Lee DH, Chun EJ, Hur JH, Min SH, Lee JE, Oh TJ, Kim KM, Jang HC, Han SJ, Kang DK, Kim HJ, Lim S.
* This article originally appeared in the February 2017 issue of Atherosclerosis.
Background and Aims
Sarpogrelate, a 5-hydroxytryptamine type 2A antagonist, is a potential antiplatelet agent. We performed a randomized study to evaluate the effect of sarpogrelate on vascular health in Korean patients with diabetes.
Methods
Forty diabetic patients aged 58.6 ± 6.8 years with 10-75% coronary artery stenosis, as assessed by coronary computed tomography angiography, were randomly assigned to sarpogrelate 300 mg/day plus aspirin 100 mg/day (SPG + ASA group) or aspirin 100 mg/day alone (ASA group) for six months. The primary endpoint of this study was the change in coronary artery disease including the calcium score (CACS), maximal stenosis, and plaque volume (calcified vs. non-calcified). The secondary endpoints were changes in biochemical parameters related to glucose and lipid metabolism, and in subclinical atherosclerosis assessed by ankle-brachial index and pulse wave velocity.
Results
After six-month treatment, there was no significant difference in the changes in CACS, coronary stenosis, ankle-brachial index, and pulse wave velocity, between groups. The total plaque volume decreased from 82.4 ± 14.5 mm³ to 74.6 ± 14.4 mm³ in the SPG + ASA group, but increased from 64.9 ± 16.0 mm³ to 68.6 ± 16.3 mm³ in the ASA group (p < 0.05), mainly driven by changes in the non-calcified component (SPG + ASA group 15.6 ± 4.6 mm³ to 11.2 ± 3.7 mm³ vs. ASA group 21.2 ± 6.2 mm³ to 22.8 ± 6.6 mm³, p < 0.01). Serum C-reactive protein levels and homeostasis model assessment of insulin resistance tended to decrease in the SPG + ASA group, but they were not altered in the ASA group.
Conclusions
The present study demonstrated that sarpogrelate treatment may decrease coronary artery plaque volume, particularly the non-calcified portion, in patients with diabetes.
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