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  5. Carotid Plaque Inflammation Imaged by 18 F-Fluorodeoxyglucose Positron Emission Tomography and Risk of Early Recurrent Stroke
 
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Carotid Plaque Inflammation Imaged by 18 F-Fluorodeoxyglucose Positron Emission Tomography and Risk of Early Recurrent Stroke

Author(s)
Kelly, Peter  
Camps-Renom, Pol  
Giannotti, Nicola  
Murphy, S. (Sean)  
McNulty, Jonathan P.  
Barry, Mary  
Foley, Shane J.  
Horgan, Gillian  
Kavanagh, Eoin  
Marnane, Michael  
McDonnell, Ciaran  
O’Donohoe, Martin  
O'Connell, Martin  
et al.  
Uri
http://hdl.handle.net/10197/24480
Date Issued
2019-07
Date Available
2023-06-15T16:02:26Z
Abstract
Background and Purpose-Plaque inflammation contributes to stroke and coronary events. 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) identifies plaque inflammation-related metabolism. Almost no prospective data exist on the relationship of carotid 18F-FDG uptake and early recurrent stroke. Methods-We did a multicenter prospective cohort study BIOVASC (Biomarkers/Imaging Vulnerable Atherosclerosis in Symptomatic Carotid disease) of patients with carotid stenosis and recent stroke/transient ischemic attack with 90-day follow-up. On coregistered carotid 18F-FDG PET/computed tomography angiography, 18F-FDG uptake was expressed as maximum standardized uptake value (SUVmax) in the axial single hottest slice. We then conducted a systematic review of similar studies and pooled unpublished individual-patient data with 2 highly similar independent studies (Dublin and Barcelona). We analyzed the association of SUVmax with all recurrent nonprocedural stroke (before and after PET) and with recurrent stroke after PET only. Results-In BIOVASC (n=109, 14 recurrent strokes), after adjustment (for age, sex, stenosis severity, antiplatelets, statins, diabetes mellitus, hypertension, and smoking), the hazard ratio for recurrent stroke per 1 g/mL SUVmax was 2.2 (CI, 1.1-4.5; P=0.025). Findings were consistent in the independent Dublin (n=52, hazard ratio, 2.2; CI, 1.1-4.3) and Barcelona studies (n=35, hazard ratio, 2.8; CI, 0.98-5.5). In the pooled cohort (n=196), 37 recurrent strokes occurred (29 before and 8 after PET). Plaque SUVmax was higher in patients with all recurrence (P<0.0001) and post-PET recurrence (P=0.009). The fully adjusted hazard ratio of any recurrent stroke was 2.19 (CI, 1.41-3.39; P<0.001) and for post-PET recurrent stroke was 4.57 (CI, 1.5-13.96; P=0.008). Recurrent stroke risk increased across SUVmax quartiles (log-rank P=0.003). The area under receiver operating curve for all recurrence was 0.70 (CI, 0.59-0.78) and for post-PET recurrence was 0.80 (CI, 0.64-0.96). Conclusions-Plaque inflammation-related 18F-FDG uptake independently predicted future recurrent stroke post-PET. Although further studies are needed, 18F-FDG PET may improve patient selection for carotid revascularization and suggest that anti-inflammatory agents may have benefit for poststroke vascular prevention.
Other Sponsorship
Health Research Board Ireland Clinician Scientist and Clinical Trials Network Awards
Fondo de Investigaciones Sanitarias Instituto de Salud Carlos III
Type of Material
Journal Article
Publisher
Lippincott Williams & Wilkins
Journal
Stroke
Volume
50
Issue
7
Start Page
1766
End Page
1773
Copyright (Published Version)
2019 American Heart Association
Subjects

Atherosclerosis

Stroke

Metabolism

Angiography

Inflammation

DOI
10.1161/STROKEAHA.119.025422
Language
English
Status of Item
Peer reviewed
ISSN
0039-2499
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by-nc-nd/3.0/ie/
File(s)
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current version, 4.12.18.docx

Size

64.65 KB

Format

Unknown

Checksum (MD5)

5e9bc90c9e0319eaa462846e4218b872

Owning collection
Medicine Research Collection

Item descriptive metadata is released under a CC-0 (public domain) license: https://creativecommons.org/public-domain/cc0/.
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