Endocrinology Division, Federal University of Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil.
Endocrinology Division, Faculty of Medical Sciences, State University of Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil.
Clin Endocrinol (Oxf). 2021 Oct;95(4):587-594. doi: 10.1111/cen.14533. Epub 2021 Jun 23.
Tumour-induced osteomalacia (TIO) is a rare paraneoplastic condition characterised by decreased tubular phosphate reabsorption. The purpose of this study is to evaluate bone mineral density (BMD) and microarchitecture in six TIO patients, compared with 18 healthy controls.
Volumetric BMD and microarchitecture were evaluated by high-resolution peripheral quantitative computed tomography (HR-pQCT), and areal BMD by dual-energy X-ray absorptiometry (DXA). Differences between groups were significant for p < .05.
All TIO subjects were healthy until the development of diffuse bone pain and multiple skeletal fractures and deformities. At baseline, sPi and TmPi/GFR were low and patients were on vitamin D and phosphate replacement at the study. Compared with controls, TIO patients had lower aBMD at lumbar spine and hip, and lower vBMD at trabecular, cortical and entire bone, at distal radius (R) and distal tibia (T): trabecular vBMD (R = 118.3 × 177.1; T = 72.3 × 161.3 gHA/cm ); cortical vBMD (R = 782.3 × 866.5; T = 789.1 × 900.9 gHA/cm ); total region vBMD (R = 234.5 × 317; T = 167.1 × 295.8 gHA/cm ). Bone microarchitecture was very heterogeneous among patients and significantly different from controls: lower cortical thickness (R = 0.59 × 0.80; T = 0.90 × 1.31 mm), bone volume-to-total volume ratio (R = 0.09 × 0.14; T = 0.06 × 0.13) and Tb.N (R = 1.46 × 2.10; T = 0.93 × 1.96 mm ) and also higher Tb.Sp (R = 0.70 × 0.41; T = 1.28 × 0.45 mm) and Tb.1/N.SD (R = 0.42 × 0.18; T = 0.87 × 0.20 mm).
In this original study of TIO patients, DXA and HR-pQCT evaluation identified lower areal and volumetric BMD and severely impaired microarchitecture at cortical and trabecular bones, which probably contribute to bone fragility and fractures.
肿瘤相关性骨软化症(TIO)是一种罕见的副瘤性疾病,其特征为管状磷酸盐重吸收减少。本研究的目的是评估 6 例 TIO 患者与 18 例健康对照者的骨密度(BMD)和微结构。
通过高分辨率外周定量 CT(HR-pQCT)评估体积 BMD 和微结构,通过双能 X 线吸收法(DXA)评估面积 BMD。组间差异有统计学意义(p<.05)。
所有 TIO 患者在出现弥漫性骨痛和多发性骨骼骨折和畸形之前均健康。在基线时,sPi 和 TmPi/GFR 较低,患者在研究时接受了维生素 D 和磷酸盐替代治疗。与对照组相比,TIO 患者的腰椎和髋部的 aBMD 较低,桡骨远端(R)和胫骨远端(T)的小梁、皮质和整体骨的 vBMD 较低:小梁 vBMD(R=118.3×177.1;T=72.3×161.3 gHA/cm);皮质 vBMD(R=782.3×866.5;T=789.1×900.9 gHA/cm);总区域 vBMD(R=234.5×317;T=167.1×295.8 gHA/cm)。患者的骨微结构非常不均匀,与对照组有显著差异:皮质厚度较低(R=0.59×0.80;T=0.90×1.31 mm),骨体积与总体积比(R=0.09×0.14;T=0.06×0.13)和 Tb.N(R=1.46×2.10;T=0.93×1.96 mm),Tb.Sp 也较高(R=0.70×0.41;T=1.28×0.45 mm)和 Tb.1/N.SD(R=0.42×0.18;T=0.87×0.20 mm)。
在这项对 TIO 患者的原始研究中,DXA 和 HR-pQCT 评估发现,面积和体积 BMD 较低,皮质和小梁骨的微结构严重受损,这可能导致骨骼脆弱和骨折。