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首页> 外文期刊>Bone Reports >Evaluation of bone mineralization in former preterm born children: Phalangeal quantitative ultrasound cannot replace dual-energy X-ray absorptiometry
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Evaluation of bone mineralization in former preterm born children: Phalangeal quantitative ultrasound cannot replace dual-energy X-ray absorptiometry

机译:前早产儿骨矿化的评估:指骨定量超声不能替代双能X线骨密度仪

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BackgroundPreterm infants are at risk of impaired bone health in later life. Dual-energy X-ray absorptiometry-scan (DXA) is the gold standard to determine bone mineralization. Phalangeal quantitative ultrasound (pQUS) is an alternative technique that is inexpensive, easy to use and radiation-free. The aim of this study was to investigate whether both techniques reveal equivalent results.Materials and methodsSixty former preterm infants (31 boys; 29 girls) received a DXA and pQUS at age 9 to 10?years. DXA measured bone mineral content (BMC) and bone mineral density (BMD) for total body and lumbar spine (L1-4), while pQUS measured the amplitude dependent speed of sound (AD-SoS) and bone transit time (BTT) at metacarpals II-IV providing continuous values andZ-scores based on age and sex. Four statistical methods evaluated the association between both techniques: Pearson's correlation coefficients, partial correlation coefficients adjusted for gestational age, height and BMI, Bland-Altman analysis and cross tabulation.ResultsBoth techniques showed a statistically significant weak correlation for continuous values as well asZ-scores (0.291–0.462, p?
机译:背景早产儿在以后的生活中有骨骼健康受损的风险。双能X射线吸收仪扫描(DXA)是确定骨矿化的金标准。 hal角定量超声(pQUS)是一种廉价,易于使用且无辐射的替代技术。这项研究的目的是调查这两种技术是否能显示相同的结果。材料和方法60例早产婴儿(31名男孩; 29名女孩)在9至10岁时接受了DXA和pQUS。 DXA测量了全身和腰椎的骨矿物质含量(BMC)和骨矿物质密度(BMD)(L1-4),而pQUS测量了掌骨的声速振幅(AD-SoS)和骨传输时间(BTT) II-IV根据年龄和性别提供连续的值和Z分数。四种统计方法评估了这两种技术之间的关联:皮尔逊相关系数,针对胎龄,身高和BMI调整的部分相关系数,Bland-Altman分析和交叉制表法。 (0.291–0.462,p <0.05)。男孩有显着且相对较高的相关性(0.468–0.585,p <0.05)。相比之下,女孩的相关性并不显着。计算偏相关时,相关系数进一步降低。 Bland-Altman地块显示出差的一致性。敏感性范围为33%至92%,特异性范围为16%至68%。阳性和阴性预测值的范围分别为4%至38%和82%至97%。结论我们发现DXA和pQUS测量值之间存在统计学上的显着弱相关性和较差的一致性。 DXA不等同于pQUS,因此在9至10岁的早产儿中不能用该技术替代。

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