Glycemic Control, Cardiac Autoimmunity, and Long-Term Risk of Cardiovascular Disease in Type 1 Diabetes Mellitus A DCCT/EDIC Cohort-Based Study

Article

关键词: CORONARY-ARTERY CALCIFICATION;    COMPLICATIONS TRIAL/EPIDEMIOLOGY;    NATIONAL INSTITUTE;    CHAGAS-DISEASE;    ALPHA-MYOSIN;    HEART;    INTERVENTIONS;    INFLAMMATION;    MORTALITY;    PROTEIN;   

DOI  :  10.1161/CIRCULATIONAHA.118.036068

来源: SCIE

【 摘 要 】

BACKGROUND: Poor glycemic control is associated with increased risk of cardiovascular disease (CVD) in type 1 diabetes mellitus (T1DM); however, little is known about mechanisms specific to T1DM. In T1DM, myocardial injury can induce persistent cardiac autoimmunity. Chronic hyperglycemia causes myocardial injury, raising the possibility that hyperglycemia-induced cardiac autoimmunity could contribute to long-term CVD complications in T1DM. METHODS: We measured the prevalence and profiles of cardiac autoantibodies (AAbs) in longitudinal samples from the DCCT (Diabetes Control and Complications Trial) in participants with mean hemoglobin A(1c) (HbA(1c)) >= 9.0% (n=83) and <= 7.0% (n=83) during DCCT. We assessed subsequent coronary artery calcification (measured once during years 7-9 in the post-DCCT EDIC [Epidemiology of Diabetes Interventions and Complications] observational study), high-sensitivity C-reactive protein (measured during EDIC years 4-6), and CVD events (defined as nonfatal myocardial infarction, stroke, death resulting from CVD, heart failure, or coronary artery bypass graft) over a 26-year median follow-up. Cardiac AAbs were also measured in matched patients with type 2 diabetes mellitus with HbA(1c) >= 9.0% (n=70) and <= 7.0% (n=140) and, as a control for cardiac autoimmunity, patients with Chagas cardiomyopathy (n=51). RESULTS: Apart from HbA(1c) levels, the DCCT groups shared similar CVD risk factors at the beginning and end of DCCT. The DCCT HbA(1c) >= 9.0% group showed markedly higher cardiac AAb levels than the HbA(1c) <= 7.0% group during DCCT, with a progressive increase and decrease in AAb levels over time in the 2 groups, respectively (P<0.001). In the HbA(1c) >= 9.0% group, 46%, 22%, and 11% tested positive for >= 1, >= 2, and >= 3 different cardiac AAb types, respectively, similar to patients with Chagas cardiomyopathy, compared with 2%, 1%, and 0% in the HbA(1c) <= 7.0% group. Glycemic control was not associated with AAb prevalence in type 2 diabetes mellitus. Positivity for >= 2 AAbs during DCCT was associated with increased risk of CVD events (4 of 6; hazard ratio, 16.1; 95% CI, 3.0-88.2) and, in multivariable analyses, with detectable coronary artery calcification (13 of 31; odds ratio, 60.1; 95% CI, 8.4-410.0). Patients with >= 2 AAbs subsequently also showed elevated high-sensitivity C-reactive protein levels (6.0 mg/L versus 1.4 mg/L in patients with <= 1 AAbs; P=0.003). CONCLUSIONS: Poor glycemic control is associated with cardiac autoimmunity in T1DM. Furthermore, cardiac AAb positivity is associated with an increased risk of CVD decades later, suggesting a role for autoimmune mechanisms in the development of CVD in T1DM, possibly through inflammatory pathways.

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