Impact of sitagliptin on carotid intima-media thickness in patients with coronary
artery disease and impaired glucose tolerance or mild diabetes mellitus.
Author(s): Ishikawa S(1), Shimano M(2), Watarai M(3), Koyasu M(3), Uchikawa T(3), Ishii
H(4), Inden Y(4), Takemoto K(3), Murohara T(4).
Affiliation(s): Author information:
(1)Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya,
Japan; Department of Cardiology, Cardiovascular Center, Anjyo Kosei Hospital,
Anjyo, Japan.
(2)Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya,
Japan; Department of Cardiology, Japanese Red Cross Nagoya Daiichi Hospital,
Nagoya, Japan. Electronic address: mshimano@med.nagoya-u.ac.jp.
(3)Department of Cardiology, Cardiovascular Center, Anjyo Kosei Hospital, Anjyo,
Japan.
(4)Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya,
Japan.
Publication date & source: 2014, Am J Cardiol. , 114(3):384-8
Sitagliptin has been widely used for the treatment of diabetes and shown recently
to have beneficial pleiotropic outcomes on cardiovascular systems in experimental
studies. However, little is known about the influence of sitagliptin on
atherosclerosis-related cardiovascular diseases in a clinical setting. This study
examined the effect of sitagliptin on carotid intima-media thickness (IMT). A
total of 76 patients with clinically stable and documented coronary artery
disease, who were newly diagnosed with impaired glucose tolerance or mild type 2
diabetes mellitus, were allocated, randomly, to receive either sitagliptin
100 mg/day or the placebo control. Common carotid IMT, glucose profiles,
glycosylated hemoglobin (HbA1c), and lipid profiles were measured at baseline and
repeated at 12 months. Sitagliptin-treated patients showed less IMT progression
than the control group (p = 0.02). In addition, the sitagliptin group showed
greater reductions in body weight (2.2%), 2-hour glucose levels on the 75-g oral
glucose tolerance test (17.3%), HbA1c (4.7%), and low-density lipoprotein
cholesterol levels (7.9%) from that at baseline. In conclusion, treatment with
sitagliptin for 12 months was associated with a beneficial effect in the
prevention of carotid IMT progression, compared with the diet control.
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