Ultrasound shoulder assessment of calcium pyrophosphate disease with suspected polymyalgia rheumatica.


Journal

Clinical and experimental rheumatology
ISSN: 0392-856X
Titre abrégé: Clin Exp Rheumatol
Pays: Italy
ID NLM: 8308521

Informations de publication

Date de publication:
Historique:
received: 15 11 2019
accepted: 20 01 2020
pubmed: 7 3 2020
medline: 15 12 2020
entrez: 7 3 2020
Statut: ppublish

Résumé

Polymyalgia rheumatica (PMR) is characterised by inflammatory pain of shoulders and the pelvic girdle that affects older people. Conditions that can mimic PMR include rheumatoid arthritis (RA), spondyloarthritis (SpA) and calcium pyrophosphate disease (CPPD). In this study, we aimed to define the prevalence of CPPD among patients with polymyalgic syndrome with suspected PMR according to recent ACR/EULAR criteria. This was an observational study in which we included patients with polymyalgic syndrome (inflammatory pain of shoulders, elevated C-reactive protein (CRP) level, and age >50 years). All patients were tested for RA antibodies and underwent ultrasonography (US) of shoulders [gleno-humeral effusion, biceps tenosynovitis, sub-acromiodeltoid (SAD) bursitis, synovitis and CPPD of the acromio-clavicular (AC) joint and humeral bone erosion]. We included 94 patients with polymyalgic syndrome (mean age 69.4±11.3 years, 67% female); 27 had a diagnosis of RA and 14 SpA. The remaining 52 were considered to have PMR according to ACR/EULAR criteria for PMR; 25 had a diagnosis of CPPD. As compared with PMR patients without CPPD, those with CPPD more frequently had humeral bone erosion (p=0.003), synovitis and CPPD of the AC joint (p<0.0001 for both) and less frequently SAD bursitis (p=0.0098). For PMR diagnosis, the most sensitive US features were SAD bursitis (96.3%) and biceps tenosynovitis (85.2%), despite low specificity. For CPPD diagnosis, CPPD of the AC joint had the best ratio of sensitivity to specificity (sensitivity: 85.2%; specificity: 97.1%). Detection of CPPD is relatively frequent with suspected PMR. Adding US assessment of the AC joint to usual US screening might help the clinician better distinguish PMR from other conditions, notably CPPD.

Identifiants

pubmed: 32141428
pii: 15000

Substances chimiques

Calcium Pyrophosphate X69NU20D19

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1170-1175

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Sébastien Ottaviani (S)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France. sebastien.ottaviani@aphp.fr.

Julia Goossens (J)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France.

Lucie Demaria (L)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France.

Marine Forien (M)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France.

Elisabeth Palazzo (E)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France.

Philippe Dieudé (P)

Service de Rhumatologie, Université Paris Diderot, Hôpital Bichat, APHP, Paris, France.

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Classifications MeSH