The anemia of familial Mediterranean fever disease

Tiraje Celkan1, Mehmet Celik, Ozgür Kasapçopur

  • 1Department of Pediatric Hematology-Oncology, Istanbul University Faculty of Medicine, Istanbul, Turkey. tirajecelkan@yahoo.com

Insights

Anemia is common in children with familial Mediterranean fever (FMF), primarily linked to iron status rather than interleukins. Colchicine therapy improves anemia and FMF disease activity.

Area of Science:

  • Pediatric Rheumatology
  • Hematology
  • Immunology

Background:

  • Familial Mediterranean fever (FMF) is a genetic autoinflammatory disorder.
  • Anemia is a frequent comorbidity in FMF patients, impacting disease management.
  • The interplay between FMF, anemia, inflammation, and treatment requires further investigation.

Purpose of the Study:

  • To determine the incidence of anemia in pediatric FMF patients.
  • To assess the influence of disease activity and colchicine therapy on anemia.
  • To evaluate the role of serum transferrin receptor (sTfR) and interleukin-6 (IL-6) in diagnosing anemia in FMF.

Main Methods:

  • Cross-sectional study involving 172 FMF patients and 17 healthy controls.
  • Categorization into newly diagnosed FMF, FMF on colchicine therapy, and healthy controls.
  • Analysis of hematological parameters, iron status (including sTfR), and IL-6 levels.

Main Results:

  • Anemia detected in 63.4% of FMF patients.
  • Anemia incidence was 53% in newly diagnosed and 31% in colchicine-treated groups.
  • Anemia correlated more with iron status than IL-6; colchicine therapy improved hemoglobin levels and reduced disease activity.

Conclusions:

  • Anemia in pediatric FMF is predominantly related to iron status.
  • Colchicine therapy positively impacts both anemia and FMF disease activity.
  • Correction of anemia, alongside decreased erythrocyte sedimentation rate (ESR), correlates with FMF symptom resolution.

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