Association of anti-Ro52, anti-Ro60 and anti-La antibodies with diagnostic, clinical and laboratory features in a referral hospital in Jerez, Spain

被引:21
|
作者
Menor Almagro, Raul [1 ]
Jurado Roger, Aurora [2 ]
Rodriguez Gutierrez, Francisco Javier [3 ]
Solis Diaz, Rocio [4 ]
Humberto Cardiel, Mario [5 ]
Salaberri Maestrojuan, Jose Javier [1 ]
机构
[1] Hosp Jerez, Dept Rheumatol, Jerez de la Frontera, Spain
[2] Hosp Reina Sofia, Dept Immunol, Cordoba, Spain
[3] Hosp Jerez, Dept Immunol, Jerez de la Frontera, Spain
[4] Hosp Comarcal Virgen Camino, Sanlucar, Spain
[5] Ctr Invest Clin Morelia SC, Morelia, Michoacan, Mexico
来源
REUMATOLOGIA CLINICA | 2016年 / 12卷 / 05期
关键词
Anti-Ro/SS-A antibodies; Anti-La/SS-B antibodies; Autoimmune disease; Immunofluorescence patterns;
D O I
10.1016/j.reuma.2015.10.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Several antibodies have proven to be useful in autoimmune diseases, as markers for diagnosis, prognosis or clinical manifestations. Our objective was to evaluate the diagnosis and manifestations associated for antibodies anti-Ro52, anti-Ro60 and anti-La at a referral hospital in Spain. Methods: We retrospectively analyzed the antigenic specificities of the consecutive samples submitted to the Immunology Unit for antinuclear antibody screening between 2002 and 2012. We included patients with more than one positive sample for some of the autoantibodies anti-Ro52, anti-Ro60 or anti-La. We also reviewed diagnosis, clinical and laboratory features. As dependent variable we evaluated possible combinations of anti-Ro52, anti-Ro60 and anti-La. Results: 322 patients, 91% females, were studied (age 44.3 +/- 15.51 years). The most frequent diagnosis was Sjogren's syndrome (40.06%) and systemic lupus erythematosus (SLE) (36.6%). The most prevalent pattern by indirect immunofluorescence was the fine speckled (69.9%). Anti-Ro52+/anti-Ro60+/anti-La+ combination was positively associated with fine speckled pattern (p: 0.001) and negatively with homogeneous (p: 0.016) and cytoplasmic pattern (p: 0.002). Isolated anti-Ro52+ was negatively associated with fine speckled pattern (p<0.001) and positively with the cytoplasmic one (p<0.001). The main positive associations with clinical symptoms were xerostomia and xerophthalmia with anti-Ro52+/anti-Ro60+/anti-La+ (p<0.001), oral ulcers with anti-Ro52+/anti-Ro60+/anti-La- (p: 0.002) and alopecia with anti-Ro52-/anti-Ro60+/anti-La- (p: 0.003). Negative associations were xerophthalmia and photosensitivity with anti-Ro52+/anti-Ro60-/anti-La- (p: 0.003). Laboratory positive associations were hypergammaglobulinemia with anti-Ro52+/anti-Ro60+/anti-La+ (p: 0.003), and hypocomplementemia with anti-Ro52-/anti-Ro60+/anti-La- (p: 0.003). Leucopenia was negatively associated with anti-Ro52+/anti-Ro60-/anti-La- (p: 0.003). Conclusion: Our study found significant relationships between clinical and laboratory manifestations with different patterns of antibodies to anti-Ro52, anti-Ro60 and anti-La. The combination of antibodies might be clinically useful due to prognostic and therapeutic implications. (C) 2015 Elsevier Espana, S.L.U. and Sociedad Espanola de Reumatologia y Colegio Mexicano de Reumatologia. All rights reserved.
引用
收藏
页码:256 / 262
页数:7
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