Immunosuppressive therapy for Vogt-Koyanagi-Harada disease: a retrospective study and review of literature

被引:5
|
作者
Rahman, Najiha [1 ]
Artiaga, Jose Carlo M. [1 ]
Bouras, Konstantinos [1 ]
Luis, Joshua [2 ]
Rees, Angela [1 ]
Westcott, Mark [1 ,3 ]
机构
[1] Moorfields Eye Hosp, Uveitis Serv, 162 City Rd, London EC1V 2PD, England
[2] Univ Coll London UCL, Inst Ophthalmol, London, England
[3] Queen Mary Univ London, William Harvey Res Inst, London, England
关键词
Uveitis; Vogt-Koyanagi-Harada; Immunosuppressive; Treatment; Mycophenolate mofetil; Adalimumab; Azathioprine; Ciclosporin; MYCOPHENOLATE-MOFETIL; INFLIXIMAB THERAPY; IMMUNOMODULATORY THERAPY; SYSTEMIC CORTICOSTEROIDS; CLINICAL-TRIAL; UVEITIS; EFFICACY; ADALIMUMAB; MANAGEMENT; RITUXIMAB;
D O I
10.1186/s12348-023-00333-6
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
BackgroundVogt-Koyanagi-Harada (VKH) disease is an idiopathic autoimmune disease which targets melanin-containing tissues such as the uvea, meninges, ear and skin. This typically presents in the eye with acute findings of granulomatous anterior uveitis, diffuse choroidal thickening, multiple focal areas of sub-retinal fluid and, in severe cases, optic nerve involvement with bullous serous retinal detachment can occur.Early initiation of treatment has been advocated to prevent progression to the chronic stage of the disease, which can result to a sunset glow fundus with devastatingly poor visual outcome. Treatment is usually initiated with corticosteroids followed by an early introduction of immunosuppressive treatment (IMT) to achieve immediate response after disease presentation, although the choice of IMT for VKH can vary.Main FindingsWe conducted a retrospective case-series to investigate the management trend of treating VKH over a 20-year period. Twenty-six patients were included and we found a shift from steroid monotherapy to combined IMT/low-dose steroid for the management of acute initial-onset of VKH in the last 10 years. Our average time from diagnosis to initiation of IMT was 2.1 months. 81% (21 of 26 patients) of our patients treated with combined IMT/steroid were able to achieve disease stability with significant good visual outcome at 24 months (Median VA(pre-IMT) = 0.3 Logmar vs VA(post-IMT) = 0.0 Logmar, p = 0.0001). MMF monotherapy was the most common IMT used and it was well-tolerated by our patients. Even so, 50% of our patients who were treated with MMF did not achieve disease control.We then performed a literature review to identify any IMT which could be superior in the treatment of VKH. We also share our experience (where applicable) on the various treatment options found from the literature review.Short conclusionOur study found that patients with VKH who were treated with combined IMT/low-dose steroids achieved significantly better visual improvement at 24 months compared to steroid monotherapy. We frequently chose MMF and this appears to be well tolerated by our patients. Since its introduction, anti-TNF agents are increasingly becoming a popular choice of treatment for VKH as these have been shown to be safe and effective. However, more data is required to provide evidence that anti-TNF agents can be used as first-line treatment and as monotherapy.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Immunosuppressive therapy for Vogt-Koyanagi-Harada disease: a retrospective study and review of literature
    Najiha Rahman
    Jose Carlo M Artiaga
    Konstantinos Bouras
    Joshua Luis
    Angela Rees
    Mark Westcott
    Journal of Ophthalmic Inflammation and Infection, 13
  • [2] Vogt-Koyanagi-Harada disease: a retrospective and multicentric study of 41 patients
    Diallo, K.
    Revuz, S.
    Clavel-Refregiers, G.
    Sene, T.
    Titah, C.
    Gerfaud-Valentin, M.
    Seve, P.
    Jaussaud, R.
    BMC OPHTHALMOLOGY, 2020, 20 (01)
  • [3] Adalimumab in Vogt-Koyanagi-Harada Disease Refractory to Conventional Therapy
    Yang, Shizhao
    Tao, Tianyu
    Huang, Zhaohao
    Liu, Xiuxing
    Li, He
    Xie, Lihui
    Wen, Feng
    Chi, Wei
    Su, Wenru
    FRONTIERS IN MEDICINE, 2022, 8
  • [4] Vogt-Koyanagi-Harada disease
    O'Keefe, Ghazala A. Datoo
    Rao, Narsing A.
    SURVEY OF OPHTHALMOLOGY, 2017, 62 (01) : 1 - 25
  • [5] Vogt-Koyanagi-Harada disease in Spain
    Arriola-Villalobos, Pedro
    Moll-Udina, Aina
    Carrasco-Lopez-Brea, Mario
    Sacristan, Cristina
    Jose Capella, Maria
    Peiteado, Diana
    Garrote-Llorden, Ana
    Albert Fort, Mara
    Jodar Marquez, Margarita
    Gonzalez Guijarro, Juan Jacobo
    Demetrio-Pablo, Rosalia
    Sanchez Sevilla, Juan Luis
    Carreno, Ester
    Gonzalez-Lopez, Julio
    Miguel-Escuder, Lucia
    Cuadros, Carlos
    Diaz-Valle, David
    Adan, Alfredo
    Benitez del Castillo, Jose M.
    Fonollosa, Alejandro
    Cordero, Miguel
    Martinez Costa, Lucia
    Blanco-Alonso, Ricardo
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2022, 32 (03) : 1547 - 1554
  • [6] Vogt-Koyanagi-Harada disease
    Joye, Ashlin
    Suhler, Eric
    CURRENT OPINION IN OPHTHALMOLOGY, 2021, 32 (06) : 574 - 582
  • [7] Vogt-Koyanagi-Harada Disease
    Cunningham, Emmett T., Jr.
    Rathinam, Sivakumar R.
    Tugal-Tutkun, Ilknur
    Muccioli, Cristina
    Zierhut, Manfred
    OCULAR IMMUNOLOGY AND INFLAMMATION, 2014, 22 (04) : 249 - 252
  • [8] Vogt-Koyanagi-Harada disease: a retrospective and multicentric study of 41 patients
    K. Diallo
    S. Revuz
    G. Clavel-Refregiers
    T. Sené
    C. Titah
    M. Gerfaud-Valentin
    P. Seve
    R. Jaussaud
    BMC Ophthalmology, 20
  • [9] Vogt-Koyanagi-Harada Disease and COVID
    Manni, Priscilla
    Saturno, Maria Carmela
    Accorinti, Massimo
    JOURNAL OF CLINICAL MEDICINE, 2023, 12 (19)
  • [10] Bibliometric analysis of the Vogt-Koyanagi-Harada disease literature
    Li, Liangpin
    Yuan, Liyun
    Zhou, Xueyan
    Hua, Xia
    Yuan, Xiaoyong
    INTERNATIONAL OPHTHALMOLOGY, 2023, 43 (11) : 4137 - 4150