Vitamin D Deficiency and Avascular Necrosis in Patients With Sickle Cell Disease: A Retrospective Cohort Study

Abdullah J Tammas1, Luluh B Albehlal2, Fahad Alabbas1

  • 1Pediatric Hematology/Oncology, Prince Sultan Medical Military City, Riyadh, SAU.

Cureus
|November 25, 2024
PubMed

Insights

Vitamin D deficiency (VDD) significantly increases the risk of avascular necrosis (AVN) in sickle cell disease (SCD) patients. This study found VDD is an independent risk factor for AVN, highlighting the need for further research on vitamin D supplementation.

Area of Science:

  • Hematology
  • Orthopedics
  • Endocrinology

Background:

  • Sickle cell disease (SCD) is a complex inherited blood disorder with multi-systemic complications.
  • Avascular necrosis (AVN) is a common and debilitating complication in SCD patients.
  • Vitamin D deficiency (VDD) is prevalent in SCD patients, but its role in AVN development is under-researched.

Purpose of the Study:

  • To investigate the association between VDD and AVN in SCD patients.
  • To identify patterns of AVN presentation, risk factors, diagnosis, and treatment in this cohort.
  • To determine if VDD is an independent risk factor for AVN in SCD.

Main Methods:

  • Retrospective cohort study of 711 SCD patients with confirmed VDD from January 2020 to December 2022.
  • Inclusion criteria: confirmed SCD and VDD testing; exclusion: bone marrow transplant recipients.
  • Statistical analysis included chi-square tests and multivariate logistic regression to assess associations and control for confounders.

Main Results:

  • AVN was diagnosed in 17.9% of the cohort, with a mean age of 30.9 years.
  • Chronic joint pain was the primary symptom (>95%), with the hip being the most affected joint (86%).
  • SCD patients with VDD had 9.79 times higher odds of developing AVN (OR 9.79; 95% CI: 5.25-18.26), independent of other risk factors like frequent vaso-occlusive crises, older age, acute chest syndrome, and high BMI.

Conclusions:

  • AVN is a significant cause of morbidity in the studied SCD cohort, often diagnosed at advanced stages (III/IV).
  • Vitamin D deficiency is identified as an independent risk factor for AVN in sickle cell disease.
  • Further randomized controlled trials are warranted to evaluate the efficacy of vitamin D supplementation in preventing AVN in SCD patients.

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