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Familial hypophosphatemic rickets: bone mass measurements in children following therapy with calcitriol and supplemental phosphate
Familial hypophosphatemic rickets is characterized by defective skeletal mineralization resulting in abnormal growth and development. The pathologic and radiologic correlates of this syndrome have been given some investigation, but the effect of this mineralization defect on bone mineral density has...
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Published in: | Calcified tissue international 1989-02, Vol.44 (2), p.86-92 |
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description | Familial hypophosphatemic rickets is characterized by defective skeletal mineralization resulting in abnormal growth and development. The pathologic and radiologic correlates of this syndrome have been given some investigation, but the effect of this mineralization defect on bone mineral density has not been adequately assessed. We measured axial and appendicular bone mineral in 17 children (mean age 5.59 +/- 4.87) with familial hypophosphatemia at baseline and at 6-month intervals after initiation of therapy with vitamin D3 (calcitriol) and phosphate supplementation. Noninvasive quantitative techniques included single photon absorptiometry (SPA) of the radius, combined cortical thickness (CCT) of the second metacarpal, and quantitative computed tomography (QCT) of vertebral trabecular bone. Thoraco-lumbar and hand/wrist radiographs were qualitatively assessed for the prevalence and severity of osteosclerosis, rickets, and other parameters indicative of metabolic bone disease as well as skeletal age. Quantitative determinations of bone mineral by each technique were compared with normal values for age and sex, and individual standardized scores (z-scores) were calculated at each measurement interval. Standard scores were also calculated for bone age-adjusted mineral values. At baseline, spinal trabecular bone by QCT was not significantly different from normal values; however, measurements of peripheral cortical bone by either SPA or CCT were significantly lower than values for normal children of the same age and sex (P = 0.05 and P = 0.01, respectively). Following therapy with calcitriol and phosphate, peripheral bone mass was not shown to improve significantly when contiguous standard scores were compared even when values were adjusted for bone age. |
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E ; PIEL, C. F ; SELVIDGE, R ; GENANT, H. K</creator><creatorcontrib>BLOCK, J. E ; PIEL, C. F ; SELVIDGE, R ; GENANT, H. K</creatorcontrib><description>Familial hypophosphatemic rickets is characterized by defective skeletal mineralization resulting in abnormal growth and development. The pathologic and radiologic correlates of this syndrome have been given some investigation, but the effect of this mineralization defect on bone mineral density has not been adequately assessed. We measured axial and appendicular bone mineral in 17 children (mean age 5.59 +/- 4.87) with familial hypophosphatemia at baseline and at 6-month intervals after initiation of therapy with vitamin D3 (calcitriol) and phosphate supplementation. Noninvasive quantitative techniques included single photon absorptiometry (SPA) of the radius, combined cortical thickness (CCT) of the second metacarpal, and quantitative computed tomography (QCT) of vertebral trabecular bone. Thoraco-lumbar and hand/wrist radiographs were qualitatively assessed for the prevalence and severity of osteosclerosis, rickets, and other parameters indicative of metabolic bone disease as well as skeletal age. Quantitative determinations of bone mineral by each technique were compared with normal values for age and sex, and individual standardized scores (z-scores) were calculated at each measurement interval. Standard scores were also calculated for bone age-adjusted mineral values. At baseline, spinal trabecular bone by QCT was not significantly different from normal values; however, measurements of peripheral cortical bone by either SPA or CCT were significantly lower than values for normal children of the same age and sex (P = 0.05 and P = 0.01, respectively). Following therapy with calcitriol and phosphate, peripheral bone mass was not shown to improve significantly when contiguous standard scores were compared even when values were adjusted for bone age.</description><identifier>ISSN: 0171-967X</identifier><identifier>EISSN: 1432-0827</identifier><identifier>DOI: 10.1007/bf02556466</identifier><identifier>PMID: 2492895</identifier><identifier>CODEN: CTINDZ</identifier><language>eng</language><publisher>New York, NY: Springer-Verlag</publisher><subject>Adolescent ; Age Determination by Skeleton ; Biological and medical sciences ; Bone and Bones - diagnostic imaging ; Bone and Bones - pathology ; Calcitriol - therapeutic use ; Child ; Child, Preschool ; General and cellular metabolism. Vitamins ; Humans ; Hypophosphatemia, Familial - complications ; Infant ; Medical sciences ; Minerals - metabolism ; Pharmacology. Drug treatments ; Phosphates - therapeutic use ; Radionuclide Imaging ; Rickets - drug therapy ; Rickets - etiology ; Rickets - pathology ; Space life sciences ; Tomography, X-Ray Computed</subject><ispartof>Calcified tissue international, 1989-02, Vol.44 (2), p.86-92</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-d8ab127c5c9cb0c60a7c98d324216da6610894db68f7751e92ba7a054b9460cf3</citedby><cites>FETCH-LOGICAL-c371t-d8ab127c5c9cb0c60a7c98d324216da6610894db68f7751e92ba7a054b9460cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7243868$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2492895$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BLOCK, J. E</creatorcontrib><creatorcontrib>PIEL, C. F</creatorcontrib><creatorcontrib>SELVIDGE, R</creatorcontrib><creatorcontrib>GENANT, H. K</creatorcontrib><title>Familial hypophosphatemic rickets: bone mass measurements in children following therapy with calcitriol and supplemental phosphate</title><title>Calcified tissue international</title><addtitle>Calcif Tissue Int</addtitle><description>Familial hypophosphatemic rickets is characterized by defective skeletal mineralization resulting in abnormal growth and development. The pathologic and radiologic correlates of this syndrome have been given some investigation, but the effect of this mineralization defect on bone mineral density has not been adequately assessed. We measured axial and appendicular bone mineral in 17 children (mean age 5.59 +/- 4.87) with familial hypophosphatemia at baseline and at 6-month intervals after initiation of therapy with vitamin D3 (calcitriol) and phosphate supplementation. Noninvasive quantitative techniques included single photon absorptiometry (SPA) of the radius, combined cortical thickness (CCT) of the second metacarpal, and quantitative computed tomography (QCT) of vertebral trabecular bone. Thoraco-lumbar and hand/wrist radiographs were qualitatively assessed for the prevalence and severity of osteosclerosis, rickets, and other parameters indicative of metabolic bone disease as well as skeletal age. Quantitative determinations of bone mineral by each technique were compared with normal values for age and sex, and individual standardized scores (z-scores) were calculated at each measurement interval. Standard scores were also calculated for bone age-adjusted mineral values. At baseline, spinal trabecular bone by QCT was not significantly different from normal values; however, measurements of peripheral cortical bone by either SPA or CCT were significantly lower than values for normal children of the same age and sex (P = 0.05 and P = 0.01, respectively). Following therapy with calcitriol and phosphate, peripheral bone mass was not shown to improve significantly when contiguous standard scores were compared even when values were adjusted for bone age.</description><subject>Adolescent</subject><subject>Age Determination by Skeleton</subject><subject>Biological and medical sciences</subject><subject>Bone and Bones - diagnostic imaging</subject><subject>Bone and Bones - pathology</subject><subject>Calcitriol - therapeutic use</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Humans</subject><subject>Hypophosphatemia, Familial - complications</subject><subject>Infant</subject><subject>Medical sciences</subject><subject>Minerals - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphates - therapeutic use</subject><subject>Radionuclide Imaging</subject><subject>Rickets - drug therapy</subject><subject>Rickets - etiology</subject><subject>Rickets - pathology</subject><subject>Space life sciences</subject><subject>Tomography, X-Ray Computed</subject><issn>0171-967X</issn><issn>1432-0827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNqFkTFP3TAUhS0Eog_owl7JA-qAFLAdx3bYKOorSEgsILFFN47TuHXi4JsIvbW_nLS8vpXpDue750jnEHLK2QVnTF_WLRNFoaRSe2TFZS4yZoTeJyvGNc9KpZ8_kSPEX4zxhVGH5FDIUpiyWJE_a-h98BBotxnj2EUcO5hc7y1N3v52E17ROg6O9oBIewc4J9e7YULqB2o7H5rkBtrGEOKrH37SqXMJxg199VNHLQTrp-RjoDA0FOdxDP--l7xd1gk5aCGg-7y9x-Rp_f3x5ja7f_hxd3N9n9lc8ylrDNRcaFvY0tbMKgbalqbJhRRcNaAUZ6aUTa1Mq3XBXSlq0MAKWZdSMdvmx-Tru--Y4svscKp6j9aFAIOLM1bamKUcIT4EecGlyDlbwPN30KaImFxbjcn3kDYVZ9XfZapv6__LLPCXretc967ZodspFv1sqwMuvbUJButxh2khc6NM_gZP9phl</recordid><startdate>19890201</startdate><enddate>19890201</enddate><creator>BLOCK, J. E</creator><creator>PIEL, C. F</creator><creator>SELVIDGE, R</creator><creator>GENANT, H. K</creator><general>Springer-Verlag</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>7QP</scope><scope>7X8</scope></search><sort><creationdate>19890201</creationdate><title>Familial hypophosphatemic rickets: bone mass measurements in children following therapy with calcitriol and supplemental phosphate</title><author>BLOCK, J. E ; PIEL, C. F ; SELVIDGE, R ; GENANT, H. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-d8ab127c5c9cb0c60a7c98d324216da6610894db68f7751e92ba7a054b9460cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adolescent</topic><topic>Age Determination by Skeleton</topic><topic>Biological and medical sciences</topic><topic>Bone and Bones - diagnostic imaging</topic><topic>Bone and Bones - pathology</topic><topic>Calcitriol - therapeutic use</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Humans</topic><topic>Hypophosphatemia, Familial - complications</topic><topic>Infant</topic><topic>Medical sciences</topic><topic>Minerals - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphates - therapeutic use</topic><topic>Radionuclide Imaging</topic><topic>Rickets - drug therapy</topic><topic>Rickets - etiology</topic><topic>Rickets - pathology</topic><topic>Space life sciences</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BLOCK, J. E</creatorcontrib><creatorcontrib>PIEL, C. F</creatorcontrib><creatorcontrib>SELVIDGE, R</creatorcontrib><creatorcontrib>GENANT, H. K</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>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Calcified tissue international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BLOCK, J. E</au><au>PIEL, C. F</au><au>SELVIDGE, R</au><au>GENANT, H. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Familial hypophosphatemic rickets: bone mass measurements in children following therapy with calcitriol and supplemental phosphate</atitle><jtitle>Calcified tissue international</jtitle><addtitle>Calcif Tissue Int</addtitle><date>1989-02-01</date><risdate>1989</risdate><volume>44</volume><issue>2</issue><spage>86</spage><epage>92</epage><pages>86-92</pages><issn>0171-967X</issn><eissn>1432-0827</eissn><coden>CTINDZ</coden><abstract>Familial hypophosphatemic rickets is characterized by defective skeletal mineralization resulting in abnormal growth and development. The pathologic and radiologic correlates of this syndrome have been given some investigation, but the effect of this mineralization defect on bone mineral density has not been adequately assessed. We measured axial and appendicular bone mineral in 17 children (mean age 5.59 +/- 4.87) with familial hypophosphatemia at baseline and at 6-month intervals after initiation of therapy with vitamin D3 (calcitriol) and phosphate supplementation. Noninvasive quantitative techniques included single photon absorptiometry (SPA) of the radius, combined cortical thickness (CCT) of the second metacarpal, and quantitative computed tomography (QCT) of vertebral trabecular bone. Thoraco-lumbar and hand/wrist radiographs were qualitatively assessed for the prevalence and severity of osteosclerosis, rickets, and other parameters indicative of metabolic bone disease as well as skeletal age. Quantitative determinations of bone mineral by each technique were compared with normal values for age and sex, and individual standardized scores (z-scores) were calculated at each measurement interval. Standard scores were also calculated for bone age-adjusted mineral values. At baseline, spinal trabecular bone by QCT was not significantly different from normal values; however, measurements of peripheral cortical bone by either SPA or CCT were significantly lower than values for normal children of the same age and sex (P = 0.05 and P = 0.01, respectively). Following therapy with calcitriol and phosphate, peripheral bone mass was not shown to improve significantly when contiguous standard scores were compared even when values were adjusted for bone age.</abstract><cop>New York, NY</cop><pub>Springer-Verlag</pub><pmid>2492895</pmid><doi>10.1007/bf02556466</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Age Determination by Skeleton Biological and medical sciences Bone and Bones - diagnostic imaging Bone and Bones - pathology Calcitriol - therapeutic use Child Child, Preschool General and cellular metabolism. Vitamins Humans Hypophosphatemia, Familial - complications Infant Medical sciences Minerals - metabolism Pharmacology. Drug treatments Phosphates - therapeutic use Radionuclide Imaging Rickets - drug therapy Rickets - etiology Rickets - pathology Space life sciences Tomography, X-Ray Computed |
title | Familial hypophosphatemic rickets: bone mass measurements in children following therapy with calcitriol and supplemental phosphate |
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