Carla Gaggiano , Mojca Zajc Avramovič , Antonio Vitale , Nina Emeršič , Jurgen Sota , Nataša Toplak , Stefano Gentileschi , Valeria Caggiano , Maria Tarsia , Gašper Markelj , Tina Vesel Tajnšek , Claudia Fabiani , Anja Koren Jeverica , Bruno Frediani , Maria Antonietta Mazzei , Luca Cantarini , Tadej Avčin
{"title":"脊柱关节炎患者的全身自身炎症表现。","authors":"Carla Gaggiano , Mojca Zajc Avramovič , Antonio Vitale , Nina Emeršič , Jurgen Sota , Nataša Toplak , Stefano Gentileschi , Valeria Caggiano , Maria Tarsia , Gašper Markelj , Tina Vesel Tajnšek , Claudia Fabiani , Anja Koren Jeverica , Bruno Frediani , Maria Antonietta Mazzei , Luca Cantarini , Tadej Avčin","doi":"10.1016/j.jbspin.2024.105772","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>(1) characterizing a group of spondyloarthritis (SpA) patients with systemic auto-inflammatory 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).</div></div><div><h3>Methods</h3><div>Retrospective observational study. Clinical data of adult and pediatric patients with S-SpA, SD or SpA were collected retrospectively and analyzed.</div></div><div><h3>Results</h3><div>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 (<em>P</em> <!-->=<!--> <!-->0.01) and uveitis less frequent (<em>P</em> <!--><<!--> <!-->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 (<em>P</em> <!--><<!--> <!-->0.05) and inflammation at the facet joints (<em>P</em> <!--><<!--> <!-->0.01), more interspinous enthesitis (<em>P</em> <!-->=<!--> <!-->0.01) and inter-apophyseal capsulitis (<em>P</em> <!--><<!--> <!-->0.01). Compared to SD, S-SpA patients had lower-grade fever (<em>P</em> <!--><<!--> <!-->0.01), less rash (<em>P</em> <!--><<!--> <!-->0.01) and weight loss (<em>P</em> <!--><<!--> <!-->0.05), but more pharyngitis (<em>P</em> <!--><<!--> <!-->0.01), gastrointestinal symptoms (<em>P</em> <!--><<!--> <!-->0.01) and chest pain (<em>P</em> <!--><<!--> <!-->0.05). ESR, CRP, WBC, ANC, LDH tested higher in SD (<em>P</em> <!--><<!--> <!-->0.01). Resolution of systemic symptoms was less frequent in S-SpA than SD on corticosteroid (<em>P</em> <!--><<!--> <!-->0.01) and methotrexate (<em>P</em> <!--><<!--> <!-->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]).</div></div><div><h3>Conclusions</h3><div>SpA should be actively investigated in patients with auto-inflammatory manifestations, including undifferentiated auto-inflammatory disease and SD.</div></div>","PeriodicalId":54902,"journal":{"name":"Joint Bone Spine","volume":"91 6","pages":"Article 105772"},"PeriodicalIF":3.8000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Systemic auto-inflammatory manifestations in patients with spondyloarthritis\",\"authors\":\"Carla Gaggiano , Mojca Zajc Avramovič , Antonio Vitale , Nina Emeršič , Jurgen Sota , Nataša Toplak , Stefano Gentileschi , Valeria Caggiano , Maria Tarsia , Gašper Markelj , Tina Vesel Tajnšek , Claudia Fabiani , Anja Koren Jeverica , Bruno Frediani , Maria Antonietta Mazzei , Luca Cantarini , Tadej Avčin\",\"doi\":\"10.1016/j.jbspin.2024.105772\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>(1) characterizing a group of spondyloarthritis (SpA) patients with systemic auto-inflammatory 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).</div></div><div><h3>Methods</h3><div>Retrospective observational study. Clinical data of adult and pediatric patients with S-SpA, SD or SpA were collected retrospectively and analyzed.</div></div><div><h3>Results</h3><div>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 (<em>P</em> <!-->=<!--> <!-->0.01) and uveitis less frequent (<em>P</em> <!--><<!--> <!-->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 (<em>P</em> <!--><<!--> <!-->0.05) and inflammation at the facet joints (<em>P</em> <!--><<!--> <!-->0.01), more interspinous enthesitis (<em>P</em> <!-->=<!--> <!-->0.01) and inter-apophyseal capsulitis (<em>P</em> <!--><<!--> <!-->0.01). Compared to SD, S-SpA patients had lower-grade fever (<em>P</em> <!--><<!--> <!-->0.01), less rash (<em>P</em> <!--><<!--> <!-->0.01) and weight loss (<em>P</em> <!--><<!--> <!-->0.05), but more pharyngitis (<em>P</em> <!--><<!--> <!-->0.01), gastrointestinal symptoms (<em>P</em> <!--><<!--> <!-->0.01) and chest pain (<em>P</em> <!--><<!--> <!-->0.05). ESR, CRP, WBC, ANC, LDH tested higher in SD (<em>P</em> <!--><<!--> <!-->0.01). Resolution of systemic symptoms was less frequent in S-SpA than SD on corticosteroid (<em>P</em> <!--><<!--> <!-->0.01) and methotrexate (<em>P</em> <!--><<!--> <!-->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]).</div></div><div><h3>Conclusions</h3><div>SpA should be actively investigated in patients with auto-inflammatory manifestations, including undifferentiated auto-inflammatory disease and SD.</div></div>\",\"PeriodicalId\":54902,\"journal\":{\"name\":\"Joint Bone Spine\",\"volume\":\"91 6\",\"pages\":\"Article 105772\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Joint Bone Spine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1297319X24000836\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Joint Bone Spine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1297319X24000836","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
Systemic auto-inflammatory manifestations in patients with spondyloarthritis
Objectives
(1) characterizing a group of spondyloarthritis (SpA) patients with systemic auto-inflammatory 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.
期刊介绍:
Bimonthly e-only international journal, Joint Bone Spine publishes in English original research articles and all the latest advances that deal with disorders affecting the joints, bones, and spine and, more generally, the entire field of rheumatology.
All submitted manuscripts to the journal are subjected to rigorous peer review by international experts: under no circumstances does the journal guarantee publication before the editorial board makes its final decision. (Surgical techniques and work focusing specifically on orthopedic surgery are not within the scope of the journal.)Joint Bone Spine is indexed in the main international databases and is accessible worldwide through the ScienceDirect and ClinicalKey platforms.