Systemic auto-inflammatory manifestations in patients with spondyloarthritis

被引:1
|
作者
Gaggiano, Carla [1 ]
Avramovic, Mojca Zajc [2 ,3 ,4 ,5 ]
Vitale, Antonio [1 ]
Emersic, Nina [2 ,3 ,4 ,5 ]
Sota, Jurgen [1 ]
Toplak, Natasa [2 ,3 ,4 ,5 ]
Gentileschi, Stefano [1 ]
Caggiano, Valeria [1 ]
Tarsia, Maria [2 ,6 ]
Markelj, Gasper [2 ,3 ,4 ,5 ]
Tajnsek, Tina Vesel [2 ,3 ,4 ,5 ]
Fabiani, Claudia [2 ,7 ]
Jeverica, Anja Koren [2 ,3 ,4 ]
Frediani, Bruno [1 ]
Mazzei, Maria Antonietta [2 ,8 ]
Cantarini, Luca [1 ]
Avcin, Tadej [2 ,3 ,4 ,5 ]
机构
[1] Univ Siena, Dept Med Sci Surg & Neurosci, Rheumatol Unit, Viale Mario Bracci 16, I-53100 Siena, Italy
[2] Azienda Osped Univ Senese, Viale Mario Bracci 16, I-53100 Siena, Italy
[3] Univ Ljubljana, Univ Childrens Hosp, Dept Allergol Rheumatol & Clin Immunol, Bohoriceva Ul 20, Ljubljana 1000, Slovenia
[4] Univ Med Ctr Ljubljana, Bohoriceva Ul 20, Ljubljana 1000, Slovenia
[5] Univ Ljubljana, Fac Med, Dept Pediat, Bohoriceva Ul 20, Ljubljana 1000, Slovenia
[6] Univ Siena, Dept Mol Med & Dev, Clin Pediat, Viale Mario Bracci 16, I-53100 Siena, Italy
[7] Univ Siena, Dept Med Sci Surg & Neurosci, Ophthalmol Unit, Viale Mario Bracci 16, I-53100 Siena, Italy
[8] Univ Siena, Dept Med Sci Surg & Neurosci, Unit Diagnost Imaging, Viale Mario Bracci 16, I-53100 Siena, Italy
关键词
Spondyloarthritis; Febrile spondyloarthritis; Still's disease; Systemic juvenile idiopathic arthritis; Adult-onset Still's disease; Auto-inflammatory diseases; JUVENILE IDIOPATHIC ARTHRITIS; ANKYLOSING-SPONDYLITIS; CLASSIFICATION CRITERIA;
D O I
10.1016/j.jbspin.2024.105772
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. - (1) characterizing a group of spondyloarthritis (SpA) patients with systemic autoinflammatory symptoms (S-SpA); (2) comparing SpA features with and without auto-inflammatory symptoms; (3) comparing the auto-inflammatory features of S-SpA and Still's disease (SD). Methods. - Retrospective observational study. Clinical data of adult and pediatric patients with S-SpA, SD or SpA were collected retrospectively and analyzed. Results. - Forty-one subjects with S-SpA, 39 with SD and 42 with SpA were enrolled. The median latency between systemic and articular manifestations in S-SpA was 4.4 (IQR: 7.2) years. S-SpA and SpA had similar frequency of peripheral arthritis and enthesitis (N.S.), while tenosynovitis was more frequent (P = 0.01) and uveitis less frequent (P < 0.01) in S-SpA. MRI showed signs of sacroiliac inflammation and damage in both S-SpA and SpA equally (N.S.). S-SpA patients had less corner inflammatory lesions (P < 0.05) and inflammation at the facet joints (P < 0.01), more interspinous enthesitis (P = 0.01) and inter-apophyseal capsulitis (P < 0.01). Compared to SD, S-SpA patients had lower-grade fever (P < 0.01), less rash (P < 0.01) and weight loss (P < 0.05), but more pharyngitis (P < 0.01), gastrointestinal symptoms (P < 0.01) and chest pain (P < 0.05). ESR, CRP, WBC, ANC, LDH tested higher in SD (P < 0.01). Resolution of systemic symptoms was less frequent in S-SpA than SD on corticosteroid (P < 0.01) and methotrexate (P < 0.05) treatment. When considering all SD patients, a complete response to corticosteroids in the systemic phase significantly reduced the likelihood of developing SpA (OR = 0.06, coefficient -2.87 [CI: -5.0 to -0.8]). Conclusions. - SpA should be actively investigated in patients with auto-inflammatory manifestations, including undifferentiated auto-inflammatory disease and SD (c) 2024 Les Auteurs. Publie<acute accent> par Elsevier Masson SAS au nom de Soci o<acute accent>t o<acute accent> Fran o<acute accent>aise de Rhumatologie. Cet article est publie<acute accent> en Open Access sous licence CC BY (http://creativecommons.org/licenses/by/4.0/).
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页数:10
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