Preventive cardiology
Association of Electrocardiographic Abnormalities With Coronary Artery Calcium and Carotid Artery Intima–Media Thickness in Individuals Without Clinical Coronary Heart Disease (from the Multi-Ethnic Study of Atherosclerosis [MESA])

https://doi.org/10.1016/j.amjcard.2009.05.060Get rights and content

Isolated minor nonspecific ST-segment and T-wave abnormalities (NSSTAs), minor and major electrocardiographic (ECG) abnormalities are established, independent risk markers for incident cardiovascular events. Their association with subclinical atherosclerosis has been postulated but is not clearly defined. The aim of this study was to define the association between ECG abnormalities and measurements of subclinical atherosclerosis. We studied participants from MESA, a multiethnic sample of men and women 45 to 84 years of age and free of clinical cardiovascular disease at enrollment. Baseline examination included measurement of traditional risk factors, 12-lead electrocardiograms at rest, coronary artery calcium (CAC) measurement, and common carotid intima–media thickness (CC-IMT). Electrocardiograms were coded using Novacode criteria and were defined as having minor abnormalities (e.g., minor NSSTTAs, first-degree atrioventricular block, and QRS-axis deviations) or major abnormalities (e.g., pathologic Q waves, major STTAs, significant dysrhythmias, and conduction system delays). Multivariable logistic and linear regressions were used to determine cross-sectional associations of ECG abnormalities with CAC and CC-IMT. Of 6,710 participants, 52.7% were women, with a mean age of 62 years. After multivariable adjustment, isolated minor STTAs and minor and major ECG abnormalities were not associated with presence of CAC (>0) in men (odds ratio 1.04, 95% confidence interval 0.81 to 1.33; 1.10, 0.91 to 1.32; and 1.03, 0.81 to 1.31, respectively) or women (1.01, 0.82 to 1.24; 1.04, 0.87 to 1.23; and 0.94, 0.73 to 1.22, respectively). Lack of association remained consistent when using log CAC and CC-IMT as continuous variables. In conclusion, ECG abnormalities are not associated with markers of subclinical atherosclerosis in a large multiethnic cohort.

Section snippets

Methods

The MESA cohort was initiated to investigate the prevalence, correlates, and progression of subclinical cardiovascular disease (i.e., disease detected by noninvasive means before it has manifested in clinical signs and symptoms). Details about the study design have previously been published.18 Briefly, from July 2000 to August 2002, 6,814 men and women 45 to 84 years old, self-identified as white, black, Hispanic, or Chinese and free of clinically apparent cardiovascular disease were recruited

Results

The study sample consisted of 6,710 subjects, of whom 52.7% were women, with a mean age of 62 years; 856 (12.8%) participants had major ECG abnormalities and were excluded from the minor ECG category, leaving 5,848 participants for inclusion in the minor and isolated minor NSTTA ECG analyses. Baseline characteristics of the study cohort stratified by gender are listed in Table 1.

Table 2 displays the proportion of participants, stratified by gender, across the 3 measurements of subclinical

Discussion

In this cross-sectional analysis of a large, multiethnic sample composed of men and women 45 to 84 years old, isolated minor NSSTAs and minor and major ECG abnormalities were not associated with the presence of subclinical atherosclerosis as indicated by the presence of CAC (Agatston score >0), extent of CAC in those with CAC, or amount of CC-IMT.

The lack of association between ECG abnormalities and subclinical atherosclerosis was observed fairly consistently across all gender and ethnic

Acknowledgment

The authors thank the other investigators, the staff, and the participants of the MESA study for their valuable contributions. A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org.

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    This research was supported by Contracts N01-HC-95159 through N01-HC-95165 and N01-HC-95169 from the National Heart, Lung and Blood Institute, Bethesda, Maryland.

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