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Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results.

Publication ,  Journal Article
Hasan, DM; Chalouhi, N; Jabbour, P; Dumont, AS; Kung, DK; Magnotta, VA; Young, WL; Hashimoto, T; Richard Winn, H; Heistad, D
Published in: J Am Heart Assoc
February 22, 2013

BACKGROUND: Inflammatory cells and molecules may play a critical role in formation and rupture of cerebral aneurysms. Recently, an epidemiologic study reported that acetylsalicylic acid (ASA) decreases the risk of aneurysm rupture. The goal of this study was to determine the effects of ASA on inflammatory cells and molecules in the walls of human cerebral aneurysms, using radiographic and histological techniques. METHODS AND RESULTS: Eleven prospectively enrolled patients harboring unruptured intracranial aneurysms were randomized into an ASA-treated (81 mg daily) group (n=6) and an untreated (control) group (n=5). Aneurysms were imaged at baseline using ferumoxytol-enhanced MRI to estimate uptake by macrophages. After 3 months, patients were reimaged before undergoing microsurgical clipping. Aneurysm tissues were collected for immunostaining with monoclonal antibodies for cyclooxygenase-1 (COX-1), cyclooxygenase-2 (COX-2), microsomal prostaglandin E2 synthase-1 (mPGES-1), and macrophages. A decrease in signal intensity on ferumoxytol-enhanced MRI was observed after 3 months of ASA treatment. Expression of COX-2 (but not COX-1), mPGES-1, and macrophages was lower in the ASA group than in the control group. CONCLUSIONS: This study provides preliminary radiographical and histological evidence that ASA may attenuate the inflammatory process in the walls of human cerebral aneurysms. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01710072.

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Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

February 22, 2013

Volume

2

Issue

1

Start / End Page

e000019

Location

England

Related Subject Headings

  • Treatment Outcome
  • Tomography, X-Ray Computed
  • Time Factors
  • Prostaglandin-E Synthases
  • Prospective Studies
  • Middle Aged
  • Male
  • Magnetic Resonance Imaging
  • Macrophages
  • Iowa
 

Citation

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Hasan, D. M., Chalouhi, N., Jabbour, P., Dumont, A. S., Kung, D. K., Magnotta, V. A., … Heistad, D. (2013). Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results. J Am Heart Assoc, 2(1), e000019. https://doi.org/10.1161/JAHA.112.000019
Hasan, David M., Nohra Chalouhi, Pascal Jabbour, Aaron S. Dumont, David K. Kung, Vincent A. Magnotta, William L. Young, Tomoki Hashimoto, H. Richard Winn, and Donald Heistad. “Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results.J Am Heart Assoc 2, no. 1 (February 22, 2013): e000019. https://doi.org/10.1161/JAHA.112.000019.
Hasan DM, Chalouhi N, Jabbour P, Dumont AS, Kung DK, Magnotta VA, et al. Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results. J Am Heart Assoc. 2013 Feb 22;2(1):e000019.
Hasan, David M., et al. “Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results.J Am Heart Assoc, vol. 2, no. 1, Feb. 2013, p. e000019. Pubmed, doi:10.1161/JAHA.112.000019.
Hasan DM, Chalouhi N, Jabbour P, Dumont AS, Kung DK, Magnotta VA, Young WL, Hashimoto T, Richard Winn H, Heistad D. Evidence that acetylsalicylic acid attenuates inflammation in the walls of human cerebral aneurysms: preliminary results. J Am Heart Assoc. 2013 Feb 22;2(1):e000019.
Journal cover image

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

February 22, 2013

Volume

2

Issue

1

Start / End Page

e000019

Location

England

Related Subject Headings

  • Treatment Outcome
  • Tomography, X-Ray Computed
  • Time Factors
  • Prostaglandin-E Synthases
  • Prospective Studies
  • Middle Aged
  • Male
  • Magnetic Resonance Imaging
  • Macrophages
  • Iowa