TY - JOUR
T1 - Are ultrasound salivary parenchymal lesions more severe in primary Sjögren patients with a longer disease duration? A cross-sectional study
AU - Tison, Alice
AU - Jousse-Joulin, Sandrine
AU - Consigny, Maëlys
AU - Moog, Philipp
AU - Hofauer, Benedikt
AU - Hachulla, Eric
AU - Lamotte, Christophe
AU - Morel, Jacques
AU - Mouterde, Gaël
AU - Milic, Vera
AU - Bootsma, Hendrika
AU - Stel, Alja
AU - Fisher, Benjamin A
AU - Maybury, Marc
AU - Baer, Alan
AU - DiRenzo, Dana
AU - Kim, Hae-Rim
AU - Min, Hong-Ki
AU - Lee, Shin-Seok
AU - Choi, Sung-Eun
AU - Alegria, Guillermo Carvajal
AU - Boisramé, Sylvie
AU - Guellec, Dewi
AU - Cornec, Divi
AU - Quéré, Baptiste
AU - Jonsson, Malin
AU - Hammenfors, Daniel
AU - Saraux, Alain
AU - Devauchelle-Pensec, Valérie
N1 - © The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: [email protected].
PY - 2024/12/19
Y1 - 2024/12/19
N2 - OBJECTIVES: Salivary gland ultrasound (SGUS) has an interest in primary Sjögren's disease (pSD) for diagnosis, but the evolution of parenchymal lesions over time is unknown. The objective of this study was to assess the severity of ultrasound abnormalities in relation to pSD duration from the time of buccal dryness onset.METHODS: In this cross-sectional international multicentre study, patients with pSD according to the 2002 or 2016 ACR/EULAR classification criteria were included. Parenchymal abnormalities were classified according to the semiquantitative score as defined by OMERACT. Patients were separated into 4 groups (Group A: < 5 years, Group B: 5-9 years, Group C: 10-20 years, and Group D: > 20 years from the onset of buccal dryness). The association between disease duration groups and SGUS lesions was quantified in terms of odds ratios and 95% confidence intervals.RESULTS: A total of 247 patients were consecutively included between May 2019 and February 2022. Eighty-nine percent of patients had a focus score ≥1/4 mm2, and 85% had positive anti-Ro/SSA. pSD duration was associated with a pathological OMERACT score (score 2 or 3): OR for 5-year duration: 1.23 [95% CI 1.04; 1.47], p= 0.0383). Considering each US item, the only statistical association with pSD duration was found regarding the presence of hyperechoic bands (25% or more): OR for five-year duration 1.18 [95% CI 1.03; 1.36], p= 0.038), independent of an older age.CONCLUSION: pSD duration was associated with the presence of hyperechoic bands, but not with hypoechoic areas, suggesting a progressive fibro-adipose evolution.
AB - OBJECTIVES: Salivary gland ultrasound (SGUS) has an interest in primary Sjögren's disease (pSD) for diagnosis, but the evolution of parenchymal lesions over time is unknown. The objective of this study was to assess the severity of ultrasound abnormalities in relation to pSD duration from the time of buccal dryness onset.METHODS: In this cross-sectional international multicentre study, patients with pSD according to the 2002 or 2016 ACR/EULAR classification criteria were included. Parenchymal abnormalities were classified according to the semiquantitative score as defined by OMERACT. Patients were separated into 4 groups (Group A: < 5 years, Group B: 5-9 years, Group C: 10-20 years, and Group D: > 20 years from the onset of buccal dryness). The association between disease duration groups and SGUS lesions was quantified in terms of odds ratios and 95% confidence intervals.RESULTS: A total of 247 patients were consecutively included between May 2019 and February 2022. Eighty-nine percent of patients had a focus score ≥1/4 mm2, and 85% had positive anti-Ro/SSA. pSD duration was associated with a pathological OMERACT score (score 2 or 3): OR for 5-year duration: 1.23 [95% CI 1.04; 1.47], p= 0.0383). Considering each US item, the only statistical association with pSD duration was found regarding the presence of hyperechoic bands (25% or more): OR for five-year duration 1.18 [95% CI 1.03; 1.36], p= 0.038), independent of an older age.CONCLUSION: pSD duration was associated with the presence of hyperechoic bands, but not with hypoechoic areas, suggesting a progressive fibro-adipose evolution.
U2 - 10.1093/rheumatology/keae690
DO - 10.1093/rheumatology/keae690
M3 - Article
C2 - 39700419
SN - 1462-0324
JO - Rheumatology
JF - Rheumatology
M1 - keae690
ER -