Imaging Biomarkers and Prevalence of Complex Aortic Plaque in Cryptogenic Stroke: A Systematic Review

Author:

Sakai Yu1,Cao Quy2ORCID,Rubin Jeremy2ORCID,Witsch Jens3ORCID,Cohen‐Addad Dan4ORCID,de Macedo Rodrigues Katyucia5ORCID,Coco‐Martin Maria Begoña6ORCID,Pasyar Pouyan1,Juega Jesús7ORCID,Fan Zhaoyang8ORCID,Kasner Scott E.3ORCID,Cucchiara Brett L.3ORCID,Song Jae W.1ORCID

Affiliation:

1. Department of Radiology University of Pennsylvania Philadelphia PA USA

2. Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

3. Department of Neurology University of Pennsylvania Philadelphia PA USA

4. Department of Radiology and Imaging Sciences Emory University Atlanta GA USA

5. Greensboro Radiology Greensboro NC USA

6. Department of Neurology University of Valladolid Valladolid Spain

7. Department of Neurology Vall d’Hebron University Hospital Barcelona Spain

8. Departments of Radiology, Biomedical Engineering, and Radiation Oncology University of Southern California Los Angeles CA USA

Abstract

Background Complex aortic plaque (CAP) is a potential embolic source in patients with cryptogenic stroke (CS). We review CAP imaging criteria for transesophageal echocardiogram (TEE), computed tomography angiography (CTA), and magnetic resonance imaging and calculate CAP prevalence in patients with acute CS. Methods and Results PubMed and EMBASE databases were searched up to December 2022 in accordance with the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guideline. Two independent reviewers extracted data on study design, imaging techniques, CAP criteria, and prevalence. The Cochrane Collaboration tool and Guideline for Reporting Reliability and Agreement Studies were used to assess risk of bias and reporting completeness, respectively. From 2293 studies, 45 were reviewed for CAP imaging biomarker criteria in patients with acute CS (N=37 TEE; N=9 CTA; N=6 magnetic resonance imaging). Most studies (74%) used ≥4 mm plaque thickness as the imaging criterion for CAP although ≥1 mm (N=1, CTA), ≥5 mm (N=5, TEE), and ≥6 mm (N=2, CTA) were also reported. Additional features included mobility, ulceration, thrombus, protrusions, and assessment of plaque composition. From 23 prospective studies, CAP was detected in 960 of 2778 patients with CS (0.32 [95% CI, 0.24–0.41], I 2 =94%). By modality, prevalence estimates were 0.29 (95% CI, 0.20–0.40; I 2 =95%) for TEE; 0.23 (95% CI, 0.15–0.34; I 2 =87%) for CTA and 0.22 (95% CI, 0.06–0.54; I 2 =92%) for magnetic resonance imaging. Conclusions TEE was commonly used to assess CAP in patients with CS. The most common CAP imaging biomarker was ≥4 mm plaque thickness. CAP was observed in one‐third of patients with acute CS. However, high study heterogeneity suggests a need for reproducible imaging methods.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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