Literature DB >> 9060512

Bone histomorphometry in adults with type IA osteogenesis imperfecta.

E F McCarthy1, K Earnest, K Rossiter, J Shapiro.   

Abstract

A histologic and histomorphometric analysis was performed on undecalcified bone from 8 adult patients, ages 34 to 64 years, with Type IA osteogenesis imperfecta. Complete histomorphometric data, including static and dynamic parameters of bone remodeling, could be generated on 6 patients, and partial data were obtained from the other 2 patients. Findings in some patients of reduced eroded surfaces and reduced osteoid surfaces suggested low bone turnover. Other findings included normal or slightly reduced labeled surfaces, slightly reduced bone formation rate, decreased cortical thickness, and decreased bone volume. Histologic examination results showed lamellar bone with mature cortical Haversian systems. Trabeculae showed qualitatively normal connectedness despite low trabecular volume. The finding of normal or reduced bone turnover in adults with Type IA osteogenesis imperfecta has not been reported. Earlier histomorphometric studies, performed without correlation with a specific age or phenotype, indicated high bone turnover. The present study suggests that future research should correlate histopathologic changes with specific phenotypes. The finding of normal or slightly reduced bone turnover in Type IA osteogenesis imperfecta may have important therapeutic implications for this phenotype.

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Year:  1997        PMID: 9060512     DOI: 10.1097/00003086-199703000-00034

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  5 in total

1.  Increased resorptive activity and accompanying morphological alterations in osteoclasts derived from the oim/oim mouse model of osteogenesis imperfecta.

Authors:  Hao Zhang; Stephen B Doty; Christine Hughes; David Dempster; Nancy Pleshko Camacho
Journal:  J Cell Biochem       Date:  2007-11-01       Impact factor: 4.429

2.  Bulbous epiphysis and popcorn calcification as related to growth plate differentiation in osteogenesis imperfecta.

Authors:  Evelise Brizola; Edward McCarthy; Jay Robert Shapiro
Journal:  Clin Cases Miner Bone Metab       Date:  2015-10-26

3.  Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.

Authors:  Jessica S Albert; Nisan Bhattacharyya; Lynne A Wolfe; William P Bone; Valerie Maduro; John Accardi; David R Adams; Charles E Schwartz; Joy Norris; Tim Wood; Rachel I Gafni; Michael T Collins; Laura L Tosi; Thomas C Markello; William A Gahl; Cornelius F Boerkoel
Journal:  Orphanet J Rare Dis       Date:  2015-03-07       Impact factor: 4.123

4.  A Clinical Perspective on Advanced Developments in Bone Biopsy Assessment in Rare Bone Disorders.

Authors:  Sanne Treurniet; Elisabeth M W Eekhoff; Felix N Schmidt; Dimitra Micha; Björn Busse; Nathalie Bravenboer
Journal:  Front Endocrinol (Lausanne)       Date:  2020-06-23       Impact factor: 5.555

5.  Histopathology of osteogenesis imperfecta bone. Supramolecular assessment of cells and matrices in the context of woven and lamellar bone formation using light, polarization and ultrastructural microscopy.

Authors:  Frederic Shapiro; Kathleen Maguire; Srilatha Swami; Hui Zhu; Evelyn Flynn; Jamie Wang; Joy Y Wu
Journal:  Bone Rep       Date:  2020-12-01
  5 in total

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