首页> 外文期刊>JAMA: the Journal of the American Medical Association >Prevention of estrogen deficiency-related bone loss with human parathyroid hormone-(1-34): a randomized controlled trial.
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Prevention of estrogen deficiency-related bone loss with human parathyroid hormone-(1-34): a randomized controlled trial.

机译:用人甲状旁腺激素(1-34)预防与雌激素缺乏有关的骨质流失:一项随机对照试验。

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CONTEXT: Short-term intermittent administration of parathyroid hormone (PTH) prevents bone loss from the spine in women treated with a gonadotropin-releasing hormone (GnRH) analog. However, the effects of a longer period of PTH administration on bone mass in estrogen-deficient women, particularly on the hip and on cortical bone of the total body, are unknown. OBJECTIVE: To determine whether more prolonged PTH administration can prevent estrogen deficiency bone loss from the hip, spine, and total body in young women with endometriosis receiving GnRH analog (nafarelin acetate) therapy. DESIGN: Randomized controlled trial. SETTING: General Clinical Research Center of a tertiary care, university-affiliated hospital. PATIENTS: Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis. INTERVENTION: Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily). MAIN OUTCOME MEASURES: The primary end points were bone mineral density (BMD) of the anterior-posterior and lateral spine, femoral neck, trochanter, radial shaft, and total body at 12 months of treatment. RESULTS: In the women who received nafarelin alone, the mean (SEM) BMDs of the anterior-posterior spine, lateral spine, femoral neck, trochanter, and total body were 4.9% (0.6%) (P<.001), 4.9% (0.8%) (P<.001), 4.7% (1.1%) (P<.001), 4.3% (0.9%) (P<.001), and 2.0% (0.6%) (P= .003) lower than at baseline after 12 months of therapy. In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency. Radial shaft BMD did not change significantly in either group. Serum bone-specific alkaline phosphatase and osteocalcin concentrations and urinary excretion of hydroxyproline and deoxypyridinoline increased 2-fold to 3-fold during the first 6 to 9 months of therapy in the women who received nafarelin plus hPTH-(1-34) and then declined. Changes in urinary deoxypyridinolone excretion were strongly predictive (r= 0.85) of changes in spinal BMD in the women who received nafarelin plus hPTH-(1-34). CONCLUSIONS: Parathyroid hormone prevents bone loss from the proximal femur and total body and increases lumbar spinal BMD in young women with GnRH analog-induced estrogen deficiency.
机译:语境:短期间歇性给予甲状旁腺激素(PTH)可以防止接受促性腺激素释放激素(GnRH)类似物治疗的女性的脊柱骨质流失。但是,长期服用PTH对缺乏雌激素的女性,特别是对整个身体的臀部和皮质骨的骨质的影响尚不清楚。目的:确定长期服用PTH是否可以预防接受GnRH类似物(醋酸萘法林)治疗的子宫内膜异位症年轻女性的雌激素缺乏症,使其从臀部,脊柱和全身骨质流失。设计:随机对照试验。单位:大学附属医院三级医疗综合临床研究中心。患者:43名年龄在21至45岁之间的有症状子宫内膜异位的女性。干预措施:单独使用那法瑞林(每天两次鼻内200微克,每天两次)或那法瑞林加人甲状旁腺激素-(1-34)(hPTH- [1-34])(每天皮下40微克)。主要观察指标:治疗的主要终点是治疗12个月时前后脊柱和外侧脊柱,股骨颈,转子,radial骨和全身的骨矿物质密度(BMD)。结果:仅接受那法瑞林治疗的女性中,前后脊柱,外侧脊柱,股骨颈,转子和全身的平均BMD为4.9%(0.6%)(P <.001),4.9% (0.8%)(P <.001),4.7%(1.1%)(P <.001),4.3%(0.9%)(P <.001)和2.0%(0.6%)(P = .003)在治疗12个月后低于基线。相比之下,hPTH-(1-34)的共同给药使前后脊柱的BMD增加2.1%(1.1%)(P = .09),外侧脊柱的BMD增加7.5%(1.9%)(P = .002)和尽管存在严重的雌激素缺乏症,但仍可防止股骨颈,转子和全身骨质流失。两组的骨骨密度均无明显变化。在接受那法瑞林加hPTH-(1-34)治疗的妇女中,在治疗的前6到9个月内,血清骨特异性碱性磷酸酶和骨钙素浓度以及尿中羟脯氨酸和脱氧吡啶啉的排泄量增加了2倍至3倍,然后下降了。接受纳法瑞林加hPTH-(1-34)的女性的尿中脱氧吡啶酮的排泄变化强烈预测(b = 0.85)脊柱BMD的变化。结论:甲状旁腺激素可防止GnRH类似物引起的雌激素缺乏的年轻女性从股骨近端和整个身体骨质流失,并增加腰椎BMD。

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