Your browser doesn't support javascript.
loading
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.
  • 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.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article