Bone mineral disease in children after renal transplantation in steroid-free and steroid-treated patients - a prospective study

Grenda R, Karczmarewicz E, Rubik J, Matusik H, Płudowski P, Kiliszek M, Piskorski J. Bone mineral disease in children after renal transplantation in steroid‐free and steroid‐treated patients – a prospective study. Pediatr Transplantation 2011: 15:205–213. © 2010 John Wiley & Sons A/S. :  Bone di...

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Veröffentlicht in:Pediatric transplantation 2011-03, Vol.15 (2), p.205-213
Hauptverfasser: Grenda, Ryszard, Karczmarewicz, Elżbieta, Rubik, Jacek, Matusik, Halina, Płudowski, Paweł, Kiliszek, Małgorzata, Piskorski, Jarosław
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container_end_page 213
container_issue 2
container_start_page 205
container_title Pediatric transplantation
container_volume 15
creator Grenda, Ryszard
Karczmarewicz, Elżbieta
Rubik, Jacek
Matusik, Halina
Płudowski, Paweł
Kiliszek, Małgorzata
Piskorski, Jarosław
description Grenda R, Karczmarewicz E, Rubik J, Matusik H, Płudowski P, Kiliszek M, Piskorski J. Bone mineral disease in children after renal transplantation in steroid‐free and steroid‐treated patients – a prospective study. Pediatr Transplantation 2011: 15:205–213. © 2010 John Wiley & Sons A/S. :  Bone disease may persist after transplantation. Different approaches aiming to ameliorate this problem have been investigated. The aim of the study was to compare the long‐term effect of three medical interventions: (i) two prophylactic oral doses of 50 mg ibandronate; (ii) daily oral dose of 0.25 μg of 1α‐OHD3 (both of these regimens in patients receiving steroids), and (iii) steroid minimization immunosuppressive protocol in patients with no other specific prophylaxis. Patients: A total of 37 children, at a mean age of 13.33 ± 3.49 yr, dialyzed for 15.93 ± 16.7 months before transplantation, were divided into three groups, depending on medical intervention. Bone mineral content and density (BMC, BMD, DXA), serum markers of bone resorption and formation (CTX, P1NP), calcium, phosphate, 25OHD3/1.25 (OH)2D3 and PTH concentration were evaluated during two yr of follow‐up. The mean values of BMD in the whole population and among the three subgroups remained within the age‐ and gender‐matched normal range during follow‐up. Patients from groups II (alphacalcidiol) and III (steroid minimization) showed a significant decrease in BMD Z‐scores over time, and this effect was determined with increasing age using multivariate analysis. Patients receiving two doses of ibandronate maintained unchanged Z‐scores for BMD and BMC over time.
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Bone mineral disease in children after renal transplantation in steroid‐free and steroid‐treated patients – a prospective study. Pediatr Transplantation 2011: 15:205–213. © 2010 John Wiley &amp; Sons A/S. :  Bone disease may persist after transplantation. Different approaches aiming to ameliorate this problem have been investigated. The aim of the study was to compare the long‐term effect of three medical interventions: (i) two prophylactic oral doses of 50 mg ibandronate; (ii) daily oral dose of 0.25 μg of 1α‐OHD3 (both of these regimens in patients receiving steroids), and (iii) steroid minimization immunosuppressive protocol in patients with no other specific prophylaxis. Patients: A total of 37 children, at a mean age of 13.33 ± 3.49 yr, dialyzed for 15.93 ± 16.7 months before transplantation, were divided into three groups, depending on medical intervention. Bone mineral content and density (BMC, BMD, DXA), serum markers of bone resorption and formation (CTX, P1NP), calcium, phosphate, 25OHD3/1.25 (OH)2D3 and PTH concentration were evaluated during two yr of follow‐up. The mean values of BMD in the whole population and among the three subgroups remained within the age‐ and gender‐matched normal range during follow‐up. Patients from groups II (alphacalcidiol) and III (steroid minimization) showed a significant decrease in BMD Z‐scores over time, and this effect was determined with increasing age using multivariate analysis. Patients receiving two doses of ibandronate maintained unchanged Z‐scores for BMD and BMC over time.</description><identifier>ISSN: 1397-3142</identifier><identifier>EISSN: 1399-3046</identifier><identifier>DOI: 10.1111/j.1399-3046.2010.01448.x</identifier><identifier>PMID: 21199211</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Adolescent ; Age ; Age Factors ; Analysis of Variance ; Biological and medical sciences ; Bisphosphonates ; Bone Demineralization, Pathologic - diagnosis ; Bone Demineralization, Pathologic - drug therapy ; Bone Demineralization, Pathologic - etiology ; Bone Density - drug effects ; Bone Density - physiology ; bone disease ; Bone diseases ; Bone mineral content ; Bone mineral density ; Bone resorption ; Calcifediol - administration &amp; dosage ; Calcium phosphate ; Child ; Children ; Cohort Studies ; Collagen ; Diphosphonates - administration &amp; dosage ; Diseases of the osteoarticular system ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Dual energy X-ray absorptiometry ; Female ; Follow-Up Studies ; General aspects ; Humans ; Ibandronic acid ; Immunosuppressive Agents - administration &amp; dosage ; Immunosuppressive Agents - adverse effects ; Kidney transplantation ; Kidney Transplantation - adverse effects ; Kidney Transplantation - methods ; Long-term effects ; Male ; Medical sciences ; Multivariate Analysis ; Osteoporosis. Osteomalacia. Paget disease ; Parathyroid hormone ; Prophylaxis ; Prospective Studies ; renal transplantation ; Risk Assessment ; Sex Factors ; Steroid hormones ; steroid minimization ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Treatment Outcome</subject><ispartof>Pediatric transplantation, 2011-03, Vol.15 (2), p.205-213</ispartof><rights>2010 John Wiley &amp; Sons A/S</rights><rights>2015 INIST-CNRS</rights><rights>2010 John Wiley &amp; Sons A/S.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4698-26b88ec37921329c19d4df98a74a255de59a37cdc50ee70bb84b2523065963803</citedby><cites>FETCH-LOGICAL-c4698-26b88ec37921329c19d4df98a74a255de59a37cdc50ee70bb84b2523065963803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1399-3046.2010.01448.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1399-3046.2010.01448.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23854581$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21199211$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grenda, Ryszard</creatorcontrib><creatorcontrib>Karczmarewicz, Elżbieta</creatorcontrib><creatorcontrib>Rubik, Jacek</creatorcontrib><creatorcontrib>Matusik, Halina</creatorcontrib><creatorcontrib>Płudowski, Paweł</creatorcontrib><creatorcontrib>Kiliszek, Małgorzata</creatorcontrib><creatorcontrib>Piskorski, Jarosław</creatorcontrib><title>Bone mineral disease in children after renal transplantation in steroid-free and steroid-treated patients - a prospective study</title><title>Pediatric transplantation</title><addtitle>Pediatr Transplant</addtitle><description>Grenda R, Karczmarewicz E, Rubik J, Matusik H, Płudowski P, Kiliszek M, Piskorski J. Bone mineral disease in children after renal transplantation in steroid‐free and steroid‐treated patients – a prospective study. Pediatr Transplantation 2011: 15:205–213. © 2010 John Wiley &amp; Sons A/S. :  Bone disease may persist after transplantation. Different approaches aiming to ameliorate this problem have been investigated. The aim of the study was to compare the long‐term effect of three medical interventions: (i) two prophylactic oral doses of 50 mg ibandronate; (ii) daily oral dose of 0.25 μg of 1α‐OHD3 (both of these regimens in patients receiving steroids), and (iii) steroid minimization immunosuppressive protocol in patients with no other specific prophylaxis. Patients: A total of 37 children, at a mean age of 13.33 ± 3.49 yr, dialyzed for 15.93 ± 16.7 months before transplantation, were divided into three groups, depending on medical intervention. Bone mineral content and density (BMC, BMD, DXA), serum markers of bone resorption and formation (CTX, P1NP), calcium, phosphate, 25OHD3/1.25 (OH)2D3 and PTH concentration were evaluated during two yr of follow‐up. The mean values of BMD in the whole population and among the three subgroups remained within the age‐ and gender‐matched normal range during follow‐up. Patients from groups II (alphacalcidiol) and III (steroid minimization) showed a significant decrease in BMD Z‐scores over time, and this effect was determined with increasing age using multivariate analysis. Patients receiving two doses of ibandronate maintained unchanged Z‐scores for BMD and BMC over time.</description><subject>Administration, Oral</subject><subject>Adolescent</subject><subject>Age</subject><subject>Age Factors</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Bisphosphonates</subject><subject>Bone Demineralization, Pathologic - diagnosis</subject><subject>Bone Demineralization, Pathologic - drug therapy</subject><subject>Bone Demineralization, Pathologic - etiology</subject><subject>Bone Density - drug effects</subject><subject>Bone Density - physiology</subject><subject>bone disease</subject><subject>Bone diseases</subject><subject>Bone mineral content</subject><subject>Bone mineral density</subject><subject>Bone resorption</subject><subject>Calcifediol - administration &amp; dosage</subject><subject>Calcium phosphate</subject><subject>Child</subject><subject>Children</subject><subject>Cohort Studies</subject><subject>Collagen</subject><subject>Diphosphonates - administration &amp; dosage</subject><subject>Diseases of the osteoarticular system</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Dual energy X-ray absorptiometry</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>General aspects</subject><subject>Humans</subject><subject>Ibandronic acid</subject><subject>Immunosuppressive Agents - administration &amp; dosage</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Kidney transplantation</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Kidney Transplantation - methods</subject><subject>Long-term effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multivariate Analysis</subject><subject>Osteoporosis. Osteomalacia. Paget disease</subject><subject>Parathyroid hormone</subject><subject>Prophylaxis</subject><subject>Prospective Studies</subject><subject>renal transplantation</subject><subject>Risk Assessment</subject><subject>Sex Factors</subject><subject>Steroid hormones</subject><subject>steroid minimization</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Treatment Outcome</subject><issn>1397-3142</issn><issn>1399-3046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhi0Eoh_wF5AviFMWf8b2BYlWbUFaKEJFHC3Hnggv2STYWdg98dfrdJflWh_s0cwzr8d-EcKULGhZb1cLyo2pOBH1gpGSJVQIvdg-QafHwtOHWFWcCnaCznJeEUJrocVzdMIoNaZsp-jvxdADXscekutwiBlcBhx77H_ELiTosWsnSLhEpT4l1-exc_3kpjj0M5dLdYihahMAdn04JqYEboKAx4JCP2VcYYfHNOQR_BR_QwE3YfcCPWtdl-Hl4TxH366v7i4_VMvbm4-X75eVF7XRFasbrcFzVabmzHhqggit0U4Jx6QMII3jygcvCYAiTaNFwyTjpJam5prwc_Rmr1sm-LWBPNl1zB668hYYNtkaxhnh5BGkllQoTdVM6j3py6tygtaOKa5d2llK7OyTXdnZDjvbYWef7INPdltaXx0u2TRrCMfGf8YU4PUBcNm7ri0f72P-z3EthdQz927P_Ykd7B49gP1ydfd1DotAtReIxbjtUcCln7ZWXEn7_fONJRdKfpLL0s7vAYB6vec</recordid><startdate>201103</startdate><enddate>201103</enddate><creator>Grenda, Ryszard</creator><creator>Karczmarewicz, Elżbieta</creator><creator>Rubik, Jacek</creator><creator>Matusik, Halina</creator><creator>Płudowski, Paweł</creator><creator>Kiliszek, Małgorzata</creator><creator>Piskorski, Jarosław</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7X8</scope><scope>7QP</scope></search><sort><creationdate>201103</creationdate><title>Bone mineral disease in children after renal transplantation in steroid-free and steroid-treated patients - a prospective study</title><author>Grenda, Ryszard ; Karczmarewicz, Elżbieta ; Rubik, Jacek ; Matusik, Halina ; Płudowski, Paweł ; Kiliszek, Małgorzata ; Piskorski, Jarosław</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4698-26b88ec37921329c19d4df98a74a255de59a37cdc50ee70bb84b2523065963803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Oral</topic><topic>Adolescent</topic><topic>Age</topic><topic>Age Factors</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Bisphosphonates</topic><topic>Bone Demineralization, Pathologic - diagnosis</topic><topic>Bone Demineralization, Pathologic - drug therapy</topic><topic>Bone Demineralization, Pathologic - etiology</topic><topic>Bone Density - drug effects</topic><topic>Bone Density - physiology</topic><topic>bone disease</topic><topic>Bone diseases</topic><topic>Bone mineral content</topic><topic>Bone mineral density</topic><topic>Bone resorption</topic><topic>Calcifediol - administration &amp; dosage</topic><topic>Calcium phosphate</topic><topic>Child</topic><topic>Children</topic><topic>Cohort Studies</topic><topic>Collagen</topic><topic>Diphosphonates - administration &amp; dosage</topic><topic>Diseases of the osteoarticular system</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Dual energy X-ray absorptiometry</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>General aspects</topic><topic>Humans</topic><topic>Ibandronic acid</topic><topic>Immunosuppressive Agents - administration &amp; dosage</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Kidney transplantation</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Kidney Transplantation - methods</topic><topic>Long-term effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multivariate Analysis</topic><topic>Osteoporosis. Osteomalacia. Paget disease</topic><topic>Parathyroid hormone</topic><topic>Prophylaxis</topic><topic>Prospective Studies</topic><topic>renal transplantation</topic><topic>Risk Assessment</topic><topic>Sex Factors</topic><topic>Steroid hormones</topic><topic>steroid minimization</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grenda, Ryszard</creatorcontrib><creatorcontrib>Karczmarewicz, Elżbieta</creatorcontrib><creatorcontrib>Rubik, Jacek</creatorcontrib><creatorcontrib>Matusik, Halina</creatorcontrib><creatorcontrib>Płudowski, Paweł</creatorcontrib><creatorcontrib>Kiliszek, Małgorzata</creatorcontrib><creatorcontrib>Piskorski, Jarosław</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>MEDLINE - Academic</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><jtitle>Pediatric transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grenda, Ryszard</au><au>Karczmarewicz, Elżbieta</au><au>Rubik, Jacek</au><au>Matusik, Halina</au><au>Płudowski, Paweł</au><au>Kiliszek, Małgorzata</au><au>Piskorski, Jarosław</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone mineral disease in children after renal transplantation in steroid-free and steroid-treated patients - a prospective study</atitle><jtitle>Pediatric transplantation</jtitle><addtitle>Pediatr Transplant</addtitle><date>2011-03</date><risdate>2011</risdate><volume>15</volume><issue>2</issue><spage>205</spage><epage>213</epage><pages>205-213</pages><issn>1397-3142</issn><eissn>1399-3046</eissn><abstract>Grenda R, Karczmarewicz E, Rubik J, Matusik H, Płudowski P, Kiliszek M, Piskorski J. Bone mineral disease in children after renal transplantation in steroid‐free and steroid‐treated patients – a prospective study. Pediatr Transplantation 2011: 15:205–213. © 2010 John Wiley &amp; Sons A/S. :  Bone disease may persist after transplantation. Different approaches aiming to ameliorate this problem have been investigated. The aim of the study was to compare the long‐term effect of three medical interventions: (i) two prophylactic oral doses of 50 mg ibandronate; (ii) daily oral dose of 0.25 μg of 1α‐OHD3 (both of these regimens in patients receiving steroids), and (iii) steroid minimization immunosuppressive protocol in patients with no other specific prophylaxis. Patients: A total of 37 children, at a mean age of 13.33 ± 3.49 yr, dialyzed for 15.93 ± 16.7 months before transplantation, were divided into three groups, depending on medical intervention. Bone mineral content and density (BMC, BMD, DXA), serum markers of bone resorption and formation (CTX, P1NP), calcium, phosphate, 25OHD3/1.25 (OH)2D3 and PTH concentration were evaluated during two yr of follow‐up. The mean values of BMD in the whole population and among the three subgroups remained within the age‐ and gender‐matched normal range during follow‐up. Patients from groups II (alphacalcidiol) and III (steroid minimization) showed a significant decrease in BMD Z‐scores over time, and this effect was determined with increasing age using multivariate analysis. Patients receiving two doses of ibandronate maintained unchanged Z‐scores for BMD and BMC over time.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21199211</pmid><doi>10.1111/j.1399-3046.2010.01448.x</doi><tpages>9</tpages></addata></record>
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identifier ISSN: 1397-3142
ispartof Pediatric transplantation, 2011-03, Vol.15 (2), p.205-213
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source MEDLINE; Wiley Online Library All Journals
subjects Administration, Oral
Adolescent
Age
Age Factors
Analysis of Variance
Biological and medical sciences
Bisphosphonates
Bone Demineralization, Pathologic - diagnosis
Bone Demineralization, Pathologic - drug therapy
Bone Demineralization, Pathologic - etiology
Bone Density - drug effects
Bone Density - physiology
bone disease
Bone diseases
Bone mineral content
Bone mineral density
Bone resorption
Calcifediol - administration & dosage
Calcium phosphate
Child
Children
Cohort Studies
Collagen
Diphosphonates - administration & dosage
Diseases of the osteoarticular system
Dose-Response Relationship, Drug
Drug Administration Schedule
Dual energy X-ray absorptiometry
Female
Follow-Up Studies
General aspects
Humans
Ibandronic acid
Immunosuppressive Agents - administration & dosage
Immunosuppressive Agents - adverse effects
Kidney transplantation
Kidney Transplantation - adverse effects
Kidney Transplantation - methods
Long-term effects
Male
Medical sciences
Multivariate Analysis
Osteoporosis. Osteomalacia. Paget disease
Parathyroid hormone
Prophylaxis
Prospective Studies
renal transplantation
Risk Assessment
Sex Factors
Steroid hormones
steroid minimization
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the urinary system
Treatment Outcome
title Bone mineral disease in children after renal transplantation in steroid-free and steroid-treated patients - a prospective study
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