Very early and early systemic sclerosis in the Spanish scleroderma Registry (RESCLE) cohort
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Trapiella-Martínez L
- Díaz-López JB
- Caminal-Montero L
- Tolosa-Vilella C
- Guillén-Del Castillo A
- Colunga-Argüelles D
- Rubio-Rivas M
- Iniesta-Arandia N
- Castillo-Palma MJ
- Sáez-Comet L
- Egurbide-Arberas MV
- Ortego-Centeno N
- Freire M
- Vargas-Hitos JA
- Ríos-Blanco JJ
- Rodríguez-Carballeira M
- Marín-Ballvé A
- Chamorro-Fernández AJ
- Pla-Salas X
- Madroñero-Vuelta AB
- Ruiz-Muñóz M
- Fonollosa-Pla V
- Simeón-Aznar CP
Grupos
Abstract
Objectives: According to the existence of subclinical organ involvement pre-scleroderma should be divided into two subsets: very early and early disease. Pre-scleroderma patients included in the Spanish Scleroderma Registry (RESCLE) Cohort were reclassified into subsets. Differences were evaluated and the risk of progression to definite systemic sclerosis was estimated. Methods: The characteristics of very early and early SSc patients were compared. A logistic regression model was used to determine the risk factors of progression. Results: 1632 patients were included, 36 (2.2%) in the very early subset and 111 (6.8%) in the early subset. There were no differences in sex, age at disease onset, duration of Raynaud's phenomenon, antinuclear antibodies or capillaroscopic findings. Three (8.3%) very early SSc patients evolved to definite SSc, 2 (5.6%) of them meeting the ACR/EULAR 2013 criteria, unlike 31 (28%) early SSc patients, 20 (24%) of them meeting the criteria (p = 0.034). Digestive involvement was an independent risk factor of progression (OR 17; 95% CI, 6.1-47.2). Conclusions: The classification of early forms of sderoderma identifies patients with different prognostic risk of progression. The evolution to definite SSc is more frequent in early than in very early SSc patients. Digestive involvement is a risk factor of progression. An active assessment of organ damage in preclinical stages allows a correct classification and risk stratification, with implications for monitoring and treatment. (C) 2017 Elsevier B.V. All rights reserved.
Datos de la publicación
- ISSN/ISSNe:
- 1568-9972, 1873-0183
- Tipo:
- Review
- Páginas:
- 796-802
- PubMed:
- 28564618
- Factor de Impacto:
- 2,648 SCImago ℠
- Cuartil:
- Q1 SCImago ℠
AUTOIMMUNITY REVIEWS ELSEVIER SCIENCE BV
Citas Recibidas en Web of Science: 17
Documentos
- No hay documentos
Filiaciones
Keywords
- Early systemic sclerosis; Very early systemic sclerosis; Pre-scleroderma
Proyectos y Estudios Clínicos
ENSAYO MULTICÉNTRICO, ABIERTO Y CON UN SOLO GRUPO PARA EVALUAR LA EFICACIA, LA FARMACOCINÉTICA, LA SEGURIDAD Y LA TOLERABILIDAD DE IGSC AL 20 % EN SUJETOS CON INMUNODEFICIENCIA PRIMARIA.
Investigador Principal: PEDRO MORAL MORAL
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PREVENCIÓN DE EPISODIOS DE TROMBOEMBOLIA - REGISTRO EUROPEO SOBRE TROMBOEMBOLIA VENOSA.
Investigador Principal: JOSÉ ANTONIO TODOLÍ PARRA
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ENSAYO CLINICO FASE III, DE GRUPOS PARALELOS, RANDOMIZADO, CONTROLADO CON PLACEBO, DOBLE CIEGO Y MULTICENTRICO, PARA EVALUAR LA EFICACIA Y SEGURIDAD DE LA ADMINISTRACION DE TOCILIZUMAB EN PACIENTES DIAGNOSTICADOS DE ORBITOPATÍA TIROIDEA (OT) MODERADA A SE VERA O QUE AMENAZA LA VISTA, QUE NO HAN RESPONDIDO ADECUADAMENTE AL TRATAMIENTO CON PULSOS DE CORTICOIDES.
Investigador Principal: ENRIQUE ESPAÑA GREGORI
GRC-TCL-2010-01 . 2013
Cita
Trapiella L,Díaz JB,Caminal L,Tolosa C,Guillén A,Colunga D,Rubio M,Iniesta N,Castillo MJ,Sáez L,Egurbide MV,Ortego N,Freire M,Vargas JA,Ríos JJ,Todolí JA,Rodríguez M,Marín A,Chamorro AJ,Pla X,Madroñero AB,Ruiz M,Fonollosa V,Simeón CP. Very early and early systemic sclerosis in the Spanish scleroderma Registry (RESCLE) cohort. Autoimmun Rev. 2017. 16(8):p. 796-802. IF:8,745. (1).