Impact of conventional and biological disease-modifying anti-rheumatic drugs on arterial lesions in Takayasu arteritis

被引:1
|
作者
Bletry, Diego [1 ,2 ]
Meyblum, Louis [3 ]
Desseaux, Kristell [4 ]
Vautier, Mathieu [1 ,2 ]
Chiche, Laurent [5 ]
Le Joncour, Alexandre [1 ,2 ]
Redheuil, Alban [6 ]
Roux, Charles [3 ]
Cacoub, Patrice [1 ,2 ]
Gaudric, Julien [5 ]
Biard, Lucie [4 ]
Saadoun, David [1 ,2 ]
机构
[1] Sorbonne Univ, Ctr Reference Malad Autoimmunes Syst Rares, Ctr Reference Malad Autoinflammatoires & Amylose i, Dept Internal Med & Clin Immunol, Paris, France
[2] Grp Hosp Pitie Salpetriere, AP HP, INSERM, UMR S 959, Paris, France
[3] Sorbonne Univ, Pitie Salpetriere Univ Hosp, Dept Intervent Radiol, Paris, France
[4] Univ Paris, AP HP, St Louis Univ Hosp, Dept Biostat & Med Informat,ECSTRRA Team,CRESS UMR, Paris, France
[5] Grp Hosp Pitie Salpetriere, AP HP, Dept Vasc Surg, Paris, France
[6] Sorbonne Univ, Pitie Salpetriere Univ Hosp, Dept Cardiovasc Imaging, Paris, France
关键词
Takayasu arteritis; vasculitis; biotherapies; imaging; vascular lesions; THERAPY; PROGNOSIS; CRITERIA; CT;
D O I
10.1093/rheumatology/keae331
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 (i.e. vessel wall thickening and stenosis) under conventional 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 in arterial wall thickness in 73% of cases and 31% had >25% relative decrease in the wall thickness. 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 seem to be more effective than cDMARDs to improve arterial lesions in TAK.
引用
收藏
页数:7
相关论文
共 50 条
  • [1] EFFICACY AND SAFETY OF DISEASE-MODIFYING ANTI-RHEUMATIC DRUGS IN THE TREATMENT OF TAKAYASU ARTERITIS
    Huang, Q.
    Wu, Y.
    Zhou, B.
    Cui, Q.
    Xie, F.
    ANNALS OF THE RHEUMATIC DISEASES, 2024, 83
  • [2] GUIDELINE ON CONVENTIONAL DISEASE-MODIFYING ANTI-RHEUMATIC DRUGS
    Galloway, James
    RHEUMATOLOGY, 2016, 55 : 14 - 14
  • [3] Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
    Durga Prasanna Misra
    Upendra Rathore
    Pallavi Patro
    Vikas Agarwal
    Aman Sharma
    Clinical Rheumatology, 2021, 40 : 4391 - 4416
  • [4] An update on the use of conventional and biological disease-modifying anti-rheumatic drugs in hand osteoarthritis
    Tenti, Sara
    Bruyere, Olivier
    Cheleschi, Sara
    Reginster, Jean-Yves
    Veronese, Nicola
    Fioravanti, Antonella
    THERAPEUTIC ADVANCES IN MUSCULOSKELETAL DISEASE, 2023, 15
  • [5] Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis-a systematic review and meta-analysis
    Misra, Durga Prasanna
    Rathore, Upendra
    Patro, Pallavi
    Agarwal, Vikas
    Sharma, Aman
    CLINICAL RHEUMATOLOGY, 2021, 40 (11) : 4391 - 4416
  • [6] The use of conventional disease-modifying anti-rheumatic drugs in established RA
    Jurgens, M. S.
    Jacobs, J. W. G.
    Bijlsma, J. W. J.
    BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2011, 25 (04): : 523 - 533
  • [7] Pharmacogenetics of disease-modifying anti-rheumatic drugs
    Tanaka, E
    Taniguchi, A
    Urano, W
    Yamanaka, H
    Kamatani, N
    BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2004, 18 (02): : 233 - 247
  • [8] Disease-modifying anti-rheumatic drugs - Cyclosporin
    Chaudhuri, K
    Torley, H
    Madhok, R
    BRITISH JOURNAL OF RHEUMATOLOGY, 1997, 36 (09): : 1016 - 1021
  • [9] Conventional, biological disease-modifying anti-rheumatic drugs and Janus kinase inhibitors and varicella zoster virus
    Atzeni, Fabiola
    Gozza, Francesco
    Riva, Agostino
    Alciati, Alessandra
    Galloway, James
    EXPERT OPINION ON PHARMACOTHERAPY, 2023, 24 (06) : 679 - 689
  • [10] THE EFFECT OF BIOLOGICAL AND CONVENTIONAL DISEASE-MODIFYING ANTI-RHEUMATIC DRUGS ON FATIGUE IN FIBROMYALGIC RHEUMATOID ARTHRITIS PATIENTS
    Hizmetli, S.
    Durmaz, Y.
    Kaptanoglu, E.
    Cengiz, A. K.
    Peksen, H.
    ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 : 864 - 864