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Discriminative power of salivary gland ultrasound in relation to symptom-based endotypes in suspected and definite primary Sjogren's Syndrome
被引:5
|作者:
Deroo, Liselotte
[1
,2
,3
]
Achten, Helena
[1
,2
,3
]
De Boeck, Kristel
[1
,3
]
Genbrugge, Eva
[4
]
Bauters, Wouter
[4
]
Roels, Dimitri
[5
]
Dochy, Frederick
[6
]
Creytens, David
[7
,8
]
De Craemer, Ann-Sophie
[1
,2
,3
]
Van den Bosch, Filip
[1
,2
,3
]
Elewaut, Dirk
[1
,2
,3
]
Peene, Isabelle
[1
,3
,9
]
机构:
[1] Ghent Univ Hosp, Dept Internal Med & Pediat, Dept Rheumatol, C Heymanslaan 10, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Internal Med & Pediat, Fac Med & Hlth Sci, Sint Pietersnieuwstr 25, B-9000 Ghent, Belgium
[3] VIB UGent, Inflammat Res Ctr, Rijvisschestr 71, B-9052 Zwijnaarde, Belgium
[4] Ghent Univ Hosp, Dept Radiol, C Heymanslaan 10, B-9000 Ghent, Belgium
[5] Ghent Univ Hosp, Dept Ophthalmol, C Heymanslaan 10, B-9000 Ghent, Belgium
[6] Ghent Univ Hosp, Dept Head & Neck Surg, C Heymanslaan 10, B-9000 Ghent, Belgium
[7] Ghent Univ Hosp, Dept Pathol, C Heymanslaan 10, B-9000 Ghent, Belgium
[8] Univ Ghent, Dept Diagnost Sci, Fac Med & Hlth Sci, Sint Pietersnieuwstr 25, B-9000 Ghent, Belgium
[9] Acad Hosp St Jan, Dept Rheurnatol, Ruddershove 10, B-8000 Brugge, Belgium
关键词:
Primary Sjogren's Syndrome;
Biomarkers;
Ultrasonography;
Diagnostic imaging;
CONSENSUS;
ONSET;
D O I:
10.1016/j.semarthrit.2022.152075
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives: Salivary gland ultrasound (SGUS) is emerging as essential tool in primary Sjogren's Syndrome (pSS), but its link to symptom-based endotypes is unknown. Therefore, we explored SGUS outcomes in relation to endotypes in patients with definite and suspected pSS. Methods: Definite pSS patients (n = 171) fulfilling the 2016 ACR/EULAR classification criteria, and suspected pSS patients (n = 119), positive for at least one criterion, were included in the Belgian Sjogren's Syndrome Transition Trial (BeSSTT). Stratification into endotypes according to the Newcastle Sjogren's Stratification Tool resulted in low symptom burden (LSB), pain dominant with fatigue (PDF), dryness dominant with fatigue (DDF) and high symptom burden (HSB). SGUS was assessed with Hocevar score (0-48). The dataset was randomly divided into a discovery (n = 203) and replication (n = 87) cohort. Results: SGUS had strong discriminative power for pSS classification (AUC=0.74), especially in DDF (AUC=0.89). In definite pSS, Hocevar scores in DDF were high compared to other endotypes (38 (20-44) versus 18 (9-33); p < 0.001). Patients with highest SGUS-scores showed more sicca and laboratory abnormalities. Moreover, a subset of young, anti-SSA/Ro positive patients not fulfilling classification criteria showed clear SGUS abnormalities. Replication showed similar results. Conclusions: SGUS-scores were significantly higher in definite pSS with DDF endotype, providing the first evidence of imaging abnormalities in salivary glands matching distinct biological profiles ascribed to pSS endotypes. Additionally, a subset of patients with potential early disease was detected based on presence of anti-SSA antibodies and high SGUS-scores. These results underscore the role of SGUS as powerful tool both in pSS classification and stratification.
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