Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients

Objective. The aim of this study was to assess the efficacy of anti-TNF-alpha therapy in refractory uveitis due to Behcet's disease (BD). Methods. We performed a multicentre study of 124 patients with BD uveitis refractory to conventional treatment including high-dose corticosteroids and at lea...

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Autores: Calvo-Rio, V, Blanco, R, Sanchez-Burson, J, Mesquida, M, Adan, A, Hernandez, MV, Garfella, MH, Pascual, EV, Martinez-Costa, L, Sellas-Fernandez, A, Coma, MC, Diaz-Llopis, M, Gallego, R, Salom, D, Serrano, JLG, Ortego, N, Herreras, JM, Fonollosa, A, Garcia-Aparicio, AM, Maiz, O, Blanco, A, Torre, I, Fernandez-Espartero, C, Jovani, V, Peiteado-Lopez, D, Pato, E, Cruz, J, Fernandez-Cid, C, Aurrecoechea, E, Garcia, M, Caracuel, MA, Montilla, C, Atanes, A, Hernandez, FF, Insua, S, Gonzalez-Suarez, S, Sanchez-Andrade, A, Gamero, F, Linares, L, Romero-Bueno, F, Garcia, AJ, Almodovar, R, Minguez, E, Cubero, CC, Olive, A, Vazquez, J, Moreno, OR, Jimenez-Zorzo, F, Manero, J, Fernandez, SM, Rueda-Gotor, J, Gonzalez-Gay, MA
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:r-FISABIO. Repositorio Institucional de Producción Científica
OAI Identifier:oai:fisabio.fundanetsuite.com:p14939
Acceso en línea:https://fisabio.portalinvestigacion.com/publicaciones/14939
Access Level:acceso abierto
Palabra clave:Behcet's disease
uveitis
anti-TNF therapy
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spelling Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patientsCalvo-Rio, VBlanco, RSanchez-Burson, JMesquida, MAdan, AHernandez, MVGarfella, MHPascual, EVMartinez-Costa, LSellas-Fernandez, AComa, MCDiaz-Llopis, MGallego, RSalom, DSerrano, JLGOrtego, NHerreras, JMFonollosa, AGarcia-Aparicio, AMMaiz, OBlanco, ATorre, IFernandez-Espartero, CJovani, VPeiteado-Lopez, DPato, ECruz, JFernandez-Cid, CAurrecoechea, EGarcia, MCaracuel, MAMontilla, CAtanes, AHernandez, FFInsua, SGonzalez-Suarez, SSanchez-Andrade, AGamero, FLinares, LRomero-Bueno, FGarcia, AJAlmodovar, RMinguez, ECubero, CCOlive, AVazquez, JMoreno, ORJimenez-Zorzo, FManero, JFernandez, SMRueda-Gotor, JGonzalez-Gay, MABehcet's diseaseuveitisanti-TNF therapyObjective. The aim of this study was to assess the efficacy of anti-TNF-alpha therapy in refractory uveitis due to Behcet's disease (BD). Methods. We performed a multicentre study of 124 patients with BD uveitis refractory to conventional treatment including high-dose corticosteroids and at least one standard immunosuppressive agent. Patients were treated for at least 12 months with infliximab (IFX) (3-5 mg/kg at 0, 2 and 6 weeks and then every 4-8 weeks) or adalimumab (ADA) (usually 40 mg every 2 weeks). The main outcome measures were degree of anterior and posterior chamber inflammation, visual acuity, macular thickness and immunosuppression load. Results. Sixty-eight men and 56 women (221 affected eyes) were studied. The mean age was 38.6 years (S.D. 10.4). HLA-B51 was positive in 66.1% of patients and uveitis was bilateral in 78.2%. IFX was the first biologic agent in 77 cases (62%) and ADA was first in 47 (38%). In most cases anti-TNF-alpha drugs were used in combination with conventional immunosuppressive drugs. At the onset of anti-TNF-alpha therapy, anterior chamber and vitreous inflammation was observed in 57% and 64.4% of patients, respectively. In both conditions the damage decreased significantly after 1 year. At baseline, 50 patients (80 eyes) had macular thickening [optical coherence tomography (OCT) >250 mu m] and 35 (49 eyes) had cystoid macular oedema (OCT > 300 mu m) that improved from 420 mm (S.D. 119.5) at baseline to 271 mu m (S.D. 45.6) at month 12 (P < 0.01). The best-corrected visual acuity and the suppression load also showed significant improvement. After 1 year of follow-up, 67.7% of patients were inactive. Biologic therapy was well tolerated in most cases. Conclusion. Anti-TNF-alpha therapy is effective and relatively safe in refractory BD uveitis.OXFORD UNIV PRESS2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://fisabio.portalinvestigacion.com/publicaciones/14939RHEUMATOLOGYISSN: 14620324ISSNe: 14620332reponame:r-FISABIO. Repositorio Institucional de Producción Científicainstname:Consejo Superior de Investigaciones Científicas (CSIC)Inglésinfo:eu-repo/semantics/openAccessoai:fisabio.fundanetsuite.com:p149392026-06-11T12:45:17Z
dc.title.none.fl_str_mv Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
title Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
spellingShingle Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
Calvo-Rio, V
Behcet's disease
uveitis
anti-TNF therapy
title_short Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
title_full Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
title_fullStr Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
title_full_unstemmed Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
title_sort Anti-TNF-alpha therapy in patients with refractory uveitis due to Behcet's disease: a 1-year follow-up study of 124 patients
dc.creator.none.fl_str_mv Calvo-Rio, V
Blanco, R
Sanchez-Burson, J
Mesquida, M
Adan, A
Hernandez, MV
Garfella, MH
Pascual, EV
Martinez-Costa, L
Sellas-Fernandez, A
Coma, MC
Diaz-Llopis, M
Gallego, R
Salom, D
Serrano, JLG
Ortego, N
Herreras, JM
Fonollosa, A
Garcia-Aparicio, AM
Maiz, O
Blanco, A
Torre, I
Fernandez-Espartero, C
Jovani, V
Peiteado-Lopez, D
Pato, E
Cruz, J
Fernandez-Cid, C
Aurrecoechea, E
Garcia, M
Caracuel, MA
Montilla, C
Atanes, A
Hernandez, FF
Insua, S
Gonzalez-Suarez, S
Sanchez-Andrade, A
Gamero, F
Linares, L
Romero-Bueno, F
Garcia, AJ
Almodovar, R
Minguez, E
Cubero, CC
Olive, A
Vazquez, J
Moreno, OR
Jimenez-Zorzo, F
Manero, J
Fernandez, SM
Rueda-Gotor, J
Gonzalez-Gay, MA
author Calvo-Rio, V
author_facet Calvo-Rio, V
Blanco, R
Sanchez-Burson, J
Mesquida, M
Adan, A
Hernandez, MV
Garfella, MH
Pascual, EV
Martinez-Costa, L
Sellas-Fernandez, A
Coma, MC
Diaz-Llopis, M
Gallego, R
Salom, D
Serrano, JLG
Ortego, N
Herreras, JM
Fonollosa, A
Garcia-Aparicio, AM
Maiz, O
Blanco, A
Torre, I
Fernandez-Espartero, C
Jovani, V
Peiteado-Lopez, D
Pato, E
Cruz, J
Fernandez-Cid, C
Aurrecoechea, E
Garcia, M
Caracuel, MA
Montilla, C
Atanes, A
Hernandez, FF
Insua, S
Gonzalez-Suarez, S
Sanchez-Andrade, A
Gamero, F
Linares, L
Romero-Bueno, F
Garcia, AJ
Almodovar, R
Minguez, E
Cubero, CC
Olive, A
Vazquez, J
Moreno, OR
Jimenez-Zorzo, F
Manero, J
Fernandez, SM
Rueda-Gotor, J
Gonzalez-Gay, MA
author_role author
author2 Blanco, R
Sanchez-Burson, J
Mesquida, M
Adan, A
Hernandez, MV
Garfella, MH
Pascual, EV
Martinez-Costa, L
Sellas-Fernandez, A
Coma, MC
Diaz-Llopis, M
Gallego, R
Salom, D
Serrano, JLG
Ortego, N
Herreras, JM
Fonollosa, A
Garcia-Aparicio, AM
Maiz, O
Blanco, A
Torre, I
Fernandez-Espartero, C
Jovani, V
Peiteado-Lopez, D
Pato, E
Cruz, J
Fernandez-Cid, C
Aurrecoechea, E
Garcia, M
Caracuel, MA
Montilla, C
Atanes, A
Hernandez, FF
Insua, S
Gonzalez-Suarez, S
Sanchez-Andrade, A
Gamero, F
Linares, L
Romero-Bueno, F
Garcia, AJ
Almodovar, R
Minguez, E
Cubero, CC
Olive, A
Vazquez, J
Moreno, OR
Jimenez-Zorzo, F
Manero, J
Fernandez, SM
Rueda-Gotor, J
Gonzalez-Gay, MA
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Behcet's disease
uveitis
anti-TNF therapy
topic Behcet's disease
uveitis
anti-TNF therapy
description Objective. The aim of this study was to assess the efficacy of anti-TNF-alpha therapy in refractory uveitis due to Behcet's disease (BD). Methods. We performed a multicentre study of 124 patients with BD uveitis refractory to conventional treatment including high-dose corticosteroids and at least one standard immunosuppressive agent. Patients were treated for at least 12 months with infliximab (IFX) (3-5 mg/kg at 0, 2 and 6 weeks and then every 4-8 weeks) or adalimumab (ADA) (usually 40 mg every 2 weeks). The main outcome measures were degree of anterior and posterior chamber inflammation, visual acuity, macular thickness and immunosuppression load. Results. Sixty-eight men and 56 women (221 affected eyes) were studied. The mean age was 38.6 years (S.D. 10.4). HLA-B51 was positive in 66.1% of patients and uveitis was bilateral in 78.2%. IFX was the first biologic agent in 77 cases (62%) and ADA was first in 47 (38%). In most cases anti-TNF-alpha drugs were used in combination with conventional immunosuppressive drugs. At the onset of anti-TNF-alpha therapy, anterior chamber and vitreous inflammation was observed in 57% and 64.4% of patients, respectively. In both conditions the damage decreased significantly after 1 year. At baseline, 50 patients (80 eyes) had macular thickening [optical coherence tomography (OCT) >250 mu m] and 35 (49 eyes) had cystoid macular oedema (OCT > 300 mu m) that improved from 420 mm (S.D. 119.5) at baseline to 271 mu m (S.D. 45.6) at month 12 (P < 0.01). The best-corrected visual acuity and the suppression load also showed significant improvement. After 1 year of follow-up, 67.7% of patients were inactive. Biologic therapy was well tolerated in most cases. Conclusion. Anti-TNF-alpha therapy is effective and relatively safe in refractory BD uveitis.
publishDate 2014
dc.date.none.fl_str_mv 2014
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://fisabio.portalinvestigacion.com/publicaciones/14939
url https://fisabio.portalinvestigacion.com/publicaciones/14939
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv OXFORD UNIV PRESS
publisher.none.fl_str_mv OXFORD UNIV PRESS
dc.source.none.fl_str_mv RHEUMATOLOGY
ISSN: 14620324
ISSNe: 14620332
reponame:r-FISABIO. Repositorio Institucional de Producción Científica
instname:Consejo Superior de Investigaciones Científicas (CSIC)
instname_str Consejo Superior de Investigaciones Científicas (CSIC)
reponame_str r-FISABIO. Repositorio Institucional de Producción Científica
collection r-FISABIO. Repositorio Institucional de Producción Científica
repository.name.fl_str_mv
repository.mail.fl_str_mv
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