Evidence map›Paper›PMID 42158291›Full record

ArticleEJHaem2026

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

Jahnavi Gollamudi, Chengzhou Wu, Guolian Kang, Michael Sexton Lamonica, Pei-Lin Chen, Ragha Srinivasan, Khalid El-Bashir, Jane Hankins, Parul Rai, Clifford Takemoto and 4 more

Abstract read
In one paragraph

Article in EJHaem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Jahnavi GollamudiDivision of Hematology/Oncology Department of Internal Medicine University of Cincinnati College of Medicine Cincinnati Ohio USA.ORCID https://orcid.org/0000-0003-2992-6264
Chengzhou WuDepartment of Biostatistics St. Jude Children's Research Hospital Memphis Tennessee USA.
Guolian KangDepartment of Biostatistics St. Jude Children's Research Hospital Memphis Tennessee USA.
Michael Sexton LamonicaDivision of Hematology/Oncology Department of Internal Medicine University of Cincinnati College of Medicine Cincinnati Ohio USA.
Pei-Lin ChenDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Ragha SrinivasanDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Khalid El-BashirDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Jane HankinsDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Parul RaiDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Clifford TakemotoDepartment of Hematology St. Jude Children's Research Hospital Memphis Tennessee USA.
Hyacinth I HyacinthDepartment of Neurology and Rehabilitation University of Cincinnati College of Medicine Cincinnati Ohio USA.
Matthew R AllenDepartment of Anatomy, Cell Biology and Physiology Indiana University School of Medicine Indianapolis Indiana USA.
Babette S ZemelDivision of Gastroenterology, Hepatology, and Nutrition The Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.
Oyebimpe AdesinaDivision of Hematology and Oncology University of California Davis Comprehensive Cancer Center Sacramento California USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 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.

Identifiers

PMID42158291
PMCPMC13181915

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.