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Updated: May 21, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease
Jahnavi Gollamudi1, Chengzhou Wu2, Guolian Kang2
1Division of Hematology/Oncology Department of Internal Medicine University of Cincinnati College of Medicine Cincinnati Ohio USA.
Introduction:
Skeletal complications are common in sickle cell disease (SCD). We previously showed that the prevalence of low areal bone mineral density (aBMD) increased with age in a pediatric SCD cohort, even after adjusting for short stature. Data on age-related aBMD trends in young adults is lacking.
Methods:
Using retrospective data from the Sickle Cell Clinical Research and Intervention Program (SCCRIP), we converted lumbar spine (LS) and total body (TB) aBMD from 713 SCCRIP participants (49.2% females, ages 6-24 years) to age-, sex-, ancestry-, and height-adjusted Z-scores, using data from healthy African American controls enrolled in the Bone Mineral Density in Childhood Study.
Results:
Low TB bone density prevalence rates increased with age: 29.5% in children (6-< 12 years), 36.7% in adolescents (12-< 18 years), and 42.2% in young adults (18-24 years). LS aBMD followed a similar age-related trend. Multivariable analysis revealed older age (OR 1.10, 95% CI 1.06-1.16), lower hemoglobin (OR 0.833, 95% CI 0.740-0.936), and higher eGFR (OR 1.01, 95% CI 1.00-1.02) as independent predictors for low TB BMD.
Conclusion:
These findings highlight the progressive decline of aBMD in SCD and underscore the need for early screening to mitigate morbidity due to SCD-related skeletal complications. Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.
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