American Heart Journal
Volume 157, Issue 1 , Pages 77-83, January 2009

Ethnic differences in the treatment of depression in patients with ischemic heart disease

Duke University Medical Center, Durham, NC

Received 14 July 2008; accepted 13 August 2008. published online 22 October 2008.

Objective

The aim of this study is to examine ethnic differences in depressive symptoms and antidepressant treatment in a cohort of patients undergoing diagnostic coronary angiography.

Background

Coronary heart disease (CHD) is the leading cause of mortality in the United States, with an excess of mortality in African Americans. Traditional risk factors occur more frequently among African Americans but do not fully account for this increased risk. Elevated depressive symptoms have been shown to be associated with higher morbidity and mortality in patients with CHD.

Methods

A consecutive series of 864 patients (727 whites, 137 African Americans) completed the Beck Depression Inventory to assess depressive symptoms. Data describing cardiovascular risk factors and type of medications including antidepressants were obtained from chart review at the time of study enrollment.

Results

There was no difference in the severity of depressive symptoms between whites (P = .50); the prevalence of elevated depressive symptoms also was similar for African Americans (35%) and whites (27%) (P = .20). However, the rate of antidepressant use was 21% for whites but only 11.7% for African Americans (P = .016). The odds ratio for ethnicity (African American vs whites) in predicting antidepressant use was 0.43 (95% confidence interval 0.24-0.76, P = .004) after adjustment for Beck Depression Inventory scores.

Conclusions

African Americans with CHD are less likely to be treated with antidepressant medications compared with whites despite having similar levels of depression. The ethnic differences in the psychopharmacological management of depression suggests that more careful assessment of depression, especially in African Americans, is necessary to optimize care of patients with CHD.

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 This study was supported by grant MH 49679 from the National Institutes of Health (Bethesda, MD) and grant M01-RR-30 from the Duke Clinical Research Unit Program, National Center for Research Resources, National Institutes of Health.

 Guest editor: Hector O. Ventura, MD.

PII: S0002-8703(08)00720-5

doi:10.1016/j.ahj.2008.08.013

American Heart Journal
Volume 157, Issue 1 , Pages 77-83, January 2009