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Therapy of Hypoparathyroidism With PTH(1-84): A Prospective Six Year Investigation of Efficacy and Safety.甲状旁腺激素(1-84)治疗甲状旁腺功能减退症:一项为期六年的疗效与安全性前瞻性研究。
J Clin Endocrinol Metab. 2016 Jul;101(7):2742-50. doi: 10.1210/jc.2015-4135. Epub 2016 May 4.
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Noninvasive Assessment of Skeletal Microstructure and Estimated Bone Strength in Hypoparathyroidism.甲状旁腺功能减退症患者骨骼微结构及估计骨强度的无创评估
J Bone Miner Res. 2016 Feb;31(2):308-16. doi: 10.1002/jbmr.2609. Epub 2015 Sep 3.
3
PTH(1-84) Administration in Hypoparathyroidism Transiently Reduces Bone Matrix Mineralization.甲状旁腺功能减退症患者给予全段甲状旁腺激素(1-84)可短暂降低骨基质矿化。
J Bone Miner Res. 2016 Jan;31(1):180-9. doi: 10.1002/jbmr.2588. Epub 2015 Jul 28.
4
The Epidemiology of Nonsurgical Hypoparathyroidism in Denmark: A Nationwide Case Finding Study.丹麦非手术性甲状旁腺功能减退症的流行病学:一项全国性病例发现研究。
J Bone Miner Res. 2015 Sep;30(9):1738-44. doi: 10.1002/jbmr.2501. Epub 2015 May 31.
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Literature review: The effects of teriparatide therapy at the hip in patients with osteoporosis.文献综述:特立帕肽治疗对骨质疏松症患者髋部的影响。
Bone. 2014 Oct;67:246-56. doi: 10.1016/j.bone.2014.07.014. Epub 2014 Jul 15.
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Bone quality of the newest bone formed after two years of teriparatide therapy in patients who were previously treatment-naïve or on long-term alendronate therapy.在既往未经治疗或接受长期阿仑膦酸盐治疗的患者中,接受特立帕肽治疗两年后形成的最新骨骼的骨质量。
Osteoporos Int. 2014 Dec;25(12):2709-19. doi: 10.1007/s00198-014-2814-2. Epub 2014 Jul 19.
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Postsurgical hypoparathyroidism--risk of fractures, psychiatric diseases, cancer, cataract, and infections.术后甲状旁腺功能减退——骨折、精神疾病、癌症、白内障及感染的风险。
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Effects of teriparatide on cortical histomorphometric variables in postmenopausal women with or without prior alendronate treatment.特立帕肽对有或无既往阿伦膦酸钠治疗的绝经后妇女皮质组织形态计量学变量的影响。
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10
Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee.骨组织形态计量学的标准化命名、符号和单位:美国骨矿研究学会(ASBMR)组织形态计量学命名委员会2012年报告更新版
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甲状旁腺功能减退症患者长期给予 rhPTH(1-84)治疗的骨组织形态计量学研究

The Effects of Long-term Administration of rhPTH(1-84) in Hypoparathyroidism by Bone Histomorphometry.

机构信息

Department of Medicine, Metabolic Bone Diseases Unit, Division of Endocrinology, College of Physicians & Surgeons, Columbia University, New York, NY, USA.

Regional Bone Center, Helen Hayes Hospital, West Haverstraw, New York, USA.

出版信息

J Bone Miner Res. 2018 Nov;33(11):1931-1939. doi: 10.1002/jbmr.3543. Epub 2018 Aug 16.

DOI:10.1002/jbmr.3543
PMID:29972871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6546298/
Abstract

Hypoparathyroidism is a rare disorder that is associated with abnormal bone properties. Recombinant human parathyroid hormone (1-84) [rhPTH(1-84)] in short-term studies has beneficial skeletal effects. Although rhPTH(1-84) will likely be used indefinitely, long-term effects on skeletal microstructure are unknown. We therefore studied histomorphometric changes with transiliac crest bone biopsies before and after 8.3 ± 1 years of rhPTH(1-84) in 13 hypoparathyroid subjects compared with 45 controls. Before institution of rhPTH(1-84), skeletal remodeling indices were markedly suppressed. With long-term treatment, indices of bone remodeling increased. Mineralizing surface increased by 26-fold (0.3 ± 1 to 7.9 ± 7%, p = 0.003), bone formation rate increased by 15-fold (0.003 ± 0.01 to 0.047 ± 0.05 μm /μm/day, p = 0.007), osteoid width doubled (1.9 ± 1 to 4.3 ± 1 lamellae, p = 0.017), and osteoid surface tripled (3.3 ± 3 to 10.8 ± 6%, p = 0.011). Bone resorption as measured by eroded surface increased (4.6 ± 2 to 7.5 ± 3%, p = 0.021). Structural changes demonstrated intratrabecular tunneling, with increases in cancellous bone volume (19.6 ± 5 to 29.1 ± 11%, p = 0.017) and trabecular number (1.8 ± 1 to 2.5 ± 1 #/mm, p = 0.025). Cortical porosity tended to increase (6.3 ± 5 to 9.5 ± 3%, p = 0.07). Mineralizing surface, osteoid surface, and eroded surface surpassed control levels, as did cancellous bone volume, trabecular number, and cortical porosity. These data, the first to reflect such long exposure of any PTH for any disease, illustrate that PTH establishes and maintains a new skeletal state for at least 8 years in hypoparathyroidism. © 2018 American Society for Bone and Mineral Research.

摘要

甲状旁腺功能减退症是一种罕见的疾病,与骨骼异常有关。在短期研究中,重组人甲状旁腺激素(1-84)[rhPTH(1-84)]对骨骼具有有益的作用。尽管 rhPTH(1-84)可能会被无限期使用,但对骨骼微观结构的长期影响尚不清楚。因此,我们在 13 名甲状旁腺功能减退症患者中进行了髂嵴骨活检的组织形态计量学研究,这些患者在接受 rhPTH(1-84)治疗 8.3±1 年后,与 45 名对照者进行了比较。在开始使用 rhPTH(1-84)之前,骨骼重塑指数明显受到抑制。随着长期治疗,骨重塑指数增加。矿化表面增加了 26 倍(0.3±1 至 7.9±7%,p=0.003),骨形成率增加了 15 倍(0.003±0.01 至 0.047±0.05μm/μm/day,p=0.007),骨样组织宽度增加了一倍(1.9±1 至 4.3±1 层,p=0.017),骨样组织表面增加了两倍(3.3±3 至 10.8±6%,p=0.011)。骨吸收表面(4.6±2 至 7.5±3%,p=0.021)的侵蚀表面增加。结构变化显示出骨小梁内隧道,松质骨体积(19.6±5 至 29.1±11%,p=0.017)和骨小梁数量(1.8±1 至 2.5±1#/mm,p=0.025)增加。皮质骨的孔隙度也有增加的趋势(6.3±5 至 9.5±3%,p=0.07)。矿化表面、骨样组织表面和侵蚀表面超过了对照水平,松质骨体积、骨小梁数量和皮质骨孔隙度也超过了对照水平。这些数据首次反映了任何疾病中任何甲状旁腺激素的长期暴露情况,表明甲状旁腺激素在甲状旁腺功能减退症中至少建立并维持了 8 年的新骨骼状态。© 2018 美国骨矿研究协会。