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Choline intake influences phosphatidylcholine DHA enrichment in nonpregnant women but not in pregnant women in the third trimester

Background: Phosphatidylcholine (PC) produced via the S-adenosylmethionine–dependent phosphatidylethanolamine (PE) N-methyltransferase (PEMT) pathway is enriched with docosahexaenoic acid (DHA). DHA plays a critical role in fetal development and is linked to health endpoints in adulthood. It is unkn...

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Published in:The American journal of clinical nutrition 2013-04, Vol.97 (4), p.718-727
Main Authors: West, Allyson A, Yan, Jian, Jiang, Xinyin, Perry, Cydne A, Innis, Sheila M, Caudill, Marie A
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container_title The American journal of clinical nutrition
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creator West, Allyson A
Yan, Jian
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Caudill, Marie A
description Background: Phosphatidylcholine (PC) produced via the S-adenosylmethionine–dependent phosphatidylethanolamine (PE) N-methyltransferase (PEMT) pathway is enriched with docosahexaenoic acid (DHA). DHA plays a critical role in fetal development and is linked to health endpoints in adulthood. It is unknown whether choline, which can serve as a source of S-adenosylmethionine methyl groups, influences PC-DHA or the PC:PE ratio in pregnant and nonpregnant women.Objective: This study tested whether choline intake affects indicators of choline-related lipid metabolism, including erythrocyte and plasma PC-DHA and PC:PE ratios, in pregnant women in the third trimester and nonpregnant women.Design: Pregnant (n = 26) and nonpregnant (n = 21) women consumed 480 or 930 mg choline/d and a daily DHA supplement for 12 wk. Blood was collected at baseline and at the midpoint and end of the study. PC-DHA was analyzed as the proportion of total PC fatty acids.Results: Pregnant women had greater (P = 0.002) PC-DHA concentrations than did nonpregnant women at baseline. The proportion of erythrocyte and plasma PC-DHA increased (P ≤ 0.002) in pregnant and nonpregnant women regardless of choline intake. However, in nonpregnant women, consumption of 930 mg choline/d led to greater (P < 0.001) erythrocyte PC-DHA and a more rapid increase (P < 0.001) in plasma PC-DHA. Lower (P = 0.001–0.024) erythrocyte and plasma PC:PE in pregnant women was not modified by choline intake.Conclusions: A higher choline intake may increase PEMT activity, resulting in greater PC-DHA enrichment of the PC molecule in nonpregnant women. Increased production of PC-DHA during pregnancy indicates elevated PEMT activity and a higher demand for methyl donors. This trial was registered at clinicaltrials.gov as NCT01127022.
doi_str_mv 10.3945/ajcn.112.050211
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DHA plays a critical role in fetal development and is linked to health endpoints in adulthood. It is unknown whether choline, which can serve as a source of S-adenosylmethionine methyl groups, influences PC-DHA or the PC:PE ratio in pregnant and nonpregnant women.Objective: This study tested whether choline intake affects indicators of choline-related lipid metabolism, including erythrocyte and plasma PC-DHA and PC:PE ratios, in pregnant women in the third trimester and nonpregnant women.Design: Pregnant (n = 26) and nonpregnant (n = 21) women consumed 480 or 930 mg choline/d and a daily DHA supplement for 12 wk. Blood was collected at baseline and at the midpoint and end of the study. PC-DHA was analyzed as the proportion of total PC fatty acids.Results: Pregnant women had greater (P = 0.002) PC-DHA concentrations than did nonpregnant women at baseline. The proportion of erythrocyte and plasma PC-DHA increased (P ≤ 0.002) in pregnant and nonpregnant women regardless of choline intake. However, in nonpregnant women, consumption of 930 mg choline/d led to greater (P &lt; 0.001) erythrocyte PC-DHA and a more rapid increase (P &lt; 0.001) in plasma PC-DHA. Lower (P = 0.001–0.024) erythrocyte and plasma PC:PE in pregnant women was not modified by choline intake.Conclusions: A higher choline intake may increase PEMT activity, resulting in greater PC-DHA enrichment of the PC molecule in nonpregnant women. Increased production of PC-DHA during pregnancy indicates elevated PEMT activity and a higher demand for methyl donors. This trial was registered at clinicaltrials.gov as NCT01127022.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.3945/ajcn.112.050211</identifier><identifier>PMID: 23446897</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Clinical Nutrition</publisher><subject>adulthood ; Biological and medical sciences ; choline ; Choline - pharmacology ; clinical nutrition ; Dietary Supplements ; docosahexaenoic acid ; Docosahexaenoic Acids - blood ; Erythrocytes ; Erythrocytes - metabolism ; Fatty acids ; Feeding. Feeding behavior ; Female ; fetal development ; Fundamental and applied biological sciences. Psychology ; Humans ; lipid metabolism ; Lipid Metabolism - drug effects ; Lipids ; Lipotropic Agents - pharmacology ; Metabolism ; phosphatidylcholines ; Phosphatidylcholines - blood ; Phosphatidylethanolamine N-Methyltransferase - metabolism ; phosphatidylethanolamines ; Phosphatidylethanolamines - blood ; Pregnancy ; Pregnancy - blood ; Pregnancy - metabolism ; Pregnancy Trimester, Third ; pregnant women ; S-adenosylmethionine ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Women</subject><ispartof>The American journal of clinical nutrition, 2013-04, Vol.97 (4), p.718-727</ispartof><rights>2014 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. Apr 1, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-8e9a78f0b595799083a2d51a7e89f322cd9b826d62c9e1bf7152fd7deb38cc923</citedby><cites>FETCH-LOGICAL-c420t-8e9a78f0b595799083a2d51a7e89f322cd9b826d62c9e1bf7152fd7deb38cc923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27165561$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23446897$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>West, Allyson A</creatorcontrib><creatorcontrib>Yan, Jian</creatorcontrib><creatorcontrib>Jiang, Xinyin</creatorcontrib><creatorcontrib>Perry, Cydne A</creatorcontrib><creatorcontrib>Innis, Sheila M</creatorcontrib><creatorcontrib>Caudill, Marie A</creatorcontrib><title>Choline intake influences phosphatidylcholine DHA enrichment in nonpregnant women but not in pregnant women in the third trimester</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Background: Phosphatidylcholine (PC) produced via the S-adenosylmethionine–dependent phosphatidylethanolamine (PE) N-methyltransferase (PEMT) pathway is enriched with docosahexaenoic acid (DHA). DHA plays a critical role in fetal development and is linked to health endpoints in adulthood. It is unknown whether choline, which can serve as a source of S-adenosylmethionine methyl groups, influences PC-DHA or the PC:PE ratio in pregnant and nonpregnant women.Objective: This study tested whether choline intake affects indicators of choline-related lipid metabolism, including erythrocyte and plasma PC-DHA and PC:PE ratios, in pregnant women in the third trimester and nonpregnant women.Design: Pregnant (n = 26) and nonpregnant (n = 21) women consumed 480 or 930 mg choline/d and a daily DHA supplement for 12 wk. Blood was collected at baseline and at the midpoint and end of the study. PC-DHA was analyzed as the proportion of total PC fatty acids.Results: Pregnant women had greater (P = 0.002) PC-DHA concentrations than did nonpregnant women at baseline. The proportion of erythrocyte and plasma PC-DHA increased (P ≤ 0.002) in pregnant and nonpregnant women regardless of choline intake. However, in nonpregnant women, consumption of 930 mg choline/d led to greater (P &lt; 0.001) erythrocyte PC-DHA and a more rapid increase (P &lt; 0.001) in plasma PC-DHA. Lower (P = 0.001–0.024) erythrocyte and plasma PC:PE in pregnant women was not modified by choline intake.Conclusions: A higher choline intake may increase PEMT activity, resulting in greater PC-DHA enrichment of the PC molecule in nonpregnant women. Increased production of PC-DHA during pregnancy indicates elevated PEMT activity and a higher demand for methyl donors. 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Psychology</subject><subject>Humans</subject><subject>lipid metabolism</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipids</subject><subject>Lipotropic Agents - pharmacology</subject><subject>Metabolism</subject><subject>phosphatidylcholines</subject><subject>Phosphatidylcholines - blood</subject><subject>Phosphatidylethanolamine N-Methyltransferase - metabolism</subject><subject>phosphatidylethanolamines</subject><subject>Phosphatidylethanolamines - blood</subject><subject>Pregnancy</subject><subject>Pregnancy - blood</subject><subject>Pregnancy - metabolism</subject><subject>Pregnancy Trimester, Third</subject><subject>pregnant women</subject><subject>S-adenosylmethionine</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Women</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpdkU1v1DAQhi0EotvCmRtEQpW4ZOuPOLGP1fJRpEocoGfLccZNlqwd7ESoV345E3YBqYfRyDOP37HnJeQVo1uhK3ll9y5sGeNbKiln7AnZMC1UKThtnpINpZSXmtXyjJznvKeU8UrVz8kZF1VVK91syK9dH8chQDGE2X5fkx8XCA5yMfUxT72dh-5hdCfq_c11ASENrj9AmJEuQgxTgvtg8fgzYrVolxmrf5qPOliZe8AYUlfMaThAniG9IM-8HTO8POULcvfxw7fdTXn75dPn3fVt6SpO51KBto3ytJVaNlpTJSzvJLMNKO0F567TreJ1V3OngbW-YZL7rumgFco5zcUFeXfUnVL8seBocxiyg3G0AeKSDRMMdyVwj4i-fYTu45ICvm6llBYVkwKpqyPlUsw5gTcT_smmB8OoWe0xqz0G7TFHe_DG65Pu0h6g-8f_9QOByxNgs7OjTza4If_nGjRT1qvQmyPnbTT2PiFz95VTJukadVWL30yPo0E</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>West, Allyson A</creator><creator>Yan, Jian</creator><creator>Jiang, Xinyin</creator><creator>Perry, Cydne A</creator><creator>Innis, Sheila M</creator><creator>Caudill, Marie A</creator><general>American Society for Clinical Nutrition</general><general>American Society for Nutrition</general><general>American Society for Clinical Nutrition, Inc</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>7X8</scope></search><sort><creationdate>20130401</creationdate><title>Choline intake influences phosphatidylcholine DHA enrichment in nonpregnant women but not in pregnant women in the third trimester</title><author>West, Allyson A ; Yan, Jian ; Jiang, Xinyin ; Perry, Cydne A ; Innis, Sheila M ; Caudill, Marie A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-8e9a78f0b595799083a2d51a7e89f322cd9b826d62c9e1bf7152fd7deb38cc923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>adulthood</topic><topic>Biological and medical sciences</topic><topic>choline</topic><topic>Choline - pharmacology</topic><topic>clinical nutrition</topic><topic>Dietary Supplements</topic><topic>docosahexaenoic acid</topic><topic>Docosahexaenoic Acids - blood</topic><topic>Erythrocytes</topic><topic>Erythrocytes - metabolism</topic><topic>Fatty acids</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>fetal development</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>lipid metabolism</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipids</topic><topic>Lipotropic Agents - pharmacology</topic><topic>Metabolism</topic><topic>phosphatidylcholines</topic><topic>Phosphatidylcholines - blood</topic><topic>Phosphatidylethanolamine N-Methyltransferase - metabolism</topic><topic>phosphatidylethanolamines</topic><topic>Phosphatidylethanolamines - blood</topic><topic>Pregnancy</topic><topic>Pregnancy - blood</topic><topic>Pregnancy - metabolism</topic><topic>Pregnancy Trimester, Third</topic><topic>pregnant women</topic><topic>S-adenosylmethionine</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>West, Allyson A</creatorcontrib><creatorcontrib>Yan, Jian</creatorcontrib><creatorcontrib>Jiang, Xinyin</creatorcontrib><creatorcontrib>Perry, Cydne A</creatorcontrib><creatorcontrib>Innis, Sheila M</creatorcontrib><creatorcontrib>Caudill, Marie A</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>MEDLINE - Academic</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>West, Allyson A</au><au>Yan, Jian</au><au>Jiang, Xinyin</au><au>Perry, Cydne A</au><au>Innis, Sheila M</au><au>Caudill, Marie A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choline intake influences phosphatidylcholine DHA enrichment in nonpregnant women but not in pregnant women in the third trimester</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>97</volume><issue>4</issue><spage>718</spage><epage>727</epage><pages>718-727</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><coden>AJCNAC</coden><abstract>Background: Phosphatidylcholine (PC) produced via the S-adenosylmethionine–dependent phosphatidylethanolamine (PE) N-methyltransferase (PEMT) pathway is enriched with docosahexaenoic acid (DHA). DHA plays a critical role in fetal development and is linked to health endpoints in adulthood. It is unknown whether choline, which can serve as a source of S-adenosylmethionine methyl groups, influences PC-DHA or the PC:PE ratio in pregnant and nonpregnant women.Objective: This study tested whether choline intake affects indicators of choline-related lipid metabolism, including erythrocyte and plasma PC-DHA and PC:PE ratios, in pregnant women in the third trimester and nonpregnant women.Design: Pregnant (n = 26) and nonpregnant (n = 21) women consumed 480 or 930 mg choline/d and a daily DHA supplement for 12 wk. Blood was collected at baseline and at the midpoint and end of the study. PC-DHA was analyzed as the proportion of total PC fatty acids.Results: Pregnant women had greater (P = 0.002) PC-DHA concentrations than did nonpregnant women at baseline. The proportion of erythrocyte and plasma PC-DHA increased (P ≤ 0.002) in pregnant and nonpregnant women regardless of choline intake. However, in nonpregnant women, consumption of 930 mg choline/d led to greater (P &lt; 0.001) erythrocyte PC-DHA and a more rapid increase (P &lt; 0.001) in plasma PC-DHA. Lower (P = 0.001–0.024) erythrocyte and plasma PC:PE in pregnant women was not modified by choline intake.Conclusions: A higher choline intake may increase PEMT activity, resulting in greater PC-DHA enrichment of the PC molecule in nonpregnant women. Increased production of PC-DHA during pregnancy indicates elevated PEMT activity and a higher demand for methyl donors. This trial was registered at clinicaltrials.gov as NCT01127022.</abstract><cop>Bethesda, MD</cop><pub>American Society for Clinical Nutrition</pub><pmid>23446897</pmid><doi>10.3945/ajcn.112.050211</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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ispartof The American journal of clinical nutrition, 2013-04, Vol.97 (4), p.718-727
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subjects adulthood
Biological and medical sciences
choline
Choline - pharmacology
clinical nutrition
Dietary Supplements
docosahexaenoic acid
Docosahexaenoic Acids - blood
Erythrocytes
Erythrocytes - metabolism
Fatty acids
Feeding. Feeding behavior
Female
fetal development
Fundamental and applied biological sciences. Psychology
Humans
lipid metabolism
Lipid Metabolism - drug effects
Lipids
Lipotropic Agents - pharmacology
Metabolism
phosphatidylcholines
Phosphatidylcholines - blood
Phosphatidylethanolamine N-Methyltransferase - metabolism
phosphatidylethanolamines
Phosphatidylethanolamines - blood
Pregnancy
Pregnancy - blood
Pregnancy - metabolism
Pregnancy Trimester, Third
pregnant women
S-adenosylmethionine
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Women
title Choline intake influences phosphatidylcholine DHA enrichment in nonpregnant women but not in pregnant women in the third trimester
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