Publication:
Monitoring Achilles enthesitis in ankylosing spondylitis during TNF-alpha antagonist therapy: an ultrasound study

dc.contributor.authorDİRESKENELİ, RAFİ HANER
dc.contributor.authorsAydin, Sibel Zehra; Karadag, Omer; Filippucci, Emilio; Atagunduz, Pamir; Akdogan, Ali; Kalyoncu, Umut; Grassi, Walter; Direskeneli, Haner
dc.date.accessioned2022-03-14T10:05:28Z
dc.date.accessioned2026-01-10T18:09:41Z
dc.date.available2022-03-14T10:05:28Z
dc.date.issued2010-03-01
dc.description.abstractObjective. Enthesitis is considered as the primary anatomical lesion in ankylosing spondylitis (AS). Therapeutic effects of TNF-alpha antagonist treatments for enthesitis on imaging changes are still limited to case reports or small sample-sized trials. We aimed to investigate the potential of ultrasonography (US) to detect early changes after TNF-alpha antagonist therapy of Achilles enthesis of AS patients. Methods. Forty-three AS patients with active disease, requiring TNF-alpha antagonist therapy, were included. Physical examination was performed to detect Achilles enthesitis and/or retrocalcaneal bursitis. US of the Achilles tendon was performed bilaterally. Grey-scale (GS) and power Doppler (PD) scores on a 0-2 semi-quantitative scale and total additive scores (TS) were calculated. Follow-up US examinations were performed 2 months after the initiation of therapy. Results. At baseline, 11 patients (26.2%) were symptomatic in physical examination for either Achilles enthesitis or retrocalcaneal bursitis, whereas 36 (83%) had GS US pathological findings and 10 (23.3%) had PD signal. GS score and TS decreased significantly [3.6 (3.0) vs 2.3 (2.2), P < 0.001 and 4.7 (4.9) vs 2.7 (3.3), P < 0.001, respectively], whereas the decrease in PD score was not significant after 2 months of follow-up. The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), ESR and CRP levels also showed significant improvements. Conclusions. Subclinical Achilles enthesitis, detected only with GS US, is present in a subset of AS patients and a significant improvement can be demonstrated after 2 months of TNF-alpha antagonist therapy. In addition to standard outcome measures, US might be an additional useful tool to monitor therapy in SpA patients with Achilles enthesitis.
dc.identifier.doi10.1093/rheumatology/kep410
dc.identifier.issn1462-0324
dc.identifier.pubmed20040527
dc.identifier.urihttps://hdl.handle.net/11424/244028
dc.identifier.wosWOS:000274487000024
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS
dc.relation.ispartofRHEUMATOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectUltrasonography
dc.subjectEnthesitis
dc.subjectAchilles tendon
dc.subjectAnkylosing spondylitis
dc.subjectTNF-alpha antagonist therapy
dc.subjectPOWER DOPPLER SONOGRAPHY
dc.subjectRHEUMATOID-ARTHRITIS
dc.subjectMUSCULOSKELETAL ULTRASOUND
dc.subjectCLINICAL MEASUREMENT
dc.subjectLOWER-LIMB
dc.subjectSPONDYLARTHROPATHY
dc.subjectULTRASONOGRAPHY
dc.subjectSPONDYLOARTHROPATHY
dc.subjectABNORMALITIES
dc.subjectENTHESOPATHY
dc.titleMonitoring Achilles enthesitis in ankylosing spondylitis during TNF-alpha antagonist therapy: an ultrasound study
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage582
oaire.citation.issue3
oaire.citation.startPage578
oaire.citation.titleRHEUMATOLOGY
oaire.citation.volume49

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