The Association of Coronary Artery Calcification With Subsequent Incidence of Cardiovascular Disease in Type 1 Diabetes The DCCT/EDIC Trials

被引:56
作者
Budoff, Matthew [1 ]
Backlund, Jye-Yu C. [2 ]
Bluemke, David A. [3 ]
Polak, Joseph [4 ,5 ]
Bebu, Ionut [2 ]
Schade, David [6 ]
Strowig, Suzanne [7 ]
Raskin, Philip [7 ]
Lachin, John M. [2 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Los Angeles Biomed Res Inst Harbor, Torrance, CA USA
[2] George Washington Univ, Dept Biostat, Rockville, MD USA
[3] Univ Wisconsin, Dept Radiol, Sch Med & Publ Hlth, Madison, WI 53706 USA
[4] Lemuel Shattuck Hosp, Dept Med, Boston, MA USA
[5] Tufts Univ, Sch Med, Boston, MA 02111 USA
[6] Univ New Mexico, Dept Med, Albuquerque, NM 87131 USA
[7] Univ Texas Southwestern Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
cardiovascular disease; coronary artery calcification; major adverse cardiovascular event; type; 1; diabetes; RISK-FACTORS; METABOLIC SYNDROME; PROGNOSTIC VALUE; CALCIUM; ATHEROSCLEROSIS; INTERVENTIONS; INDIVIDUALS; PROGRESSION; MELLITUS; ADULTS;
D O I
10.1016/j.jcmg.2019.01.014
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVES This study sought to determine the relationship between coronary artery calcium (CAC) scores and subsequent cardiovascular disease (CVD) events in DCCT (Diabetes Control and Complications Trial)/EDIC (Epidemiology of Diabetes Interventions and Complications) participants. BACKGROUND The CAC score has been validated for improved risk stratification in general populations; however, this association has not been well studied in type 1 diabetes (T1DM). METHODS Computed tomography (CT) to measure CAC was performed in 1,205 DCCT/EDIC participants at a mean of 42.8 years of age during EDIC years 7 to 9, after the end of DCCT. This study analyzed the association between CAC and time to the first subsequent CVD event or to the first major adverse cardiac event (MACE), a follow-up of 10 to 13 years. CAC was categorized as: 0, >0 to 100, >100 to 300, or >300 Agatston units. RESULTS Of 1,156 participants at risk for subsequent CVD, 105 had an initial CVD event (8.5 per 1,000 patient-years); and of 1,187 participants at risk for MACE, 51 had an initial MACE event (3.9 per 1,000 patient-years). Event rates among those with scores of zero (n = 817 [70.7%]) were very low for CVD (5.6 per 1,000 patient years). CAC scores >100 to 300 (hazard ratio [HR]: 4.17, 5.40) and >300 (HR: 6.06, 6.91) were associated with higher risks of CVD and MACE, respectively, compared to CAC of 0 (p < 0.0001). CAC scores >0 to 100 were nominally associated with CVD (HR: 1.71; p = 0.0415) but not with MACE (HR: 1.11; p = 0.8134). Similar results were observed when also adjusted for mean HbA(1c) and conventional CVD risk factors. The increment in the AUC due to CAC was modest. CONCLUSIONS CAC scores >100 Agatston units were significantly associated with an increased risk of the subsequent occurrence of CVD and MACE in DCCT/EDIC cohort. Diabetes Control and Complications Trial [DCCT]; NCT00360815; Epidemiology of Diabetes Interventions and Complications [EDIC]; NCT00360893)(C) 2019 by the American College of Cardiology Foundation.
引用
收藏
页码:1341 / 1349
页数:9
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