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重组人生长激素-1 序贯利塞膦酸钠治疗神经性厌食症女性患者增加脊柱骨密度:一项随机、安慰剂对照试验。

Sequential Therapy With Recombinant Human IGF-1 Followed by Risedronate Increases Spine Bone Mineral Density in Women With Anorexia Nervosa: A Randomized, Placebo-Controlled Trial.

机构信息

Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

J Bone Miner Res. 2021 Nov;36(11):2116-2126. doi: 10.1002/jbmr.4420. Epub 2021 Sep 2.

Abstract

Anorexia nervosa is complicated by low bone mineral density (BMD) and increased fracture risk associated with low bone formation and high bone resorption. The lumbar spine is most severely affected. Low bone formation is associated with relative insulin-like growth factor 1 (IGF-1) deficiency. Our objective was to determine whether bone anabolic therapy with recombinant human (rh) IGF-1 used off-label followed by antiresorptive therapy with risedronate would increase BMD more than risedronate or placebo in women with anorexia nervosa. We conducted a 12-month, randomized, placebo-controlled study of 90 ambulatory women with anorexia nervosa and low areal BMD (aBMD). Participants were randomized to three groups: 6 months of rhIGF-1 followed by 6 months of risedronate ("rhIGF-1/Risedronate") (n = 33), 12 months of risedronate ("Risedronate") (n = 33), or double placebo ("Placebo") (n = 16). Outcome measures were lumbar spine (1° endpoint: postero-anterior [PA] spine), hip, and radius aBMD by dual-energy X-ray absorptiometry (DXA), and vertebral, tibial, and radial volumetric BMD (vBMD) and estimated strength by high-resolution peripheral quantitative computed tomography (HR-pCT) (for extremity measurements) and multi-detector computed tomography (for vertebral measurements). At baseline, mean age, body mass index (BMI), aBMD, and vBMD were similar among groups. At 12 months, mean PA lumbar spine aBMD was higher in the rhIGF-1/Risedronate (p = 0.03) group and trended toward being higher in the Risedronate group than Placebo. Mean lateral lumbar spine aBMD was higher, in the rhIGF-1/Risedronate than the Risedronate or Placebo groups (p < 0.05). Vertebral vBMD was higher, and estimated strength trended toward being higher, in the rhIGF-1/Risedronate than Placebo group (p < 0.05). Neither hip or radial aBMD or vBMD, nor radial or tibial estimated strength, differed among groups. rhIGF-1 was well tolerated. Therefore, sequential therapy with rhIGF-1 followed by risedronate increased lateral lumbar spine aBMD more than risedronate or placebo. Strategies that are anabolic and antiresorptive to bone may be effective at increasing BMD in women with anorexia nervosa. © 2021 American Society for Bone and Mineral Research (ASBMR).

摘要

神经性厌食症的特点是骨密度(BMD)低,骨折风险增加,这与骨形成减少和骨吸收增加有关。腰椎受影响最严重。骨形成减少与相对胰岛素样生长因子 1(IGF-1)缺乏有关。我们的目的是确定在神经性厌食症女性中,使用重组人生长激素(rhIGF-1)进行骨合成代谢治疗,然后使用利塞膦酸盐进行抗吸收治疗,是否比利塞膦酸盐或安慰剂更能增加 BMD。我们进行了一项为期 12 个月、随机、安慰剂对照的研究,纳入了 90 名患有神经性厌食症且骨密度(aBMD)较低的门诊女性患者。参与者被随机分为三组:rhIGF-1 治疗 6 个月,然后利塞膦酸盐治疗 6 个月(rhIGF-1/利塞膦酸盐)(n=33),利塞膦酸盐治疗 12 个月(利塞膦酸盐)(n=33),或双安慰剂(n=16)。主要结局为腰椎(1°终点:前后位[PA]脊柱)、髋部和桡骨的双能 X 射线吸收仪(DXA)aBMD,以及通过高分辨率外周定量计算机断层扫描(HR-pCT)(四肢测量)和多探测器计算机断层扫描(椎体测量)评估的椎体、胫骨和桡骨体积 BMD(vBMD)和估计强度。在基线时,各组的平均年龄、体重指数(BMI)、aBMD 和 vBMD 相似。在 12 个月时,rhIGF-1/利塞膦酸盐组的 PA 腰椎 aBMD 较高(p=0.03),利塞膦酸盐组的趋势也高于安慰剂组。rhIGF-1/利塞膦酸盐组的侧位腰椎 aBMD 高于利塞膦酸盐组或安慰剂组(p<0.05)。rhIGF-1/利塞膦酸盐组的椎体 vBMD 较高,估计强度也有升高的趋势(p<0.05)。各组间髋部或桡骨的 aBMD 或 vBMD ,或桡骨或胫骨的估计强度均无差异。rhIGF-1 耐受性良好。因此,rhIGF-1 序贯利塞膦酸盐治疗可使腰椎侧位 aBMD 增加,高于利塞膦酸盐或安慰剂。对骨骼具有合成代谢和抗吸收作用的策略可能会有效增加神经性厌食症女性的 BMD。

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