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Vitamin B-12 and neural tube defects: the Canadian experience
Although early epidemiologic studies showed a protective effect of adequate maternal folic acid (FA) status against neural tube defects (NTDs), the role of adequate vitamin B-12 nutrition in the putative reduction of NTD frequency has remained uncertain. Evaluating vitamin B-12 status was complicate...
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Published in: | The American journal of clinical nutrition 2009-02, Vol.89 (2), p.697S-701S |
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creator | Thompson, Miles D Cole, David EC Ray, Joel G |
description | Although early epidemiologic studies showed a protective effect of adequate maternal folic acid (FA) status against neural tube defects (NTDs), the role of adequate vitamin B-12 nutrition in the putative reduction of NTD frequency has remained uncertain. Evaluating vitamin B-12 status was complicated by the need to control for altered FA status after fortification in Canada. More recent studies have made use of better biomarkers of vitamin B-12 status, including methylmalonic acid and holotranscobalamin (holoTC). HoloTC provides a useful measure of vitamin B-12 status because it represents the bioavailable fraction of circulating vitamin B-12. By assessing bioavailable vitamin B-12 status in a large Canadian cohort accrued before and after FA fortification, we found a 3-fold increase in the risk of NTDs in mothers who had vitamin B-12 status in the lower quartile, regardless of FA fortification. Our work suggests that vitamin B-12 fortification, analogous to the FA fortification program, may reduce NTDs more than FA fortification alone. A multicenter randomized controlled trial comparing periconceptional vitamin B-12 in combination with FA against FA alone is warranted. |
doi_str_mv | 10.3945/ajcn.2008.26947B |
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Evaluating vitamin B-12 status was complicated by the need to control for altered FA status after fortification in Canada. More recent studies have made use of better biomarkers of vitamin B-12 status, including methylmalonic acid and holotranscobalamin (holoTC). HoloTC provides a useful measure of vitamin B-12 status because it represents the bioavailable fraction of circulating vitamin B-12. By assessing bioavailable vitamin B-12 status in a large Canadian cohort accrued before and after FA fortification, we found a 3-fold increase in the risk of NTDs in mothers who had vitamin B-12 status in the lower quartile, regardless of FA fortification. Our work suggests that vitamin B-12 fortification, analogous to the FA fortification program, may reduce NTDs more than FA fortification alone. A multicenter randomized controlled trial comparing periconceptional vitamin B-12 in combination with FA against FA alone is warranted.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.3945/ajcn.2008.26947B</identifier><identifier>PMID: 19116334</identifier><language>eng</language><publisher>United States: American Society for Clinical Nutrition</publisher><subject>Adult ; Biological Availability ; biomarkers ; Biomarkers - blood ; Canada ; Clinical trials ; cohort studies ; Dietary supplements ; epidemiological studies ; Epidemiology ; Female ; fetal development ; fetus ; Flour ; folic acid ; Folic Acid - administration & dosage ; food additives ; food fortification ; Food, Fortified ; Humans ; literature reviews ; maternal nutrition ; methylmalonic acid ; Methylmalonic Acid - blood ; neural tube defects ; Neural Tube Defects - epidemiology ; Neural Tube Defects - etiology ; Neural Tube Defects - prevention & control ; nutrient availability ; nutrient intake ; nutrient-nutrient interactions ; Nutrition ; nutrition assessment ; Nutritional Status ; Pregnancy ; pregnant women ; protective effect ; Randomized Controlled Trials as Topic ; risk factors ; Studies ; Transcobalamins ; Vitamin B ; Vitamin B 12 - administration & dosage ; Vitamin B 12 - blood ; Vitamin B 12 - pharmacokinetics ; Vitamin B 12 Deficiency - complications ; Vitamin B 12 Deficiency - epidemiology ; Vitamin B Complex - administration & dosage ; Vitamin B Complex - blood ; vitamin B12 ; Vitamin deficiency</subject><ispartof>The American journal of clinical nutrition, 2009-02, Vol.89 (2), p.697S-701S</ispartof><rights>Copyright American Society for Clinical Nutrition, Inc. Feb 1, 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-85d16ee59ce96ac94d2b898969a99746f915a47d69b17675217c6956126193e23</citedby><cites>FETCH-LOGICAL-c421t-85d16ee59ce96ac94d2b898969a99746f915a47d69b17675217c6956126193e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19116334$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thompson, Miles D</creatorcontrib><creatorcontrib>Cole, David EC</creatorcontrib><creatorcontrib>Ray, Joel G</creatorcontrib><title>Vitamin B-12 and neural tube defects: the Canadian experience</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Although early epidemiologic studies showed a protective effect of adequate maternal folic acid (FA) status against neural tube defects (NTDs), the role of adequate vitamin B-12 nutrition in the putative reduction of NTD frequency has remained uncertain. Evaluating vitamin B-12 status was complicated by the need to control for altered FA status after fortification in Canada. More recent studies have made use of better biomarkers of vitamin B-12 status, including methylmalonic acid and holotranscobalamin (holoTC). HoloTC provides a useful measure of vitamin B-12 status because it represents the bioavailable fraction of circulating vitamin B-12. By assessing bioavailable vitamin B-12 status in a large Canadian cohort accrued before and after FA fortification, we found a 3-fold increase in the risk of NTDs in mothers who had vitamin B-12 status in the lower quartile, regardless of FA fortification. Our work suggests that vitamin B-12 fortification, analogous to the FA fortification program, may reduce NTDs more than FA fortification alone. A multicenter randomized controlled trial comparing periconceptional vitamin B-12 in combination with FA against FA alone is warranted.</description><subject>Adult</subject><subject>Biological Availability</subject><subject>biomarkers</subject><subject>Biomarkers - blood</subject><subject>Canada</subject><subject>Clinical trials</subject><subject>cohort studies</subject><subject>Dietary supplements</subject><subject>epidemiological studies</subject><subject>Epidemiology</subject><subject>Female</subject><subject>fetal development</subject><subject>fetus</subject><subject>Flour</subject><subject>folic acid</subject><subject>Folic Acid - administration & dosage</subject><subject>food additives</subject><subject>food fortification</subject><subject>Food, Fortified</subject><subject>Humans</subject><subject>literature reviews</subject><subject>maternal nutrition</subject><subject>methylmalonic acid</subject><subject>Methylmalonic Acid - blood</subject><subject>neural tube defects</subject><subject>Neural Tube Defects - epidemiology</subject><subject>Neural Tube Defects - etiology</subject><subject>Neural Tube Defects - prevention & control</subject><subject>nutrient availability</subject><subject>nutrient intake</subject><subject>nutrient-nutrient interactions</subject><subject>Nutrition</subject><subject>nutrition assessment</subject><subject>Nutritional Status</subject><subject>Pregnancy</subject><subject>pregnant women</subject><subject>protective effect</subject><subject>Randomized Controlled Trials as Topic</subject><subject>risk factors</subject><subject>Studies</subject><subject>Transcobalamins</subject><subject>Vitamin B</subject><subject>Vitamin B 12 - administration & dosage</subject><subject>Vitamin B 12 - blood</subject><subject>Vitamin B 12 - pharmacokinetics</subject><subject>Vitamin B 12 Deficiency - complications</subject><subject>Vitamin B 12 Deficiency - epidemiology</subject><subject>Vitamin B Complex - administration & dosage</subject><subject>Vitamin B Complex - blood</subject><subject>vitamin B12</subject><subject>Vitamin deficiency</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpdkEtLw0AUhQdRtD72rjS4cJc6d17JFVxo8QWCCx_bYTq50ZR2UmcS0H9vSguCq7v5zuGej7Fj4GOJSl-4mQ9jwXk5FgZVcbPFRoCyzKXgxTYbcc5FjmD0HttPacY5CFWaXbYHCGCkVCN29d50btGE7CYHkblQZYH66OZZ108pq6gm36XLrPukbOKCqxoXMvpeUmwoeDpkO7WbJzra3AP2dnf7OnnIn57vHyfXT7lXArq81BUYIo2e0DiPqhLTEks06BALZWoE7VRRGZxCYQotoPAGtQFhhjkk5AE7X_cuY_vVU-rsokme5nMXqO2TFVyWCFwP4Nk_cNb2MQy_WSEBh_mwauNryMc2pUi1XcZm4eKPBW5XXu3Kq115tWuvQ-Rk09tPF1T9BTYiB-B0DdSute4jNsm-vQgOkoMuQSstfwFdHHle</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Thompson, Miles D</creator><creator>Cole, David EC</creator><creator>Ray, Joel G</creator><general>American Society for Clinical Nutrition</general><general>American Society for Clinical Nutrition, Inc</general><scope>FBQ</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>7TK</scope></search><sort><creationdate>20090201</creationdate><title>Vitamin B-12 and neural tube defects: the Canadian experience</title><author>Thompson, Miles D ; Cole, David EC ; Ray, Joel G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-85d16ee59ce96ac94d2b898969a99746f915a47d69b17675217c6956126193e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Biological Availability</topic><topic>biomarkers</topic><topic>Biomarkers - blood</topic><topic>Canada</topic><topic>Clinical trials</topic><topic>cohort studies</topic><topic>Dietary supplements</topic><topic>epidemiological studies</topic><topic>Epidemiology</topic><topic>Female</topic><topic>fetal development</topic><topic>fetus</topic><topic>Flour</topic><topic>folic acid</topic><topic>Folic Acid - administration & dosage</topic><topic>food additives</topic><topic>food fortification</topic><topic>Food, Fortified</topic><topic>Humans</topic><topic>literature reviews</topic><topic>maternal nutrition</topic><topic>methylmalonic acid</topic><topic>Methylmalonic Acid - blood</topic><topic>neural tube defects</topic><topic>Neural Tube Defects - epidemiology</topic><topic>Neural Tube Defects - etiology</topic><topic>Neural Tube Defects - prevention & control</topic><topic>nutrient availability</topic><topic>nutrient intake</topic><topic>nutrient-nutrient interactions</topic><topic>Nutrition</topic><topic>nutrition assessment</topic><topic>Nutritional Status</topic><topic>Pregnancy</topic><topic>pregnant women</topic><topic>protective effect</topic><topic>Randomized Controlled Trials as Topic</topic><topic>risk factors</topic><topic>Studies</topic><topic>Transcobalamins</topic><topic>Vitamin B</topic><topic>Vitamin B 12 - administration & dosage</topic><topic>Vitamin B 12 - blood</topic><topic>Vitamin B 12 - pharmacokinetics</topic><topic>Vitamin B 12 Deficiency - complications</topic><topic>Vitamin B 12 Deficiency - epidemiology</topic><topic>Vitamin B Complex - administration & dosage</topic><topic>Vitamin B Complex - blood</topic><topic>vitamin B12</topic><topic>Vitamin deficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thompson, Miles D</creatorcontrib><creatorcontrib>Cole, David EC</creatorcontrib><creatorcontrib>Ray, Joel G</creatorcontrib><collection>AGRIS</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>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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thompson, Miles D</au><au>Cole, David EC</au><au>Ray, Joel G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vitamin B-12 and neural tube defects: the Canadian experience</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>89</volume><issue>2</issue><spage>697S</spage><epage>701S</epage><pages>697S-701S</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><abstract>Although early epidemiologic studies showed a protective effect of adequate maternal folic acid (FA) status against neural tube defects (NTDs), the role of adequate vitamin B-12 nutrition in the putative reduction of NTD frequency has remained uncertain. Evaluating vitamin B-12 status was complicated by the need to control for altered FA status after fortification in Canada. More recent studies have made use of better biomarkers of vitamin B-12 status, including methylmalonic acid and holotranscobalamin (holoTC). HoloTC provides a useful measure of vitamin B-12 status because it represents the bioavailable fraction of circulating vitamin B-12. By assessing bioavailable vitamin B-12 status in a large Canadian cohort accrued before and after FA fortification, we found a 3-fold increase in the risk of NTDs in mothers who had vitamin B-12 status in the lower quartile, regardless of FA fortification. Our work suggests that vitamin B-12 fortification, analogous to the FA fortification program, may reduce NTDs more than FA fortification alone. A multicenter randomized controlled trial comparing periconceptional vitamin B-12 in combination with FA against FA alone is warranted.</abstract><cop>United States</cop><pub>American Society for Clinical Nutrition</pub><pmid>19116334</pmid><doi>10.3945/ajcn.2008.26947B</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological Availability biomarkers Biomarkers - blood Canada Clinical trials cohort studies Dietary supplements epidemiological studies Epidemiology Female fetal development fetus Flour folic acid Folic Acid - administration & dosage food additives food fortification Food, Fortified Humans literature reviews maternal nutrition methylmalonic acid Methylmalonic Acid - blood neural tube defects Neural Tube Defects - epidemiology Neural Tube Defects - etiology Neural Tube Defects - prevention & control nutrient availability nutrient intake nutrient-nutrient interactions Nutrition nutrition assessment Nutritional Status Pregnancy pregnant women protective effect Randomized Controlled Trials as Topic risk factors Studies Transcobalamins Vitamin B Vitamin B 12 - administration & dosage Vitamin B 12 - blood Vitamin B 12 - pharmacokinetics Vitamin B 12 Deficiency - complications Vitamin B 12 Deficiency - epidemiology Vitamin B Complex - administration & dosage Vitamin B Complex - blood vitamin B12 Vitamin deficiency |
title | Vitamin B-12 and neural tube defects: the Canadian experience |
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