Hostility and platelet reactivity in individuals without a history of cardiovascular disease events.

Published

Journal Article

OBJECTIVE: To examine the association between hostility and platelet reactivity in individuals without a prior history of cardiovascular disease (CVD) events. Hostility is associated with incident CVD events, independent of traditional risk factors. Increased platelet reactivity and thrombus formation over a disrupted coronary plaque are fundamental for CVD event onset. METHODS: Hypertensive patients (n = 42) without concomitant CVD event history completed the 50-item Cook-Medley Hostility Scale, and a subset score of 27 items (Barefoot Ho) was derived. We examined the relationship between Barefoot Ho scores and platelet aggregation. We also examined individual components of Barefoot Ho (aggressive responding, cynicism, and hostile affect) and their associations with platelet aggregation. Platelet reactivity, induced by adenosine diphosphate (ADP), was assessed by standard light transmission aggregometry, the current gold standard method of platelet aggregation assessment. RESULTS: Barefoot Ho scores were related significantly to increased rate of platelet aggregation in response to ADP. Of the three Barefoot Ho components, only aggressive responding was associated independently with increased platelet aggregation rate. The strength of these relationships did not diminish after adjusting for several standard CVD risk factors. CONCLUSIONS: These data demonstrate that hostility, particularly the aggressive responding subtype, is associated with platelet reactivity-a key pathophysiological pathway in the onset of CVD events.

Full Text

Duke Authors

Cited Authors

  • Shimbo, D; Chaplin, W; Kuruvilla, S; Wasson, LT; Abraham, D; Burg, MM

Published Date

  • September 2009

Published In

Volume / Issue

  • 71 / 7

Start / End Page

  • 741 - 747

PubMed ID

  • 19592519

Pubmed Central ID

  • 19592519

Electronic International Standard Serial Number (EISSN)

  • 1534-7796

Digital Object Identifier (DOI)

  • 10.1097/PSY.0b013e3181ad18b6

Language

  • eng

Conference Location

  • United States