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DXA and pQCT derived parameters in Indian children with beta thalassemia major - A case controlled study

机译:印度儿童DXA和PQCT衍生的参数,具有Beta Thalassemia专业 - 一个案例控制研究

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Children with beta thalassemia major (BTM) are known to have reduced bone mass which increases incidence of non-traumatic fractures. Few studies have assessed prevalence of fractures and bone health in underprivileged children with BTM. Our objectives were to 1) determine prevalence of fractures in underprivileged Indian children with BTM, 2) assess size corrected bone density and bone geometry using Dual x-ray absorptiometry (DXA) and peripheral quantitative computerized tomography (pQCT) in these children and healthy controls 3) determine predictors of fractures in children with BTM 4) compare differences in bone density between children with BMT with and without fractures. Bone mineral content and areal bone mineral density (aBMD) of lumbar spine and whole body and vertebral fracture assessment (VFA) was performed by DXA in 334 children (3-18 years, 167 BTM + 167 controls). Volumetric BMD (vBMD) and bone geometry were assessed by pQCT (subset, 70 BTM, 70 healthy) at distal radius. Children with BTM had higher prevalence of vertebral and long bone fractures (p < 0.05). DXA aBMD was lower in children with BTM (p 0.05), whereas, lumbar spine bone mineral apparent density (LSBMAD) was higher (p 0.05). Children with BTM had lower total distal radial vBMD, cortical vBMD and strength strain index (SSI) at 66% site whereas, distal radial trabecular vBMD at 4% was higher (p < 0.05). On height adjustment, children with BTM had lower muscle area and cortical thickness and higher marrow area (p < 0.05) at 66% site. Age, body size, total body less head (TBLH) aBMD and strength strain index (SSI) were important predictors of fractures in children with BTM. Thus, children with BTM had higher prevalence of nontraumatic fractures. Despite lower areal and volumetric densities, they had higher LSBMAD and trabecular densities which may be attributed to erythroid hyperplasia and iron deposition due to inadequate transfusion and chelation. As LSBMAD is raised in these children, it is unlikely to identify BTM subjects at risk of fracture; VFA thus maybe useful in identifying asymptomatic vertebral fractures.
机译:众所周知,含有β的孩子们的主要(BTM)具有降低的骨质量,这增加了非创伤性骨折的发生率。少数研究评估了BTM贫困儿童骨折和骨骼健康的患病率。我们的目标是1)确定使用双X射线吸收计(DXA)和周边定量计算机断层扫描(DXA)和健康控制中的双X射线吸收测量(DXA)和外围定量计算机断层扫描(DXA)和健康对照中的弱势印度儿童骨折骨折的骨折骨折3)确定BTM 4患儿骨折的预测因子)在没有骨折的情况下比较患有BMT的儿童骨密度的差异。腰椎和全身和椎体骨质密度(ABMD)的骨矿物质含量和椎体骨折评估(VFA)于334名儿童(3-18岁,167年BTM + 167对照)进行。通过远端半径的PQCT(子集,70 btm,70健康)评估体积BMD(VBMD)和骨几何。 BTM的儿童具有更高的椎体和长骨骨折患病率(P <0.05)。 DXA ABMD在BTM的儿童中较低(P 0.05),而腰椎骨矿物明显密度(LSBMAD)较高(P 0.05)。 BTM的儿童总远端径向VBMD,皮质VBMD和强度应变指数(SSI)在66%位点,而4%的远端径向小梁VBMD(P <0.05)。在高度调整上,BTM的儿童在66%位点上具有较低的肌肉区域和皮质厚度和更高的骨髓区域(P <0.05)。年龄,体型,总体较小的头部(TBLH)ABMD和强度应变指数(SSI)是BTM儿童骨折的重要预测因子。因此,BTM的儿童具有更高的非吸引性裂缝的患病率。尽管面积和体积密度较低,但由于输血和螯合不足,它们具有较高的LSBMAD和小梁沉积,其可能归因于红细胞增生和铁沉积。随着LSBMAD在这些儿童中提出,它不太可能识别骨折风险的BTM受试者;因此,VFA可能用于识别无症状的椎骨骨折。

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