Dynamic and Structural Properties of the Skeleton in Hypoparathyroidism
Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty‐three subjects with hypoparathyroidism and 33 age‐ and sex‐matched control subjects with no known...
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Published in | Journal of bone and mineral research Vol. 23; no. 12; pp. 2018 - 2024 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)
01.12.2008
Amer Soc Bone & Mineral Res |
Subjects | |
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Abstract | Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty‐three subjects with hypoparathyroidism and 33 age‐ and sex‐matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double‐labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean ± SD; BV/TV: 23.5 ± 8 versus 19.7 ± 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 ± 37 versus 119.3 ± 21 μm, p = 0.03), and cortical width (Ct.Wi: 923.4 ± 420 versus 753.5 ± 246 μm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 ± 1.58 versus 4.27 ± 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 ± 0.014 versus 0.032 ± 0.028 μm3/μm2/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. |
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AbstractList | Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean ± SD; BV/TV: 23.5 ± 8 versus 19.7 ± 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 ± 37 versus 119.3 ± 21 μm, p = 0.03), and cortical width (Ct.Wi: 923.4 ± 420 versus 753.5 ± 246 μm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 ± 1.58 versus 4.27 ± 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 ± 0.014 versus 0.032 ± 0.028 μm3/μm2/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean ± SD; BV/TV: 23.5 ± 8 versus 19.7 ± 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 ± 37 versus 119.3 ± 21 μm, p = 0.03), and cortical width (Ct.Wi: 923.4 ± 420 versus 753.5 ± 246 μm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 ± 1.58 versus 4.27 ± 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 ± 0.014 versus 0.032 ± 0.028 μm 3 /μm 2 /d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean plus or minus SD; BV/TV: 23.5 plus or minus 8 versus 19.7 plus or minus 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 plus or minus 37 versus 119.3 plus or minus 21 mu m, p = 0.03), and cortical width (Ct.Wi: 923.4 plus or minus 420 versus 753.5 plus or minus 246 mu m, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 plus or minus 1.58 versus 4.27 plus or minus 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 plus or minus 0.014 versus 0.032 plus or minus 0.028 mu m super(3)/ mu m super(2)/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean +/- SD; BV/TV: 23.5 +/- 8 versus 19.7 +/- 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 +/- 37 versus 119.3 +/- 21 microm, p = 0.03), and cortical width (Ct.Wi: 923.4 +/- 420 versus 753.5 +/- 246 microm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 +/- 1.58 versus 4.27 +/- 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 +/- 0.014 versus 0.032 +/- 0.028 microm(3)/microm(2)/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone.Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean +/- SD; BV/TV: 23.5 +/- 8 versus 19.7 +/- 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 +/- 37 versus 119.3 +/- 21 microm, p = 0.03), and cortical width (Ct.Wi: 923.4 +/- 420 versus 753.5 +/- 246 microm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 +/- 1.58 versus 4.27 +/- 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 +/- 0.014 versus 0.032 +/- 0.028 microm(3)/microm(2)/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of the skeleton in hypoparathyroidism. Thirty-three subjects with hypoparathyroidism and 33 age- and sex-matched control subjects with no known metabolic diseases underwent percutaneous iliac crest bone biopsies after double-labeling with tetracycline. The main outcome was histomorphometric assessment of structural and dynamic skeletal parameters. Subjects with hypoparathyroidism had greater cancellous bone volume (mean +/- SD; BV/TV: 23.5 +/- 8 versus 19.7 +/- 5%, p = 0.02), trabecular width (Tb.Wi: 136.1 +/- 37 versus 119.3 +/- 21 microm, p = 0.03), and cortical width (Ct.Wi: 923.4 +/- 420 versus 753.5 +/- 246 microm, p = 0.05) than control subjects. Dynamic skeletal indices, including mineralizing surface (MS: 0.85 +/- 1.58 versus 4.27 +/- 3.32%, p < 0.0001) and bone formation rate (BFR/BS: 0.006 +/- 0.014 versus 0.032 +/- 0.028 microm(3)/microm(2)/d, p < 0.0001), were profoundly suppressed in the hypoparathyroid subjects. We conclude that hypoparathyroidism is characterized by markedly unusual structural and dynamic properties of bone. |
Author | Rubin, Mishaela R Zhou, Hua Shane, Elizabeth Bilezikian, John P Dempster, David W Nickolas, Thomas Sliney, James Silverberg, Shonni J |
AuthorAffiliation | College of Physicians and Surgeons, Columbia University, New York, New York, USA |
AuthorAffiliation_xml | – name: College of Physicians and Surgeons, Columbia University, New York, New York, USA |
Author_xml | – sequence: 1 givenname: Mishaela R surname: Rubin fullname: Rubin, Mishaela R – sequence: 2 givenname: David W surname: Dempster fullname: Dempster, David W – sequence: 3 givenname: Hua surname: Zhou fullname: Zhou, Hua – sequence: 4 givenname: Elizabeth surname: Shane fullname: Shane, Elizabeth – sequence: 5 givenname: Thomas surname: Nickolas fullname: Nickolas, Thomas – sequence: 6 givenname: James surname: Sliney fullname: Sliney, James – sequence: 7 givenname: Shonni J surname: Silverberg fullname: Silverberg, Shonni J – sequence: 8 givenname: John P surname: Bilezikian fullname: Bilezikian, John P |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18684087$$D View this record in MEDLINE/PubMed |
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Notes | Dr Bilezikian states financial conflicts with Mercy & Co., Eli Lilly & Co., and Novartis Pharmaceuticals. All other authors state that they have no conflicts of interest. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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References | 1998; 49 2004; 145 1987; 33 1987; 2 1989; 4 1986; 119 1991; 1 1996; 18 1997; 21 2000; 9 2005; 115 2004; 89 2003; 14 1999; 140 2003; 18 1999; 84 1995; 310 1990; 322 1981; 60 2003; 33 2004; 112 1982; 69 1988; 3 1995; 80 1989; 148 1993; 76 1999; 282 1997; 34 1997; 12 1996; 81 1996; 335 2007; 22 1992; 67 1988; 82 2003; 142 Kao (2024020319465919300_bib8) 1992; 67 Clarke (2024020319465919300_bib20) 1996; 81 Parisien (2024020319465919300_bib18) 1997; 12 Dempster (2024020319465919300_bib23) 1999; 84 Recker (2024020319465919300_bib17) 1988; 3 Mayer (2024020319465919300_bib1) 2004; 89 Sunthornthepvarakul (2024020319465919300_bib7) 1999; 84 Schneider (2024020319465919300_bib35) 2004; 112 Seeman (2024020319465919300_bib15) 1982; 69 Silverberg (2024020319465919300_bib22) 1989; 4 Fujiyama (2024020319465919300_bib14) 1995; 80 Kleerekoper (2024020319465919300_bib27) 1991; 1 Miao (2024020319465919300_bib37) 2004; 145 Michelangeli (2024020319465919300_bib9) 1997; 34 Langdahl (2024020319465919300_bib10) 1996; 18 Ettinger (2024020319465919300_bib26) 1999; 282 Ahonen (2024020319465919300_bib2) 1990; 322 Malluche (2024020319465919300_bib25) 1986; 119 Currey (2024020319465919300_bib31) 2003; 18 Miao (2024020319465919300_bib38) 2004; 145 Abugassa (2024020319465919300_bib13) 1993; 76 Kruse (2024020319465919300_bib11) 1989; 148 Muller (2024020319465919300_bib29) 2003; 14 Saaf (2024020319465919300_bib34) 1999; 140 Brauner (2024020319465919300_bib33) 2003; 142 Touliatos (2024020319465919300_bib16) 1995; 310 Dempster (2024020319465919300_bib28) 2003; 14 Neufield (2024020319465919300_bib3) 1981; 60 Nussbaum (2024020319465919300_bib21) 1987; 33 Meunier (2024020319465919300_bib32) 1997; 21 Scambler (2024020319465919300_bib4) 2000; 9 Parfitt (2024020319465919300_bib24) 1987; 2 Heaney (2024020319465919300_bib36) 2003; 33 Mizunashi (2024020319465919300_bib12) 1988; 82 Burr (2024020319465919300_bib30) 2003; 14 Cohen (2024020319465919300_bib19) 2007; 22 Martin (2024020319465919300_bib40) 2005; 115 Brown (2024020319465919300_bib5) 1998; 49 Pearce (2024020319465919300_bib6) 1996; 335 Miao (2024020319465919300_bib39) 2005; 115 10229902 - Eur J Endocrinol. 1999 May;140(5):390-9 14504707 - Osteoporos Int. 2003 Sep;14 Suppl 5:S54-6 14504709 - Osteoporos Int. 2003 Sep;14 Suppl 5:S67-72 15090463 - Endocrinology. 2004 Aug;145(8):3554-62 15372365 - Exp Clin Endocrinol Diabetes. 2004 Sep;112(8):444-50 2348835 - N Engl J Med. 1990 Jun 28;322(26):1829-36 14701672 - Endocrinology. 2004 Apr;145(4):2046-53 7631643 - Am J Med Sci. 1995 Aug;310(2):56-60 14504712 - Osteoporos Int. 2003 Sep;14 Suppl 5:S89-95; discussion S95-9 9022895 - Ann Clin Biochem. 1997 Jan;34 ( Pt 1):97-103 2763869 - J Bone Miner Res. 1989 Jun;4(3):283-91 8833203 - Bone. 1996 Feb;18(2):103-8 1434896 - Mayo Clin Proc. 1992 Jul;67(7):637-45 10323380 - J Clin Endocrinol Metab. 1999 May;84(5):1562-6 3755395 - Endocrinology. 1986 Sep;119(3):1298-304 3213608 - J Bone Miner Res. 1988 Apr;3(2):133-44 10523031 - J Clin Endocrinol Metab. 1999 Oct;84(10):3792-6 8501170 - J Clin Endocrinol Metab. 1993 Jun;76(6):1617-21 3608153 - Clin Chem. 1987 Aug;33(8):1364-7 3455637 - J Bone Miner Res. 1987 Dec;2(6):595-610 16138187 - J Clin Invest. 2005 Sep;115(9):2322-4 16138191 - J Clin Invest. 2005 Sep;115(9):2402-11 7085876 - J Clin Invest. 1982 Jun;69(6):1302-9 12674319 - J Bone Miner Res. 2003 Apr;18(4):591-8 8964862 - J Clin Endocrinol Metab. 1996 Jun;81(6):2264-70 11005797 - Hum Mol Genet. 2000 Oct;9(16):2421-6 14555248 - Bone. 2003 Oct;33(4):457-65 2744015 - Eur J Pediatr. 1989 Apr;148(6):535-9 1790403 - Osteoporos Int. 1991 Jun;1(3):155-61 7608266 - J Clin Endocrinol Metab. 1995 Jul;80(7):2135-8 2843573 - J Clin Invest. 1988 Sep;82(3):861-5 9509247 - Annu Rev Med. 1998;49:15-29 10517716 - JAMA. 1999 Aug 18;282(7):637-45 15356052 - J Clin Endocrinol Metab. 2004 Sep;89(9):4484-8 8813042 - N Engl J Med. 1996 Oct 10;335(15):1115-22 7024719 - Medicine (Baltimore). 1981 Sep;60(5):355-62 9356729 - Bone. 1997 Nov;21(5):373-7 9169355 - J Bone Miner Res. 1997 Jun;12(6):948-57 12756381 - J Pediatr. 2003 May;142(5):504-8 |
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Snippet | Hypoparathyroidism, a disorder in which PTH is absent, is associated with BMD that is above average. We studied associated structural and dynamic properties of... |
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StartPage | 2018 |
SubjectTerms | Adult Animals Biopsy Bone and Bones - metabolism Bone and Bones - pathology bone densitometry Bone Density bone histomorphometry Case-Control Studies Cohort Studies Densitometry - methods Female Humans hypoparathyroidism Hypoparathyroidism - pathology Male Middle Aged Original parathyroid Postmenopause Premenopause |
Title | Dynamic and Structural Properties of the Skeleton in Hypoparathyroidism |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1359%2Fjbmr.080803 https://www.ncbi.nlm.nih.gov/pubmed/18684087 https://www.proquest.com/docview/19663433 https://www.proquest.com/docview/69826247 https://pubmed.ncbi.nlm.nih.gov/PMC2686925 |
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