New perspectives in the imaging of Raynaud's phenomenon.


Journal

European journal of rheumatology
ISSN: 2147-9720
Titre abrégé: Eur J Rheumatol
Pays: Turkey
ID NLM: 101656068

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 30 06 2019
accepted: 05 03 2020
entrez: 9 11 2020
pubmed: 10 11 2020
medline: 10 11 2020
Statut: ppublish

Résumé

The last 10-20 years have seen huge strides in imaging science. The aim of this review article is to share with the reader the key recent advances in non-invasive imaging of the digital (finger) vasculature in patients with Raynaud's phenomenon (RP), including in systemic sclerosis (SSc)-related digital vasculopathy. For the rheumatologist, seeing a patient with RP is an opportunity for early diagnosis of an underlying SSc-spectrum disorder or (conversely) for reassuring the patient with primary (idiopathic) RP. Non-invasive imaging techniques can help to provide diagnostic certainty. In addition, they can provide new insights into pathophysiology and have the potential to facilitate the development of much needed effective treatments by providing primary and secondary endpoints for randomized controlled trials: validation studies are ongoing. This review article focuses on nailfold capillaroscopy, thermography, and laser Doppler methods but also discusses (briefly) other technologies, including optical coherence tomography, multispectral imaging, and photoacoustic imaging. Key recent advances are the increasing use/availability of nailfold capillaroscopy (and better understanding of the role of low-cost hand-held devices), increased accessibility of thermography (including mobile phone thermography), and increased application of laser Doppler methods to the study of RP/digital vasculopathy (in particular of laser Doppler imaging and laser speckle contrast imaging, both of which measure blood flow over an area rather than at a single site). In an era of precision medicine, non-invasive imaging techniques can help stratify risk of (a) SSc in the patient with RP and (b) digital vascular disease progression in the patient with an SSc-spectrum disorder.

Identifiants

pubmed: 33164735
pii: eurjrheum.2020.19124
doi: 10.5152/eurjrheum.2020.19124
pmc: PMC7647685
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

S212-S221

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Auteurs

Ariane L Herrick (AL)

Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Salford Royal NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, UK.

Graham Dinsdale (G)

Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Salford Royal NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, UK.

Andrea Murray (A)

Division of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Salford Royal NHS Foundation Trust, Manchester Academic Health Science Centre, Salford, UK.

Classifications MeSH