Normal salivary gland ultrasonography could rule out the diagnosis of Sjögren's syndrome in anti-SSA-negative patients with sicca syndrome.


Journal

RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038

Informations de publication

Date de publication:
01 2021
Historique:
received: 31 10 2020
revised: 07 01 2021
accepted: 14 01 2021
entrez: 29 1 2021
pubmed: 30 1 2021
medline: 1 9 2021
Statut: ppublish

Résumé

To evaluate the relevance of salivary gland ultrasound (SGUS) and its place in the diagnostic algorithm in patients referred with dry syndrome (DS) for a suspicion of Sjögren's syndrome (SS). We included all patients assessed at our dedicated DS clinic from June 2015 to September 2019 for which a SGUS has been carried out. Images were read blindly and the worst salivary gland was scored according to OMERACT classification. Clinical features, disease activity and treatments were collected. 337 patients were seen from June 2015 to September 2019. 269 patients underwent SGUS. 77 patients were diagnosed with SS and 192 did not meet the ACR/EULAR criteria for SS: non-Sjögren's DS (NSDS). Of these 192 patients, 60 had another possible cause of DS, and 132 patients were diagnosed with SAPS (sicca, asthenia, polyalgia syndrome).SGUS abnormalities were significantly higher in patients with SS versus NSDS: 51% vs 8% for a score ≥2 (p<0.0001), and 43% vs 3% for a score ≥3 (p<0.0001). SGUS score ≥2 had a specificity (Sp) of 91%, sensitivity (Se) of 57%, positive predictive value (PPV) of 72% and negative predictive value (NPV) of 82% for SS diagnosis. SGUS's characteristics in SSA-negative patients were similar to the whole population (Se=42%, Sp=91%, PPV=42%, NPV=92%). The high specificity and NPV in this population could avoid labial salivary gland biopsy (LSGB) in SSA-negative patients with normal SGUS (186 patients, 69%). SGUS is useful for SS diagnosis. If anti-SSA antibodies are negative and SGUS score <2, the diagnosis of SS is very improbable and LSGB could be avoided.

Identifiants

pubmed: 33510043
pii: rmdopen-2020-001503
doi: 10.1136/rmdopen-2020-001503
pmc: PMC7845729
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Omar Al Tabaa (O)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Hélène Gouze (H)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Sabrina Hamroun (S)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Elisabeth Bergé (E)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Rakiba Belkhir (R)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Stephan Pavy (S)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France.

Sandrine Jousse-Joulin (S)

Rheumatology, University and Regional Hospital Centre Brest, Inserm, LBAI, UMR 1227, Brest, France.

Xavier Mariette (X)

Rheumatology, Assistance Publique - Hôpitaux de Paris, Hospital Bicetre, Le Kremlin-Bicetre, France xavier.mariette@aphp.fr.
Center for Immunology of Viral Infections and Auto-immune Diseases (IMVA), Institut pour la Santé et la Recherche Médicale (INSERM) UMR 1184, Université Paris-Saclay, Le Kremlin Bicêtre, France.

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