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Abstract Number: 2014

Serum 25(OH)D Levels in Adolescents and Young Adults with Juvenile Idiopathic Arthritis and Juvenile Onset Systemic Lupus Erythematosus: Prevalence and Association with Disease Activity

Fernanda Falcini1, Stefano Stagi2, Loredana Cavalli3, Giulia Carnesecchi1, Federico Bertini1, Laura Masi3, Marco Matucci-Cerinic1 and Maria Luisa Brandi3, 1Department of Internal Medicine, Rheumatology Section, Transition Clinic, University of Florence, Florence, Italy, 2Pediatric Endocrinology Unit, Anna Meyer Children’s Hospital, University of Florence, Firenze, Italy, 3Department of Internal Medicine, Endocrinology Unit, University of Florence, Firenze, Italy

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: 25 OH D Vitamin insufficiency, juvenile idiopathic arthritis (JIA) and systemic lupus erythematosus (SLE)

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Session Information

Title: Pediatric Rheumatology - Clinical and Therapeutic Aspects: Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Diseases

Session Type: Abstract Submissions (ACR)

Background/Purpose: Numerous data are available in literature on 25 (OH)D serum levels in general population, few and contradictory in Juvenile Idiopathic Arthritis (JIA), and scarce in Juvenile onset Systemic Lupus Erythematosus (JSLE) pts. Our goals are:1- to evaluate the serum  25(OH)D status  in a large cohort of JIA and JSLE pts; 2- to correlate the 25(OH)D  levels with the variables associated with JIA and JSLE. 3.To compare  the  pts results with healthy controls.

Methods: 144 JIA pts (122 F, 22 M, median age 15.5 ± 7.2 yrs: 78 oligo, 30 poly, 12 systemic and 24 Entesitis-arthritis [ERA]) onsets, and 46 JSLE  pts (38 F, 8M, median age 16.9 ± 6.8 yrs)  were studied after informed consent and Ethical approval. In all, serum 25( OH)D, serum intact parathyroid hormone (PTH),  calcium, phosphorus, and bone alkaline phosphatase were measured. 100 sex-matched healthy subjects acted as controls.

Results: No significant  difference of  25(OH)D levels has been detected in JIA and JSLE pts in comparison to controls as regard the percentage of  those with VD deficiency and insufficiency. Of note,  in JIA and JSLE pts with deficiency or  insufficiency,  a significant difference in comparison to controls with deficit or insufficiency, as regard the percentage  of subjects with increased PTH and alkaline bone phosphatase levels (p < 0.0001) was detected. In addition, among 25(OH)D levels and JIA subtypes, the  lowest levels were found  in systemic and poly than in oligo and ERA onsets. Moreover, systmic and poly pts have a significant lower  increase of  25 (OH)D levels after supplementation  than oligo, ERA pts, and controls with a high percentage of those who remains with insufficiency (p < 0.001). The same results have been observed in JSLE pts who showed a high percentage of insufficiency, despite supplementation, of 25(OH)D than controls. The persistent low 25 (OH)D levels, despite supplementation, are significantly higher in patients with persistent active disease.

Conclusion: Serum 25 (OH) D levels and the percentage with persistent VD insufficiency seem to correlate to type of disease and disease activity. These preliminary results suggest  a  higher consumption  and a higher request of 25(OH)D in patients with active JIA and JSLE.


Disclosure:

F. Falcini,
None;

S. Stagi,
None;

L. Cavalli,
None;

G. Carnesecchi,
None;

F. Bertini,
None;

L. Masi,
None;

M. Matucci-Cerinic,
None;

M. L. Brandi,
None.

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