Predicting longitudinal trajectory of bone mineral density in paediatric systemic lupus erythematosus patients

Objectives (1) To identify the average lumbar spine (LS) bone mineral density (BMD) trajectory in paediatric systemic lupus erythematosus (pSLE) patients, and (2) to identify predictors of BMD trajectory. Methods 68 consecutive newly diagnosed pSLE patients prospectively followed in our lupus cohort...

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Veröffentlicht in:Annals of the rheumatic diseases 2012-10, Vol.71 (10), p.1686-1691
Hauptverfasser: Lim, Lily Siok Hoon, Benseler, Susanne M, Tyrrell, Pascal N, Harvey, Elizabeth, Herbert, Diane, Charron, Martin, Silverman, Earl D
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container_end_page 1691
container_issue 10
container_start_page 1686
container_title Annals of the rheumatic diseases
container_volume 71
creator Lim, Lily Siok Hoon
Benseler, Susanne M
Tyrrell, Pascal N
Harvey, Elizabeth
Herbert, Diane
Charron, Martin
Silverman, Earl D
description Objectives (1) To identify the average lumbar spine (LS) bone mineral density (BMD) trajectory in paediatric systemic lupus erythematosus (pSLE) patients, and (2) to identify predictors of BMD trajectory. Methods 68 consecutive newly diagnosed pSLE patients prospectively followed in our lupus cohort with three annual dual energy x-ray absorptiometry (DEXA) examinations were studied. Low LS BMD was defined as z-score ≤−2.0. Baseline and longitudinal clinical features including disease activity, treatment and bone physiology markers were collected. Hierarchical linear modelling was used to model trajectory of LS BMD and identify predictors. Results Women constituted 84% of the cohort and median age at diagnosis was 13.1 years. The mean LS BMD z-scores decreased over time (−0.42 at first, −1.02 at second and −1.11 at third DEXA). Initially 9% of patients had a low BMD, which increased to 19% by 3 years after diagnosis. 35% of patients deteriorated in BMD category from the first to third DEXA. LS BMD (adjusted by height-for-age z-score) followed a general deteriorating trajectory of −0.06 z-score/year from diagnosis. Increased rate of deterioration of BMD trajectory was predicted by pubertal status at diagnosis, increased interval cumulative steroid exposure and decreased weight z-scores. Conclusions The LS BMD of pSLE patients followed a general deteriorating trend over time and could be predicted by a combination of pubertal status at diagnosis, interval cumulative doses of steroids and weight z-scores. Interval cumulative steroid dose represents an important target that clinicians may modify to ameliorate deteriorating BMD trajectory over time.
doi_str_mv 10.1136/annrheumdis-2011-200805
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Methods 68 consecutive newly diagnosed pSLE patients prospectively followed in our lupus cohort with three annual dual energy x-ray absorptiometry (DEXA) examinations were studied. Low LS BMD was defined as z-score ≤−2.0. Baseline and longitudinal clinical features including disease activity, treatment and bone physiology markers were collected. Hierarchical linear modelling was used to model trajectory of LS BMD and identify predictors. Results Women constituted 84% of the cohort and median age at diagnosis was 13.1 years. The mean LS BMD z-scores decreased over time (−0.42 at first, −1.02 at second and −1.11 at third DEXA). Initially 9% of patients had a low BMD, which increased to 19% by 3 years after diagnosis. 35% of patients deteriorated in BMD category from the first to third DEXA. LS BMD (adjusted by height-for-age z-score) followed a general deteriorating trajectory of −0.06 z-score/year from diagnosis. Increased rate of deterioration of BMD trajectory was predicted by pubertal status at diagnosis, increased interval cumulative steroid exposure and decreased weight z-scores. Conclusions The LS BMD of pSLE patients followed a general deteriorating trend over time and could be predicted by a combination of pubertal status at diagnosis, interval cumulative doses of steroids and weight z-scores. Interval cumulative steroid dose represents an important target that clinicians may modify to ameliorate deteriorating BMD trajectory over time.</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2011-200805</identifier><identifier>PMID: 22440826</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><subject>Absorptiometry, Photon ; Adolescent ; Biological and medical sciences ; Bone Density ; Child ; Cohort Studies ; Disease Progression ; Diseases of the osteoarticular system ; Female ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Lumbar Vertebrae - diagnostic imaging ; Lupus ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - diagnostic imaging ; Male ; Medical sciences ; Osteoarticular system. Muscles ; Osteoporosis ; Osteoporosis - diagnostic imaging ; Osteoporosis - epidemiology ; Osteoporosis - etiology ; Radiodiagnosis. Nmr imagery. Nmr spectrometry ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Vitamin D</subject><ispartof>Annals of the rheumatic diseases, 2012-10, Vol.71 (10), p.1686-1691</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2012 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b485t-e5fc296e787ed651b886947000b00878e83808f9da6ef53fa4383a722bc36c43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/71/10/1686.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/71/10/1686.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26359488$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22440826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lim, Lily Siok Hoon</creatorcontrib><creatorcontrib>Benseler, Susanne M</creatorcontrib><creatorcontrib>Tyrrell, Pascal N</creatorcontrib><creatorcontrib>Harvey, Elizabeth</creatorcontrib><creatorcontrib>Herbert, Diane</creatorcontrib><creatorcontrib>Charron, Martin</creatorcontrib><creatorcontrib>Silverman, Earl D</creatorcontrib><title>Predicting longitudinal trajectory of bone mineral density in paediatric systemic lupus erythematosus patients</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Objectives (1) To identify the average lumbar spine (LS) bone mineral density (BMD) trajectory in paediatric systemic lupus erythematosus (pSLE) patients, and (2) to identify predictors of BMD trajectory. Methods 68 consecutive newly diagnosed pSLE patients prospectively followed in our lupus cohort with three annual dual energy x-ray absorptiometry (DEXA) examinations were studied. Low LS BMD was defined as z-score ≤−2.0. Baseline and longitudinal clinical features including disease activity, treatment and bone physiology markers were collected. Hierarchical linear modelling was used to model trajectory of LS BMD and identify predictors. Results Women constituted 84% of the cohort and median age at diagnosis was 13.1 years. The mean LS BMD z-scores decreased over time (−0.42 at first, −1.02 at second and −1.11 at third DEXA). Initially 9% of patients had a low BMD, which increased to 19% by 3 years after diagnosis. 35% of patients deteriorated in BMD category from the first to third DEXA. LS BMD (adjusted by height-for-age z-score) followed a general deteriorating trajectory of −0.06 z-score/year from diagnosis. Increased rate of deterioration of BMD trajectory was predicted by pubertal status at diagnosis, increased interval cumulative steroid exposure and decreased weight z-scores. Conclusions The LS BMD of pSLE patients followed a general deteriorating trend over time and could be predicted by a combination of pubertal status at diagnosis, interval cumulative doses of steroids and weight z-scores. Interval cumulative steroid dose represents an important target that clinicians may modify to ameliorate deteriorating BMD trajectory over time.</description><subject>Absorptiometry, Photon</subject><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Bone Density</subject><subject>Child</subject><subject>Cohort Studies</subject><subject>Disease Progression</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Lumbar Vertebrae - diagnostic imaging</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - diagnostic imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Osteoarticular system. Muscles</subject><subject>Osteoporosis</subject><subject>Osteoporosis - diagnostic imaging</subject><subject>Osteoporosis - epidemiology</subject><subject>Osteoporosis - etiology</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Vitamin D</subject><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkV2L1TAQhoMo7tnVv6AFEfammo82SS_l-LHi4hcHvQxpO93NsU27SQr23zuHHg_ijUJIMswzbybzEvKU0ReMCfnSeh9uYR5aF3NOGcONalreIxtWSI2RpPfJhlIq8qKS6oycx7jHkGqmH5IzzouCai43xH8O0LomOX-T9aO_cWlunbd9loLdQ5PGsGRjl9Wjh2xwHgKmWvDRpSVzPpssVtsUXJPFJSYY8NLP0xwzCEu6hcGmMWI02eTAp_iIPOhsH-Hx8bwgu7dvdtur_PrTu_fbV9d5Xegy5VB2Da8kKK2glSWrtZZVobD_Gr-gNGihqe6q1kroStHZQmhhFed1I2RTiAtyucpOYbybISYzuNhA31sP4xwNkwwXL6j4N0pFhRNWrET02V_ofpwDDgsppTSVirPD22qlmjDGGKAzU3CDDQtKmYN55g_zzME8s5qHlU-O-nM9QHuq--0WAs-PgI2N7btgfYMaJ06Ksiq0Ri5fOYeW_DzlbfhhpBKqNB-_bc3VV_Z996F6bb4gz1e-Hvb_3e0vIw3GSw</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Lim, Lily Siok Hoon</creator><creator>Benseler, Susanne M</creator><creator>Tyrrell, Pascal N</creator><creator>Harvey, Elizabeth</creator><creator>Herbert, Diane</creator><creator>Charron, Martin</creator><creator>Silverman, Earl D</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>BMJ Publishing Group</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QP</scope></search><sort><creationdate>20121001</creationdate><title>Predicting longitudinal trajectory of bone mineral density in paediatric systemic lupus erythematosus patients</title><author>Lim, Lily Siok Hoon ; Benseler, Susanne M ; Tyrrell, Pascal N ; Harvey, Elizabeth ; Herbert, Diane ; Charron, Martin ; Silverman, Earl D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b485t-e5fc296e787ed651b886947000b00878e83808f9da6ef53fa4383a722bc36c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Absorptiometry, Photon</topic><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Bone Density</topic><topic>Child</topic><topic>Cohort Studies</topic><topic>Disease Progression</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Lumbar Vertebrae - diagnostic imaging</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - diagnostic imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Osteoarticular system. Muscles</topic><topic>Osteoporosis</topic><topic>Osteoporosis - diagnostic imaging</topic><topic>Osteoporosis - epidemiology</topic><topic>Osteoporosis - etiology</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Vitamin D</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lim, Lily Siok Hoon</creatorcontrib><creatorcontrib>Benseler, Susanne M</creatorcontrib><creatorcontrib>Tyrrell, Pascal N</creatorcontrib><creatorcontrib>Harvey, Elizabeth</creatorcontrib><creatorcontrib>Herbert, Diane</creatorcontrib><creatorcontrib>Charron, Martin</creatorcontrib><creatorcontrib>Silverman, Earl D</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lim, Lily Siok Hoon</au><au>Benseler, Susanne M</au><au>Tyrrell, Pascal N</au><au>Harvey, Elizabeth</au><au>Herbert, Diane</au><au>Charron, Martin</au><au>Silverman, Earl D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predicting longitudinal trajectory of bone mineral density in paediatric systemic lupus erythematosus patients</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>71</volume><issue>10</issue><spage>1686</spage><epage>1691</epage><pages>1686-1691</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Objectives (1) To identify the average lumbar spine (LS) bone mineral density (BMD) trajectory in paediatric systemic lupus erythematosus (pSLE) patients, and (2) to identify predictors of BMD trajectory. Methods 68 consecutive newly diagnosed pSLE patients prospectively followed in our lupus cohort with three annual dual energy x-ray absorptiometry (DEXA) examinations were studied. Low LS BMD was defined as z-score ≤−2.0. Baseline and longitudinal clinical features including disease activity, treatment and bone physiology markers were collected. Hierarchical linear modelling was used to model trajectory of LS BMD and identify predictors. Results Women constituted 84% of the cohort and median age at diagnosis was 13.1 years. The mean LS BMD z-scores decreased over time (−0.42 at first, −1.02 at second and −1.11 at third DEXA). Initially 9% of patients had a low BMD, which increased to 19% by 3 years after diagnosis. 35% of patients deteriorated in BMD category from the first to third DEXA. LS BMD (adjusted by height-for-age z-score) followed a general deteriorating trajectory of −0.06 z-score/year from diagnosis. Increased rate of deterioration of BMD trajectory was predicted by pubertal status at diagnosis, increased interval cumulative steroid exposure and decreased weight z-scores. Conclusions The LS BMD of pSLE patients followed a general deteriorating trend over time and could be predicted by a combination of pubertal status at diagnosis, interval cumulative doses of steroids and weight z-scores. Interval cumulative steroid dose represents an important target that clinicians may modify to ameliorate deteriorating BMD trajectory over time.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><pmid>22440826</pmid><doi>10.1136/annrheumdis-2011-200805</doi><tpages>6</tpages></addata></record>
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subjects Absorptiometry, Photon
Adolescent
Biological and medical sciences
Bone Density
Child
Cohort Studies
Disease Progression
Diseases of the osteoarticular system
Female
Humans
Investigative techniques, diagnostic techniques (general aspects)
Lumbar Vertebrae - diagnostic imaging
Lupus
Lupus Erythematosus, Systemic - complications
Lupus Erythematosus, Systemic - diagnostic imaging
Male
Medical sciences
Osteoarticular system. Muscles
Osteoporosis
Osteoporosis - diagnostic imaging
Osteoporosis - epidemiology
Osteoporosis - etiology
Radiodiagnosis. Nmr imagery. Nmr spectrometry
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Vitamin D
title Predicting longitudinal trajectory of bone mineral density in paediatric systemic lupus erythematosus patients
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