Pediatric rheumatology

Bone mineral density in egyptian children with juvenile idiopathic arthritis: possible correlation to serum RANKL / osteoprotegerin (OPG) ratio and OPG gene polymorphisms

Pediatr Rheumatol Online JPublished Case-control study

Authors' conclusion

Egyptian children with JIA have decreased BMD. rs2073617 TT genotype and T allele, RANKL/OPG ratio are possible determinants of reduced BMD in JIA.

Study context

Population
Egyptian children with juvenile idiopathic arthritis (JIA) (mean age 12.05 ± 3.2 years; 38 females; systemic-onset JIA most frequent, 38%) and matched healthy controls
Participants
60 vs 100
Comparison
JIA children vs matched healthy controls; within JIA, bone mineral density (BMD) z-score below vs above −2
  • JIAn = 60
  • Controlsn = 100reference
Outcome
BMD (lumbar DEXA z-score) and its association with OPG gene polymorphisms (rs2073617, rs3134069), serum RANKL, OPG and RANKL/OPG ratio
Methodological detailsmatched healthy controls
  • Matched healthy controls

Main finding

As reported in the abstract

BMD z-score below −2 (lumbar DEXA) in JIA patients

Patients with BMD z-score below −2

31%

Observational data: associations, not effects.

Further findings

OutcomeP value
OPG polymorphisms and serum markers, JIA vs controlsJIA vs ControlsP = < 0.001
OPG polymorphisms and serum markers, JIA vs controlsJIA vs Controls0.03
OPG polymorphisms and serum markers, JIA vs controls — Genotype and allele frequencies of the 2 polymorphisms did not differ between patients and controls
p > 0.05 for all

Original publication

Bone mineral density in egyptian children with juvenile idiopathic arthritis: possible correlation to serum RANKL / osteoprotegerin (OPG) ratio and OPG gene polymorphisms. Pediatr Rheumatol Online J. Published 16 June 2023. doi:10.1186/s12969-023-00843-6

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