Bone Mineral Density and Microarchitecture in Patients With Autosomal Dominant Osteopetrosis: A Report of Two Cases
ABSTRACT The aim of this case study is to describe changes in areal bone mineral density (aBMD) by dual‐energy X‐ray absorptiometry (DXA) scan, as well as volumetric bone density and microarchitecture by high‐resolution peripheral quantitative computed tomography (HR‐pQCT) in two patients with autos...
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Veröffentlicht in: | Journal of bone and mineral research 2016-03, Vol.31 (3), p.657-662 |
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creator | Arruda, Mariana Coelho, Maria Caroline Alves Moraes, Aline Barbosa de Paula Paranhos‐Neto, Francisco Madeira, Miguel Farias, Maria Lucia Fleiuss Neto, Leonardo Vieira |
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The aim of this case study is to describe changes in areal bone mineral density (aBMD) by dual‐energy X‐ray absorptiometry (DXA) scan, as well as volumetric bone density and microarchitecture by high‐resolution peripheral quantitative computed tomography (HR‐pQCT) in two patients with autosomal dominant osteopetrosis (ADO) and compare with 20 healthy subjects. We describe a 44‐year‐old male patient with six low‐impact fractures since he was age 16 years, and a 32‐year‐old female patient with four low‐impact fractures on her past history. Radiographic changes were typical of ADO. Consistent with the much higher aBMD, total volumetric BMD (average bone density of the whole bone, including trabecular and cortical compartments) at distal radius and tibia (HR‐pQCT) was more than twice the mean values found in healthy subjects in both patients. Trabecular number and thickness were higher, leading to an evident increase in trabecular bone volume to tissue volume. Also, an enormous increase in cortical thickness was found. Most important, a great heterogeneity in bone microstructure of the affected patients was evident on HR‐pQCT images: islets of very dense bone were interposed with areas with apparent normal density. The increase in aBMD, volumetric BMD, and most indices of trabecular and cortical bone, associated with the great heterogeneity on bone tridimensional microarchitecture, reflect the accumulation of old and fragile bone randomly distributed along the skeleton. These alterations in bone microstructure probably compromise bone quality, which might justify the high prevalence of low‐impact fractures in patients with ADO, despite abnormally elevated BMD. © 2015 American Society for Bone and Mineral Research. |
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The aim of this case study is to describe changes in areal bone mineral density (aBMD) by dual‐energy X‐ray absorptiometry (DXA) scan, as well as volumetric bone density and microarchitecture by high‐resolution peripheral quantitative computed tomography (HR‐pQCT) in two patients with autosomal dominant osteopetrosis (ADO) and compare with 20 healthy subjects. We describe a 44‐year‐old male patient with six low‐impact fractures since he was age 16 years, and a 32‐year‐old female patient with four low‐impact fractures on her past history. Radiographic changes were typical of ADO. Consistent with the much higher aBMD, total volumetric BMD (average bone density of the whole bone, including trabecular and cortical compartments) at distal radius and tibia (HR‐pQCT) was more than twice the mean values found in healthy subjects in both patients. Trabecular number and thickness were higher, leading to an evident increase in trabecular bone volume to tissue volume. Also, an enormous increase in cortical thickness was found. Most important, a great heterogeneity in bone microstructure of the affected patients was evident on HR‐pQCT images: islets of very dense bone were interposed with areas with apparent normal density. The increase in aBMD, volumetric BMD, and most indices of trabecular and cortical bone, associated with the great heterogeneity on bone tridimensional microarchitecture, reflect the accumulation of old and fragile bone randomly distributed along the skeleton. These alterations in bone microstructure probably compromise bone quality, which might justify the high prevalence of low‐impact fractures in patients with ADO, despite abnormally elevated BMD. © 2015 American Society for Bone and Mineral Research.</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1002/jbmr.2715</identifier><identifier>PMID: 26387875</identifier><identifier>CODEN: JBMREJ</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Absorptiometry, Photon ; Adult ; Bone Density ; BONE QCT/µCT ; Case-Control Studies ; DXA ; Female ; FRACTURE RISK ASSESSMENT ; Genes, Dominant ; Humans ; Male ; OSTEOPETROSIS ; Osteopetrosis - pathology ; Osteopetrosis - physiopathology ; Radius - pathology ; Tibia - pathology ; Tomography, X-Ray Computed</subject><ispartof>Journal of bone and mineral research, 2016-03, Vol.31 (3), p.657-662</ispartof><rights>2015 American Society for Bone and Mineral Research</rights><rights>2015 American Society for Bone and Mineral Research.</rights><rights>2016 American Society for Bone and Mineral Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4215-31aea4fa23c56130ed112b94c348c8b9193945f5458ae26fbb461439834d80633</citedby><cites>FETCH-LOGICAL-c4215-31aea4fa23c56130ed112b94c348c8b9193945f5458ae26fbb461439834d80633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbmr.2715$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbmr.2715$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26387875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arruda, Mariana</creatorcontrib><creatorcontrib>Coelho, Maria Caroline Alves</creatorcontrib><creatorcontrib>Moraes, Aline Barbosa</creatorcontrib><creatorcontrib>de Paula Paranhos‐Neto, Francisco</creatorcontrib><creatorcontrib>Madeira, Miguel</creatorcontrib><creatorcontrib>Farias, Maria Lucia Fleiuss</creatorcontrib><creatorcontrib>Neto, Leonardo Vieira</creatorcontrib><title>Bone Mineral Density and Microarchitecture in Patients With Autosomal Dominant Osteopetrosis: A Report of Two Cases</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>ABSTRACT
The aim of this case study is to describe changes in areal bone mineral density (aBMD) by dual‐energy X‐ray absorptiometry (DXA) scan, as well as volumetric bone density and microarchitecture by high‐resolution peripheral quantitative computed tomography (HR‐pQCT) in two patients with autosomal dominant osteopetrosis (ADO) and compare with 20 healthy subjects. We describe a 44‐year‐old male patient with six low‐impact fractures since he was age 16 years, and a 32‐year‐old female patient with four low‐impact fractures on her past history. Radiographic changes were typical of ADO. Consistent with the much higher aBMD, total volumetric BMD (average bone density of the whole bone, including trabecular and cortical compartments) at distal radius and tibia (HR‐pQCT) was more than twice the mean values found in healthy subjects in both patients. Trabecular number and thickness were higher, leading to an evident increase in trabecular bone volume to tissue volume. Also, an enormous increase in cortical thickness was found. Most important, a great heterogeneity in bone microstructure of the affected patients was evident on HR‐pQCT images: islets of very dense bone were interposed with areas with apparent normal density. The increase in aBMD, volumetric BMD, and most indices of trabecular and cortical bone, associated with the great heterogeneity on bone tridimensional microarchitecture, reflect the accumulation of old and fragile bone randomly distributed along the skeleton. These alterations in bone microstructure probably compromise bone quality, which might justify the high prevalence of low‐impact fractures in patients with ADO, despite abnormally elevated BMD. © 2015 American Society for Bone and Mineral Research.</description><subject>Absorptiometry, Photon</subject><subject>Adult</subject><subject>Bone Density</subject><subject>BONE QCT/µCT</subject><subject>Case-Control Studies</subject><subject>DXA</subject><subject>Female</subject><subject>FRACTURE RISK ASSESSMENT</subject><subject>Genes, Dominant</subject><subject>Humans</subject><subject>Male</subject><subject>OSTEOPETROSIS</subject><subject>Osteopetrosis - pathology</subject><subject>Osteopetrosis - physiopathology</subject><subject>Radius - pathology</subject><subject>Tibia - pathology</subject><subject>Tomography, X-Ray Computed</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0U9rFDEYBvAgFrtWD34BCXjRw7R5828y3rZr1ZaWSql4HDKz79AsM8k2yVD223fGrR4EoeTwQvjlgTcPIe-AHQNj_GTTDPGYl6BekAUoLgqpDbwkC2aMLJgUcEhep7RhjGml9StyyLUwpSnVgqTT4JFeOY_R9vQL-uTyjlq_nu7aGGxs71zGNo8RqfP0h80OfU70l8t3dDnmkMIwPwyD89Znep0yhi3mGJJLn-mS3uA2xExDR28fAl3ZhOkNOehsn_Dt0zwiP7-e3a6-F5fX385Xy8uilRxUIcCilZ3lolUaBMM1AG8q2QppWtNUUIlKqk5JZSxy3TWN1CBFZYRcG6aFOCIf97nbGO5HTLkeXGqx763HMKYaSsMUNwLgGbQspTFa6Il--Iduwhj9tMistAYznUl92qvpE1OK2NXb6AYbdzWwei6tnkur59Im-_4pcWwGXP-Vf1qawMkePLged_9Pqi9Or25-Rz4CSoSfvQ</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Arruda, Mariana</creator><creator>Coelho, Maria Caroline Alves</creator><creator>Moraes, Aline Barbosa</creator><creator>de Paula Paranhos‐Neto, Francisco</creator><creator>Madeira, Miguel</creator><creator>Farias, Maria Lucia Fleiuss</creator><creator>Neto, Leonardo Vieira</creator><general>Wiley Subscription Services, Inc</general><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>7TS</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201603</creationdate><title>Bone Mineral Density and Microarchitecture in Patients With Autosomal Dominant Osteopetrosis: A Report of Two Cases</title><author>Arruda, Mariana ; Coelho, Maria Caroline Alves ; Moraes, Aline Barbosa ; de Paula Paranhos‐Neto, Francisco ; Madeira, Miguel ; Farias, Maria Lucia Fleiuss ; Neto, Leonardo Vieira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4215-31aea4fa23c56130ed112b94c348c8b9193945f5458ae26fbb461439834d80633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Absorptiometry, Photon</topic><topic>Adult</topic><topic>Bone Density</topic><topic>BONE QCT/µCT</topic><topic>Case-Control Studies</topic><topic>DXA</topic><topic>Female</topic><topic>FRACTURE RISK ASSESSMENT</topic><topic>Genes, Dominant</topic><topic>Humans</topic><topic>Male</topic><topic>OSTEOPETROSIS</topic><topic>Osteopetrosis - pathology</topic><topic>Osteopetrosis - physiopathology</topic><topic>Radius - pathology</topic><topic>Tibia - pathology</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arruda, Mariana</creatorcontrib><creatorcontrib>Coelho, Maria Caroline Alves</creatorcontrib><creatorcontrib>Moraes, Aline Barbosa</creatorcontrib><creatorcontrib>de Paula Paranhos‐Neto, Francisco</creatorcontrib><creatorcontrib>Madeira, Miguel</creatorcontrib><creatorcontrib>Farias, Maria Lucia Fleiuss</creatorcontrib><creatorcontrib>Neto, Leonardo Vieira</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arruda, Mariana</au><au>Coelho, Maria Caroline Alves</au><au>Moraes, Aline Barbosa</au><au>de Paula Paranhos‐Neto, Francisco</au><au>Madeira, Miguel</au><au>Farias, Maria Lucia Fleiuss</au><au>Neto, Leonardo Vieira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone Mineral Density and Microarchitecture in Patients With Autosomal Dominant Osteopetrosis: A Report of Two Cases</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2016-03</date><risdate>2016</risdate><volume>31</volume><issue>3</issue><spage>657</spage><epage>662</epage><pages>657-662</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>ABSTRACT
The aim of this case study is to describe changes in areal bone mineral density (aBMD) by dual‐energy X‐ray absorptiometry (DXA) scan, as well as volumetric bone density and microarchitecture by high‐resolution peripheral quantitative computed tomography (HR‐pQCT) in two patients with autosomal dominant osteopetrosis (ADO) and compare with 20 healthy subjects. We describe a 44‐year‐old male patient with six low‐impact fractures since he was age 16 years, and a 32‐year‐old female patient with four low‐impact fractures on her past history. Radiographic changes were typical of ADO. Consistent with the much higher aBMD, total volumetric BMD (average bone density of the whole bone, including trabecular and cortical compartments) at distal radius and tibia (HR‐pQCT) was more than twice the mean values found in healthy subjects in both patients. Trabecular number and thickness were higher, leading to an evident increase in trabecular bone volume to tissue volume. Also, an enormous increase in cortical thickness was found. Most important, a great heterogeneity in bone microstructure of the affected patients was evident on HR‐pQCT images: islets of very dense bone were interposed with areas with apparent normal density. The increase in aBMD, volumetric BMD, and most indices of trabecular and cortical bone, associated with the great heterogeneity on bone tridimensional microarchitecture, reflect the accumulation of old and fragile bone randomly distributed along the skeleton. These alterations in bone microstructure probably compromise bone quality, which might justify the high prevalence of low‐impact fractures in patients with ADO, despite abnormally elevated BMD. © 2015 American Society for Bone and Mineral Research.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>26387875</pmid><doi>10.1002/jbmr.2715</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Absorptiometry, Photon Adult Bone Density BONE QCT/µCT Case-Control Studies DXA Female FRACTURE RISK ASSESSMENT Genes, Dominant Humans Male OSTEOPETROSIS Osteopetrosis - pathology Osteopetrosis - physiopathology Radius - pathology Tibia - pathology Tomography, X-Ray Computed |
title | Bone Mineral Density and Microarchitecture in Patients With Autosomal Dominant Osteopetrosis: A Report of Two Cases |
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