Evidence map›Paper›PMID 42174354›Full record

ArticleArchives of osteoporosis2026

Osteoporosis risk in alpha and beta thalassemia: An age- and sex-specific retrospective cohort study.

Yuan-Sheng Hsu, Sheng-Chieh Tseng, Tze-Fan Chao, Kun-Hui Chen

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

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4 authors.

Yuan-Sheng HsuDepartment of Orthopedic Surgery, Taichung Veterans General Hospital, 1650, Sec. 4, Taiwan Blvd., Xitun Dist., Taichung City, 407219, Taiwan.
Sheng-Chieh TsengDepartment of Orthopedic Surgery, Taichung Veterans General Hospital, 1650, Sec. 4, Taiwan Blvd., Xitun Dist., Taichung City, 407219, Taiwan.
Tze-Fan ChaoDivision of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Kun-Hui ChenDepartment of Orthopedic Surgery, Taichung Veterans General Hospital, 1650, Sec. 4, Taiwan Blvd., Xitun Dist., Taichung City, 407219, Taiwan. orthochen@gmail.com.

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6 · The paper itself

Abstract

rationaleDifferential skeletal risks between alpha- and beta-thalassemia subtypes remain unclear. MAIN

resultBeta-thalassemia correlates with higher fracture risk than alpha-thalassemia. Notably, males aged 18-50 with beta-thalassemia show a 14-fold increase in osteoporosis. SIGNIFICANCE: Identifies a notably elevated osteoporosis risk in young males, supporting consideration of earlier skeletal surveillance. PURPOSE: The differences in osteoporosis and fracture risk between alpha- and beta-thalassemia subtypes, and how these differences vary by age and sex, remain poorly understood. We conducted a large-scale analysis to characterize these risks and guide risk-stratified protocols.

methodsThis retrospective cohort study used the TriNetX health research network. Patients with alpha- and beta-thalassemia (identified by ICD-10 codes) were matched 1:1 with non-anemic controls by age, sex, race, and comorbidities (chronic kidney disease, diabetes mellitus, rheumatoid arthritis, malnutrition, and endocrine dysfunction) using propensity scores. We assessed the risk of osteoporosis, fractures, and mortality from Kaplan-Meier analyses.

resultsBeta-thalassemia patients have a significantly greater risk of osteoporosis (HR = 1.26, 95% CI: 1.11-1.43) than alpha-thalassemia patients. Within the beta-thalassemia group, males demonstrated a risk of osteoporosis that was more than three times higher than that of controls (HR = 3.28, 95% CI: 2.51-4.28), which was notably higher than that observed in females (HR = 1.42, 95% CI: 1.26-1.60). Young males (aged 18-50) demonstrated a markedly elevated risk of osteoporosis (HR = 13.97, 95% CI: 7.30-26.73) and mortality (HR = 6.31, 95% CI: 3.62-11.01) compared to matched controls.

conclusionBeta-thalassemia is associated with worse skeletal outcomes than alpha-thalassemia. Young male patients demonstrate substantially elevated risk of osteoporosis and mortality. These findings highlight the need for age- and sex-specific risk assessment in thalassemia patients.

Indexed as

alpha-Thalassemiabeta-ThalassemiaOsteoporosisAdolescentAdultAge FactorsFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSex FactorsYoung AdultBeta thalassemiaOsteoporosisReal-world dataThalassemiaThalassemia-associated osteoporosis

Identifiers

PMID42174354
PMCPMC13197373

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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 OpenQuestion graph.