Focal osteoporosis defects play a key role in hip fracture

Abstract Background Hip fractures are mainly caused by accidental falls and trips, which magnify forces in well-defined areas of the proximal femur. Unfortunately, the same areas are at risk of rapid bone loss with ageing, since they are relatively stress-shielded during walking and sitting. Focal o...

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Veröffentlicht in:Bone (New York, N.Y.) N.Y.), 2017-01, Vol.94, p.124-134
Hauptverfasser: Poole, Kenneth, Skingle, Linda, Gee, Andrew, Turmezei, Thomas, Johannesdottir, Fjola, Blesic, Karen, Rose, Collette, Vindlacheruvu, Madhavi, Donell, Simon, Vaculik, Jan, Dungl, Pavel, Horak, Martin, Stepan, Jan, Reeve, Jonathan, Treece, Graham
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container_end_page 134
container_issue
container_start_page 124
container_title Bone (New York, N.Y.)
container_volume 94
creator Poole, Kenneth
Skingle, Linda
Gee, Andrew
Turmezei, Thomas
Johannesdottir, Fjola
Blesic, Karen
Rose, Collette
Vindlacheruvu, Madhavi
Donell, Simon
Vaculik, Jan
Dungl, Pavel
Horak, Martin
Stepan, Jan
Reeve, Jonathan
Treece, Graham
description Abstract Background Hip fractures are mainly caused by accidental falls and trips, which magnify forces in well-defined areas of the proximal femur. Unfortunately, the same areas are at risk of rapid bone loss with ageing, since they are relatively stress-shielded during walking and sitting. Focal osteoporosis in those areas may contribute to fracture, and targeted 3D measurements might enhance hip fracture prediction. In the FEMCO case-control clinical study, Cortical Bone Mapping (CBM) was applied to clinical computed tomography (CT) scans to define 3D cortical and trabecular bone defects in patients with acute hip fracture compared to controls. Direct measurements of trabecular bone volume were then made in biopsies of target regions removed at operation. Methods The sample consisted of CT scans from 313 female and 40 male volunteers (158 with proximal femoral fracture, 145 age-matched controls and 50 fallers without hip fracture). Detailed Cortical Bone Maps (c.5580 measurement points on the unfractured hip) were created before registering each hip to an average femur shape to facilitate statistical parametric mapping (SPM). Areas where cortical and trabecular bone differed from controls were visualised in 3D for location, magnitude and statistical significance. Measures from the novel regions created by the SPM process were then tested for their ability to classify fracture versus control by comparison with traditional CT measures of areal Bone Mineral Density (aBMD). In women we used the surgical classification of fracture location (‘femoral neck’ or ‘trochanteric’) to discover whether focal osteoporosis was specific to fracture type. To explore whether the focal areas were osteoporotic by histological criteria, we used micro CT to measure trabecular bone parameters in targeted biopsies taken from the femoral heads of 14 cases. Results Hip fracture patients had distinct patterns of focal osteoporosis that determined fracture type, and CBM measures classified fracture type better than aBMD parameters. CBM measures however improved only minimally on aBMD for predicting any hip fracture and depended on the inclusion of trabecular bone measures alongside cortical regions. Focal osteoporosis was confirmed on biopsy as reduced sub-cortical trabecular bone volume. Conclusion Using 3D imaging methods and targeted bone biopsy, we discovered focal osteoporosis affecting trabecular and cortical bone of the proximal femur, among men and women with hip fracture.
doi_str_mv 10.1016/j.bone.2016.10.020
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Unfortunately, the same areas are at risk of rapid bone loss with ageing, since they are relatively stress-shielded during walking and sitting. Focal osteoporosis in those areas may contribute to fracture, and targeted 3D measurements might enhance hip fracture prediction. In the FEMCO case-control clinical study, Cortical Bone Mapping (CBM) was applied to clinical computed tomography (CT) scans to define 3D cortical and trabecular bone defects in patients with acute hip fracture compared to controls. Direct measurements of trabecular bone volume were then made in biopsies of target regions removed at operation. Methods The sample consisted of CT scans from 313 female and 40 male volunteers (158 with proximal femoral fracture, 145 age-matched controls and 50 fallers without hip fracture). Detailed Cortical Bone Maps (c.5580 measurement points on the unfractured hip) were created before registering each hip to an average femur shape to facilitate statistical parametric mapping (SPM). Areas where cortical and trabecular bone differed from controls were visualised in 3D for location, magnitude and statistical significance. Measures from the novel regions created by the SPM process were then tested for their ability to classify fracture versus control by comparison with traditional CT measures of areal Bone Mineral Density (aBMD). In women we used the surgical classification of fracture location (‘femoral neck’ or ‘trochanteric’) to discover whether focal osteoporosis was specific to fracture type. To explore whether the focal areas were osteoporotic by histological criteria, we used micro CT to measure trabecular bone parameters in targeted biopsies taken from the femoral heads of 14 cases. Results Hip fracture patients had distinct patterns of focal osteoporosis that determined fracture type, and CBM measures classified fracture type better than aBMD parameters. CBM measures however improved only minimally on aBMD for predicting any hip fracture and depended on the inclusion of trabecular bone measures alongside cortical regions. Focal osteoporosis was confirmed on biopsy as reduced sub-cortical trabecular bone volume. Conclusion Using 3D imaging methods and targeted bone biopsy, we discovered focal osteoporosis affecting trabecular and cortical bone of the proximal femur, among men and women with hip fracture.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/j.bone.2016.10.020</identifier><identifier>PMID: 27777119</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Area Under Curve ; Biopsy ; Cortical Bone - pathology ; Female ; Femur Neck - pathology ; Fracture prediction ; Full Length ; Hip fracture ; Hip Fractures - etiology ; Hip Fractures - pathology ; Humans ; Male ; Odds Ratio ; Orthopedics ; Osteoporosis ; Osteoporosis - complications ; Osteoporosis - pathology ; Pathogenesis ; ROC Curve</subject><ispartof>Bone (New York, N.Y.), 2017-01, Vol.94, p.124-134</ispartof><rights>2016 The Authors</rights><rights>Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>2016 The Authors 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c613t-ea68c4a8ad9eedf151f5523c988424c7e8d945654f63ce4dabf6465df02a77fe3</citedby><cites>FETCH-LOGICAL-c613t-ea68c4a8ad9eedf151f5523c988424c7e8d945654f63ce4dabf6465df02a77fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bone.2016.10.020$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27777119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poole, Kenneth</creatorcontrib><creatorcontrib>Skingle, Linda</creatorcontrib><creatorcontrib>Gee, Andrew</creatorcontrib><creatorcontrib>Turmezei, Thomas</creatorcontrib><creatorcontrib>Johannesdottir, Fjola</creatorcontrib><creatorcontrib>Blesic, Karen</creatorcontrib><creatorcontrib>Rose, Collette</creatorcontrib><creatorcontrib>Vindlacheruvu, Madhavi</creatorcontrib><creatorcontrib>Donell, Simon</creatorcontrib><creatorcontrib>Vaculik, Jan</creatorcontrib><creatorcontrib>Dungl, Pavel</creatorcontrib><creatorcontrib>Horak, Martin</creatorcontrib><creatorcontrib>Stepan, Jan</creatorcontrib><creatorcontrib>Reeve, Jonathan</creatorcontrib><creatorcontrib>Treece, Graham</creatorcontrib><title>Focal osteoporosis defects play a key role in hip fracture</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><description>Abstract Background Hip fractures are mainly caused by accidental falls and trips, which magnify forces in well-defined areas of the proximal femur. Unfortunately, the same areas are at risk of rapid bone loss with ageing, since they are relatively stress-shielded during walking and sitting. Focal osteoporosis in those areas may contribute to fracture, and targeted 3D measurements might enhance hip fracture prediction. In the FEMCO case-control clinical study, Cortical Bone Mapping (CBM) was applied to clinical computed tomography (CT) scans to define 3D cortical and trabecular bone defects in patients with acute hip fracture compared to controls. Direct measurements of trabecular bone volume were then made in biopsies of target regions removed at operation. Methods The sample consisted of CT scans from 313 female and 40 male volunteers (158 with proximal femoral fracture, 145 age-matched controls and 50 fallers without hip fracture). Detailed Cortical Bone Maps (c.5580 measurement points on the unfractured hip) were created before registering each hip to an average femur shape to facilitate statistical parametric mapping (SPM). Areas where cortical and trabecular bone differed from controls were visualised in 3D for location, magnitude and statistical significance. Measures from the novel regions created by the SPM process were then tested for their ability to classify fracture versus control by comparison with traditional CT measures of areal Bone Mineral Density (aBMD). In women we used the surgical classification of fracture location (‘femoral neck’ or ‘trochanteric’) to discover whether focal osteoporosis was specific to fracture type. To explore whether the focal areas were osteoporotic by histological criteria, we used micro CT to measure trabecular bone parameters in targeted biopsies taken from the femoral heads of 14 cases. Results Hip fracture patients had distinct patterns of focal osteoporosis that determined fracture type, and CBM measures classified fracture type better than aBMD parameters. CBM measures however improved only minimally on aBMD for predicting any hip fracture and depended on the inclusion of trabecular bone measures alongside cortical regions. Focal osteoporosis was confirmed on biopsy as reduced sub-cortical trabecular bone volume. Conclusion Using 3D imaging methods and targeted bone biopsy, we discovered focal osteoporosis affecting trabecular and cortical bone of the proximal femur, among men and women with hip fracture.</description><subject>Aged</subject><subject>Area Under Curve</subject><subject>Biopsy</subject><subject>Cortical Bone - pathology</subject><subject>Female</subject><subject>Femur Neck - pathology</subject><subject>Fracture prediction</subject><subject>Full Length</subject><subject>Hip fracture</subject><subject>Hip Fractures - etiology</subject><subject>Hip Fractures - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Odds Ratio</subject><subject>Orthopedics</subject><subject>Osteoporosis</subject><subject>Osteoporosis - complications</subject><subject>Osteoporosis - pathology</subject><subject>Pathogenesis</subject><subject>ROC Curve</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1rFTEYhYNY7LX6B1xIlm7mmo_Jx4gUSmlVKHRRXYfc5E2b69zJmMwU7r9vhtsWddFsEt6ccxKeg9AHStaUUPl5u96kAdasnutgTRh5hVZUK94wJflrtNJKyIYzzY7R21K2hBDeKfoGHTNVF6XdCn25TM72OJUJ0phyKrFgDwHcVPDY2z22-DfscU494DjguzjikK2b5gzv0FGwfYH3j_sJ-nV58fP8e3N1_e3H-dlV4yTlUwNWatdabX0H4AMVNAjBuOu0blnrFGjftUKKNkjuoPV2E2QrhQ-EWaUC8BN0esgd580OvINhyrY3Y447m_cm2Wj-vRninblN90ZQLhgTNeDTY0BOf2Yok9nF4qDv7QBpLoZqQZTiWixSdpC6iqJkCM_PUGIW6GZrFuhmgb7MKvRq-vj3B58tT5Sr4OtBABXTfYRsioswOPAxV9LGp_hy_ul_dtfHIdbeajVQtmnOQy3AUFOYIeZmqX1pnUpOOJWKPwBJiKjs</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Poole, Kenneth</creator><creator>Skingle, Linda</creator><creator>Gee, Andrew</creator><creator>Turmezei, Thomas</creator><creator>Johannesdottir, Fjola</creator><creator>Blesic, Karen</creator><creator>Rose, Collette</creator><creator>Vindlacheruvu, Madhavi</creator><creator>Donell, Simon</creator><creator>Vaculik, Jan</creator><creator>Dungl, Pavel</creator><creator>Horak, Martin</creator><creator>Stepan, Jan</creator><creator>Reeve, Jonathan</creator><creator>Treece, Graham</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>5PM</scope></search><sort><creationdate>20170101</creationdate><title>Focal osteoporosis defects play a key role in hip fracture</title><author>Poole, Kenneth ; 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Calcified Tissue Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poole, Kenneth</au><au>Skingle, Linda</au><au>Gee, Andrew</au><au>Turmezei, Thomas</au><au>Johannesdottir, Fjola</au><au>Blesic, Karen</au><au>Rose, Collette</au><au>Vindlacheruvu, Madhavi</au><au>Donell, Simon</au><au>Vaculik, Jan</au><au>Dungl, Pavel</au><au>Horak, Martin</au><au>Stepan, Jan</au><au>Reeve, Jonathan</au><au>Treece, Graham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Focal osteoporosis defects play a key role in hip fracture</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>94</volume><spage>124</spage><epage>134</epage><pages>124-134</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>Abstract Background Hip fractures are mainly caused by accidental falls and trips, which magnify forces in well-defined areas of the proximal femur. Unfortunately, the same areas are at risk of rapid bone loss with ageing, since they are relatively stress-shielded during walking and sitting. Focal osteoporosis in those areas may contribute to fracture, and targeted 3D measurements might enhance hip fracture prediction. In the FEMCO case-control clinical study, Cortical Bone Mapping (CBM) was applied to clinical computed tomography (CT) scans to define 3D cortical and trabecular bone defects in patients with acute hip fracture compared to controls. Direct measurements of trabecular bone volume were then made in biopsies of target regions removed at operation. Methods The sample consisted of CT scans from 313 female and 40 male volunteers (158 with proximal femoral fracture, 145 age-matched controls and 50 fallers without hip fracture). Detailed Cortical Bone Maps (c.5580 measurement points on the unfractured hip) were created before registering each hip to an average femur shape to facilitate statistical parametric mapping (SPM). Areas where cortical and trabecular bone differed from controls were visualised in 3D for location, magnitude and statistical significance. Measures from the novel regions created by the SPM process were then tested for their ability to classify fracture versus control by comparison with traditional CT measures of areal Bone Mineral Density (aBMD). In women we used the surgical classification of fracture location (‘femoral neck’ or ‘trochanteric’) to discover whether focal osteoporosis was specific to fracture type. To explore whether the focal areas were osteoporotic by histological criteria, we used micro CT to measure trabecular bone parameters in targeted biopsies taken from the femoral heads of 14 cases. Results Hip fracture patients had distinct patterns of focal osteoporosis that determined fracture type, and CBM measures classified fracture type better than aBMD parameters. CBM measures however improved only minimally on aBMD for predicting any hip fracture and depended on the inclusion of trabecular bone measures alongside cortical regions. Focal osteoporosis was confirmed on biopsy as reduced sub-cortical trabecular bone volume. Conclusion Using 3D imaging methods and targeted bone biopsy, we discovered focal osteoporosis affecting trabecular and cortical bone of the proximal femur, among men and women with hip fracture.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27777119</pmid><doi>10.1016/j.bone.2016.10.020</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Aged
Area Under Curve
Biopsy
Cortical Bone - pathology
Female
Femur Neck - pathology
Fracture prediction
Full Length
Hip fracture
Hip Fractures - etiology
Hip Fractures - pathology
Humans
Male
Odds Ratio
Orthopedics
Osteoporosis
Osteoporosis - complications
Osteoporosis - pathology
Pathogenesis
ROC Curve
title Focal osteoporosis defects play a key role in hip fracture
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