Age related clinical presentation and laboratory parameters in juvenile SLE: a Hungarian multicenter study
Pediatric Rheumatology volume 9, Article number: P265 (2011)
Several studies on SLE suggest that age at onset modifies the expression of the disease in terms of clinical presentation, pattern of organ involvement and laboratory findings. There are only few data about the age-related differences within the pediatric SLE group.
To determine the different clinical manifestations and laboratory characteristics of juvenile SLE (jSLE) in the pre- and postpubertal age in patients fulfilling the 1997 ARA criteria for SLE.
Retrospective multicenter analysis of data of 77 jSLE patients, divided into two groups according to the age. Mean age at disease onset was 8.9±1.9 (range 4-11y), follow-up period 7,1±4.3y in the prepubertal (n=30), and 14.7±1.2 (range 11-16y) follow-up period 6.0 ±4.3y in the postpubertal (n=47) group. Various clinical and laboratory parameters were analysed and compared between groups.
Female:Male ratio was 9:1 in both groups. The most common initial manifestations as butterfly rash occured in 60%/62%, cytopenias 60%/57%, kidney involvement 47%/43%, serositis 27%/23%, in the pre/postpubertal group. Arthritis was significantly more common in the older group (57%/77%). General symptomes like fever 47%/57%, weight loss 23%/30%, increased infection rate 20%/13% were also similar in the two age groups, as did ANA, anti-dsDNA, anti-Sm, anti-SSA, anti-SSB positivity and low C3 and C4 levels. Anti-RNP antibody was more common in the younger ages (33%/10%). Mean SLEDAI score was 12 in both groups. Zero SLICC damage index is significantly more common (68%/43%) in the older group after comparable follow-up period.
There are no prominent clinical differences except arthritis at onset and higher percentage of 0 SLICC damage score in older jSLE patients as compared to youngers.
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Derfalvi, B., Malik, A., Kreko, M. et al. Age related clinical presentation and laboratory parameters in juvenile SLE: a Hungarian multicenter study. Pediatr Rheumatol 9 (Suppl 1), P265 (2011). https://doi.org/10.1186/1546-0096-9-S1-P265