Effect of dipeptidyl peptidase-4 inhibitor on the progression of coronary artery disease evaluated by computed tomography in patients receiving insulin therapy for type 2 diabetes mellitus

被引:0
|
作者
Choi, Young [1 ,2 ]
Ko, Seung-Hyun [3 ]
Chang, Kiyuk [1 ,2 ]
Yoo, Ki Dong [2 ,4 ]
Ihm, Sang-Hyun [2 ,5 ,6 ]
机构
[1] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Div Cardiol,Dept Internal Med, Seoul, South Korea
[2] Catholic Univ Korea, Cardiovasc Res Inst Intractable Dis, Coll Med, Seoul, South Korea
[3] Catholic Univ Korea, St Vincents Hosp, Dept Internal Med, Div Endocrinol & Metab,Coll Med, Seoul, South Korea
[4] Catholic Univ Korea, St Vincents Hosp, Coll Med, Div Cardiol,Dept Internal Med, Seoul, South Korea
[5] Catholic Univ Korea, Bucheon St Marys Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[6] Bucheon St Marys Hosp, 327 Sosa Ro, Bucheon 14647, South Korea
关键词
computed tomography; coronary artery disease; diabetes mellitus; dipeptidyl peptidase-4 inhibitor; insulin; ADVERSE CARDIOVASCULAR EVENTS; DPP-4; INHIBITORS; INCREASED RISK; MORTALITY; ATHEROSCLEROSIS; SITAGLIPTIN; ROSIGLITAZONE; ANGIOGRAPHY; RESISTANCE; OUTCOMES;
D O I
10.1111/1753-0407.13449
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundWe evaluated the effect of a dipeptidyl peptidase-4 inhibitor (DPP-4i) on the progression of obstructive coronary artery disease (OCAD) in patients with type 2 diabetes mellitus (T2DM) receiving insulin therapy. MethodsUsing a multicenter clinical data warehouse, we analyzed the patients receiving insulin therapy for T2DM who underwent coronary computed tomography angiography (CCTA) for & GE;2 times. The patients were divided into two groups according to the presence of DPP-4i prescription between the two CCTA examinations. The prevalence of OCAD (>50% stenosis on CCTA), new revascularization rates, and changes in the coronary calcium score (CCS) were analyzed. ResultsA total of 623 patients were included, and a DPP-4i was prescribed to 380 (60.9%) patients. The median time difference between the two CCTAs was 39.0 (17.0-61.4) months. Newly developed OCAD at the follow-up CCTA was detected in 62 (16.3%) patients in the DPP-4i group and 76 (31.3%) patients in the no DPP-4i group (p < 0.001). The risk of new OCAD or new revascularization was lower in the DPP-4i group (19.7% vs. 38.7%; p < 0.001). After propensity score matching, the prevalence of new OCAD (15.9% vs. 29.5%; p = 0.001) and the composite rate of new OCAD or new revascularization (18.7% vs. 37.3%; p < 0.001) were lower in the DPP-4i group. The change in CCS per year did not differ significantly between the two groups (9.1 [0.1-56.8] vs. 13.5 [0.0-78.6]; p = 0.715). ConclusionsAdd-on DPP-4i therapy would be beneficial in preventing coronary artery disease progression in patients with T2DM receiving insulin therapy.
引用
收藏
页码:944 / 954
页数:11
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