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Updated: Jun 6, 2025

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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.
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.
Abstract:
Introduction Sickle cell disease (SCD) is an inherited hemoglobinopathy with complex multi-systemic involvement. Avascular necrosis (AVN) is a devastating complication among patients with SCD. Vitamin D deficiency (VDD) is a common finding in SCD patients. However, there is a paucity of research that evaluates the potential role of VDD as a risk factor for AVN in patients with SCD. This study aimed to assess the association between VDD and AVN and determine the patterns of presentation, risk factors, diagnosis, and treatment of AVN in patients with SCD. Methods We conducted a retrospective cohort study of consecutive SCD patients diagnosed with VDD from January 2020 to December 2022 at Prince Sultan Medical Military City (PSMMC), Riyadh, Saudi Arabia. Inclusion criteria: (1) adults and children with confirmed SCD and (2) tested for VDD. We excluded patients who underwent bone marrow transplants. The associations were assessed using the chi-square test. Logistic regression was performed to control for confounding. Results The study included 711 eligible patients; 271 (38%) were children. VDD affected 301/711 (42.3%). VDD was noticed in 32.2% and 48.1% of children and adults, respectively. AVN was diagnosed in 127/711 (17.9%) patients. The mean age at AVN diagnosis was 30.9 ± 11 years. The most common presentation of AVN was chronic joint pain (> 95%). The most frequently affected joint was the hip (86%). The majority of patients (76.4%) were late in stage at diagnosis of AVN (III/IV). Patients with a history of VDD were significantly associated with a higher risk of AVN (p < 0.001). Using multivariate logistic regression, SCD patients with VDD have 9.79 times the odds of AVN compared with SCD patients without VDD (OR 9.79; 95% CI: 5.25 - 18.26). Other statistically significant risk factors for AVN included frequent vaso-occlusive crises, older age, history of acute chest syndrome, and high body mass index. Conclusion AVN is a significant cause of morbidity in our SCD cohort. Most of the patients had advanced AVN disease. VDD is an independent risk factor for the occurrence of AVN. Well-designed randomized trials are required to determine the effect of vitamin D supplementation in reducing AVN in patients with SCD.
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