Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease

ABSTRACT 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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Journal
eJHaem
Published
2026-05-18
DOI
https://doi.org/10.1002/jha2.70306
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
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0.00

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article

Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease

Mario Lamonica, Parul Rai, Pei‐Lin Chen, Babette S. Zemel et al.
eJHaem
Hemoglobinopathies and Related Disorders
article

Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease

Mario Lamonica, Parul Rai, Pei‐Lin Chen, Babette S. Zemel, Ragha Srinivasan, Clifford Takemoto, Hyacinth I. Hyacinth, Jane Hankins, Khalid El‐Bashir, Jahnavi Gollamudi, Guolian Kang, Oyebimpe Adesina, Chengzhou Wu, Matthew R. Allen
article en

Abstract

ABSTRACT 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

eJHaemVol. 7(3)
St. Jude Children's Research Hospital (US), Children's Hospital of Philadelphia (US), University of California Davis Medical Center (US), Indiana University – Purdue University Indianapolis (US), University of Pennsylvania (US), University of Cincinnati Medical Center (US)
National Heart, Lung, and Blood Institute
Openalex Percentile: Top 6%
Hemoglobinopathies and Related Disorders
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