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Impact of conventional and biological disease-modifying anti-rheumatic drugs on arterial lesions in Takayasu arteritis.
Bletry, Diego; Meyblum, Louis; Desseaux, Kristell; Vautier, Mathieu; Chiche, Laurent; Le Joncour, Alexandre; Redheuil, Alban; Roux, Charles; Cacoub, Patrice; Gaudric, Julien; Biard, Lucie; Saadoun, David.
Afiliación
  • Bletry D; Sorbonne Universités, Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Centre de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire (CEREMAIA), F-75013, Paris, France; INSERM, UMR_S 959, F-75013, AP-HP, Gr
  • Meyblum L; Department of interventional radiology, Sorbonne Universités, Pitié-Salpêtrière University Hospital, Paris, France, Paris, France.
  • Desseaux K; Department of Biostatistics and Medical Information, AP-HP Saint-Louis University Hospital, ECSTRRA Team, CRESS UMR 1153, INSERM, University of Paris, Paris, France.
  • Vautier M; Sorbonne Universités, Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Centre de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire (CEREMAIA), F-75013, Paris, France; INSERM, UMR_S 959, F-75013, AP-HP, Gr
  • Chiche L; Department of vascular surgery, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, F-75005, France.
  • Le Joncour A; Sorbonne Universités, Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Centre de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire (CEREMAIA), F-75013, Paris, France; INSERM, UMR_S 959, F-75013, AP-HP, Gr
  • Redheuil A; Department of cardiovascular imaging, Sorbonne Universités, Pitié-Salpêtrière University Hospital, Paris, France, Paris, France.
  • Roux C; Department of interventional radiology, Sorbonne Universités, Pitié-Salpêtrière University Hospital, Paris, France, Paris, France.
  • Cacoub P; Sorbonne Universités, Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Centre de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire (CEREMAIA), F-75013, Paris, France; INSERM, UMR_S 959, F-75013, AP-HP, Gr
  • Gaudric J; Department of vascular surgery, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, F-75005, France.
  • Biard L; Department of Biostatistics and Medical Information, AP-HP Saint-Louis University Hospital, ECSTRRA Team, CRESS UMR 1153, INSERM, University of Paris, Paris, France.
  • Saadoun D; Sorbonne Universités, Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Centre de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire (CEREMAIA), F-75013, Paris, France; INSERM, UMR_S 959, F-75013, AP-HP, Gr
Article en En | MEDLINE | ID: mdl-38970381
ABSTRACT

BACKGROUND:

The definition of Takayasu arteritis (TAK) remission and disease activity is still unclear. Vascular imaging is an essential tool for following-up patients. Herein, we aimed to compare the evolution of vascular lesions (ie vessel wall thickening and stenosis) under conventional disease-modifying anti-rheumatic drugs (cDMARDs) relatively to biological DMARDs (bDMARDs) in TAK patients followed with the same CT angiography modalities.

METHOD:

We compared 75 lines of therapy in TAK patients who received cDMARDs (n = 40 lines) and bDMARDs (n = 35 lines) using CT angiography. We established 1-3 main target vessels with vessel wall thickening and/or stenosis. Every targeted vessel had its thickness and its lumen diameter measured at the initiation of immunosuppressive treatment and at 12 months.

RESULTS:

We observed an overall reduction of arterial wall thickness in 73% of cases and 31% had >25% of wall thickness relative decrease. Using a linear mixed effects model, first line immunosuppressive therapy (p= 0.012) and bDMARDs relatively to cDMARDs (p= 0.026) were independently associated with vessel wall thickness reduction in TAK. Thirty-eight percent of the stenotic vessels had a > 25% relative increase in lumen diameter under immunosuppressive therapy. The relative increase >25% in lumen diameter was noted in 56% vs 17% with bDMARDs compared with cDMARDs.

CONCLUSION:

Immunosuppressive treatments can reduce arterial wall thickness and widen lumen diameter in TAK. bDMARDs seems to be more effective than cDMARDs to improve arterial lesions in TAK.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article