Serum vitamin D metabolites and bone mineralization in young children with chronic low to moderate lead exposure
One hundred five children (49 male, 99 black) with known lead exposure indices from birth and adequate nutrient intake of calcium, phosphorus, and vitamin D were studied at 1 of 3 ages (21, 27, or 33 months) to determine the effects of chronic low to moderate lead exposure on circulating concentrati...
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Veröffentlicht in: | Pediatrics (Evanston) 1991-05, Vol.87 (5), p.680-687 |
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description | One hundred five children (49 male, 99 black) with known lead exposure indices from birth and adequate nutrient intake of calcium, phosphorus, and vitamin D were studied at 1 of 3 ages (21, 27, or 33 months) to determine the effects of chronic low to moderate lead exposure on circulating concentrations of vitamin D metabolites and bone mineral content as determined by photon absorptiometry. Univariate multiple regression analyses showed no direct relationship of blood lead levels to vitamin D metabolites or bone mineral content. Structural equation analyses which took into account potential covariates of age, season, race, and sex showed estimated declines in serum concentrations of total calcium (from 9.72 to 9.61 mg/dL), phosphorus (from 5.4 to 4.67 mg/dL), and 25-hydroxyvitamin D (from 27.24 to 25.8 ng/mL) and estimated increases in concentrations of parathyroid hormones (from 73.03 to 83.14 microL Eq/mL), 1,25-dihydroxyvitamin D (from 62.39 to 62.69 pg/mL), and bone mineral content (from 222.66 to 234.91 mg/cm) over the observed range of average lifetime blood lead concentrations (4.76 to 23.61 micrograms/dL, geometric mean 9.74 micrograms/dL). However, the only statistically significant effect of average lifetime blood lead concentration was that for phosphorus, and the multivariate test of the combined effects of lead on these six outcomes was not statistically significant (P = 0.2). It is concluded that significant alterations in vitamin D metabolism, calcium and phosphorus homeostasis, and bone mineral content are not present in children whose nutritional status is adequate and who experience low to moderate lead exposure |
doi_str_mv | 10.1542/peds.87.5.680 |
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(University of Cincinnati, OH) ; Succop, P.A ; Bornschein, R.L ; Krug-Wispe, S.K ; Steinchen, J.J ; Tsang, R.C ; Berger, O.G</creator><creatorcontrib>Koo, W.W.K. (University of Cincinnati, OH) ; Succop, P.A ; Bornschein, R.L ; Krug-Wispe, S.K ; Steinchen, J.J ; Tsang, R.C ; Berger, O.G</creatorcontrib><description>One hundred five children (49 male, 99 black) with known lead exposure indices from birth and adequate nutrient intake of calcium, phosphorus, and vitamin D were studied at 1 of 3 ages (21, 27, or 33 months) to determine the effects of chronic low to moderate lead exposure on circulating concentrations of vitamin D metabolites and bone mineral content as determined by photon absorptiometry. Univariate multiple regression analyses showed no direct relationship of blood lead levels to vitamin D metabolites or bone mineral content. Structural equation analyses which took into account potential covariates of age, season, race, and sex showed estimated declines in serum concentrations of total calcium (from 9.72 to 9.61 mg/dL), phosphorus (from 5.4 to 4.67 mg/dL), and 25-hydroxyvitamin D (from 27.24 to 25.8 ng/mL) and estimated increases in concentrations of parathyroid hormones (from 73.03 to 83.14 microL Eq/mL), 1,25-dihydroxyvitamin D (from 62.39 to 62.69 pg/mL), and bone mineral content (from 222.66 to 234.91 mg/cm) over the observed range of average lifetime blood lead concentrations (4.76 to 23.61 micrograms/dL, geometric mean 9.74 micrograms/dL). However, the only statistically significant effect of average lifetime blood lead concentration was that for phosphorus, and the multivariate test of the combined effects of lead on these six outcomes was not statistically significant (P = 0.2). It is concluded that significant alterations in vitamin D metabolism, calcium and phosphorus homeostasis, and bone mineral content are not present in children whose nutritional status is adequate and who experience low to moderate lead exposure</description><identifier>ISSN: 0031-4005</identifier><identifier>EISSN: 1098-4275</identifier><identifier>DOI: 10.1542/peds.87.5.680</identifier><identifier>PMID: 2020514</identifier><identifier>CODEN: PEDIAU</identifier><language>eng</language><publisher>Elk Grove Village, IL: American Academy of Pediatrics</publisher><subject>ABSORCION DE SUBSTANCIAS NUTRITIVAS ; ABSORPTION DE SUBSTANCES NUTRITIVES ; Biological and medical sciences ; Bone density ; Bone Density - physiology ; Bones ; Calcification, Physiologic - physiology ; CALCIO ; Calcitonin - blood ; CALCITONINA ; CALCITONINE ; CALCIUM ; Calcium - blood ; Child, Preschool ; Chronic Disease ; Cohort Studies ; Density ; ENFANT ; Female ; FORMACION OSEA ; FORMATION DES OS ; FOSFORO ; HORMONAS ; HORMONE ; Humans ; Hydroxycholecalciferols - blood ; Infant ; Lead - blood ; Lead in the body ; Lead Poisoning - blood ; Lead Poisoning - metabolism ; MAGNESIO ; MAGNESIUM ; Magnesium - blood ; Male ; Medical sciences ; Mineral metabolism ; MODELE ; MODELOS ; NINOS ; OHIO ; Parathyroid Hormone - blood ; PEPTIDE ; PEPTIDOS ; PHOSPHORE ; Phosphorus - blood ; Physiological aspects ; PLOMB ; PLOMO ; Regression Analysis ; SERUM SANGUIN ; SUERO SANGUINEO ; Toxicology ; Vitamin D ; Vitamin D metabolism ; Vitamin metabolism ; VITAMINA D ; VITAMINE D</subject><ispartof>Pediatrics (Evanston), 1991-05, Vol.87 (5), p.680-687</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-dc4e865bbe7f18d86b63206c346961782e277a64a38f4601ecee354355a8c7333</citedby></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=4403853$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2020514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koo, W.W.K. (University of Cincinnati, OH)</creatorcontrib><creatorcontrib>Succop, P.A</creatorcontrib><creatorcontrib>Bornschein, R.L</creatorcontrib><creatorcontrib>Krug-Wispe, S.K</creatorcontrib><creatorcontrib>Steinchen, J.J</creatorcontrib><creatorcontrib>Tsang, R.C</creatorcontrib><creatorcontrib>Berger, O.G</creatorcontrib><title>Serum vitamin D metabolites and bone mineralization in young children with chronic low to moderate lead exposure</title><title>Pediatrics (Evanston)</title><addtitle>Pediatrics</addtitle><description>One hundred five children (49 male, 99 black) with known lead exposure indices from birth and adequate nutrient intake of calcium, phosphorus, and vitamin D were studied at 1 of 3 ages (21, 27, or 33 months) to determine the effects of chronic low to moderate lead exposure on circulating concentrations of vitamin D metabolites and bone mineral content as determined by photon absorptiometry. Univariate multiple regression analyses showed no direct relationship of blood lead levels to vitamin D metabolites or bone mineral content. Structural equation analyses which took into account potential covariates of age, season, race, and sex showed estimated declines in serum concentrations of total calcium (from 9.72 to 9.61 mg/dL), phosphorus (from 5.4 to 4.67 mg/dL), and 25-hydroxyvitamin D (from 27.24 to 25.8 ng/mL) and estimated increases in concentrations of parathyroid hormones (from 73.03 to 83.14 microL Eq/mL), 1,25-dihydroxyvitamin D (from 62.39 to 62.69 pg/mL), and bone mineral content (from 222.66 to 234.91 mg/cm) over the observed range of average lifetime blood lead concentrations (4.76 to 23.61 micrograms/dL, geometric mean 9.74 micrograms/dL). However, the only statistically significant effect of average lifetime blood lead concentration was that for phosphorus, and the multivariate test of the combined effects of lead on these six outcomes was not statistically significant (P = 0.2). It is concluded that significant alterations in vitamin D metabolism, calcium and phosphorus homeostasis, and bone mineral content are not present in children whose nutritional status is adequate and who experience low to moderate lead exposure</description><subject>ABSORCION DE SUBSTANCIAS NUTRITIVAS</subject><subject>ABSORPTION DE SUBSTANCES NUTRITIVES</subject><subject>Biological and medical sciences</subject><subject>Bone density</subject><subject>Bone Density - physiology</subject><subject>Bones</subject><subject>Calcification, Physiologic - physiology</subject><subject>CALCIO</subject><subject>Calcitonin - blood</subject><subject>CALCITONINA</subject><subject>CALCITONINE</subject><subject>CALCIUM</subject><subject>Calcium - blood</subject><subject>Child, Preschool</subject><subject>Chronic Disease</subject><subject>Cohort Studies</subject><subject>Density</subject><subject>ENFANT</subject><subject>Female</subject><subject>FORMACION OSEA</subject><subject>FORMATION DES OS</subject><subject>FOSFORO</subject><subject>HORMONAS</subject><subject>HORMONE</subject><subject>Humans</subject><subject>Hydroxycholecalciferols - blood</subject><subject>Infant</subject><subject>Lead - blood</subject><subject>Lead in the body</subject><subject>Lead Poisoning - blood</subject><subject>Lead Poisoning - metabolism</subject><subject>MAGNESIO</subject><subject>MAGNESIUM</subject><subject>Magnesium - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mineral metabolism</subject><subject>MODELE</subject><subject>MODELOS</subject><subject>NINOS</subject><subject>OHIO</subject><subject>Parathyroid Hormone - blood</subject><subject>PEPTIDE</subject><subject>PEPTIDOS</subject><subject>PHOSPHORE</subject><subject>Phosphorus - blood</subject><subject>Physiological aspects</subject><subject>PLOMB</subject><subject>PLOMO</subject><subject>Regression Analysis</subject><subject>SERUM SANGUIN</subject><subject>SUERO SANGUINEO</subject><subject>Toxicology</subject><subject>Vitamin D</subject><subject>Vitamin D metabolism</subject><subject>Vitamin metabolism</subject><subject>VITAMINA D</subject><subject>VITAMINE D</subject><issn>0031-4005</issn><issn>1098-4275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90c1rHCEYBnApLek27bGXQsFDj52tn6NzDNtPCOSQ5iyO887G4uigbpP0r6_LLjmJPD_15RGh95RsqRTsywpT2Wq1ldtekxdoQ8mgO8GUfIk2hHDaCULka_SmlD-EECEVu0AXjDAiqdig9RbyYcF_fbWLj_grXqDaMQVfoWAbJzymCLhFkG3w_2z1KeIGn9Ih7rG792HKEPGDr_dtl1P0Dof0gGvCS5raoQo4gJ0wPK6pHDK8Ra9mGwq8O6-X6O77t9-7n931zY9fu6vrznHFazc5AbqX4whqpnrS_dhzRnrHRT_0VGkGTCnbC8v1LHpCwQFwKbiUVjvFOb9En0_37m0A46NLscJjdSkE2INpb-1uzBUlWjA2yMa7E3c5lZJhNmv2i81PhhJz7NkcezZaGWlaz81_PPn1MC4wPetzsS3_dM5tcTbM2UbnyzMTgnAtj1N-OLHZJmP3uZG724FKPbSv-w9iXI6G</recordid><startdate>19910501</startdate><enddate>19910501</enddate><creator>Koo, W.W.K. (University of Cincinnati, OH)</creator><creator>Succop, P.A</creator><creator>Bornschein, R.L</creator><creator>Krug-Wispe, S.K</creator><creator>Steinchen, J.J</creator><creator>Tsang, R.C</creator><creator>Berger, O.G</creator><general>American Academy of Pediatrics</general><scope>FBQ</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></search><sort><creationdate>19910501</creationdate><title>Serum vitamin D metabolites and bone mineralization in young children with chronic low to moderate lead exposure</title><author>Koo, W.W.K. (University of Cincinnati, OH) ; Succop, P.A ; Bornschein, R.L ; Krug-Wispe, S.K ; Steinchen, J.J ; Tsang, R.C ; Berger, O.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-dc4e865bbe7f18d86b63206c346961782e277a64a38f4601ecee354355a8c7333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>ABSORCION DE SUBSTANCIAS NUTRITIVAS</topic><topic>ABSORPTION DE SUBSTANCES NUTRITIVES</topic><topic>Biological and medical sciences</topic><topic>Bone density</topic><topic>Bone Density - physiology</topic><topic>Bones</topic><topic>Calcification, Physiologic - physiology</topic><topic>CALCIO</topic><topic>Calcitonin - blood</topic><topic>CALCITONINA</topic><topic>CALCITONINE</topic><topic>CALCIUM</topic><topic>Calcium - blood</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Cohort Studies</topic><topic>Density</topic><topic>ENFANT</topic><topic>Female</topic><topic>FORMACION OSEA</topic><topic>FORMATION DES OS</topic><topic>FOSFORO</topic><topic>HORMONAS</topic><topic>HORMONE</topic><topic>Humans</topic><topic>Hydroxycholecalciferols - blood</topic><topic>Infant</topic><topic>Lead - blood</topic><topic>Lead in the body</topic><topic>Lead Poisoning - blood</topic><topic>Lead Poisoning - metabolism</topic><topic>MAGNESIO</topic><topic>MAGNESIUM</topic><topic>Magnesium - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mineral metabolism</topic><topic>MODELE</topic><topic>MODELOS</topic><topic>NINOS</topic><topic>OHIO</topic><topic>Parathyroid Hormone - blood</topic><topic>PEPTIDE</topic><topic>PEPTIDOS</topic><topic>PHOSPHORE</topic><topic>Phosphorus - blood</topic><topic>Physiological aspects</topic><topic>PLOMB</topic><topic>PLOMO</topic><topic>Regression Analysis</topic><topic>SERUM SANGUIN</topic><topic>SUERO SANGUINEO</topic><topic>Toxicology</topic><topic>Vitamin D</topic><topic>Vitamin D metabolism</topic><topic>Vitamin metabolism</topic><topic>VITAMINA D</topic><topic>VITAMINE D</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koo, W.W.K. (University of Cincinnati, OH)</creatorcontrib><creatorcontrib>Succop, P.A</creatorcontrib><creatorcontrib>Bornschein, R.L</creatorcontrib><creatorcontrib>Krug-Wispe, S.K</creatorcontrib><creatorcontrib>Steinchen, J.J</creatorcontrib><creatorcontrib>Tsang, R.C</creatorcontrib><creatorcontrib>Berger, O.G</creatorcontrib><collection>AGRIS</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><jtitle>Pediatrics (Evanston)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koo, W.W.K. (University of Cincinnati, OH)</au><au>Succop, P.A</au><au>Bornschein, R.L</au><au>Krug-Wispe, S.K</au><au>Steinchen, J.J</au><au>Tsang, R.C</au><au>Berger, O.G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum vitamin D metabolites and bone mineralization in young children with chronic low to moderate lead exposure</atitle><jtitle>Pediatrics (Evanston)</jtitle><addtitle>Pediatrics</addtitle><date>1991-05-01</date><risdate>1991</risdate><volume>87</volume><issue>5</issue><spage>680</spage><epage>687</epage><pages>680-687</pages><issn>0031-4005</issn><eissn>1098-4275</eissn><coden>PEDIAU</coden><abstract>One hundred five children (49 male, 99 black) with known lead exposure indices from birth and adequate nutrient intake of calcium, phosphorus, and vitamin D were studied at 1 of 3 ages (21, 27, or 33 months) to determine the effects of chronic low to moderate lead exposure on circulating concentrations of vitamin D metabolites and bone mineral content as determined by photon absorptiometry. Univariate multiple regression analyses showed no direct relationship of blood lead levels to vitamin D metabolites or bone mineral content. Structural equation analyses which took into account potential covariates of age, season, race, and sex showed estimated declines in serum concentrations of total calcium (from 9.72 to 9.61 mg/dL), phosphorus (from 5.4 to 4.67 mg/dL), and 25-hydroxyvitamin D (from 27.24 to 25.8 ng/mL) and estimated increases in concentrations of parathyroid hormones (from 73.03 to 83.14 microL Eq/mL), 1,25-dihydroxyvitamin D (from 62.39 to 62.69 pg/mL), and bone mineral content (from 222.66 to 234.91 mg/cm) over the observed range of average lifetime blood lead concentrations (4.76 to 23.61 micrograms/dL, geometric mean 9.74 micrograms/dL). However, the only statistically significant effect of average lifetime blood lead concentration was that for phosphorus, and the multivariate test of the combined effects of lead on these six outcomes was not statistically significant (P = 0.2). It is concluded that significant alterations in vitamin D metabolism, calcium and phosphorus homeostasis, and bone mineral content are not present in children whose nutritional status is adequate and who experience low to moderate lead exposure</abstract><cop>Elk Grove Village, IL</cop><pub>American Academy of Pediatrics</pub><pmid>2020514</pmid><doi>10.1542/peds.87.5.680</doi><tpages>8</tpages></addata></record> |
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subjects | ABSORCION DE SUBSTANCIAS NUTRITIVAS ABSORPTION DE SUBSTANCES NUTRITIVES Biological and medical sciences Bone density Bone Density - physiology Bones Calcification, Physiologic - physiology CALCIO Calcitonin - blood CALCITONINA CALCITONINE CALCIUM Calcium - blood Child, Preschool Chronic Disease Cohort Studies Density ENFANT Female FORMACION OSEA FORMATION DES OS FOSFORO HORMONAS HORMONE Humans Hydroxycholecalciferols - blood Infant Lead - blood Lead in the body Lead Poisoning - blood Lead Poisoning - metabolism MAGNESIO MAGNESIUM Magnesium - blood Male Medical sciences Mineral metabolism MODELE MODELOS NINOS OHIO Parathyroid Hormone - blood PEPTIDE PEPTIDOS PHOSPHORE Phosphorus - blood Physiological aspects PLOMB PLOMO Regression Analysis SERUM SANGUIN SUERO SANGUINEO Toxicology Vitamin D Vitamin D metabolism Vitamin metabolism VITAMINA D VITAMINE D |
title | Serum vitamin D metabolites and bone mineralization in young children with chronic low to moderate lead exposure |
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