Depressive Symptoms and Risk of Stroke in a National Cohort of Black and White Participants From REGARDS

The purpose of this study was to examine depressive symptoms as a risk factor for incident stroke and determine whether depressive symptomatology was differentially predictive of stroke among Black and White participants. The study comprised 9,529 Black and 14,516 White stroke-free participants, age...

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Published in:Neurology. Clinical practice Vol. 11; no. 4; pp. e454 - e461
Main Authors: Ford, Cassandra D., Gray, Marquita S., Crowther, Martha R., Wadley, Virginia G., Austin, Audrey L., Crowe, Michael G., Pulley, LeaVonne, Unverzagt, Frederick, Kleindorfer, Dawn O., Kissela, Brett M., Howard, Virginia J.
Format: Journal Article
Language:English
Published: United States Lippincott Williams & Wilkins 01-08-2021
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Summary:The purpose of this study was to examine depressive symptoms as a risk factor for incident stroke and determine whether depressive symptomatology was differentially predictive of stroke among Black and White participants. The study comprised 9,529 Black and 14,516 White stroke-free participants, aged 45 and older, enrolled in the REasons for Geographic and Racial Differences in Stroke (2003-2007). Incident stroke was the first occurrence of stroke. Association between baseline depressive symptoms (assessed via the 4-item Center for Epidemiologic Studies Depression Scale [CES-D-4]: 0, 1-3, or ≥4) and incident stroke was analyzed with Cox proportional hazards models adjusted for demographics, stroke risk factors, and social factors. There were 1,262 strokes over an average follow-up of 9.21 (SD 4.0) years. Compared to participants with no depressive symptoms, after demographic adjustment, participants with CES-D-4 scores of 1-3 had 39% increased stroke risk (hazard ratio [HR] = 1.39, 95% confidence interval [CI] = 1.23-1.57), with slight attenuation after full adjustment (HR = 1.27, 95% CI = 1.11-1.43). Participants with CES-D-4 scores of ≥4 experienced 54% higher risk of stroke after demographic adjustment (HR = 1.54, 95% CI = 1.27-1.85), with risk attenuated in the full model similar to risk with 1-3 symptoms (HR = 1.25, 95% CI = 1.03-1.51). There was no evidence of a differential effect by race ( = 0.53). The association of depressive symptoms with increased stroke risk was similar among a national sample of Black and White participants. These findings suggest that assessment of depressive symptoms should be considered in primary stroke prevention for both Black and White participants.
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Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/cp.
ISSN:2163-0402
2163-0933
DOI:10.1212/CPJ.0000000000000983