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rdf:type |
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lifeskim:mentions |
umls-concept:C0007789,
umls-concept:C0008059,
umls-concept:C0015811,
umls-concept:C0016658,
umls-concept:C0026850,
umls-concept:C0079809,
umls-concept:C0177804,
umls-concept:C0205108,
umls-concept:C0205653,
umls-concept:C0339510,
umls-concept:C0439849,
umls-concept:C0917713,
umls-concept:C1414083,
umls-concept:C1510486,
umls-concept:C1826421,
umls-concept:C2699549
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pubmed:issue |
3
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pubmed:dateCreated |
2010-5-24
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pubmed:abstractText |
Children with limited or no ability to ambulate frequently sustain fragility fractures. Joint contractures, scoliosis, hip dysplasia, and metallic implants often prevent reliable measures of bone mineral density (BMD) in the proximal femur and lumbar spine, where BMD is commonly measured. Further, the relevance of lumbar spine BMD to fracture risk in this population is questionable. In an effort to obtain bone density measures that are both technically feasible and clinically relevant, a technique was developed involving dual-energy X-ray absorptiometry (DXA) measures of the distal femur projected in the lateral plane. The purpose of this study is to test the hypothesis that these new measures of BMD correlate with fractures in children with limited or no ability to ambulate. The relationship between distal femur BMD Z-scores and fracture history was assessed in a cross-sectional study of 619 children aged 6 to 18 years with muscular dystrophy or moderate to severe cerebral palsy compiled from eight centers. There was a strong correlation between fracture history and BMD Z-scores in the distal femur; 35% to 42% of those with BMD Z-scores less than -5 had fractured compared with 13% to 15% of those with BMD Z-scores greater than -1. Risk ratios were 1.06 to 1.15 (95% confidence interval 1.04-1.22), meaning a 6% to 15% increased risk of fracture with each 1.0 decrease in BMD Z-score. In clinical practice, DXA measure of BMD in the distal femur is the technique of choice for the assessment of children with impaired mobility.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-10641693,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-10824241,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-11028455,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-12093955,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-1497045,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-15174534,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-15537440,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-15973316,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-16785082,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-16932102,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-16939408,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-17627820,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-17643769,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-18157055,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-19321369,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-2137720,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-3817311,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-5942801,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-7593076,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-9183259,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-9342815,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-9443800,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-9545479,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19821773-9724682
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1523-4681
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pubmed:author |
pubmed-author:BerglundLisa MLM,
pubmed-author:GrossbergRichard IRI,
pubmed-author:HarckeH TheodoreHT,
pubmed-author:HendersonRichard CRC,
pubmed-author:JohnsonJulieJ,
pubmed-author:KecskemethyHeidi HHH,
pubmed-author:PlotkinHoracioH,
pubmed-author:ReadA FAF,
pubmed-author:StevensonRichard DRD,
pubmed-author:SzalayElizabethE,
pubmed-author:WongBrendaB,
pubmed-author:ZemelBabette SBS
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pubmed:copyrightInfo |
Copyright 2010 American Society for Bone and Mineral Research.
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pubmed:issnType |
Electronic
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
520-6
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pubmed:dateRevised |
2011-8-25
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pubmed:meshHeading |
pubmed-meshheading:19821773-Absorptiometry, Photon,
pubmed-meshheading:19821773-Adolescent,
pubmed-meshheading:19821773-Bone Density,
pubmed-meshheading:19821773-Cerebral Palsy,
pubmed-meshheading:19821773-Child,
pubmed-meshheading:19821773-Disabled Children,
pubmed-meshheading:19821773-Female,
pubmed-meshheading:19821773-Femur,
pubmed-meshheading:19821773-Fractures, Bone,
pubmed-meshheading:19821773-Humans,
pubmed-meshheading:19821773-Male,
pubmed-meshheading:19821773-Muscular Dystrophies
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pubmed:year |
2010
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pubmed:articleTitle |
The relationship between fractures and DXA measures of BMD in the distal femur of children and adolescents with cerebral palsy or muscular dystrophy.
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pubmed:affiliation |
Department of Orthopaedics, University of North Carolina, Chapel Hill, NC 27599-7055, USA. richard_henderson@med.unc.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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