Ultrasound to identify systemic lupus erythematosus patients with musculoskeletal symptoms who respond best to therapy: the US Evaluation For mUsculoskeletal Lupus longitudinal multicentre study
Ultrasound to identify systemic lupus erythematosus patients with musculoskeletal symptoms who respond best to therapy: the US Evaluation For mUsculoskeletal Lupus longitudinal multicentre study
Objectives
To determine whether SLE patients with inflammatory joint symptoms and US synovitis/tenosyovitis achieve better clinical responses to glucocorticoids compared with patients with normal scans. Secondary objectives included identification of clinical features predicting US synovitis/tenosynovitis.
Methods
In a longitudinal multicentre study, SLE patients with physician-diagnosed inflammatory joint pain received intramuscular methylprednisolone 120 mg once. Clinical assessments, patient-reported outcomes and bilateral hand/wrist USs were collected at 0, 2 and 6 weeks. The primary outcome (determined via internal pilot) was the early morning stiffness visual analogue scale (EMS-VAS) at 2 weeks, adjusted for baseline, comparing patients with positive (greyscale ≥2 and/or power Doppler ≥1) and negative US. Post hoc analyses excluded FM.
Results
Of 133 patients, 78 had a positive US. Only 53 (68%) of these had one or more swollen joint. Of 66 patients with one or more swollen joint, 20% had a negative US. A positive US was associated with joint swelling, symmetrical small joint distribution and serology. The primary endpoint was not met: in the full analysis set (N = 133) there was no difference in baseline-adjusted EMS-VAS at week 2 [−7.7 mm (95% CI −19.0, 3.5); P = 0.178]. After excluding 32 patients with FM, response was significantly better in patients with a positive US at baseline [baseline-adjusted EMS-VAS at 2 weeks −12.1 mm (95% CI −22.2, −0.1); P = 0.049]. This difference was greater when adjusted for treatment [−12.8 mm (95% CI −22, −3); P = 0.007]. BILAG and SLEDAI responses were higher in US-positive patients.
Conclusion
In SLE patients without FM, those with a positive US had a better clinical response to therapy. Imaging-detected synovitis/tenosynovitis may be considered to decide on therapy and enrich clinical trials.
biomarkers, clinical trials and methods, outcome measures, systemic lupus erythematosus, ultrasound
5194-5204
Mahmoud, Khaled
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Zayat, Ahmed S.
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Yusof, Md Yuzaiful Md
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Dutton, Katherine
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Teh, Lee Suan
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Yee, Chee-Seng
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D’cruz, David
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Ng, Nora
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Isenberg, David
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Ciurtin, Coziana
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Conaghan, Philip G.
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Emery, Paul
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Edwards, Christopher J.
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Hensor, Elizabeth M.A.
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Vital, Edward M.
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3 November 2021
Mahmoud, Khaled
985cb3ed-91d7-45ff-99cf-6458e664b897
Zayat, Ahmed S.
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Yusof, Md Yuzaiful Md
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Dutton, Katherine
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Teh, Lee Suan
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Yee, Chee-Seng
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D’cruz, David
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Ng, Nora
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Isenberg, David
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Ciurtin, Coziana
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Conaghan, Philip G.
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Emery, Paul
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Edwards, Christopher J.
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Hensor, Elizabeth M.A.
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Vital, Edward M.
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Mahmoud, Khaled, Zayat, Ahmed S., Yusof, Md Yuzaiful Md, Dutton, Katherine, Teh, Lee Suan, Yee, Chee-Seng, D’cruz, David, Ng, Nora, Isenberg, David, Ciurtin, Coziana, Conaghan, Philip G., Emery, Paul, Edwards, Christopher J., Hensor, Elizabeth M.A. and Vital, Edward M.
(2021)
Ultrasound to identify systemic lupus erythematosus patients with musculoskeletal symptoms who respond best to therapy: the US Evaluation For mUsculoskeletal Lupus longitudinal multicentre study.
Rheumatology, 60 (11), .
(doi:10.1093/rheumatology/keab288).
Abstract
Objectives
To determine whether SLE patients with inflammatory joint symptoms and US synovitis/tenosyovitis achieve better clinical responses to glucocorticoids compared with patients with normal scans. Secondary objectives included identification of clinical features predicting US synovitis/tenosynovitis.
Methods
In a longitudinal multicentre study, SLE patients with physician-diagnosed inflammatory joint pain received intramuscular methylprednisolone 120 mg once. Clinical assessments, patient-reported outcomes and bilateral hand/wrist USs were collected at 0, 2 and 6 weeks. The primary outcome (determined via internal pilot) was the early morning stiffness visual analogue scale (EMS-VAS) at 2 weeks, adjusted for baseline, comparing patients with positive (greyscale ≥2 and/or power Doppler ≥1) and negative US. Post hoc analyses excluded FM.
Results
Of 133 patients, 78 had a positive US. Only 53 (68%) of these had one or more swollen joint. Of 66 patients with one or more swollen joint, 20% had a negative US. A positive US was associated with joint swelling, symmetrical small joint distribution and serology. The primary endpoint was not met: in the full analysis set (N = 133) there was no difference in baseline-adjusted EMS-VAS at week 2 [−7.7 mm (95% CI −19.0, 3.5); P = 0.178]. After excluding 32 patients with FM, response was significantly better in patients with a positive US at baseline [baseline-adjusted EMS-VAS at 2 weeks −12.1 mm (95% CI −22.2, −0.1); P = 0.049]. This difference was greater when adjusted for treatment [−12.8 mm (95% CI −22, −3); P = 0.007]. BILAG and SLEDAI responses were higher in US-positive patients.
Conclusion
In SLE patients without FM, those with a positive US had a better clinical response to therapy. Imaging-detected synovitis/tenosynovitis may be considered to decide on therapy and enrich clinical trials.
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More information
Accepted/In Press date: 16 March 2021
e-pub ahead of print date: 1 April 2021
Published date: 3 November 2021
Additional Information:
Publisher Copyright:
© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology.
Keywords:
biomarkers, clinical trials and methods, outcome measures, systemic lupus erythematosus, ultrasound
Identifiers
Local EPrints ID: 450364
URI: http://eprints.soton.ac.uk/id/eprint/450364
ISSN: 1462-0324
PURE UUID: b18365bd-5ce0-455d-8d73-87e819b8361c
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Date deposited: 26 Jul 2021 16:31
Last modified: 16 Mar 2024 13:09
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Contributors
Author:
Khaled Mahmoud
Author:
Ahmed S. Zayat
Author:
Md Yuzaiful Md Yusof
Author:
Katherine Dutton
Author:
Lee Suan Teh
Author:
Chee-Seng Yee
Author:
David D’cruz
Author:
Nora Ng
Author:
David Isenberg
Author:
Coziana Ciurtin
Author:
Philip G. Conaghan
Author:
Paul Emery
Author:
Elizabeth M.A. Hensor
Author:
Edward M. Vital
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