Correlates of low bone mass in children with generalized forms of epidermolysis bullosa
Background Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. Objectives We sought to describe the range and to...
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creator | Bruckner, Anna L., MD Bedocs, Laleh A., DO Keiser, Elizabeth, BA Tang, Jean Y., MD, PhD Doernbrack, Catherine, RN, MS, CPNP Arbuckle, H. Alan, MD Berman, Stephen, MD Kent, Kyla, BA, CBDT Bachrach, Laura K., MD |
description | Background Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. Objectives We sought to describe the range and to estimate the prevalence of low bone mass in children with generalized EB, and to identify correlates of low bone mass in this population. Methods This was a prospective, observational study of 24 patients with generalized EB. Each patient completed a history, physical examination, laboratory studies, bone age, and x-rays of the lumbar spine. Those aged 6 years and older underwent dual energy x-ray absorptiometry scans of the lumbar spine. Primary outcomes were areal bone mineral density (aBMD) based on chronologic age, bone age, and adjusted for height Z-score. Descriptive statistics were used to summarize results, and linear regression was used to determine factors associated with low aBMD. Results Mean lumbar spine aBMD Z-scores ± SD were: –2.6 ± 1.4 for chronologic age, –1.7 ± 1.3 for bone age, and –1.0 ± 1.2 after adjusting for height Z-score. aBMD Z-scores were less than or equal to –2 in 64% for chronologic age, 50% for bone age, and 28% after adjusting for height Z-score. aBMD correlated with height Z-score, weight Z-score, extensive blistering, immobility, albumin, hemoglobin, iron, erythrocyte sedimentation rate, and c-reactive protein values. Limitations Small sample size was a limitation. Conclusions Children with severe, generalized recessive dystrophic EB have low aBMD for age. Deficits in aBMD were reduced after adjusting for delayed skeletal maturation and small body size. |
doi_str_mv | 10.1016/j.jaad.2010.08.028 |
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Alan, MD ; Berman, Stephen, MD ; Kent, Kyla, BA, CBDT ; Bachrach, Laura K., MD</creator><creatorcontrib>Bruckner, Anna L., MD ; Bedocs, Laleh A., DO ; Keiser, Elizabeth, BA ; Tang, Jean Y., MD, PhD ; Doernbrack, Catherine, RN, MS, CPNP ; Arbuckle, H. Alan, MD ; Berman, Stephen, MD ; Kent, Kyla, BA, CBDT ; Bachrach, Laura K., MD</creatorcontrib><description>Background Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. Objectives We sought to describe the range and to estimate the prevalence of low bone mass in children with generalized EB, and to identify correlates of low bone mass in this population. Methods This was a prospective, observational study of 24 patients with generalized EB. Each patient completed a history, physical examination, laboratory studies, bone age, and x-rays of the lumbar spine. Those aged 6 years and older underwent dual energy x-ray absorptiometry scans of the lumbar spine. Primary outcomes were areal bone mineral density (aBMD) based on chronologic age, bone age, and adjusted for height Z-score. Descriptive statistics were used to summarize results, and linear regression was used to determine factors associated with low aBMD. Results Mean lumbar spine aBMD Z-scores ± SD were: –2.6 ± 1.4 for chronologic age, –1.7 ± 1.3 for bone age, and –1.0 ± 1.2 after adjusting for height Z-score. aBMD Z-scores were less than or equal to –2 in 64% for chronologic age, 50% for bone age, and 28% after adjusting for height Z-score. aBMD correlated with height Z-score, weight Z-score, extensive blistering, immobility, albumin, hemoglobin, iron, erythrocyte sedimentation rate, and c-reactive protein values. Limitations Small sample size was a limitation. Conclusions Children with severe, generalized recessive dystrophic EB have low aBMD for age. Deficits in aBMD were reduced after adjusting for delayed skeletal maturation and small body size.</description><identifier>ISSN: 0190-9622</identifier><identifier>EISSN: 1097-6787</identifier><identifier>DOI: 10.1016/j.jaad.2010.08.028</identifier><identifier>PMID: 21550693</identifier><identifier>CODEN: JAADDB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Absorptiometry, Photon ; Adolescent ; Age Determination by Skeleton ; Anemia - etiology ; Biological and medical sciences ; Blood Sedimentation ; Body Size ; bone ; Bone Density ; Bone Diseases, Metabolic - blood ; Bone Diseases, Metabolic - diagnostic imaging ; Bone Diseases, Metabolic - etiology ; bone mineral density ; Bullous diseases of the skin ; C-Reactive Protein - analysis ; Calcifediol - blood ; Calcium - blood ; Child ; Child, Preschool ; children ; Dermatology ; Dwarfism - etiology ; epidermolysis bullosa ; Epidermolysis Bullosa - blood ; Epidermolysis Bullosa - classification ; Epidermolysis Bullosa - complications ; Female ; fracture ; General aspects ; Hemoglobins - analysis ; Humans ; Inflammation - blood ; Inflammation - etiology ; Insulin-Like Growth Factor I - analysis ; Iron - blood ; Lumbar Vertebrae - diagnostic imaging ; Male ; Medical sciences ; Mobility Limitation ; osteoporosis ; Serum Albumin - analysis ; Young Adult</subject><ispartof>Journal of the American Academy of Dermatology, 2011-11, Vol.65 (5), p.1001-1009</ispartof><rights>American Academy of Dermatology, Inc.</rights><rights>2010 American Academy of Dermatology, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-ef5263604f58769e07b1b279624adc748205c70feb3a20da4c0f5a148127b0c53</citedby><cites>FETCH-LOGICAL-c465t-ef5263604f58769e07b1b279624adc748205c70feb3a20da4c0f5a148127b0c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaad.2010.08.028$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24750737$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21550693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bruckner, Anna L., MD</creatorcontrib><creatorcontrib>Bedocs, Laleh A., DO</creatorcontrib><creatorcontrib>Keiser, Elizabeth, BA</creatorcontrib><creatorcontrib>Tang, Jean Y., MD, PhD</creatorcontrib><creatorcontrib>Doernbrack, Catherine, RN, MS, CPNP</creatorcontrib><creatorcontrib>Arbuckle, H. Alan, MD</creatorcontrib><creatorcontrib>Berman, Stephen, MD</creatorcontrib><creatorcontrib>Kent, Kyla, BA, CBDT</creatorcontrib><creatorcontrib>Bachrach, Laura K., MD</creatorcontrib><title>Correlates of low bone mass in children with generalized forms of epidermolysis bullosa</title><title>Journal of the American Academy of Dermatology</title><addtitle>J Am Acad Dermatol</addtitle><description>Background Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. Objectives We sought to describe the range and to estimate the prevalence of low bone mass in children with generalized EB, and to identify correlates of low bone mass in this population. Methods This was a prospective, observational study of 24 patients with generalized EB. Each patient completed a history, physical examination, laboratory studies, bone age, and x-rays of the lumbar spine. Those aged 6 years and older underwent dual energy x-ray absorptiometry scans of the lumbar spine. Primary outcomes were areal bone mineral density (aBMD) based on chronologic age, bone age, and adjusted for height Z-score. Descriptive statistics were used to summarize results, and linear regression was used to determine factors associated with low aBMD. Results Mean lumbar spine aBMD Z-scores ± SD were: –2.6 ± 1.4 for chronologic age, –1.7 ± 1.3 for bone age, and –1.0 ± 1.2 after adjusting for height Z-score. aBMD Z-scores were less than or equal to –2 in 64% for chronologic age, 50% for bone age, and 28% after adjusting for height Z-score. aBMD correlated with height Z-score, weight Z-score, extensive blistering, immobility, albumin, hemoglobin, iron, erythrocyte sedimentation rate, and c-reactive protein values. Limitations Small sample size was a limitation. Conclusions Children with severe, generalized recessive dystrophic EB have low aBMD for age. Deficits in aBMD were reduced after adjusting for delayed skeletal maturation and small body size.</description><subject>Absorptiometry, Photon</subject><subject>Adolescent</subject><subject>Age Determination by Skeleton</subject><subject>Anemia - etiology</subject><subject>Biological and medical sciences</subject><subject>Blood Sedimentation</subject><subject>Body Size</subject><subject>bone</subject><subject>Bone Density</subject><subject>Bone Diseases, Metabolic - blood</subject><subject>Bone Diseases, Metabolic - diagnostic imaging</subject><subject>Bone Diseases, Metabolic - etiology</subject><subject>bone mineral density</subject><subject>Bullous diseases of the skin</subject><subject>C-Reactive Protein - analysis</subject><subject>Calcifediol - blood</subject><subject>Calcium - blood</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>children</subject><subject>Dermatology</subject><subject>Dwarfism - etiology</subject><subject>epidermolysis bullosa</subject><subject>Epidermolysis Bullosa - blood</subject><subject>Epidermolysis Bullosa - classification</subject><subject>Epidermolysis Bullosa - complications</subject><subject>Female</subject><subject>fracture</subject><subject>General aspects</subject><subject>Hemoglobins - analysis</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Inflammation - etiology</subject><subject>Insulin-Like Growth Factor I - analysis</subject><subject>Iron - blood</subject><subject>Lumbar Vertebrae - diagnostic imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mobility Limitation</subject><subject>osteoporosis</subject><subject>Serum Albumin - analysis</subject><subject>Young Adult</subject><issn>0190-9622</issn><issn>1097-6787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2L1TAUhoMoznX0D7iQbMRV75ykTZOCCMPFLxhwoeIypOmpk5o216R1uPPrTb3XGXDhKnB43pPD8xLynMGWAasvhu1gTLflkAegtsDVA7Jh0Miilko-JBtgDRRNzfkZeZLSAABNVcrH5IwzIaBuyg35tgsxojczJhp66sMNbcOEdDQpUTdRe-18F3GiN26-pt9xwmi8u8WO9iGOfzK4dx3GMfhDcom2i_chmafkUW98wmen95x8fff2y-5DcfXp_cfd5VVhq1rMBfaC12UNVS-UrBsE2bKWy3xzZTorK8VBWAk9tqXh0JnKQi8MqxTjsgUrynPy6rh3H8PPBdOsR5csem8mDEvSqlGqlLJqMsmPpI0hpYi93kc3mnjQDPTqUw969alXnxqUzj5z6MVp_dKO2N1F_grMwMsTYJI1vo9msi7dc5UUIEuZuddHDrOMXw6jTtbhZLFzEe2su-D-f8ebf-LWu8nlH3_gAdMQljhlzZrpxDXoz2vza_Fs7bypRfkbaCyoGQ</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Bruckner, Anna L., MD</creator><creator>Bedocs, Laleh A., DO</creator><creator>Keiser, Elizabeth, BA</creator><creator>Tang, Jean Y., MD, PhD</creator><creator>Doernbrack, Catherine, RN, MS, CPNP</creator><creator>Arbuckle, H. Alan, MD</creator><creator>Berman, Stephen, MD</creator><creator>Kent, Kyla, BA, CBDT</creator><creator>Bachrach, Laura K., MD</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20111101</creationdate><title>Correlates of low bone mass in children with generalized forms of epidermolysis bullosa</title><author>Bruckner, Anna L., MD ; Bedocs, Laleh A., DO ; Keiser, Elizabeth, BA ; Tang, Jean Y., MD, PhD ; Doernbrack, Catherine, RN, MS, CPNP ; Arbuckle, H. Alan, MD ; Berman, Stephen, MD ; Kent, Kyla, BA, CBDT ; Bachrach, Laura K., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-ef5263604f58769e07b1b279624adc748205c70feb3a20da4c0f5a148127b0c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Absorptiometry, Photon</topic><topic>Adolescent</topic><topic>Age Determination by Skeleton</topic><topic>Anemia - etiology</topic><topic>Biological and medical sciences</topic><topic>Blood Sedimentation</topic><topic>Body Size</topic><topic>bone</topic><topic>Bone Density</topic><topic>Bone Diseases, Metabolic - blood</topic><topic>Bone Diseases, Metabolic - diagnostic imaging</topic><topic>Bone Diseases, Metabolic - etiology</topic><topic>bone mineral density</topic><topic>Bullous diseases of the skin</topic><topic>C-Reactive Protein - analysis</topic><topic>Calcifediol - blood</topic><topic>Calcium - blood</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>children</topic><topic>Dermatology</topic><topic>Dwarfism - etiology</topic><topic>epidermolysis bullosa</topic><topic>Epidermolysis Bullosa - blood</topic><topic>Epidermolysis Bullosa - classification</topic><topic>Epidermolysis Bullosa - complications</topic><topic>Female</topic><topic>fracture</topic><topic>General aspects</topic><topic>Hemoglobins - analysis</topic><topic>Humans</topic><topic>Inflammation - blood</topic><topic>Inflammation - etiology</topic><topic>Insulin-Like Growth Factor I - analysis</topic><topic>Iron - blood</topic><topic>Lumbar Vertebrae - diagnostic imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mobility Limitation</topic><topic>osteoporosis</topic><topic>Serum Albumin - analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bruckner, Anna L., MD</creatorcontrib><creatorcontrib>Bedocs, Laleh A., DO</creatorcontrib><creatorcontrib>Keiser, Elizabeth, BA</creatorcontrib><creatorcontrib>Tang, Jean Y., MD, PhD</creatorcontrib><creatorcontrib>Doernbrack, Catherine, RN, MS, CPNP</creatorcontrib><creatorcontrib>Arbuckle, H. Alan, MD</creatorcontrib><creatorcontrib>Berman, Stephen, MD</creatorcontrib><creatorcontrib>Kent, Kyla, BA, CBDT</creatorcontrib><creatorcontrib>Bachrach, Laura K., MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Academy of Dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bruckner, Anna L., MD</au><au>Bedocs, Laleh A., DO</au><au>Keiser, Elizabeth, BA</au><au>Tang, Jean Y., MD, PhD</au><au>Doernbrack, Catherine, RN, MS, CPNP</au><au>Arbuckle, H. Alan, MD</au><au>Berman, Stephen, MD</au><au>Kent, Kyla, BA, CBDT</au><au>Bachrach, Laura K., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlates of low bone mass in children with generalized forms of epidermolysis bullosa</atitle><jtitle>Journal of the American Academy of Dermatology</jtitle><addtitle>J Am Acad Dermatol</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>65</volume><issue>5</issue><spage>1001</spage><epage>1009</epage><pages>1001-1009</pages><issn>0190-9622</issn><eissn>1097-6787</eissn><coden>JAADDB</coden><abstract>Background Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. Objectives We sought to describe the range and to estimate the prevalence of low bone mass in children with generalized EB, and to identify correlates of low bone mass in this population. Methods This was a prospective, observational study of 24 patients with generalized EB. Each patient completed a history, physical examination, laboratory studies, bone age, and x-rays of the lumbar spine. Those aged 6 years and older underwent dual energy x-ray absorptiometry scans of the lumbar spine. Primary outcomes were areal bone mineral density (aBMD) based on chronologic age, bone age, and adjusted for height Z-score. Descriptive statistics were used to summarize results, and linear regression was used to determine factors associated with low aBMD. Results Mean lumbar spine aBMD Z-scores ± SD were: –2.6 ± 1.4 for chronologic age, –1.7 ± 1.3 for bone age, and –1.0 ± 1.2 after adjusting for height Z-score. aBMD Z-scores were less than or equal to –2 in 64% for chronologic age, 50% for bone age, and 28% after adjusting for height Z-score. aBMD correlated with height Z-score, weight Z-score, extensive blistering, immobility, albumin, hemoglobin, iron, erythrocyte sedimentation rate, and c-reactive protein values. Limitations Small sample size was a limitation. Conclusions Children with severe, generalized recessive dystrophic EB have low aBMD for age. Deficits in aBMD were reduced after adjusting for delayed skeletal maturation and small body size.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>21550693</pmid><doi>10.1016/j.jaad.2010.08.028</doi><tpages>9</tpages></addata></record> |
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subjects | Absorptiometry, Photon Adolescent Age Determination by Skeleton Anemia - etiology Biological and medical sciences Blood Sedimentation Body Size bone Bone Density Bone Diseases, Metabolic - blood Bone Diseases, Metabolic - diagnostic imaging Bone Diseases, Metabolic - etiology bone mineral density Bullous diseases of the skin C-Reactive Protein - analysis Calcifediol - blood Calcium - blood Child Child, Preschool children Dermatology Dwarfism - etiology epidermolysis bullosa Epidermolysis Bullosa - blood Epidermolysis Bullosa - classification Epidermolysis Bullosa - complications Female fracture General aspects Hemoglobins - analysis Humans Inflammation - blood Inflammation - etiology Insulin-Like Growth Factor I - analysis Iron - blood Lumbar Vertebrae - diagnostic imaging Male Medical sciences Mobility Limitation osteoporosis Serum Albumin - analysis Young Adult |
title | Correlates of low bone mass in children with generalized forms of epidermolysis bullosa |
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