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Docosahexaenoic acid, eicosapentaenoic acid, arachidonic acid, and neural tube defects in Tunisian population

Objective To determine the effect of maternal status in (plasma and red blood cell) folate, vitamin B12, homocysteine, and vitamin D, as well as their interaction with MTHFR (C677T and A1298C) and MTRR A66G polymorphisms, on maternal plasma docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), an...

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Published in:Birth defects research 2024-06, Vol.116 (6), p.e2372-n/a
Main Authors: Nasri, Kaouther, Ben Jamaa, Nadia, Siala Gaigi, Soumeya, Feki, Moncef, Marrakchi, Raja
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container_title Birth defects research
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Ben Jamaa, Nadia
Siala Gaigi, Soumeya
Feki, Moncef
Marrakchi, Raja
description Objective To determine the effect of maternal status in (plasma and red blood cell) folate, vitamin B12, homocysteine, and vitamin D, as well as their interaction with MTHFR (C677T and A1298C) and MTRR A66G polymorphisms, on maternal plasma docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), and arachidonic acid (ARA) levels and the risk of neural tube defects (NTDs). Methods ARA, EPA, and DHA composition was assessed using capillary gas chromatography. Results ARA and DHA levels were higher in controls than in case mothers for low plasma folate status. For low red blood cell folate status, DHA levels were higher in controls than in case mothers. For high homocysteine levels, ARA and DHA levels were higher in controls than in case mothers. NTD mothers had lower EPA and DHA levels for low vitamin B12 levels. NTD mothers had lower DHA levels for low vitamin D levels. For low plasma folate status, DHA levels in the MTHFR C677T gene and ARA and EPA levels in MTHFR A1298C gene were different among the three genotypes in case mothers. DHA levels in the MTHFR C677T gene were different among the three genotypes in case mothers for both low and high homocysteine levels. For low vitamin B12 levels, ARA and DHA levels were different among the three genotypes of the MTHFR C677T gene in case mothers. In the MTHFR C677T gene, ARA and DHA levels were different among the three genotypes in case mothers for low vitamin D levels. Conclusions More advanced research is required to verify a suitable biochemical parameter status in relation to the genotypes in pregnant women.
doi_str_mv 10.1002/bdr2.2372
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Methods ARA, EPA, and DHA composition was assessed using capillary gas chromatography. Results ARA and DHA levels were higher in controls than in case mothers for low plasma folate status. For low red blood cell folate status, DHA levels were higher in controls than in case mothers. For high homocysteine levels, ARA and DHA levels were higher in controls than in case mothers. NTD mothers had lower EPA and DHA levels for low vitamin B12 levels. NTD mothers had lower DHA levels for low vitamin D levels. For low plasma folate status, DHA levels in the MTHFR C677T gene and ARA and EPA levels in MTHFR A1298C gene were different among the three genotypes in case mothers. DHA levels in the MTHFR C677T gene were different among the three genotypes in case mothers for both low and high homocysteine levels. For low vitamin B12 levels, ARA and DHA levels were different among the three genotypes of the MTHFR C677T gene in case mothers. In the MTHFR C677T gene, ARA and DHA levels were different among the three genotypes in case mothers for low vitamin D levels. Conclusions More advanced research is required to verify a suitable biochemical parameter status in relation to the genotypes in pregnant women.</description><identifier>ISSN: 2472-1727</identifier><identifier>EISSN: 2472-1727</identifier><identifier>DOI: 10.1002/bdr2.2372</identifier><identifier>PMID: 38877667</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Acids ; Adult ; Arachidonic acid ; Arachidonic Acid - blood ; Arachidonic Acid - metabolism ; Birth defects ; Blood levels ; Calciferol ; Case-Control Studies ; Cyanocobalamin ; Defects ; Docosahexaenoic acid ; Docosahexaenoic Acids - blood ; Eicosapentaenoic acid ; Eicosapentaenoic Acid - blood ; Erythrocytes ; Female ; Folic acid ; Folic Acid - blood ; Gas chromatography ; genetic polymorphisms ; Genotype ; Genotypes ; Homocysteine ; Homocysteine - blood ; Homocysteine - genetics ; Humans ; Methylenetetrahydrofolate reductase ; Methylenetetrahydrofolate Reductase (NADPH2) - genetics ; Neural tube defects ; Neural Tube Defects - genetics ; Plasma ; Pregnancy ; Tunisia ; Vitamin B ; Vitamin B 12 - blood ; Vitamin B12 ; Vitamin D ; Vitamin D - blood ; Vitamin D - genetics</subject><ispartof>Birth defects research, 2024-06, Vol.116 (6), p.e2372-n/a</ispartof><rights>2024 Wiley Periodicals LLC.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2432-26ff450ed0e25f1fdf84b87ef92e779d86b22fea4403a93a5fff274893d3c0fc3</cites><orcidid>0000-0001-9380-4013</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38877667$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nasri, Kaouther</creatorcontrib><creatorcontrib>Ben Jamaa, Nadia</creatorcontrib><creatorcontrib>Siala Gaigi, Soumeya</creatorcontrib><creatorcontrib>Feki, Moncef</creatorcontrib><creatorcontrib>Marrakchi, Raja</creatorcontrib><title>Docosahexaenoic acid, eicosapentaenoic acid, arachidonic acid, and neural tube defects in Tunisian population</title><title>Birth defects research</title><addtitle>Birth Defects Res</addtitle><description>Objective To determine the effect of maternal status in (plasma and red blood cell) folate, vitamin B12, homocysteine, and vitamin D, as well as their interaction with MTHFR (C677T and A1298C) and MTRR A66G polymorphisms, on maternal plasma docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), and arachidonic acid (ARA) levels and the risk of neural tube defects (NTDs). Methods ARA, EPA, and DHA composition was assessed using capillary gas chromatography. Results ARA and DHA levels were higher in controls than in case mothers for low plasma folate status. For low red blood cell folate status, DHA levels were higher in controls than in case mothers. For high homocysteine levels, ARA and DHA levels were higher in controls than in case mothers. NTD mothers had lower EPA and DHA levels for low vitamin B12 levels. NTD mothers had lower DHA levels for low vitamin D levels. For low plasma folate status, DHA levels in the MTHFR C677T gene and ARA and EPA levels in MTHFR A1298C gene were different among the three genotypes in case mothers. DHA levels in the MTHFR C677T gene were different among the three genotypes in case mothers for both low and high homocysteine levels. For low vitamin B12 levels, ARA and DHA levels were different among the three genotypes of the MTHFR C677T gene in case mothers. In the MTHFR C677T gene, ARA and DHA levels were different among the three genotypes in case mothers for low vitamin D levels. Conclusions More advanced research is required to verify a suitable biochemical parameter status in relation to the genotypes in pregnant women.</description><subject>Acids</subject><subject>Adult</subject><subject>Arachidonic acid</subject><subject>Arachidonic Acid - blood</subject><subject>Arachidonic Acid - metabolism</subject><subject>Birth defects</subject><subject>Blood levels</subject><subject>Calciferol</subject><subject>Case-Control Studies</subject><subject>Cyanocobalamin</subject><subject>Defects</subject><subject>Docosahexaenoic acid</subject><subject>Docosahexaenoic Acids - blood</subject><subject>Eicosapentaenoic acid</subject><subject>Eicosapentaenoic Acid - blood</subject><subject>Erythrocytes</subject><subject>Female</subject><subject>Folic acid</subject><subject>Folic Acid - blood</subject><subject>Gas chromatography</subject><subject>genetic polymorphisms</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Homocysteine</subject><subject>Homocysteine - blood</subject><subject>Homocysteine - genetics</subject><subject>Humans</subject><subject>Methylenetetrahydrofolate reductase</subject><subject>Methylenetetrahydrofolate Reductase (NADPH2) - genetics</subject><subject>Neural tube defects</subject><subject>Neural Tube Defects - genetics</subject><subject>Plasma</subject><subject>Pregnancy</subject><subject>Tunisia</subject><subject>Vitamin B</subject><subject>Vitamin B 12 - blood</subject><subject>Vitamin B12</subject><subject>Vitamin D</subject><subject>Vitamin D - blood</subject><subject>Vitamin D - genetics</subject><issn>2472-1727</issn><issn>2472-1727</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp10UtLxDAUBeAgiorOwj8gBTcKjiY3bZNZ-lYQBBnXJU1uMNJJatKi8-_tOL7BVcLh4xByCNlh9IhRCse1iXAEXMAK2YRcwJgJEKs_7htklNITpZRJYILLdbLBpRSiLMUmmZ0HHZJ6xFeFPjidKe3MYYZukbbou1-xiko_OhP8d-JN5rGPqsm6vsbMoEXdpcz5bNp7l5zyWRvavlGdC36brFnVJBx9nFvk4fJienY9vr27ujk7uR1ryDmMobQ2LygailBYZo2VeS0F2gmgEBMjyxrAospzytWEq8JaCyKXE264plbzLbK_7G1jeO4xddXMJY1NozyGPlWcllIUgvFyoHt_6FPoox9eNygBwAqZy0EdLJWOIaWItmqjm6k4rxitFjNUixmqxQyD3f1o7OsZmi_5-ekDOF6CF9fg_P-m6vT8Ht4r3wC7V5F6</recordid><startdate>202406</startdate><enddate>202406</enddate><creator>Nasri, Kaouther</creator><creator>Ben Jamaa, Nadia</creator><creator>Siala Gaigi, Soumeya</creator><creator>Feki, Moncef</creator><creator>Marrakchi, Raja</creator><general>John Wiley &amp; 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Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Birth defects research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nasri, Kaouther</au><au>Ben Jamaa, Nadia</au><au>Siala Gaigi, Soumeya</au><au>Feki, Moncef</au><au>Marrakchi, Raja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Docosahexaenoic acid, eicosapentaenoic acid, arachidonic acid, and neural tube defects in Tunisian population</atitle><jtitle>Birth defects research</jtitle><addtitle>Birth Defects Res</addtitle><date>2024-06</date><risdate>2024</risdate><volume>116</volume><issue>6</issue><spage>e2372</spage><epage>n/a</epage><pages>e2372-n/a</pages><issn>2472-1727</issn><eissn>2472-1727</eissn><abstract>Objective To determine the effect of maternal status in (plasma and red blood cell) folate, vitamin B12, homocysteine, and vitamin D, as well as their interaction with MTHFR (C677T and A1298C) and MTRR A66G polymorphisms, on maternal plasma docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), and arachidonic acid (ARA) levels and the risk of neural tube defects (NTDs). Methods ARA, EPA, and DHA composition was assessed using capillary gas chromatography. Results ARA and DHA levels were higher in controls than in case mothers for low plasma folate status. For low red blood cell folate status, DHA levels were higher in controls than in case mothers. For high homocysteine levels, ARA and DHA levels were higher in controls than in case mothers. NTD mothers had lower EPA and DHA levels for low vitamin B12 levels. NTD mothers had lower DHA levels for low vitamin D levels. For low plasma folate status, DHA levels in the MTHFR C677T gene and ARA and EPA levels in MTHFR A1298C gene were different among the three genotypes in case mothers. DHA levels in the MTHFR C677T gene were different among the three genotypes in case mothers for both low and high homocysteine levels. For low vitamin B12 levels, ARA and DHA levels were different among the three genotypes of the MTHFR C677T gene in case mothers. In the MTHFR C677T gene, ARA and DHA levels were different among the three genotypes in case mothers for low vitamin D levels. Conclusions More advanced research is required to verify a suitable biochemical parameter status in relation to the genotypes in pregnant women.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38877667</pmid><doi>10.1002/bdr2.2372</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-9380-4013</orcidid></addata></record>
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subjects Acids
Adult
Arachidonic acid
Arachidonic Acid - blood
Arachidonic Acid - metabolism
Birth defects
Blood levels
Calciferol
Case-Control Studies
Cyanocobalamin
Defects
Docosahexaenoic acid
Docosahexaenoic Acids - blood
Eicosapentaenoic acid
Eicosapentaenoic Acid - blood
Erythrocytes
Female
Folic acid
Folic Acid - blood
Gas chromatography
genetic polymorphisms
Genotype
Genotypes
Homocysteine
Homocysteine - blood
Homocysteine - genetics
Humans
Methylenetetrahydrofolate reductase
Methylenetetrahydrofolate Reductase (NADPH2) - genetics
Neural tube defects
Neural Tube Defects - genetics
Plasma
Pregnancy
Tunisia
Vitamin B
Vitamin B 12 - blood
Vitamin B12
Vitamin D
Vitamin D - blood
Vitamin D - genetics
title Docosahexaenoic acid, eicosapentaenoic acid, arachidonic acid, and neural tube defects in Tunisian population
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