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Sex differences in patient-reported outcomes and the association with clinical factors in axial spondyloarthritis patients treated with tumour necrosis factor inhibitors.
Hellamand, Pasoon; van de Sande, Marleen G H; Nurmohamed, Michael T; van Vollenhoven, Ronald F; Hollick, Rosemary J; Rotariu, Ovidiu; Rotar, Ziga; Pirkmajer, Katja P; Nordström, Dan; Hokkanen, Anna-Mari; Michelsen, Brigitte; Kvien, Tore K; Glintborg, Bente; Hetland, Merete L; Østergaard, Mikkel; Loft, Anne G; Pavelka, Karel; Zavada, Jakub; Castrejon, Isabel; Otero-Varela, Lucia; Gudbjornsson, Bjorn; Palsson, Olafur; Olofsson, Tor; Wallman, Johan K; Ciurea, Adrian; Nissen, Michael J; Yildirim, Tuba D; Onen, Fatos; Codreanu, Catalin; Mogosan, Corina; Santos, Maria J; Vieira-Sousa, Elsa; Iannone, Florenzo; Frediani, Bruno; Ørnbjerg, Lykke M; Twisk, Jos W R; van der Horst-Bruinsma, Irene E.
Afiliação
  • Hellamand P; Department of Clinical Immunology and Rheumatology, Amsterdam UMC, location AMC, Free University of Amsterdam, Netherlands, Amsterdam.
  • van de Sande MGH; Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands.
  • Nurmohamed MT; Department of Clinical Immunology and Rheumatology, UMC, location AMC, University of Amsterdam, Netherlands, Amsterdam, Amsterdam.
  • van Vollenhoven RF; Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands.
  • Hollick RJ; Amsterdam Rheumatology and Immunology Center (ARC), Reade and Amsterdam UMC, Amsterdam, Netherlands.
  • Rotariu O; Department of Clinical Immunology and Rheumatology, Amsterdam UMC, location AMC, Netherlands, Amsterdam.
  • Rotar Z; Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands.
  • Pirkmajer KP; Aberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, United Kingdom.
  • Nordström D; Aberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, United Kingdom.
  • Hokkanen AM; Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Michelsen B; Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Kvien TK; Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Glintborg B; Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Hetland ML; Departments of Medicine and Rheumatology, Helsinki University Hospital, Helsinki, Finland.
  • Østergaard M; Department of Medicine, Helsinki University and Helsinki University Hospital, Helsinki, Finland.
  • Loft AG; Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
  • Pavelka K; Research Unit, Sørlandet Hospital, Kristiansand, Norway.
  • Zavada J; Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Castrejon I; Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
  • Otero-Varela L; DANBIO and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Gudbjornsson B; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Palsson O; DANBIO and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Olofsson T; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Wallman JK; Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Ciurea A; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Nissen MJ; DANBIO and Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark.
  • Yildirim TD; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Onen F; Institute of Rheumatology, Prague, Czech Republic.
  • Codreanu C; Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Mogosan C; Institute of Rheumatology, Prague, Czech Republic.
  • Santos MJ; Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Vieira-Sousa E; Department of Rheumatology, Hospital General, Universitario Gregorio Marañón, Madrid, Spain.
  • Iannone F; Faculty of Medicine, Complutense University of Madrid, Madrid, Spain.
  • Frediani B; Research Unit, Spanish Society of Rheumatology, Madrid, Spain.
  • Ørnbjerg LM; Centre for Rheumatology Research, Landspitali University Hospital, Reykjavik, Iceland.
  • Twisk JWR; Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
  • van der Horst-Bruinsma IE; Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Article em En | MEDLINE | ID: mdl-39041780
ABSTRACT

OBJECTIVES:

To investigate sex differences in patient-reported outcome measures (PROMs) among axSpA patients initiating their first TNFi and identify factors contributing to these disparities over the follow-up.

METHODS:

Data were included from 15 EuroSpA registries and consisted of axSpA patients initiating their first TNFi, with ≥2 measurements for each analysed PROM (BASDAI and BASFI, scale 0-100) taken at any time point. Linear mixed models were employed to analyse sex differences in PROMs over 24 months and to evaluate how baseline characteristics were related to the observed sex differences.

RESULTS:

We analysed 13 102 (38% women) in the BASDAI analyses and 10 623 (38% women) in the BASFI analyses. At follow-up, mean sex differences in BASDAI increased from 4.3 units at baseline (95% CI, 3.5-5.1)-8.0 (7.2-8.8) at 6 months, and in BASFI from 2.2 (1.4-3.1)-4.6 (3.6-5.5), with consistently worse scores in women. Baseline characteristics could not substantially account for the observed sex differences over time; however, the magnitude of the sex differences was reduced by HLA-B27 positivity, longer disease duration, and increased CRP levels, but increased by TNFi initiation in later years and peripheral arthritis.

CONCLUSION:

In axSpA patients initiating their first TNFi, baseline sex differences in BASDAI and BASFI increased two-fold after 6 months of treatment and persisted thereafter, with worse scores in women. Several baseline characteristics moderated the sex differences, though none could fully account for them. These findings improve our understanding of sex differences and underscore their importance in axSpA.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article