Artigo Acesso aberto Produção Nacional Revisado por pares

Features of 847 Childhood‐Onset Systemic Lupus Erythematosus Patients in Three Age Groups at Diagnosis: A Brazilian Multicenter Study

2016; Wiley; Volume: 68; Issue: 11 Linguagem: Inglês

10.1002/acr.22881

ISSN

2151-4658

Autores

Roberta Gomes, Marco F. Silva, Kátia Tomie Kozu, Eloísa Bonfá, Rosa Maria Rodrigues Pereira, Maria Teresa Terreri, Cláudia Saad Magalhães, Silvana Sacchetti, Roberto Marini, Melissa Mariti Fraga, Luciana Martins de Carvalho, Cássia Maria Passarelli Lupoli Barbosa, Magda Carneiro‐Sampaio, Clóvis A. Silva,

Tópico(s)

Atherosclerosis and Cardiovascular Diseases

Resumo

To evaluate demographic data and clinical and laboratory features at disease diagnosis in 3 different age groups of childhood-onset systemic lupus erythematosus (SLE): group A, early-onset (<6 years); group B, school age (≥6 to <12 years); and group C, adolescent (≥12 to <18 years).This was a Brazilian multicenter cohort retrospective study in 10 pediatric rheumatology centers, including 847 childhood-onset SLE patients.Patients were divided into 3 groups: group A with 39 patients (4%), group B with 395 patients (47%), and group C with 413 patients (49%). Of 39 childhood-onset SLE patients in group A, 3 (8%) were ages <2 years, 4 (10%) were ≥2 to <3 years, and 32 (82%) were ≥3 and 0.05). However, the frequency of fever (78% versus 61% versus 47%; P < 0.0001), hepatomegaly (42% versus 29% versus 14%; P < 0.0001), splenomegaly (28% versus 12% versus 4%; P < 0.0001), and discoid lupus (13% versus 4% versus 4%; P = 0.020) was significantly higher in group A compared to groups B and C. The frequency of weight loss >2 kg (19% versus 28% versus 36%; P = 0.017), photosensitivity (34% versus 41% versus 51%; P = 0.006), leukopenia <4,000/mm3 (14% versus 25% versus 30%; P = 0.048), and lymphopenia <1,500/mm3 (22% versus 41% versus 47%; P = 0.011) was significantly lower in group A.Our large multicenter study identified the finding that the initial appearance of childhood-onset SLE is characterized by comparable high frequency of internal organ involvement and some distinct clinical and laboratory features in early-onset and adolescent groups.

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