Sharma Deepti K, Sawyer Rebecca K, Robertson Thomas S, Stamenkov Roumen, Solomon Lucian B, Atkins Gerald J, Clifton Peter M, Morris Howard A, Anderson Paul H
Health and Biomedical Innovation, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide 5001, Australia.
Royal Adelaide Hospital, Adelaide 5001, Australia.
J Clin Med. 2019 Nov 15;8(11):1988. doi: 10.3390/jcm8111988.
Vitamin D, along with calcium, is generally considered necessary for bone health and reduction of fractures. However, he effects of improving vitamin D status have not always been observed to improve bone mineral density (BMD). We have investigated whether varying vitamin D status in humans, as measured by serum 25(OH)D levels, relate to micro-structural and histomorphetric measures of bone quality and quantity, rather than density. Intertrochanteric trabecular bone biopsies and serum samples were collected from patients undergoing hip arthroplasty (65 females, 38 males, mean age 84.8 ± 8.3 years) at Royal Adelaide Hospital. Estimated GFR, serum ionized calcium, alkaline phosphatase, albumin, supplement and medication intake prior to surgery were taken from patient case records. Serum 25(OH)D, 1,25(OH)2D, and parathyroid hormone (PTH) levels were measured by immunoassays. Trabecular bone structural indices were determined by high-resolution micro-CT. Mean wall thickness (MWT) was measured on toluidine blue-stained histological sections. Bone mRNA levels for vitamin D metabolising enzymes CYP27B1 and CYP24A1 were measured by qRT-PCR. While serum 25(OH)D levels did not associate with bone volume/tissue volume (BV/TV%), serum 25(OH)D levels were strongly and independently associated with MWT ( = 0.81 < 0.0001) with values significantly greater in patients with higher serum 25(OH)D levels. Furthermore, serum 25(OH)D levels were negatively associated with Bone Surface/Bone Volume (BS/BV) ( = -0.206, < 0.05) and together with bone CYP27B1 and CYP24A1 mRNA accounted for 10% of the variability of BS/BV ( = 0.001). These data demonstrate that serum 25(OH)D is an independent positive predictor of micro-structural and bone formation measures and may be dependent, in part, on its metabolism within the bone.
维生素D与钙一起,通常被认为是骨骼健康和减少骨折所必需的。然而,改善维生素D状态的效果并不总是能观察到骨矿物质密度(BMD)的提高。我们研究了以血清25(OH)D水平衡量的人体不同维生素D状态是否与骨质量和数量的微观结构及组织形态测量指标相关,而非与密度相关。在皇家阿德莱德医院,从接受髋关节置换术的患者(65名女性,38名男性,平均年龄84.8±8.3岁)中采集转子间小梁骨活检样本和血清样本。术前估计的肾小球滤过率、血清离子钙、碱性磷酸酶、白蛋白、补充剂和药物摄入量取自患者病历。血清25(OH)D、1,25(OH)2D和甲状旁腺激素(PTH)水平通过免疫测定法测量。小梁骨结构指标通过高分辨率微CT确定。在甲苯胺蓝染色的组织切片上测量平均壁厚度(MWT)。通过qRT-PCR测量维生素D代谢酶CYP27B1和CYP24A1的骨mRNA水平。虽然血清25(OH)D水平与骨体积/组织体积(BV/TV%)无关,但血清25(OH)D水平与MWT呈强且独立的相关性(=0.81,<0.0001),血清25(OH)D水平较高的患者其值显著更高。此外,血清25(OH)D水平与骨表面/骨体积(BS/BV)呈负相关(=-0.206,<0.05)且与骨CYP27B1和CYP24A1 mRNA一起占BS/BV变异性的10%(=0.001)。这些数据表明血清25(OH)D是微观结构和骨形成测量指标的独立阳性预测因子,并且可能部分取决于其在骨内的代谢。