Association between vascular FDG uptake during follow-up and the development of thoracic aortic aneurysms in giant cell arteritis.

PET aneurysm aorta giant cell arteritis (GCA) vasculitis

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2024
Historique:
received: 09 02 2024
accepted: 01 03 2024
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 4 4 2024
Statut: epublish

Résumé

A positive PET scan at diagnosis was associated with a greater yearly increase in ascending and descending aortic diameter and thoracic aortic volume in patients with giant cell arteritis (GCA). Radiologic and histopathologic vascular abnormalities persist in a subset of treated patients despite clinical remission. The aim of this study was to evaluate the association between vascular FDG uptake during follow-up and the development of thoracic aortic aneurysms. We recently performed a prospective cohort study of 106 GCA patients, who underwent FDG PET and CT imaging at diagnosis and CT imaging yearly for a maximum of 10 years. In this Eighty-eight repeat PET scans were performed in 52 out of 106 GCA patients, who were included in the original prospective cohort. Fifty-five (63%) PET scans were done at the time of a relapse and 33 (38%) were done while in remission. Nine out of ten patients with an incident thoracic aortic aneurysm had both a positive PET scan at diagnosis and during follow-up. In addition to the intensity and extent of the initial vascular inflammation, ongoing aortic inflammation may contribute to the development of thoracic aortic aneurysms in GCA. However, this hypothesis should be confirmed in a large prospective trial with repeat PET scans at predefined time points during follow-up.

Sections du résumé

Background UNASSIGNED
A positive PET scan at diagnosis was associated with a greater yearly increase in ascending and descending aortic diameter and thoracic aortic volume in patients with giant cell arteritis (GCA). Radiologic and histopathologic vascular abnormalities persist in a subset of treated patients despite clinical remission. The aim of this study was to evaluate the association between vascular FDG uptake during follow-up and the development of thoracic aortic aneurysms.
Methods UNASSIGNED
We recently performed a prospective cohort study of 106 GCA patients, who underwent FDG PET and CT imaging at diagnosis and CT imaging yearly for a maximum of 10 years. In this
Results UNASSIGNED
Eighty-eight repeat PET scans were performed in 52 out of 106 GCA patients, who were included in the original prospective cohort. Fifty-five (63%) PET scans were done at the time of a relapse and 33 (38%) were done while in remission. Nine out of ten patients with an incident thoracic aortic aneurysm had both a positive PET scan at diagnosis and during follow-up.
Conclusion UNASSIGNED
In addition to the intensity and extent of the initial vascular inflammation, ongoing aortic inflammation may contribute to the development of thoracic aortic aneurysms in GCA. However, this hypothesis should be confirmed in a large prospective trial with repeat PET scans at predefined time points during follow-up.

Identifiants

pubmed: 38572159
doi: 10.3389/fmed.2024.1384533
pmc: PMC10987716
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1384533

Informations de copyright

Copyright © 2024 Blockmans, Moreel, Betrains, Vanderschueren, Coudyzer, Boeckxstaens and Van Laere.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Daniel Blockmans (D)

Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
European Reference Network for Immunodeficiency, Autoinflammatory, Autoimmune and Pediatric Rheumatic Disease (ERN-RITA), Utrecht, Netherlands.

Lien Moreel (L)

Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Albrecht Betrains (A)

Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Steven Vanderschueren (S)

Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
European Reference Network for Immunodeficiency, Autoinflammatory, Autoimmune and Pediatric Rheumatic Disease (ERN-RITA), Utrecht, Netherlands.

Walter Coudyzer (W)

Department of Radiology, University Hospitals Leuven, Leuven, Belgium.

Lennert Boeckxstaens (L)

Division of Nuclear Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, KU Leuven, Leuven, Belgium.

Koen Van Laere (K)

Division of Nuclear Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, KU Leuven, Leuven, Belgium.

Classifications MeSH