Clinical presentation and treatment response in patients with polymyalgia rheumatica and giant cell arteritis during a 40-week follow-up.

18F-fluorodeoxyglucose PET/CT Polymyalgia rheumatica giant cell arteritis temporal artery biopsy treatment response

Journal

Rheumatology advances in practice
ISSN: 2514-1775
Titre abrégé: Rheumatol Adv Pract
Pays: England
ID NLM: 101736676

Informations de publication

Date de publication:
2021
Historique:
received: 31 07 2021
accepted: 09 11 2021
entrez: 15 12 2021
pubmed: 16 12 2021
medline: 16 12 2021
Statut: epublish

Résumé

The aim was to study the clinical features of PMR/GCA and clinical predictors of treatment response during a 40-week follow-up period. Clinical data on 77 patients with newly diagnosed PMR/GCA who were treated with oral glucocorticoids were gathered at baseline and during a 40-week follow-up period. A unilateral temporal artery biopsy (TAB) and Of 77 patients [49 (63.6%) female; mean age 71.8 (8.0) years], 64 (83.1%) patients had pure PMR, 10 (13.0%) concomitant PMR and GCA, and 3 (3.9%) pure GCA. The patients reported that clinical symptoms, apart from scalp pain and duration of morning stiffness, improved significantly at week 4 and remained lower at week 40 compared with the relative frequencies at baseline. Besides, all components of physical examination showed significant improvement and remained lower at week 40 compared with the baseline. A complete response was seen in 68.7, 62.9, 44.1 and 33.3% of patients at weeks 4, 16, 28 and 40, respectively. Several clinical features, including female biological sex, younger age, fewer relapses and a lower level of baseline ESR, were significantly associated with a better treatment response. Treatment response during the follow-up period was independent of TAB results and fluorodeoxyglucose uptakes on Obtaining valid disease-specific outcome measures for evaluating treatment efficacy in PMR and GCA that can be applied universally is clearly an unmet clinical need. ClinicalTrials.gov, https://clinicaltrials.gov, NCT02985424.

Identifiants

pubmed: 34909566
doi: 10.1093/rap/rkab091
pii: rkab091
pmc: PMC8665449
doi:

Banques de données

ClinicalTrials.gov
['NCT02985424']

Types de publication

Journal Article

Langues

eng

Pagination

rkab091

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Amir Emamifar (A)

Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense.
Diagnostic Center.
Department of Rheumatology, Svendborg Hospital, OUH, Svendborg.
OPEN, Odense Patient data Explorative Network, Odense University Hospital, Odense.

Søren Hess (S)

Department of Radiology and Nuclear Medicine, Hospital of Southwest Jutland, Esbjerg.
Institute of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark.

Torkell Ellingsen (T)

Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark.

Oke Gerke (O)

Research Unit of Clinical Physiology and Nuclear Medicine, Department of Clinical Research, University of Southern Denmark.
Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.

Ziba Ahangarani Farahani (Z)

Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.

Per Syrak Hansen (P)

Diagnostic Center.

Inger Marie Jensen Hansen (IM)

Department of Rheumatology, Svendborg Hospital, OUH, Svendborg.

Peter Thye-Rønn (P)

Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense.
Diagnostic Center.

Classifications MeSH