Fluoride exposure and bone status in patients with chronic intestinal failure who are receiving home parenteral nutrition

BACKGROUND: and Objective: Metabolic bone disease is frequent in chronic intestinal failure. Because fluoride has a major effect on bones, the status of both fluoride and bone was studied in long-term home parenteral nutrition (HPN) patients. DESIGN: We studied 31 adults aged (x ± SD) 56.3 ± 15.1 y,...

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Veröffentlicht in:The American journal of clinical nutrition 2006-06, Vol.83 (6), p.1429-1437
Hauptverfasser: Boulétreau, Paul H, Bost, Muriel, Fontanges, Elisabeth, Lauverjat, Madeleine, Gutknecht, Christel, Ecochard, René, Delmas, Pierre D, Chambrier, Cécile
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container_end_page 1437
container_issue 6
container_start_page 1429
container_title The American journal of clinical nutrition
container_volume 83
creator Boulétreau, Paul H
Bost, Muriel
Fontanges, Elisabeth
Lauverjat, Madeleine
Gutknecht, Christel
Ecochard, René
Delmas, Pierre D
Chambrier, Cécile
description BACKGROUND: and Objective: Metabolic bone disease is frequent in chronic intestinal failure. Because fluoride has a major effect on bones, the status of both fluoride and bone was studied in long-term home parenteral nutrition (HPN) patients. DESIGN: We studied 31 adults aged (x ± SD) 56.3 ± 15.1 y, mainly patients with short-bowel syndrome, who had been receiving HPN for >1 y. Bone mineral density (BMD) was measured by absorptiometry, and serum fluoride was measured by using a fluoride-sensitive electrode. All patients ate and drank ad libitum. HPN (3.4 ± 1.2 times/wk) complemented oral nutrition. Potential explicative factors were estimated by using a linear regression model (mixed-effects model). RESULTS: Of 120 fluoride dosages (2-6/patient), 102 were above the upper normal limit (1.58 μmol/L) at the laboratory. Mean (± SD) daily fluoride supply was 8.03 ± 7.71 mg (US adequate intake: 3.1 mg/d for women and 3.8 for men; tolerable upper normal limit: 10 mg/d); intravenous fluoride varied from 0.06 to 1.45 mg, and oral fluoride varied from 0.09 to 27.8 mg. Serum fluoride concentrations were correlated with creatinine clearance and fluoride supply. BMD was significantly lower in the femoral neck than in the spinal area. After adjustment for sex and the duration of HPN, only the effect of serum fluoride on spinal BMD was significant. Two patients had symptoms of fluorosis, eg, calcaneum fissures, interosseous calcifications, or femoral neck osteoporosis. CONCLUSIONS: In chronic intestinal failure, high intakes of fluoride are frequent because of the beverages ingested to compensate for stool losses. Hyperfluoremia has an effect on bone metabolism and may increase skeletal fragility. The consumption of fluoride-rich beverages for extended periods is therefore not advisable.
doi_str_mv 10.1093/ajcn/83.6.1429
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Because fluoride has a major effect on bones, the status of both fluoride and bone was studied in long-term home parenteral nutrition (HPN) patients. DESIGN: We studied 31 adults aged (x ± SD) 56.3 ± 15.1 y, mainly patients with short-bowel syndrome, who had been receiving HPN for &gt;1 y. Bone mineral density (BMD) was measured by absorptiometry, and serum fluoride was measured by using a fluoride-sensitive electrode. All patients ate and drank ad libitum. HPN (3.4 ± 1.2 times/wk) complemented oral nutrition. Potential explicative factors were estimated by using a linear regression model (mixed-effects model). RESULTS: Of 120 fluoride dosages (2-6/patient), 102 were above the upper normal limit (1.58 μmol/L) at the laboratory. Mean (± SD) daily fluoride supply was 8.03 ± 7.71 mg (US adequate intake: 3.1 mg/d for women and 3.8 for men; tolerable upper normal limit: 10 mg/d); intravenous fluoride varied from 0.06 to 1.45 mg, and oral fluoride varied from 0.09 to 27.8 mg. Serum fluoride concentrations were correlated with creatinine clearance and fluoride supply. BMD was significantly lower in the femoral neck than in the spinal area. After adjustment for sex and the duration of HPN, only the effect of serum fluoride on spinal BMD was significant. Two patients had symptoms of fluorosis, eg, calcaneum fissures, interosseous calcifications, or femoral neck osteoporosis. CONCLUSIONS: In chronic intestinal failure, high intakes of fluoride are frequent because of the beverages ingested to compensate for stool losses. Hyperfluoremia has an effect on bone metabolism and may increase skeletal fragility. The consumption of fluoride-rich beverages for extended periods is therefore not advisable.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.1093/ajcn/83.6.1429</identifier><identifier>PMID: 16762955</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Nutrition</publisher><subject>Adult ; adults ; Aged ; Biological and medical sciences ; blood chemistry ; Bone and Bones - metabolism ; Bone density ; Bone Density - drug effects ; bone strength ; developmental orthopedic disease ; dietary exposure ; digestive system diseases ; feces ; Feeding. Feeding behavior ; Female ; Fluoridation ; fluorides ; Fluorides - administration &amp; dosage ; Fluorides - adverse effects ; Fluorides - blood ; fluorosis ; food intake ; Fundamental and applied biological sciences. Psychology ; Humans ; hyperfluoremia ; Life Sciences ; Linear Models ; Male ; Metabolism ; Middle Aged ; Nutrition ; oral nutrition ; Other ; parenteral feeding ; Parenteral Nutrition, Home ; patients ; regression analysis ; Retrospective Studies ; Short Bowel Syndrome - metabolism ; signs and symptoms (animals and humans) ; Small intestine ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>The American journal of clinical nutrition, 2006-06, Vol.83 (6), p.1429-1437</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. 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Because fluoride has a major effect on bones, the status of both fluoride and bone was studied in long-term home parenteral nutrition (HPN) patients. DESIGN: We studied 31 adults aged (x ± SD) 56.3 ± 15.1 y, mainly patients with short-bowel syndrome, who had been receiving HPN for &gt;1 y. Bone mineral density (BMD) was measured by absorptiometry, and serum fluoride was measured by using a fluoride-sensitive electrode. All patients ate and drank ad libitum. HPN (3.4 ± 1.2 times/wk) complemented oral nutrition. Potential explicative factors were estimated by using a linear regression model (mixed-effects model). RESULTS: Of 120 fluoride dosages (2-6/patient), 102 were above the upper normal limit (1.58 μmol/L) at the laboratory. Mean (± SD) daily fluoride supply was 8.03 ± 7.71 mg (US adequate intake: 3.1 mg/d for women and 3.8 for men; tolerable upper normal limit: 10 mg/d); intravenous fluoride varied from 0.06 to 1.45 mg, and oral fluoride varied from 0.09 to 27.8 mg. Serum fluoride concentrations were correlated with creatinine clearance and fluoride supply. BMD was significantly lower in the femoral neck than in the spinal area. After adjustment for sex and the duration of HPN, only the effect of serum fluoride on spinal BMD was significant. Two patients had symptoms of fluorosis, eg, calcaneum fissures, interosseous calcifications, or femoral neck osteoporosis. CONCLUSIONS: In chronic intestinal failure, high intakes of fluoride are frequent because of the beverages ingested to compensate for stool losses. Hyperfluoremia has an effect on bone metabolism and may increase skeletal fragility. The consumption of fluoride-rich beverages for extended periods is therefore not advisable.</description><subject>Adult</subject><subject>adults</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>blood chemistry</subject><subject>Bone and Bones - metabolism</subject><subject>Bone density</subject><subject>Bone Density - drug effects</subject><subject>bone strength</subject><subject>developmental orthopedic disease</subject><subject>dietary exposure</subject><subject>digestive system diseases</subject><subject>feces</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fluoridation</subject><subject>fluorides</subject><subject>Fluorides - administration &amp; dosage</subject><subject>Fluorides - adverse effects</subject><subject>Fluorides - blood</subject><subject>fluorosis</subject><subject>food intake</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>hyperfluoremia</subject><subject>Life Sciences</subject><subject>Linear Models</subject><subject>Male</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>Nutrition</subject><subject>oral nutrition</subject><subject>Other</subject><subject>parenteral feeding</subject><subject>Parenteral Nutrition, Home</subject><subject>patients</subject><subject>regression analysis</subject><subject>Retrospective Studies</subject><subject>Short Bowel Syndrome - metabolism</subject><subject>signs and symptoms (animals and humans)</subject><subject>Small intestine</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1v1DAQxS0EokvhyhGsSiBxyNYfiR0fq4pSpJU4QM_W-CNdr7L2Yict_e9xtCsqcRpp5vfeaOYh9J6SNSWKX8LOxsuer8Watky9QCuqeN9wRuRLtCKEsEZR0Z2hN6XsCKGs7cVrdEaFFEx13Qo93YxzysF57P8cUpmzxxAdNil6XCaY5oJDxAeYgo9TwY9h2mK7zSkGWweTL1OIMOIBwrhoH7cJQ63ZWx8eQrzH27T3VZ-r3OdKxnnKYQopvkWvBhiLf3eq5-ju5uuv69tm8-Pb9-urTWNbqabGdQNTpHWyM70RvZWSSju0BozlvXCs65wh3BqQxElDW8cAeiGlcMZTpgQ_R1-OvlsY9SGHPeQnnSDo26uNXnqEtEwqQh5oZT8f2UNOv-d6nN6HYv04QvRpLpoqplTH-wpe_Afu0pzrJ4pmnKpOSLq4rY-QzamU7Id_6ynRS3p6SU_3XAu9pFcFH06us9l794yf4qrApxMAxcI4ZIg2lGdO9vVnYrn545EbIGm4z5W5-8kI5YQSqVrZ8b_VRK2Q</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Boulétreau, Paul H</creator><creator>Bost, Muriel</creator><creator>Fontanges, Elisabeth</creator><creator>Lauverjat, Madeleine</creator><creator>Gutknecht, Christel</creator><creator>Ecochard, René</creator><creator>Delmas, Pierre D</creator><creator>Chambrier, Cécile</creator><general>American Society for Nutrition</general><general>American Society for Clinical Nutrition</general><general>American Society for Clinical Nutrition, Inc</general><general>Oxford University Press</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><scope>7QP</scope><scope>7T7</scope><scope>7TS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7U7</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-1695-789X</orcidid></search><sort><creationdate>20060601</creationdate><title>Fluoride exposure and bone status in patients with chronic intestinal failure who are receiving home parenteral nutrition</title><author>Boulétreau, Paul H ; Bost, Muriel ; Fontanges, Elisabeth ; Lauverjat, Madeleine ; Gutknecht, Christel ; Ecochard, René ; Delmas, Pierre D ; Chambrier, Cécile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-d5f2904d75b8b68c7717cf4babc386d255db03cba70d7b14d2aa86776dbe12963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>adults</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>blood chemistry</topic><topic>Bone and Bones - metabolism</topic><topic>Bone density</topic><topic>Bone Density - drug effects</topic><topic>bone strength</topic><topic>developmental orthopedic disease</topic><topic>dietary exposure</topic><topic>digestive system diseases</topic><topic>feces</topic><topic>Feeding. 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Psychology</topic><topic>Humans</topic><topic>hyperfluoremia</topic><topic>Life Sciences</topic><topic>Linear Models</topic><topic>Male</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>Nutrition</topic><topic>oral nutrition</topic><topic>Other</topic><topic>parenteral feeding</topic><topic>Parenteral Nutrition, Home</topic><topic>patients</topic><topic>regression analysis</topic><topic>Retrospective Studies</topic><topic>Short Bowel Syndrome - metabolism</topic><topic>signs and symptoms (animals and humans)</topic><topic>Small intestine</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boulétreau, Paul H</creatorcontrib><creatorcontrib>Bost, Muriel</creatorcontrib><creatorcontrib>Fontanges, Elisabeth</creatorcontrib><creatorcontrib>Lauverjat, Madeleine</creatorcontrib><creatorcontrib>Gutknecht, Christel</creatorcontrib><creatorcontrib>Ecochard, René</creatorcontrib><creatorcontrib>Delmas, Pierre D</creatorcontrib><creatorcontrib>Chambrier, Cécile</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><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boulétreau, Paul H</au><au>Bost, Muriel</au><au>Fontanges, Elisabeth</au><au>Lauverjat, Madeleine</au><au>Gutknecht, Christel</au><au>Ecochard, René</au><au>Delmas, Pierre D</au><au>Chambrier, Cécile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluoride exposure and bone status in patients with chronic intestinal failure who are receiving home parenteral nutrition</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>83</volume><issue>6</issue><spage>1429</spage><epage>1437</epage><pages>1429-1437</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><coden>AJCNAC</coden><abstract>BACKGROUND: and Objective: Metabolic bone disease is frequent in chronic intestinal failure. Because fluoride has a major effect on bones, the status of both fluoride and bone was studied in long-term home parenteral nutrition (HPN) patients. DESIGN: We studied 31 adults aged (x ± SD) 56.3 ± 15.1 y, mainly patients with short-bowel syndrome, who had been receiving HPN for &gt;1 y. Bone mineral density (BMD) was measured by absorptiometry, and serum fluoride was measured by using a fluoride-sensitive electrode. All patients ate and drank ad libitum. HPN (3.4 ± 1.2 times/wk) complemented oral nutrition. Potential explicative factors were estimated by using a linear regression model (mixed-effects model). RESULTS: Of 120 fluoride dosages (2-6/patient), 102 were above the upper normal limit (1.58 μmol/L) at the laboratory. Mean (± SD) daily fluoride supply was 8.03 ± 7.71 mg (US adequate intake: 3.1 mg/d for women and 3.8 for men; tolerable upper normal limit: 10 mg/d); intravenous fluoride varied from 0.06 to 1.45 mg, and oral fluoride varied from 0.09 to 27.8 mg. Serum fluoride concentrations were correlated with creatinine clearance and fluoride supply. BMD was significantly lower in the femoral neck than in the spinal area. After adjustment for sex and the duration of HPN, only the effect of serum fluoride on spinal BMD was significant. Two patients had symptoms of fluorosis, eg, calcaneum fissures, interosseous calcifications, or femoral neck osteoporosis. CONCLUSIONS: In chronic intestinal failure, high intakes of fluoride are frequent because of the beverages ingested to compensate for stool losses. Hyperfluoremia has an effect on bone metabolism and may increase skeletal fragility. The consumption of fluoride-rich beverages for extended periods is therefore not advisable.</abstract><cop>Bethesda, MD</cop><pub>American Society for Nutrition</pub><pmid>16762955</pmid><doi>10.1093/ajcn/83.6.1429</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1695-789X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
adults
Aged
Biological and medical sciences
blood chemistry
Bone and Bones - metabolism
Bone density
Bone Density - drug effects
bone strength
developmental orthopedic disease
dietary exposure
digestive system diseases
feces
Feeding. Feeding behavior
Female
Fluoridation
fluorides
Fluorides - administration & dosage
Fluorides - adverse effects
Fluorides - blood
fluorosis
food intake
Fundamental and applied biological sciences. Psychology
Humans
hyperfluoremia
Life Sciences
Linear Models
Male
Metabolism
Middle Aged
Nutrition
oral nutrition
Other
parenteral feeding
Parenteral Nutrition, Home
patients
regression analysis
Retrospective Studies
Short Bowel Syndrome - metabolism
signs and symptoms (animals and humans)
Small intestine
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Fluoride exposure and bone status in patients with chronic intestinal failure who are receiving home parenteral nutrition
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