion. Inclusion criteria were male and female patients with type 2 diabetes, HbA1c values ranging from 6.9 to 8.3 %, and treatment with the highest approved doses of α-GIs (100 mg acarbose or 0.3 mg voglibose at each meal) in combination with insulin or a sulfonylurea for at least 6 months, who visited the hospital between May 2007 and April 2008. The number of patients compliant with the inclusion criteria was 196 type 2 diabetic patients who visited the clinic during the study period (n = 1,136). Among these patients, we excluded from the study patients considered inappropriate, e.g.