# Utility of contrast-enhanced ultrasound for assessing disease activity in takayasu arteritis with carotid artery involvement: a scoping review

**Authors:** Carina Soto-Fajardo, Rosa-Elena Cervantes-Ramírez, Carlos-Vidal Montiel-Castañeda, Ada-Rocío Morales-Meza, Daniela-Isabel Rojas-Abarca, Fabiola-Bugambilia Sánchez-Zamudio, Hugo Sandoval, Carlos Pineda

PMC · DOI: 10.3389/fimmu.2026.1767181 · Frontiers in Immunology · 2026-02-05

## TL;DR

This review explores how contrast-enhanced ultrasound can help assess and monitor disease activity in Takayasu arteritis, especially in the carotid arteries.

## Contribution

The study provides a comprehensive synthesis of CEUS's utility in TA, highlighting its potential as a radiation-free alternative for monitoring inflammation.

## Key findings

- CEUS detects arterial wall neovascularization linked to active inflammation in TA patients.
- CEUS correlates with inflammatory biomarkers, PET-CT findings, and clinical activity scores.
- CEUS reveals subclinical inflammation and early relapses not captured by clinical symptoms or labs.

## Abstract

Takayasu arteritis (TA) is a chronic, immune-mediated vasculitis that primarily affects the large arteries, particularly the aorta and its main branches, leading to stenosis, occlusion, dilation, or aneurysms. Traditional imaging modalities, including computed tomography angiography (CTA), magnetic resonance angiography (MRA), and positron emission tomography/computed tomography (PET-CT), offer valuable diagnostic information; however, their clinical applicability has limitations, including high costs, radiation exposure, and reduced availability. In recent years, contrast-enhanced ultrasound (CEUS) has emerged as a minimally invasive, radiation-free technique capable of detecting vascular wall neovascularization as a potential surrogate imaging marker of TA inflammatory activity.

This scoping review, conducted in accordance with the Joanna Briggs Institute (JBI) methodology and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) checklist, aims to synthesize current evidence on the diagnostic and monitoring utility of CEUS in patients with TA and carotid involvement.

We systematically searched MEDLINE/PubMed, Scopus, Web of Science, LILACS and EBSCO from inception to May 2025 for original studies of adult patients with TA in whom CEUS was used to assess disease activity.

Eighteen studies (8 cross-sectional, 3 cohort, 7 case reports; 631 patients) met the eligibility criteria. Across these studies, CEUS detected arterial wall neovascularization compatible with active inflammation, particularly in the carotid arteries, and demonstrated moderate-to-strong correlations with inflammatory biomarkers, PET-CT findings, and clinical activity scores such as the Indian Takayasu Activity Score (ITAS) and the National Institutes of Health (NIH) criteria. Importantly, CEUS can reveal subclinical or residual inflammation even when clinical symptoms or laboratory markers are absent. Its ability to detect early relapses and monitor therapeutic response has been demonstrated in both observational cohorts and individual case reports. Despite this, substantial heterogeneity in imaging protocols and activity definitions limits comparability across studies and restricts integration into clinical practice.

CEUS is a minimally invasive, reproducible, and effective technique for both detecting and monitoring disease activity in TA with carotid vessel involvement, thereby facilitating early and accurate therapeutic decisions. Its future incorporation into clinical practice will require validated scoring systems, harmonized acquisition protocols, and demonstration of added value in treatment decision-making and long-term outcomes.

## Linked entities

- **Diseases:** Takayasu arteritis (MONDO:0017991)

## Full-text entities

- **Genes:** IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PTX3 (pentraxin 3) [NCBI Gene 5806] {aka TNFAIP5, TSG-14}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}
- **Diseases:** III (MESH:C537189), occlusion (MESH:D001157), atherosclerotic (MESH:D050197), Giant cell arteritis (MESH:D013700), carotid artery disease (MESH:D002340), NIH (OMIM:603663), rheumatological disease (MESH:D012216), artery (MESH:D012078), atherosclerotic plaques (MESH:D058226), TA (MESH:D013625), inflammation (MESH:D007249), large-vessel vasculitis (MESH:D014657), carotid stenosis (MESH:D016893), aneurysm (MESH:D000783), CEUS (MESH:C564835), vascular abnormalities (MESH:D014652), stenosis (MESH:D003251), ischemia (MESH:D007511)
- **Chemicals:** agents (-), saline (MESH:D012965), Sonovue (MESH:C420843)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103]
- **Mutations:** AUC of 0, C

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916648/full.md

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Source: https://tomesphere.com/paper/PMC12916648