Evaluation of relationship between biochemical parameters and osteoporosis in patients with β-thalassemia major

M. Hamidpour, Fatemeh Jafari, Mahdieh Mehrpouri, Azita Azarkyvan, Davod Bashash, Aliakbar Khadem Maboudi
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Abstract

Background: Osteoporosis is one of the late complications of β-Thalassemia major. The pathogenesis of osteoporosis depends on different factors. Ineffectiveness of hematopoiesis is the major factor, and the other factors are defected by hormonal functions or biochemical parameters. Osteoclasts hyperactivity in thalassemia increases the serum receptor activator of nuclear factor Kappa B ligand (RANKL), which plays a crucial role in bone development. This study aimed to evaluate the biochemical and hormonal parameters in patients with β-thalassemia major and their association with osteoporosis. Materials and Methods: In this case-control study, 52 patients with β-thalassemia major and 23 with thalassemia minor as controls were enrolled. The patients’ Bone Mineral Density (BMD) was measured using the Dual Energy X-ray absorptiometry (DEXA) method, and 6 mL peripheral blood of the patients and controls was obtained to detect hormonal and biochemical parameters. Data were analyzed using ANOVA, Spearman correlation coefficient, and T-test. Results:  The mean of BMD in patients was 0.59±0.01 and 0.69±0.11 in femur and vertebrae, respectively. The biochemical parameters in the (patients/ controls) including calcium and alkaline phosphatase (ALK) were 9.1/ 10.2 mg/dL and 171.1/310 IU, respectively indicating a significant decrease (P< 0.05) compared to the controls. On the contrary, the mean levels of Ferritin and Zinc were 1914.18 µg/L and 113.92 mg/mL, respectively which were significantly increased (P= 0.015 and P=0.045, respectively). There was a negative correlation between the femurs BMD of patients with the RANKL level (r= - 0.8, p = 0.034) and the vertebrae BMD of patients with a Parathormone (PTH) level (r= - 0.8, P = 0.028).  Conclusion: The study results indicated that the hyperactivity of RANKL and PTH in thalassemia patients might cause osteoporosis; therefore, detecting biomarkers mentioned above could be useful to diagnose osteoporosis.
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β-地中海贫血患者生化指标与骨质疏松关系的评价
背景:骨质疏松是重度β-地中海贫血的晚期并发症之一。骨质疏松症的发病机制取决于不同的因素。造血功能无效是主要因素,其他因素受激素功能或生化参数的影响。地中海贫血的破骨细胞过度活跃增加了核因子κ B配体(RANKL)的血清受体激活因子,这在骨发育中起着至关重要的作用。本研究旨在评价β-地中海贫血患者的生化和激素指标及其与骨质疏松症的关系。材料与方法:本病例对照研究纳入52例重度β-地中海贫血患者和23例轻度地中海贫血患者作为对照。采用双能x线骨密度仪(DEXA)测定患者骨密度(BMD),取患者及对照组外周血6 mL检测激素及生化指标。数据分析采用方差分析、Spearman相关系数和t检验。结果:患者股骨骨密度平均值为0.59±0.01,椎骨骨密度平均值为0.69±0.11。(患者/对照组)钙和碱性磷酸酶(ALK)生化指标分别为9.1/ 10.2 mg/dL和171.1/310 IU,与对照组相比显著降低(P< 0.05)。相反,铁蛋白和锌的平均含量分别为1914.18µg/L和113.92 mg/mL,显著升高(P= 0.015和P=0.045)。RANKL水平患者股骨骨密度(r= - 0.8, p = 0.034)与甲状旁激素(PTH)水平患者椎骨骨密度(r= - 0.8, p = 0.028)呈负相关。结论:地中海贫血患者RANKL和PTH的高活性可能导致骨质疏松;因此,检测上述生物标志物可能有助于骨质疏松症的诊断。
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来源期刊
CiteScore
0.80
自引率
33.30%
发文量
33
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