Deane Andrew, Constancio Leonor, Fogelman Ignac, Hampson Geeta
Department of Chemical Pathology and metabolic bone clinic, St Thomas' Hospital campus, Kings College London, London, UK.
BMC Musculoskelet Disord. 2007 Jan 10;8:3. doi: 10.1186/1471-2474-8-3.
It is still unclear whether addition of calcium/vitamin D supplements leads to an incremental benefit in patients taking bisphosphonates and whether achievement of serum level of 25 (OH) vitamin D of at least 70 nmol/L has an impact on the skeletal response to bisphosphonates. Moreover the maintenance of BMD after bisphosphonates withdrawal with the continuation of calcium/vitamin D supplements only, remains uncertain. The aims were to assess the impact of vitamin D status on changes in bone mineral density (BMD) in firstly patients with post-menopausal osteoporosis on bisphosphonates and secondly following discontinuation of bisphosphonates after long-term use.
Two patient groups were recruited. The first study population comprised of 112 women treated with a bisphosphonate. The second study population consisted of 35 women who had been on bisphosphonates for > 5 years in whom the treatment agent was discontinued. Baseline BMD, changes in BMD following treatment, duration of treatment, serum 25 (OH) vitamin D, parathyroid hormone (PTH), urine C-terminal telopeptides of type 1 collagen (CTX) were obtained on the study participants.
In the first study group, subjects with serum vitamin D concentrations (> 70 nmol/L) had a significantly lower serum PTH level (mean [SEM] 41 2 ng/L). PTH concentrations of 41 ng/L or less was associated with a significantly higher increase in BMD at the hip following treatment with bisphosphonates compared to patients with PTH > 41 ng/L (2.5% [0.9] v/s -0.2% [0.9], P = 0.04). In the second study group, discontinuation of bisphosphonate for 15 months after long-term treatment did not result in significant bone loss at the lumbar spine and total hip, although a trend towards gradual decline in BMD at the femoral neck was observed.
the data suggest that optimal serum 25 (OH) vitamin D concentration may lead to further reduction in bone loss at the hip in patients on bisphosphonates. A prospective controlled trial is needed to evaluate whether the response to bisphosphonates is influenced by vitamin D status. BMD is preserved at the lumbar spine and total hip following discontinuation of bisphosphonate for a short period following long-term treatment, although a gradual loss occurs at the femoral neck.
对于正在服用双膦酸盐的患者,补充钙/维生素D是否能带来额外益处,以及血清25(OH)维生素D水平达到至少70 nmol/L是否会影响骨骼对双膦酸盐的反应,目前仍不清楚。此外,仅通过持续补充钙/维生素D来维持双膦酸盐停药后的骨密度,情况仍不确定。本研究旨在评估维生素D状态对绝经后骨质疏松症患者在服用双膦酸盐时以及长期使用双膦酸盐停药后骨密度变化的影响。
招募了两组患者。第一个研究人群包括112名接受双膦酸盐治疗的女性。第二个研究人群由35名服用双膦酸盐超过5年且已停用治疗药物的女性组成。收集了研究参与者的基线骨密度、治疗后骨密度变化、治疗持续时间、血清25(OH)维生素D、甲状旁腺激素(PTH)、尿Ⅰ型胶原C端肽(CTX)。
在第一个研究组中,血清维生素D浓度(>70 nmol/L)的受试者血清PTH水平显著较低(平均[标准误]41±2 ng/L)。与PTH>41 ng/L的患者相比,PTH浓度为41 ng/L或更低的患者在接受双膦酸盐治疗后髋部骨密度的增加显著更高(2.5%[0.9]对-0.2%[0.9],P = 0.04)。在第二个研究组中,长期治疗后停用双膦酸盐15个月,腰椎和全髋部并未出现明显的骨质流失,尽管在股骨颈观察到骨密度有逐渐下降的趋势。
数据表明,最佳血清25(OH)维生素D浓度可能会使服用双膦酸盐的患者髋部骨质流失进一步减少。需要进行一项前瞻性对照试验来评估维生素D状态是否会影响对双膦酸盐的反应。长期治疗后短期停用双膦酸盐,腰椎和全髋部的骨密度得以保留,尽管股骨颈会逐渐出现骨质流失。