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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Veröffentlicht in:Journal of the American Academy of Dermatology 2011-11, Vol.65 (5), p.1001-1009
Hauptverfasser: 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
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container_end_page 1009
container_issue 5
container_start_page 1001
container_title Journal of the American Academy of Dermatology
container_volume 65
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. 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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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