Parathyroid Hormone: Anabolic Treatment of Osteoporosis

Osteoporosis ◽  
2013 ◽  
pp. 158-177
Author(s):  
Erik Fink Eriksen
2017 ◽  
Vol 7 (4) ◽  
pp. 482-496 ◽  
Author(s):  
Yang Yang ◽  
Ali Aghazadeh-Habashi ◽  
Arash Panahifar ◽  
Yuchin Wu ◽  
Krishna H. Bhandari ◽  
...  

2010 ◽  
Vol 54 (2) ◽  
pp. 213-219 ◽  
Author(s):  
Victória Z. Cochenski Borba ◽  
Nádila Cecyn Pietszkowski Mañas

Anabolic drugs have recently widened therapeutic options in osteoporosis treatment, as they influence processes associated with bone formation to a greater extent and earlier than bone reabsortion. They positively affect a number of skeletal properties besides bone density, as intermittent administration of parathyroid hormone (PTH) results in an increase in the number and activity of osteoblasts leading to an increase in bone mass and improvement in skeletal architecture at both the trabecular and cortical bone. Human recombinant parathyroid hormone (hrPTH 1-84) and human recombinant PTH peptide 1-34 (teriparatide) belong to this group. The objective of this paper is to review PTH actions, benefits and adverse effects, action on biochemical markers, combination therapy with antiresorptive agents, impact of antiresorptive therapy prior to anabolic treatment, sequential treatment, and effect on glucocorticoid-induced osteoporosis.


2008 ◽  
Vol 1 ◽  
pp. CCRep.S1026 ◽  
Author(s):  
Terje Forslund ◽  
Anna-Mari Koski ◽  
Arvo Koistinen ◽  
Anu Sikiö

A breakthrough in understanding of mechanisms of bone structure regulation has brought about the introduction of the new synthetic recombinant human parathyroid hormone 1–34 (PTH1-34; Teriparatide) in the treatment of osteoporosis. These mechanisms, involving the RANKL, RANK, and osteoprotegerin system, are also known to be involved in malignant myeloma (MM) and tumor and bone metastasis development. We report a case in which MM was found after treatment of osteoporosis with teriparatide. We were unable to demonstrate any direct association between the MM and teriparatide treatment. However, it seemed intriguing that similar mechanisms are activated in the development of MM as those being working during teriparatide treatment. In the view of our case, we propose that MM by examination of serum protein fraction should be searched for prior to treatment with teriparatide as it is an exclusion criterion in teriparatide treatment of secondary osteoporosis. A search for other metastatic diseases prior to teriparatide treatment should eventually also be considered. The theoretical basis for our proposal is discussed.


Peptides ◽  
2009 ◽  
Vol 30 (6) ◽  
pp. 1173-1180 ◽  
Author(s):  
Jiao Feng ◽  
Yanhua Liu ◽  
Yun Xing ◽  
Huaqian Wang ◽  
Taiming Li ◽  
...  

1998 ◽  
Vol 8 (1) ◽  
pp. 31-37 ◽  
Author(s):  
Paul Morley ◽  
James F Whitfield ◽  
Gordon Willick

2005 ◽  
Vol 26 (5) ◽  
pp. 688-703 ◽  
Author(s):  
Anthony B. Hodsman ◽  
Douglas C. Bauer ◽  
David W. Dempster ◽  
Larry Dian ◽  
David A. Hanley ◽  
...  

1976 ◽  
Vol 50 (2) ◽  
pp. 14P-14P
Author(s):  
J. Reeve ◽  
J. A. Parsons ◽  
G. W. Tregear ◽  
A. J. Darby ◽  
R. Hesp ◽  
...  

2018 ◽  
Vol 535 (1-2) ◽  
pp. 113-119 ◽  
Author(s):  
Allan J. Williams ◽  
Faron Jordan ◽  
Gareth King ◽  
Andrew L. Lewis ◽  
Lisbeth Illum ◽  
...  

2009 ◽  
Vol 84 (3) ◽  
pp. 159-170 ◽  
Author(s):  
Johannes Pleiner-Duxneuner ◽  
Elisabeth Zwettler ◽  
Eleftherios Paschalis ◽  
Paul Roschger ◽  
Valerie Nell-Duxneuner ◽  
...  

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