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Bone microarchitecture involvement and intervertebral disc alterations in patients with β-thalassemia: a retrospective study

https://doi.org/10.14341/probl201662570-71

Abstract

Background. Bone involvement in patients with β-thalassemia is well known, but only few studies have analyzed bone microarchitecture and the prevalence of intervertebral disc calcifications (IDCs) in these patients.

Aim: to evaluate the bone involvement in a group of patients with β-thalassemia in terms of geometry and bone quality; moreover, we evaluated prevalence and site of IDCs in these patients.

Methods. Our retrospective case-control study was conducted in a population of adults with β-thalassemia, aged between 18 and 50 years. The patients were divided, according with the International Society for Clinical Densitometry, into 2 groups: subjects with Zs ≤ -2.0, below the expected range for age, and subjects with Zs > -2.0, within the expected range for age. Assessment of proximal femur geometry was performed using the Hip Structural Analysis (HSA), that provides the following parameters: Hip Axis Length (HAL), Femoral Strength Index (FSI), Cross-Sectional Moment of Inertia (CSMI) Cross-Sectional Area (CSA), Section Modulus (Z), and buckling ratio (BR). Assessment of bone quality was performed using the Trabecular Bone Score (TBS), stratifying subjects into 3 groups: with abnormal (TBS ≤ 1.200), partially altered (TBS> 1.200 and <1.350), and normal (TBS ≥ 1.350) trabecular microarchitecture. Finally, we evaluated the prevalence of IDCs highlighted by images of Vertebral Fracture Assessment (VFA).

Results. We evaluated 49 patients with β-thalassemia, mean aged 35.16 ± 9.59 years, divided into two groups: 25 patients with Zs ≤ -2.0 and 24 patients with Zs > -2.0. Results demonstrated all statistically significant differences (p<0.001) between the two groups in BMD, Ts and Zs (in all examined districts), and in number of fragility fractures (p=0.0339). HSA showed that there are significant differences between groups only in FSI (p=0.0068) and CSA (p=0.0041). Furthermore, TBS of patients with Zs ≤ -2.0 was significantly lower than individuals Zs > -2.0 (p=0.0006); there was a statistically significant difference between the two groups in categorized TBS (p=0.0061). Finally, we evidenced in 7 patients (14.29%) the presence of at least one IDC.

Conclusions. Our results showed that β-thalassemia is characterized not only by a reduction in BMD, but also by a geometric and qualitative bone microarchitecture involvement. HSA and even more TBS should be included in the assessment of individuals with β-thalassemia, in order to obtain a proper management and prevention of fragility fractures; furthermore, the presence of IDCs might be better investigated in these patients.

About the Authors

Alessandro de Sire
Second University of Naples
Italy


Giovanni Iolascon
Second University of Naples
Italy


Review

For citations:


de Sire A., Iolascon G. Bone microarchitecture involvement and intervertebral disc alterations in patients with β-thalassemia: a retrospective study. Problems of Endocrinology. 2016;62(5):70-71. https://doi.org/10.14341/probl201662570-71

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ISSN 0375-9660 (Print)
ISSN 2308-1430 (Online)