1.The Dipeptidyl Peptidase-4 Inhibitor Sitagliptin Improves Vascular Endothelial Function in Type 2 Diabetes.
Yoshiaki KUBOTA ; Masaaki MIYAMOTO ; Gen TAKAGI ; Takeshi IKEDA ; Sonoko KIRINOKI-ICHIKAWA ; Kotoko TANAKA ; Kyoichi MIZUNO
Journal of Korean Medical Science 2012;27(11):1364-1370
The vascular endothelial function is impaired in the very early stage of atherosclerosis in diabetic patients. The goal of this study was to identify the mechanism underlying the improvement in vascular endothelial function by sitagliptin in type 2 diabetes mellitus patients. This study was an open-labeled prospective observational single arm trial. Forty patients were treated with 50 mg of sitagliptin once daily for 12-weeks. The flow-mediated dilation (FMD) and plasma adiponectin were measured at baseline and 12 weeks after initiating treatment. The %FMD was significantly increased after treatment (4.13 +/- 1.59 vs 5.12 +/- 1.55, P < 0.001), whereas the nitroglycerin-mediated dilation (NMD) did not change. The plasma adiponectin levels significantly increased (13.0 +/- 11.3 vs 14.3 +/- 12.8, P < 0.001). The changes in the FMD were significantly correlated with those of the plasma adiponectin (r = 0.322, P < 0.05). A multivariate linear regression analysis demonstrated that the improvement in the FMD is associated with the plasma adiponectin (P < 0.05). The treatment of type 2 diabetes mellitus patients with sitagliptin reverses vascular endothelial dysfunction, as evidenced by increase in the FMD, and improvement of the adiponectin levels (UMIN Clinical Trials Registry System as trial ID UMIN000004236).
Adiponectin/blood
;
Aged
;
Aged, 80 and over
;
Atherosclerosis/complications/drug therapy
;
Diabetes Mellitus, Type 2/complications/*drug therapy
;
Dipeptidyl-Peptidase IV Inhibitors/pharmacology/*therapeutic use
;
Drug Administration Schedule
;
Endothelium, Vascular/*drug effects/physiopathology
;
Female
;
Humans
;
Male
;
Middle Aged
;
Nitroglycerin/therapeutic use
;
Prospective Studies
;
Pyrazines/pharmacology/*therapeutic use
;
Regression Analysis
;
Triazoles/pharmacology/*therapeutic use
;
Vasodilation/drug effects
;
Vasodilator Agents/therapeutic use
2.The Dipeptidyl Peptidase-4 Inhibitor Sitagliptin Improves Vascular Endothelial Function in Type 2 Diabetes.
Yoshiaki KUBOTA ; Masaaki MIYAMOTO ; Gen TAKAGI ; Takeshi IKEDA ; Sonoko KIRINOKI-ICHIKAWA ; Kotoko TANAKA ; Kyoichi MIZUNO
Journal of Korean Medical Science 2012;27(11):1364-1370
The vascular endothelial function is impaired in the very early stage of atherosclerosis in diabetic patients. The goal of this study was to identify the mechanism underlying the improvement in vascular endothelial function by sitagliptin in type 2 diabetes mellitus patients. This study was an open-labeled prospective observational single arm trial. Forty patients were treated with 50 mg of sitagliptin once daily for 12-weeks. The flow-mediated dilation (FMD) and plasma adiponectin were measured at baseline and 12 weeks after initiating treatment. The %FMD was significantly increased after treatment (4.13 +/- 1.59 vs 5.12 +/- 1.55, P < 0.001), whereas the nitroglycerin-mediated dilation (NMD) did not change. The plasma adiponectin levels significantly increased (13.0 +/- 11.3 vs 14.3 +/- 12.8, P < 0.001). The changes in the FMD were significantly correlated with those of the plasma adiponectin (r = 0.322, P < 0.05). A multivariate linear regression analysis demonstrated that the improvement in the FMD is associated with the plasma adiponectin (P < 0.05). The treatment of type 2 diabetes mellitus patients with sitagliptin reverses vascular endothelial dysfunction, as evidenced by increase in the FMD, and improvement of the adiponectin levels (UMIN Clinical Trials Registry System as trial ID UMIN000004236).
Adiponectin/blood
;
Aged
;
Aged, 80 and over
;
Atherosclerosis/complications/drug therapy
;
Diabetes Mellitus, Type 2/complications/*drug therapy
;
Dipeptidyl-Peptidase IV Inhibitors/pharmacology/*therapeutic use
;
Drug Administration Schedule
;
Endothelium, Vascular/*drug effects/physiopathology
;
Female
;
Humans
;
Male
;
Middle Aged
;
Nitroglycerin/therapeutic use
;
Prospective Studies
;
Pyrazines/pharmacology/*therapeutic use
;
Regression Analysis
;
Triazoles/pharmacology/*therapeutic use
;
Vasodilation/drug effects
;
Vasodilator Agents/therapeutic use
3.Evaluation of neointimal coverage and thrombosis at 3 months and 2 years post sirolimus-eluting stent implantation by optical coherence tomography.
Yong XIE ; Sheng-Hu HE ; Xiang GU ; Ri-Xin XU ; Takano MASAMICHI ; Mizuno KYOICHI
Chinese Journal of Cardiology 2010;38(2):116-120
OBJECTIVETo evaluate the short- and long-term prevalence of persistent uncovered struts and in-stent thrombus after sirolimus-eluting stent (SES) implantation by optical coherence tomography (OCT).
METHODSOCT was performed for 31 SES in 21 patients at 3 months and for 30 SES in 21 patients at 2 years post SES implantation. Thickness of new intima inside each strut was measured and thickness equal to 0 microm was defined as an uncovered strut. Existence of in-stent thrombus was also evaluated.
RESULTSA total of 4545 struts and 3707 struts were evaluated at 3 months and at 2 years post SES implantation, respectively. New intima at 2 years was significantly thicker than that at 3 months [(71 +/- 93) microm vs. (29 +/- 41) microm, P < 0.01]. Percent of uncovered struts at 2 years was significantly lower than that at 3 months (5% vs. 15%, P < 0.01). Prevalence of uncovered struts was similar at 2 years and at 3 months (81% vs.95%, P > 0.05). Subclinical thrombus was recognized in 14% patients at 3 months and 2 years post SES implantation.
CONCLUSIONSNeointimal coverage inside the SES is a continuous process and the number of uncovered struts decreased from 3 months to 2 years after SES implantation. Few uncovered struts could still be visualized in the majority of patients at 2 years post SES implantation.
Aged ; Drug-Eluting Stents ; adverse effects ; Female ; Humans ; Male ; Middle Aged ; Thrombosis ; diagnosis ; etiology ; pathology ; Tomography, Optical Coherence ; methods ; Tunica Intima ; pathology