4.5 Article

Early Improvement in Carotid Plaque Echogenicity by Acarbose in Patients With Acute Coronary Syndromes

期刊

CIRCULATION JOURNAL
卷 76, 期 6, 页码 1452-1460

出版社

JAPANESE CIRCULATION SOC
DOI: 10.1253/circj.CJ-11-1524

关键词

Carotid arteries; C-reactive protein; Plaque vulnerability; Type 2 diabetes mellitus; Ultrasound

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology [(2)-15390244, 19390209, 15012222]
  2. Health and Labor Sciences Research Grants for Comprehensive Research on Aging and Health, Tokyo, Japan [H15-Choju-012]
  3. Grants-in-Aid for Scientific Research [15012222, 19390209] Funding Source: KAKEN

向作者/读者索取更多资源

Background: The resolution of hyperglycemia is associated with suppression of in-hospital cardiac complications in patients with acute coronary syndromes (ACS). This study evaluated carotid artery plaque echolucency using ultrasound in patients with ACS and type 2 diabetes mellitus (DM) to determine whether acarbose, an alpha-glucosidase inhibitor, may rapidly stabilize unstable atherosclerotic plaques. Methods and Results: ACS patients with type 2 DM and carotid plaques (n=44) were randomly assigned to treatment with acarbose (150 or 300 mg/day, n=22) or a control group (no acarbose, n=22). Acarbose treatment was initiated within 5 days after the onset of ACS. Unstable carotid plaques were assessed by measuring plaque echolucency using carotid ultrasound with integrated backscatter (IBS) before, and at 2 weeks, 1 and 6 months after the initiation of treatment. An increase in the IBS value reflected an increase in carotid plaque echogenicity. As results, the IBS value of echolucent carotid plaques showed a significant increase at 1 month and a further increase at 6 months after treatment in the acarbose group, but there was minimal change in the control group. The increase in IBS values was significantly correlated with a decrease in C-reactive protein levels. Conclusions: Acarbose rapidly improved carotid plaque echolucency within 1 month of therapy in patients with ACS and type 2 DM. (Circ J 2012; 76: 1452-1460)

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