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Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophy
Abstract This cross-sectional study examined bone mineral density, bone turnover, body composition and calciotropic hormones in 24 boys with Duchenne muscular dystrophy (DMD) (2.3–19.7 years), most of whom were being treated with prednisolone, and 24 age-matched healthy boys. Our study demonstrated...
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Published in: | Neuromuscular disorders : NMD 2007-12, Vol.17 (11), p.919-928 |
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description | Abstract This cross-sectional study examined bone mineral density, bone turnover, body composition and calciotropic hormones in 24 boys with Duchenne muscular dystrophy (DMD) (2.3–19.7 years), most of whom were being treated with prednisolone, and 24 age-matched healthy boys. Our study demonstrated lower bone mineral density in the DMD group for total body, spine, hip, heel and forearm measurements. These differences between DMD patients and controls increased with increasing age. Biochemical markers of both bone formation and resorption revealed reduced bone turnover in DMD patients. The fracture rate was not higher in DMD patients. The DMD group had low vitamin D levels but high leptin levels in comparison with the control group. Muscle strength correlated with bone mineral density assessed at the hip and heel in the DMD group. Interventions that increase bone formation should be considered, as DMD patients have reduced bone turnover in addition to their low bone mineral density. |
doi_str_mv | 10.1016/j.nmd.2007.05.008 |
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Our study demonstrated lower bone mineral density in the DMD group for total body, spine, hip, heel and forearm measurements. These differences between DMD patients and controls increased with increasing age. Biochemical markers of both bone formation and resorption revealed reduced bone turnover in DMD patients. The fracture rate was not higher in DMD patients. The DMD group had low vitamin D levels but high leptin levels in comparison with the control group. Muscle strength correlated with bone mineral density assessed at the hip and heel in the DMD group. Interventions that increase bone formation should be considered, as DMD patients have reduced bone turnover in addition to their low bone mineral density.</description><identifier>ISSN: 0960-8966</identifier><identifier>ISSN: 1873-2364</identifier><identifier>EISSN: 1873-2364</identifier><identifier>DOI: 10.1016/j.nmd.2007.05.008</identifier><identifier>PMID: 17627820</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Biomarkers - analysis ; Biomarkers - metabolism ; Bone and Bones - drug effects ; Bone and Bones - metabolism ; Bone and Bones - physiopathology ; Bone Density - drug effects ; Bone Density - physiology ; Bone markers ; Bone Resorption - chemically induced ; Bone Resorption - metabolism ; Bone Resorption - physiopathology ; Calciotropic hormones ; Calcium - metabolism ; Child ; Child, Preschool ; Children ; Cross-Sectional Studies ; Diet ; DXA ; Glucocorticoids - adverse effects ; Humans ; Leptin - metabolism ; Male ; MEDICAL AND HEALTH SCIENCES ; MEDICIN ; MEDICIN OCH HÄLSOVETENSKAP ; MEDICINE ; Muscle Strength - genetics ; Muscular Dystrophy, Duchenne - drug therapy ; Neurology ; Nutrition Assessment ; Nutritional Physiological Phenomena ; Osteogenesis - genetics ; Osteoporosis - chemically induced ; Osteoporosis - metabolism ; Osteoporosis - physiopathology ; Prednisolone - adverse effects ; Skeleton ; Steroids ; Vitamin D Deficiency - etiology ; Vitamin D Deficiency - physiopathology</subject><ispartof>Neuromuscular disorders : NMD, 2007-12, Vol.17 (11), p.919-928</ispartof><rights>Elsevier B.V.</rights><rights>2007 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-bf46c457a75a4a90d62a627ead7c0bd3003c971c17d7d388b7a3444c7e2ca3d23</citedby><cites>FETCH-LOGICAL-c546t-bf46c457a75a4a90d62a627ead7c0bd3003c971c17d7d388b7a3444c7e2ca3d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17627820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-40616$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/57044$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Söderpalm, Ann-Charlott</creatorcontrib><creatorcontrib>Magnusson, Per</creatorcontrib><creatorcontrib>Åhlander, Anne-Christine</creatorcontrib><creatorcontrib>Karlsson, Jón</creatorcontrib><creatorcontrib>Kroksmark, Anna-Karin</creatorcontrib><creatorcontrib>Tulinius, Már</creatorcontrib><creatorcontrib>Swolin-Eide, Diana</creatorcontrib><title>Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophy</title><title>Neuromuscular disorders : NMD</title><addtitle>Neuromuscul Disord</addtitle><description>Abstract This cross-sectional study examined bone mineral density, bone turnover, body composition and calciotropic hormones in 24 boys with Duchenne muscular dystrophy (DMD) (2.3–19.7 years), most of whom were being treated with prednisolone, and 24 age-matched healthy boys. Our study demonstrated lower bone mineral density in the DMD group for total body, spine, hip, heel and forearm measurements. These differences between DMD patients and controls increased with increasing age. Biochemical markers of both bone formation and resorption revealed reduced bone turnover in DMD patients. The fracture rate was not higher in DMD patients. The DMD group had low vitamin D levels but high leptin levels in comparison with the control group. Muscle strength correlated with bone mineral density assessed at the hip and heel in the DMD group. Interventions that increase bone formation should be considered, as DMD patients have reduced bone turnover in addition to their low bone mineral density.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biomarkers - analysis</subject><subject>Biomarkers - metabolism</subject><subject>Bone and Bones - drug effects</subject><subject>Bone and Bones - metabolism</subject><subject>Bone and Bones - physiopathology</subject><subject>Bone Density - drug effects</subject><subject>Bone Density - physiology</subject><subject>Bone markers</subject><subject>Bone Resorption - chemically induced</subject><subject>Bone Resorption - metabolism</subject><subject>Bone Resorption - physiopathology</subject><subject>Calciotropic hormones</subject><subject>Calcium - metabolism</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Cross-Sectional Studies</subject><subject>Diet</subject><subject>DXA</subject><subject>Glucocorticoids - adverse effects</subject><subject>Humans</subject><subject>Leptin - metabolism</subject><subject>Male</subject><subject>MEDICAL AND HEALTH SCIENCES</subject><subject>MEDICIN</subject><subject>MEDICIN OCH HÄLSOVETENSKAP</subject><subject>MEDICINE</subject><subject>Muscle Strength - genetics</subject><subject>Muscular Dystrophy, Duchenne - drug therapy</subject><subject>Neurology</subject><subject>Nutrition Assessment</subject><subject>Nutritional Physiological Phenomena</subject><subject>Osteogenesis - genetics</subject><subject>Osteoporosis - chemically induced</subject><subject>Osteoporosis - metabolism</subject><subject>Osteoporosis - physiopathology</subject><subject>Prednisolone - adverse effects</subject><subject>Skeleton</subject><subject>Steroids</subject><subject>Vitamin D Deficiency - etiology</subject><subject>Vitamin D Deficiency - physiopathology</subject><issn>0960-8966</issn><issn>1873-2364</issn><issn>1873-2364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kcFq3DAURUVpaKZpP6Cb4g-onSdbljwUCiFJ28BAF0m6fcjSm4mmHnmQ7AT_fWUcWsgiKwlx7kWcy9gnDgUHLs_3hT_YogRQBdQFQPOGrXijqryspHjLVrCWkDdrKU_Z-xj3ALxWUr1jp1zJUjUlrNjtpn_K2t5TdnCegu4ySz66Ycq0t-luAulIdkGGMfj-kULmfHY1mgfyc26MZux0yOwUh9AfH6YP7GSru0gfn88zdv_9-u7yZ7759ePm8mKTm1rIIW-3QhpRK61qLfQarCx1-hZpqwy0tgKozFpxw5VVtmqaVulKCGEUlUZXtqzO2JelNz7RcWzxGNxBhwl77XA3HjE97UaMhLUCIV7Fr9zvC-zDDjs3ogDJZcL5gpvQxxho-y_AAWf9uMekH2f9CDUm_Snzecmk_gPZ_4ln3wn4ugCUvDw6ChiNI2_IukBmQNu7V-u_vUibznlndPeHJor7Pu2ThCPHWCLg7bz_PD-oNH3T1NVfldSsXA</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Söderpalm, Ann-Charlott</creator><creator>Magnusson, Per</creator><creator>Åhlander, Anne-Christine</creator><creator>Karlsson, Jón</creator><creator>Kroksmark, Anna-Karin</creator><creator>Tulinius, Már</creator><creator>Swolin-Eide, Diana</creator><general>Elsevier B.V</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>ADTPV</scope><scope>AOWAS</scope><scope>DG8</scope><scope>F1U</scope></search><sort><creationdate>20071201</creationdate><title>Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophy</title><author>Söderpalm, Ann-Charlott ; 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Our study demonstrated lower bone mineral density in the DMD group for total body, spine, hip, heel and forearm measurements. These differences between DMD patients and controls increased with increasing age. Biochemical markers of both bone formation and resorption revealed reduced bone turnover in DMD patients. The fracture rate was not higher in DMD patients. The DMD group had low vitamin D levels but high leptin levels in comparison with the control group. Muscle strength correlated with bone mineral density assessed at the hip and heel in the DMD group. Interventions that increase bone formation should be considered, as DMD patients have reduced bone turnover in addition to their low bone mineral density.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>17627820</pmid><doi>10.1016/j.nmd.2007.05.008</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Adult Biomarkers - analysis Biomarkers - metabolism Bone and Bones - drug effects Bone and Bones - metabolism Bone and Bones - physiopathology Bone Density - drug effects Bone Density - physiology Bone markers Bone Resorption - chemically induced Bone Resorption - metabolism Bone Resorption - physiopathology Calciotropic hormones Calcium - metabolism Child Child, Preschool Children Cross-Sectional Studies Diet DXA Glucocorticoids - adverse effects Humans Leptin - metabolism Male MEDICAL AND HEALTH SCIENCES MEDICIN MEDICIN OCH HÄLSOVETENSKAP MEDICINE Muscle Strength - genetics Muscular Dystrophy, Duchenne - drug therapy Neurology Nutrition Assessment Nutritional Physiological Phenomena Osteogenesis - genetics Osteoporosis - chemically induced Osteoporosis - metabolism Osteoporosis - physiopathology Prednisolone - adverse effects Skeleton Steroids Vitamin D Deficiency - etiology Vitamin D Deficiency - physiopathology |
title | Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophy |
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