首页> 外文期刊>Journal of Bone and Mineral Metabolism >Risedronate improves proximal femur bone density and geometry in patients with osteoporosis or osteopenia and clinical risk factors of fractures: a practice-based observational study
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Risedronate improves proximal femur bone density and geometry in patients with osteoporosis or osteopenia and clinical risk factors of fractures: a practice-based observational study

机译:利塞膦酸改善骨质疏松症或骨质减少症患者的近端股骨骨密度和几何形状以及骨折的临床危险因素:一项基于实践的观察性研究

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The purpose of this practice-based observational study was to clarify the acute effect of risedronate on proximal femur bone mineral density (BMD) and structural geometry in patients with an increased risk of fractures. One hundred sixty-four patients (7 men and 157 postmenopausal women; mean age, 69.2 years) with osteoporosis or osteopenia and clinical risk factors of fractures were analyzed. All these patients were treated with risedronate for 1 year. Urinary levels of cross-linked N-terminal telopeptide of type I collagen (NTX) were measured at baseline and 4 months after the start of treatment. BMD of the lumbar spine and proximal femur and structural geometric parameters of the proximal femur were evaluated by dual-energy X-ray absorptiometry with advanced hip assessment (AHA) software at baseline and every 4 months. Urinary NTX levels significantly decreased after 4 months of treatment. BMD of the femoral neck and total hip significantly increased after 4, 8, and 12 months of treatment. Cross-sectional moment of inertia (CSMI) and cross-sectional area significantly increased after 4, 8, and 12 months of treatment. An increase in CSMI was apparently greater than those of proximal femur BMD after 4 months of treatment. These results suggest the acute (4 months) and sustained (12 months) effect of risedronate on proximal femur structural geometry as well as BMD as a result of suppression of bone resorption in patients with an increased risk of fractures.
机译:这项基于实践的观察研究的目的是阐明利塞膦酸盐对骨折风险增加的患者股骨近端骨矿物质密度(BMD)和结构几何形状的急性影响。分析了164例骨质疏松或骨质减少和骨折的临床危险因素的患者(男7例,绝经后157例;平均年龄69.2岁)。所有这些患者均接受利塞膦酸盐治疗1年。在基线和治疗开始后4个月测量尿液中I型胶原蛋白(NTX)交联的N末端端肽的尿水平。基线和每4个月,通过双能X线骨密度仪和高级髋关节评估(AHA)软件评估腰椎和股骨近端的BMD和股骨近端的结构几何参数。治疗4个月后尿NTX水平显着降低。治疗4、8和12个月后,股骨颈和全髋骨的BMD显着增加。在治疗4、8和12个月后,截面惯性矩(CSMI)和截面面积显着增加。治疗4个月后,CSMI的增加明显大于股骨近端BMD。这些结果表明,对于骨折风险增加的患者,利塞膦酸盐对股骨近端结构几何形状和骨密度的急性(4个月)和持续(12个月)作用是抑制骨吸收的结果。

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