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Published on: January 28, 2020
HbA1c, Coronary atheroma progression and cardiovascular outcomes
Iryna Dykun1,2, Ozgur Bayturan3, Julie Carlo1
1C5Research, Department of Cardiovascular Medicine, Heart, Vascular, and Thoracic Institute, Cleveland Clinic, Cleveland, OH.
Insights
Higher on-treatment hemoglobin A1c (HbA1c) levels are linked to increased coronary artery plaque buildup and major adverse cardiovascular events (MACE). This suggests glycemic control directly impacts cardiovascular health, independent of other risk factors.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Syndrome
Background:
- Glycemic control is crucial for managing diabetes and preventing complications.
- The direct impact of on-treatment hemoglobin A1c (HbA1c) on coronary atheroma progression and major adverse cardiovascular events (MACE) remains an area of investigation.
Purpose of the Study:
- To investigate the independent association between on-treatment HbA1c levels and coronary atheroma progression.
- To assess the relationship between on-treatment HbA1c levels and the incidence of MACE.
Main Methods:
- A post-hoc pooled analysis of seven prospective, randomized trials using serial coronary intravascular ultrasonography (IVUS).
- Percent atheroma volume (PAV) was measured to assess plaque burden.
- Multivariable mixed modeling and Cox proportional hazard models were employed to analyze associations.
Main Results:
- In 3,312 patients, higher on-treatment HbA1c levels were independently associated with increased annualized changes in PAV (beta: 0.13 [0.08, 0.19], p < 0.001).
- On-treatment HbA1c levels were also independently associated with a higher incidence of MACE (HR: 1.13 [1.04, 1.23], p = 0.005).
Conclusions:
- Elevated on-treatment HbA1c levels are significantly associated with coronary atheroma progression and adverse cardiovascular outcomes, irrespective of other risk factor control.
- These findings support a direct effect of glycemic control on coronary atheroma and atherosclerotic events, underscoring the rationale for therapies targeting glycemic modulation.
Background And Aims:
We tested the hypothesis that on-treatment HbA1c levels independently associate with coronary atheroma progression and major adverse cardiovascular events (MACE: death, myocardial infarction, cerebrovascular accident, coronary revascularization, or hospitalization for unstable angina) rates.
Methods:
We performed a post-hoc pooled analysis of data from seven prospective, randomized trials involving serial coronary intravascular ultrasonography (IVUS). The percent atheroma volume (PAV) was calculated as the proportion of the entire vessel wall occupied by atherosclerotic plaque. Using multivariable mixed modeling, we determined the association of on-treatment HbA1c with annualized change in PAV. Cox proportional hazard models were used to assess the association of HbA1c with incidence of MACE.
Results:
Among 3,312 patients (mean age 58.6±9years, 28.4%women) average on-treatment HbA1c was 6.2±1.1%. Overall, there was no net significant annualized change in PAV (0.12±0.19%, p = 0.52). In a fully adjusted multivariable analysis (following adjustment of age, sex, body mass index, systolic blood pressure, smoking, low- and high-density lipoprotein cholesterol, triglyceride levels, peripheral vascular disease, trial, region, and baseline PAV), higher on-treatment HbA1c levels were independently associated with annualized changes in PAV [beta-estimate (95% confidence interval): 0.13(0.08, 0.19), p < 0.001]. On-treatment HbA1c levels were independently associated with MACE [hazard ratio (95% confidence interval): 1.13(1.04, 1.23), p = 0.005].
Conclusions:
Independent of achieved cardiovascular risk factor control, greater HbA1c levels significantly associate with coronary atheroma progression rates and clinical outcomes. These results support the notion of a direct, specific effect of glycemic control upon coronary atheroma and atherosclerotic events, supporting the rationale of therapies designed to directly modulate it.
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