Zinc metabolism in adolescents with Crohn's disease
Low serum zinc concentrations have been reported in Crohn's disease (CD) and overt zinc deficiency has been described, but little is known about the effect of CD on zinc metabolism in adolescents. The aim of this study was to measure zinc absorption, endogenous fecal zinc excretion, urinary zin...
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Veröffentlicht in: | Pediatric research 2004-08, Vol.56 (2), p.235-239 |
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description | Low serum zinc concentrations have been reported in Crohn's disease (CD) and overt zinc deficiency has been described, but little is known about the effect of CD on zinc metabolism in adolescents. The aim of this study was to measure zinc absorption, endogenous fecal zinc excretion, urinary zinc excretion, and zinc balance in children with stable CD and in matched controls. Subjects were 15 children, ages 8-18 y, with stable CD, and 15 healthy matched controls. Subjects were adapted to diets providing 12 mg/d elemental zinc for 2 wk, and then admitted for a 6-d metabolic study. Stable zinc isotopes were given intravenously and orally, and urine and feces collected for 6 d. Fractional zinc absorption, endogenous fecal zinc excretion, and zinc balance were calculated using established stable isotope methods. In subjects with CD, zinc absorption (10.9% +/- 6.1 versus 23.4 +/- 15.8, p = 0.008) and plasma zinc concentration (0.85 mg/dL +/- 0.15 versus 1.25 +/- 0.35, p = 0.004) were significantly reduced, compared with controls. Despite this, there were no significant differences in endogenous fecal zinc excretion (2.0 mg +/- 1.5 versus 1.5 +/- 1.5, p = 0.34) or urinary zinc excretion (0.9 mg +/- 0.7 versus 1.0 +/- 0.7, p = 0.47). Zinc balance was significantly lower in CD (-1.5 mg +/- 1.5) than in controls (+0.6 mg +/- 3.1, p < 0.0001). In conclusion, adolescents with CD have significantly reduced zinc absorption. Despite this, they were unable to reduce endogenous fecal zinc excretion to restore normal zinc balance and had a significantly worse zinc balance and lower plasma zinc concentration than controls. |
doi_str_mv | 10.1203/01.PDR.0000132851.50841.D7 |
format | Article |
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The aim of this study was to measure zinc absorption, endogenous fecal zinc excretion, urinary zinc excretion, and zinc balance in children with stable CD and in matched controls. Subjects were 15 children, ages 8-18 y, with stable CD, and 15 healthy matched controls. Subjects were adapted to diets providing 12 mg/d elemental zinc for 2 wk, and then admitted for a 6-d metabolic study. Stable zinc isotopes were given intravenously and orally, and urine and feces collected for 6 d. Fractional zinc absorption, endogenous fecal zinc excretion, and zinc balance were calculated using established stable isotope methods. In subjects with CD, zinc absorption (10.9% +/- 6.1 versus 23.4 +/- 15.8, p = 0.008) and plasma zinc concentration (0.85 mg/dL +/- 0.15 versus 1.25 +/- 0.35, p = 0.004) were significantly reduced, compared with controls. Despite this, there were no significant differences in endogenous fecal zinc excretion (2.0 mg +/- 1.5 versus 1.5 +/- 1.5, p = 0.34) or urinary zinc excretion (0.9 mg +/- 0.7 versus 1.0 +/- 0.7, p = 0.47). Zinc balance was significantly lower in CD (-1.5 mg +/- 1.5) than in controls (+0.6 mg +/- 3.1, p < 0.0001). In conclusion, adolescents with CD have significantly reduced zinc absorption. Despite this, they were unable to reduce endogenous fecal zinc excretion to restore normal zinc balance and had a significantly worse zinc balance and lower plasma zinc concentration than controls.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1203/01.PDR.0000132851.50841.D7</identifier><identifier>PMID: 15181193</identifier><identifier>CODEN: PEREBL</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Biological and medical sciences ; Blood Chemical Analysis ; Case-Control Studies ; Child ; Crohn Disease - metabolism ; Gastroenterology. Liver. Pancreas. Abdomen ; General aspects ; Humans ; Malformations ; Medical sciences ; Other diseases. Semiology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Zinc - chemistry ; Zinc - metabolism ; Zinc Isotopes - metabolism</subject><ispartof>Pediatric research, 2004-08, Vol.56 (2), p.235-239</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-264a8ed1d0b9cf80e2b6b09724e76c8df3c8e4ba7baeaf9ca2437335dcab4b7c3</citedby><cites>FETCH-LOGICAL-c397t-264a8ed1d0b9cf80e2b6b09724e76c8df3c8e4ba7baeaf9ca2437335dcab4b7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15975407$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15181193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GRIFFIN, Ian J</creatorcontrib><creatorcontrib>KIM, Sandra C</creatorcontrib><creatorcontrib>HICKS, Penni D</creatorcontrib><creatorcontrib>LIANG, Lily K</creatorcontrib><creatorcontrib>ABRAMS, Steven A</creatorcontrib><title>Zinc metabolism in adolescents with Crohn's disease</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><description>Low serum zinc concentrations have been reported in Crohn's disease (CD) and overt zinc deficiency has been described, but little is known about the effect of CD on zinc metabolism in adolescents. The aim of this study was to measure zinc absorption, endogenous fecal zinc excretion, urinary zinc excretion, and zinc balance in children with stable CD and in matched controls. Subjects were 15 children, ages 8-18 y, with stable CD, and 15 healthy matched controls. Subjects were adapted to diets providing 12 mg/d elemental zinc for 2 wk, and then admitted for a 6-d metabolic study. Stable zinc isotopes were given intravenously and orally, and urine and feces collected for 6 d. Fractional zinc absorption, endogenous fecal zinc excretion, and zinc balance were calculated using established stable isotope methods. In subjects with CD, zinc absorption (10.9% +/- 6.1 versus 23.4 +/- 15.8, p = 0.008) and plasma zinc concentration (0.85 mg/dL +/- 0.15 versus 1.25 +/- 0.35, p = 0.004) were significantly reduced, compared with controls. Despite this, there were no significant differences in endogenous fecal zinc excretion (2.0 mg +/- 1.5 versus 1.5 +/- 1.5, p = 0.34) or urinary zinc excretion (0.9 mg +/- 0.7 versus 1.0 +/- 0.7, p = 0.47). Zinc balance was significantly lower in CD (-1.5 mg +/- 1.5) than in controls (+0.6 mg +/- 3.1, p < 0.0001). In conclusion, adolescents with CD have significantly reduced zinc absorption. Despite this, they were unable to reduce endogenous fecal zinc excretion to restore normal zinc balance and had a significantly worse zinc balance and lower plasma zinc concentration than controls.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Blood Chemical Analysis</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Crohn Disease - metabolism</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>General aspects</subject><subject>Humans</subject><subject>Malformations</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Zinc - chemistry</subject><subject>Zinc - metabolism</subject><subject>Zinc Isotopes - metabolism</subject><issn>0031-3998</issn><issn>1530-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1LxDAQhoMo7vrxF6QI6ql1pkmbxJvs-gULiujFS0jSlI30Y226iP_erltY5zKX531neAg5R0gwBXoNmLzMXxMYBmkqMkwyEAyTOd8jU8woxMAY3ydTAIoxlVJMyFEInwPOMsEOyQQzFIiSTgn98I2Natdr01Y-1JFvIl20lQvWNX2Ivn2_jGZdu2yuQlT44HRwJ-Sg1FVwp-M-Ju_3d2-zx3jx_PA0u13Elkrex2nOtHAFFmCkLQW41OQGJE-Z47kVRUmtcMxobrTTpbQ6ZZRTmhVWG2a4pcfkctu76tqvtQu9qv3wVlXpxrXroPKcU0gFH8CbLWi7NoTOlWrV-Vp3PwpBbZQpQDUoUztl6k-Zmm_CZ-OVtaldsYuOjgbgYgR0sLoqO91YH_5xkmcMOP0FXyF0wQ</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>GRIFFIN, Ian J</creator><creator>KIM, Sandra C</creator><creator>HICKS, Penni D</creator><creator>LIANG, Lily K</creator><creator>ABRAMS, Steven A</creator><general>Lippincott Williams & Wilkins</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>7X8</scope></search><sort><creationdate>20040801</creationdate><title>Zinc metabolism in adolescents with Crohn's disease</title><author>GRIFFIN, Ian J ; KIM, Sandra C ; HICKS, Penni D ; LIANG, Lily K ; ABRAMS, Steven A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-264a8ed1d0b9cf80e2b6b09724e76c8df3c8e4ba7baeaf9ca2437335dcab4b7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Blood Chemical Analysis</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Crohn Disease - metabolism</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>General aspects</topic><topic>Humans</topic><topic>Malformations</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Zinc - chemistry</topic><topic>Zinc - metabolism</topic><topic>Zinc Isotopes - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GRIFFIN, Ian J</creatorcontrib><creatorcontrib>KIM, Sandra C</creatorcontrib><creatorcontrib>HICKS, Penni D</creatorcontrib><creatorcontrib>LIANG, Lily K</creatorcontrib><creatorcontrib>ABRAMS, Steven A</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>MEDLINE - Academic</collection><jtitle>Pediatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GRIFFIN, Ian J</au><au>KIM, Sandra C</au><au>HICKS, Penni D</au><au>LIANG, Lily K</au><au>ABRAMS, Steven A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zinc metabolism in adolescents with Crohn's disease</atitle><jtitle>Pediatric research</jtitle><addtitle>Pediatr Res</addtitle><date>2004-08-01</date><risdate>2004</risdate><volume>56</volume><issue>2</issue><spage>235</spage><epage>239</epage><pages>235-239</pages><issn>0031-3998</issn><eissn>1530-0447</eissn><coden>PEREBL</coden><abstract>Low serum zinc concentrations have been reported in Crohn's disease (CD) and overt zinc deficiency has been described, but little is known about the effect of CD on zinc metabolism in adolescents. The aim of this study was to measure zinc absorption, endogenous fecal zinc excretion, urinary zinc excretion, and zinc balance in children with stable CD and in matched controls. Subjects were 15 children, ages 8-18 y, with stable CD, and 15 healthy matched controls. Subjects were adapted to diets providing 12 mg/d elemental zinc for 2 wk, and then admitted for a 6-d metabolic study. Stable zinc isotopes were given intravenously and orally, and urine and feces collected for 6 d. Fractional zinc absorption, endogenous fecal zinc excretion, and zinc balance were calculated using established stable isotope methods. In subjects with CD, zinc absorption (10.9% +/- 6.1 versus 23.4 +/- 15.8, p = 0.008) and plasma zinc concentration (0.85 mg/dL +/- 0.15 versus 1.25 +/- 0.35, p = 0.004) were significantly reduced, compared with controls. Despite this, there were no significant differences in endogenous fecal zinc excretion (2.0 mg +/- 1.5 versus 1.5 +/- 1.5, p = 0.34) or urinary zinc excretion (0.9 mg +/- 0.7 versus 1.0 +/- 0.7, p = 0.47). Zinc balance was significantly lower in CD (-1.5 mg +/- 1.5) than in controls (+0.6 mg +/- 3.1, p < 0.0001). In conclusion, adolescents with CD have significantly reduced zinc absorption. Despite this, they were unable to reduce endogenous fecal zinc excretion to restore normal zinc balance and had a significantly worse zinc balance and lower plasma zinc concentration than controls.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>15181193</pmid><doi>10.1203/01.PDR.0000132851.50841.D7</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Biological and medical sciences Blood Chemical Analysis Case-Control Studies Child Crohn Disease - metabolism Gastroenterology. Liver. Pancreas. Abdomen General aspects Humans Malformations Medical sciences Other diseases. Semiology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Zinc - chemistry Zinc - metabolism Zinc Isotopes - metabolism |
title | Zinc metabolism in adolescents with Crohn's disease |
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