Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age
Background: Brain tissue is selectively enriched with highly unsaturated fatty acids (FAs). Altering the maternal FA status in pregnancy may improve fetal neural development with lasting consequences for child development.Objective: We explored whether maternal FAs in erythrocytes, either measured d...
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description | Background: Brain tissue is selectively enriched with highly unsaturated fatty acids (FAs). Altering the maternal FA status in pregnancy may improve fetal neural development with lasting consequences for child development.Objective: We explored whether maternal FAs in erythrocytes, either measured directly or indirectly by maternal FADS genetic variants, are associated with child intelligence quotient (IQ).Design: Linear regression analyses, adjusted for 18 confounders, were used to investigate the associations in 2839 mother-child pairs from the population-based Avon Longitudinal Study of Parents and Children cohort.Results: Low levels of arachidonic acid (20:4n−6) were associated with lower performance IQ (−2.0 points; 95% CI: −3.5, −0.6 points; P = 0.007, increased R2 = 0.27%), high levels of osbond acid (22:5n−6) were associated with verbal IQ (−1.8 points; 95% CI: −3.2, −0.4 points; P = 0.014, R2 = 0.20%), and high levels of adrenic acid (22:4n−6) were associated with verbal IQ (−1.7 points; 95% CI:−3.1, −0.3 points; P = 0.016, R2 = 0.19%). There was some evidence to support a negative association of low docosahexaenoic acid (DHA; 22:6n−3) with full-scale IQ (R2 = 0.15%). Novel weak associations were also observed for low levels of osbond acid (R2 ≤ 0.29%) and FADS variants with opposite effects for intron variants and variants in the promoter region such as rs3834458 (R2 ≤ 0.38%).Conclusions: These results support the positive role of maternal arachidonic acid and DHA on fetal neural development, although the effects on child IQ by 8 y of age were small (0.1 SD), with other factors contributing more substantially. The endogenous synthesis of these FAs by FADS genes, especially FADS2, may also be important. The replication of these results is recommended. |
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Altering the maternal FA status in pregnancy may improve fetal neural development with lasting consequences for child development.Objective: We explored whether maternal FAs in erythrocytes, either measured directly or indirectly by maternal FADS genetic variants, are associated with child intelligence quotient (IQ).Design: Linear regression analyses, adjusted for 18 confounders, were used to investigate the associations in 2839 mother-child pairs from the population-based Avon Longitudinal Study of Parents and Children cohort.Results: Low levels of arachidonic acid (20:4n−6) were associated with lower performance IQ (−2.0 points; 95% CI: −3.5, −0.6 points; P = 0.007, increased R2 = 0.27%), high levels of osbond acid (22:5n−6) were associated with verbal IQ (−1.8 points; 95% CI: −3.2, −0.4 points; P = 0.014, R2 = 0.20%), and high levels of adrenic acid (22:4n−6) were associated with verbal IQ (−1.7 points; 95% CI:−3.1, −0.3 points; P = 0.016, R2 = 0.19%). There was some evidence to support a negative association of low docosahexaenoic acid (DHA; 22:6n−3) with full-scale IQ (R2 = 0.15%). Novel weak associations were also observed for low levels of osbond acid (R2 ≤ 0.29%) and FADS variants with opposite effects for intron variants and variants in the promoter region such as rs3834458 (R2 ≤ 0.38%).Conclusions: These results support the positive role of maternal arachidonic acid and DHA on fetal neural development, although the effects on child IQ by 8 y of age were small (0.1 SD), with other factors contributing more substantially. The endogenous synthesis of these FAs by FADS genes, especially FADS2, may also be important. The replication of these results is recommended.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.3945/ajcn.112.051524</identifier><identifier>PMID: 24067669</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Clinical Nutrition</publisher><subject>Adult ; arachidonic acid ; Biological and medical sciences ; brain ; Child ; Child Development ; children ; clinical nutrition ; Cohort Studies ; docosahexaenoic acid ; England ; erythrocytes ; Erythrocytes - metabolism ; Fatty Acid Desaturases - genetics ; Fatty Acid Desaturases - metabolism ; Fatty acids ; Fatty Acids, Omega-3 - blood ; Fatty Acids, Omega-3 - chemistry ; Fatty Acids, Omega-3 - metabolism ; Fatty Acids, Omega-6 - blood ; Fatty Acids, Omega-6 - chemistry ; Fatty Acids, Omega-6 - deficiency ; Fatty Acids, Omega-6 - metabolism ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; genes ; Genetic Association Studies ; highly unsaturated fatty acids ; Humans ; Intelligence ; Intelligence tests ; introns ; Language Development ; linear models ; Linkage Disequilibrium ; Longitudinal Studies ; Male ; Maternal Nutritional Physiological Phenomena ; Mothers ; neurodevelopment ; Original Research Communications ; parents ; Polymorphism ; Polymorphism, Single Nucleotide ; Pregnancy ; promoter regions ; Promoter Regions, Genetic ; Regression analysis ; Stereoisomerism ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>The American journal of clinical nutrition, 2013-12, Vol.98 (6), p.1575-1582</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. Dec 1, 2013</rights><rights>2013 American Society for Nutrition 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-44aa8f66357277f3950614471b63b5e0ea6bc8a28b03ceccd32116fc9b0d90723</citedby><cites>FETCH-LOGICAL-c475t-44aa8f66357277f3950614471b63b5e0ea6bc8a28b03ceccd32116fc9b0d90723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27952626$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24067669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steer, Colin D</creatorcontrib><creatorcontrib>Lattka, Eva</creatorcontrib><creatorcontrib>Koletzko, Berthold</creatorcontrib><creatorcontrib>Golding, Jean</creatorcontrib><creatorcontrib>Hibbeln, Joseph R</creatorcontrib><title>Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Background: Brain tissue is selectively enriched with highly unsaturated fatty acids (FAs). Altering the maternal FA status in pregnancy may improve fetal neural development with lasting consequences for child development.Objective: We explored whether maternal FAs in erythrocytes, either measured directly or indirectly by maternal FADS genetic variants, are associated with child intelligence quotient (IQ).Design: Linear regression analyses, adjusted for 18 confounders, were used to investigate the associations in 2839 mother-child pairs from the population-based Avon Longitudinal Study of Parents and Children cohort.Results: Low levels of arachidonic acid (20:4n−6) were associated with lower performance IQ (−2.0 points; 95% CI: −3.5, −0.6 points; P = 0.007, increased R2 = 0.27%), high levels of osbond acid (22:5n−6) were associated with verbal IQ (−1.8 points; 95% CI: −3.2, −0.4 points; P = 0.014, R2 = 0.20%), and high levels of adrenic acid (22:4n−6) were associated with verbal IQ (−1.7 points; 95% CI:−3.1, −0.3 points; P = 0.016, R2 = 0.19%). There was some evidence to support a negative association of low docosahexaenoic acid (DHA; 22:6n−3) with full-scale IQ (R2 = 0.15%). Novel weak associations were also observed for low levels of osbond acid (R2 ≤ 0.29%) and FADS variants with opposite effects for intron variants and variants in the promoter region such as rs3834458 (R2 ≤ 0.38%).Conclusions: These results support the positive role of maternal arachidonic acid and DHA on fetal neural development, although the effects on child IQ by 8 y of age were small (0.1 SD), with other factors contributing more substantially. The endogenous synthesis of these FAs by FADS genes, especially FADS2, may also be important. The replication of these results is recommended.</description><subject>Adult</subject><subject>arachidonic acid</subject><subject>Biological and medical sciences</subject><subject>brain</subject><subject>Child</subject><subject>Child Development</subject><subject>children</subject><subject>clinical nutrition</subject><subject>Cohort Studies</subject><subject>docosahexaenoic acid</subject><subject>England</subject><subject>erythrocytes</subject><subject>Erythrocytes - metabolism</subject><subject>Fatty Acid Desaturases - genetics</subject><subject>Fatty Acid Desaturases - metabolism</subject><subject>Fatty acids</subject><subject>Fatty Acids, Omega-3 - blood</subject><subject>Fatty Acids, Omega-3 - chemistry</subject><subject>Fatty Acids, Omega-3 - metabolism</subject><subject>Fatty Acids, Omega-6 - blood</subject><subject>Fatty Acids, Omega-6 - chemistry</subject><subject>Fatty Acids, Omega-6 - deficiency</subject><subject>Fatty Acids, Omega-6 - metabolism</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genes</subject><subject>Genetic Association Studies</subject><subject>highly unsaturated fatty acids</subject><subject>Humans</subject><subject>Intelligence</subject><subject>Intelligence tests</subject><subject>introns</subject><subject>Language Development</subject><subject>linear models</subject><subject>Linkage Disequilibrium</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Maternal Nutritional Physiological Phenomena</subject><subject>Mothers</subject><subject>neurodevelopment</subject><subject>Original Research Communications</subject><subject>parents</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Pregnancy</subject><subject>promoter regions</subject><subject>Promoter Regions, Genetic</subject><subject>Regression analysis</subject><subject>Stereoisomerism</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>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1v1DAQhi0EokvhzA0sIW7N1t92LpWqQilSqx5Kz9bEcbJeZePUziLl35Nol0IPIx_m8TujeRD6SMmal0Kew9b1a0rZmkgqmXiFVrTkpuCM6NdoRQhhRUmVPEHvct4SQpkw6i06YYIorVS5QvUdjD710OEGxnHC4EKdcejxkHzbQ--mM3x9-e0BD7GbdjENm5B3-QxDX2O3CV09s6PvutD63nn8tI9j8P2IYcQGTzg2GFr_Hr1poMv-w_E9RY_X339d3RS39z9-Xl3eFk5oORZCAJhGKS4107rhpSSKCqFppXglPfGgKmeAmYpw552rOaNUNa6sSF0SzfgpujjkDvtq52s3L5Kgs0MKO0iTjRDsy04fNraNv60SRBhJ54Avx4AUn_Y-j3Yb98t1sqVCCW2o0Wqmzg-USzHn5JvnCZTYRYtdtNhZiz1omX98-n-xZ_6vhxn4egQgO-iaNF8-5H-cLiVTbBn9-cA1EC20aWYeHxihkixljOF_AO7an1Y</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Steer, Colin D</creator><creator>Lattka, Eva</creator><creator>Koletzko, Berthold</creator><creator>Golding, Jean</creator><creator>Hibbeln, Joseph R</creator><general>American Society for Clinical Nutrition</general><general>American Society for 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>5PM</scope></search><sort><creationdate>20131201</creationdate><title>Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age</title><author>Steer, Colin D ; Lattka, Eva ; Koletzko, Berthold ; Golding, Jean ; Hibbeln, Joseph R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-44aa8f66357277f3950614471b63b5e0ea6bc8a28b03ceccd32116fc9b0d90723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>arachidonic acid</topic><topic>Biological and medical sciences</topic><topic>brain</topic><topic>Child</topic><topic>Child Development</topic><topic>children</topic><topic>clinical nutrition</topic><topic>Cohort Studies</topic><topic>docosahexaenoic acid</topic><topic>England</topic><topic>erythrocytes</topic><topic>Erythrocytes - metabolism</topic><topic>Fatty Acid Desaturases - genetics</topic><topic>Fatty Acid Desaturases - metabolism</topic><topic>Fatty acids</topic><topic>Fatty Acids, Omega-3 - blood</topic><topic>Fatty Acids, Omega-3 - chemistry</topic><topic>Fatty Acids, Omega-3 - metabolism</topic><topic>Fatty Acids, Omega-6 - blood</topic><topic>Fatty Acids, Omega-6 - chemistry</topic><topic>Fatty Acids, Omega-6 - deficiency</topic><topic>Fatty Acids, Omega-6 - metabolism</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genes</topic><topic>Genetic Association Studies</topic><topic>highly unsaturated fatty acids</topic><topic>Humans</topic><topic>Intelligence</topic><topic>Intelligence tests</topic><topic>introns</topic><topic>Language Development</topic><topic>linear models</topic><topic>Linkage Disequilibrium</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Maternal Nutritional Physiological Phenomena</topic><topic>Mothers</topic><topic>neurodevelopment</topic><topic>Original Research Communications</topic><topic>parents</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Pregnancy</topic><topic>promoter regions</topic><topic>Promoter Regions, Genetic</topic><topic>Regression analysis</topic><topic>Stereoisomerism</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steer, Colin D</creatorcontrib><creatorcontrib>Lattka, Eva</creatorcontrib><creatorcontrib>Koletzko, Berthold</creatorcontrib><creatorcontrib>Golding, Jean</creatorcontrib><creatorcontrib>Hibbeln, Joseph R</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 & 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>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steer, Colin D</au><au>Lattka, Eva</au><au>Koletzko, Berthold</au><au>Golding, Jean</au><au>Hibbeln, Joseph R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>98</volume><issue>6</issue><spage>1575</spage><epage>1582</epage><pages>1575-1582</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><coden>AJCNAC</coden><abstract>Background: Brain tissue is selectively enriched with highly unsaturated fatty acids (FAs). Altering the maternal FA status in pregnancy may improve fetal neural development with lasting consequences for child development.Objective: We explored whether maternal FAs in erythrocytes, either measured directly or indirectly by maternal FADS genetic variants, are associated with child intelligence quotient (IQ).Design: Linear regression analyses, adjusted for 18 confounders, were used to investigate the associations in 2839 mother-child pairs from the population-based Avon Longitudinal Study of Parents and Children cohort.Results: Low levels of arachidonic acid (20:4n−6) were associated with lower performance IQ (−2.0 points; 95% CI: −3.5, −0.6 points; P = 0.007, increased R2 = 0.27%), high levels of osbond acid (22:5n−6) were associated with verbal IQ (−1.8 points; 95% CI: −3.2, −0.4 points; P = 0.014, R2 = 0.20%), and high levels of adrenic acid (22:4n−6) were associated with verbal IQ (−1.7 points; 95% CI:−3.1, −0.3 points; P = 0.016, R2 = 0.19%). There was some evidence to support a negative association of low docosahexaenoic acid (DHA; 22:6n−3) with full-scale IQ (R2 = 0.15%). Novel weak associations were also observed for low levels of osbond acid (R2 ≤ 0.29%) and FADS variants with opposite effects for intron variants and variants in the promoter region such as rs3834458 (R2 ≤ 0.38%).Conclusions: These results support the positive role of maternal arachidonic acid and DHA on fetal neural development, although the effects on child IQ by 8 y of age were small (0.1 SD), with other factors contributing more substantially. The endogenous synthesis of these FAs by FADS genes, especially FADS2, may also be important. The replication of these results is recommended.</abstract><cop>Bethesda, MD</cop><pub>American Society for Clinical Nutrition</pub><pmid>24067669</pmid><doi>10.3945/ajcn.112.051524</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult arachidonic acid Biological and medical sciences brain Child Child Development children clinical nutrition Cohort Studies docosahexaenoic acid England erythrocytes Erythrocytes - metabolism Fatty Acid Desaturases - genetics Fatty Acid Desaturases - metabolism Fatty acids Fatty Acids, Omega-3 - blood Fatty Acids, Omega-3 - chemistry Fatty Acids, Omega-3 - metabolism Fatty Acids, Omega-6 - blood Fatty Acids, Omega-6 - chemistry Fatty Acids, Omega-6 - deficiency Fatty Acids, Omega-6 - metabolism Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology genes Genetic Association Studies highly unsaturated fatty acids Humans Intelligence Intelligence tests introns Language Development linear models Linkage Disequilibrium Longitudinal Studies Male Maternal Nutritional Physiological Phenomena Mothers neurodevelopment Original Research Communications parents Polymorphism Polymorphism, Single Nucleotide Pregnancy promoter regions Promoter Regions, Genetic Regression analysis Stereoisomerism Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Maternal fatty acids in pregnancy, FADS polymorphisms, and child intelligence quotient at 8 y of age |
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