Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10974
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dc.contributor.authorWang, Qingjuen
dc.contributor.authorWang, Xiao-Fangen
dc.contributor.authorIuliano-Burns, Sandraen
dc.contributor.authorGhasem-Zadeh, Alien
dc.contributor.authorZebaze, Roger M Den
dc.contributor.authorSeeman, Egoen
dc.date.accessioned2015-05-16T00:33:10Z
dc.date.available2015-05-16T00:33:10Z
dc.date.issued2010-07-01en
dc.identifier.citationJournal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research; 25(7): 1521-6en
dc.identifier.govdoc20200962en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10974en
dc.description.abstractFractures of the distal radius in children have a similar incidence to that found in postmenopausal women but occur more commonly in boys than in girls. Fractures of the distal tibia are uncommon in children and show no sex specificity. About 90% of lengthening of the radius but only 30% of lengthening of the tibia during puberty occur at the distal growth plate. We speculated that more rapid modeling at the distal radial metaphysis results in a greater dissociation between growth and mineral accrual than observed at the distal tibia. We measured the macro- and microarchitecture of the distal radial and tibial metaphysis using high-resolution peripheral quantitative computed tomography in a cross-sectional study of 69 healthy boys and 60 healthy girls aged from 5 to 18 years. Bone diameters were larger but total volumetric bone mineral density (vBMD) was lower at the distal radius (not at the distal tibia) by 20% in boys and by 15% in girls at Tanner stage III than in children of the same sex at Tanner stage I (both p < .05). In boys at Tanner stage III, total vBMD was lower because the larger radial total cross-sectional area (CSA) had a thinner cortex with lower vBMD than in boys at Tanner stage I. In girls at Tanner stage III, the larger total radial CSA was not associated with a difference in cortical thickness or cortical vBMD relative to girls in Tanner stage I. Cortical thickness and density at both sites in both sexes after Tanner stage III were greater than in younger children. Trabecular bone volume fraction (BV/TV) was higher in boys than in girls at both sites and more so after puberty because trabeculae were thicker in more mature boys but not in girls. There was no sex- or age-related differences in trabecular number at either site. We infer that longitudinal growth outpaces mineral accrual in both sexes at the distal radius, where bone grows rapidly. The dissociation produces transitory low cortical thickness and vBMD in boys but not in girls. These structural features in part may account for the site and sex specificity of metaphyseal fractures during growth.en
dc.language.isoenen
dc.subject.otherAdolescenten
dc.subject.otherBone Development.physiologyen
dc.subject.otherBone and Bones.radiographyen
dc.subject.otherChilden
dc.subject.otherCross-Sectional Studiesen
dc.subject.otherFemaleen
dc.subject.otherFractures, Bone.etiology.radiographyen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherPubertyen
dc.subject.otherRadius.growth & developmenten
dc.subject.otherSex Characteristicsen
dc.subject.otherTibia.growth & developmenten
dc.titleRapid growth produces transient cortical weakness: a risk factor for metaphyseal fractures during puberty.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Bone and Mineral Researchen
dc.identifier.affiliationEndocrine Centre, Heidelberg Repatriation Hospital, Heidelberg West, Australiaen
dc.identifier.doi10.1002/jbmr.46en
dc.description.pages1521-6en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/20200962en
dc.type.austinJournal Articleen
local.name.researcherGhasem-Zadeh, Ali
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
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