The effect of metoprolol and aspirin on cardiovascular risk in bereavement: A randomized controlled trial. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Bereavement is associated with an increased risk of cardiovascular disease; however, no reports exist of interventions to reduce risk. In a randomized, double-blind, placebo-controlled trial of 85 recently bereaved participants, we determined whether β-blocker (metoprolol 25 mg) and aspirin (100 mg) reduce cardiovascular risk markers and anxiety, without adversely affecting bereavement intensity. METHODS: Participants were spouses (n = 73) or parents (n = 12) of deceased from 5 hospitals in Sydney, Australia, 55 females, 30 males, aged 66.1 ± 9.4 years. After assessment within 2 weeks of bereavement, subjects were randomized to 6 weeks of daily treatment or placebo, and the effect evaluated using ANCOVA, adjusted for baseline values (primary analysis). RESULTS: Participants on metoprolol and aspirin had lower levels of home systolic pressure (P = .03), 24-hour average heart rate (P < .001) and anxiety (P = .01) platelet response to arachidonic acid (P < .001) and depression symptoms (P = .046) than placebo with no difference in standard deviation of NN intervals index (SDNNi), von Willebrand Factor antigen, platelet-granulocyte aggregates or bereavement intensity. No significant adverse safety impact was observed. CONCLUSIONS: In early bereavement, low dose metoprolol and aspirin for 6 weeks reduces physiological and psychological surrogate measures of cardiovascular risk. Although further research is needed, results suggest a potential preventive benefit of this approach during heightened cardiovascular risk associated with early bereavement.

publication date

  • November 13, 2019

Research

keywords

  • Adrenergic beta-1 Receptor Antagonists
  • Anti-Inflammatory Agents, Non-Steroidal
  • Aspirin
  • Bereavement
  • Cardiovascular Diseases
  • Metoprolol

Identity

Scopus Document Identifier

  • 85077655453

Digital Object Identifier (DOI)

  • 10.1016/j.ahj.2019.11.003

PubMed ID

  • 31923768

Additional Document Info

volume

  • 220