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Genetic loci associated with circulating levels of very long-chain saturated fatty acids[S]
Very long-chain saturated fatty acids (VLSFAs) are saturated fatty acids with 20 or more carbons. In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influe...
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Published in: | Journal of lipid research 2015-01, Vol.56 (1), p.176-184 |
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creator | Lemaitre, Rozenn N. King, Irena B. Kabagambe, Edmond K. Wu, Jason H.Y. McKnight, Barbara Manichaikul, Ani Guan, Weihua Sun, Qi Chasman, Daniel I. Foy, Millennia Wang, Lu Zhu, Jingwen Siscovick, David S. Tsai, Michael Y. Arnett, Donna K. Psaty, Bruce M. Djousse, Luc Chen, Yii-Der I. Tang, Weihong Weng, Lu-Chen Wu, Hongyu Jensen, Majken K. Chu, Audrey Y. Jacobs, David R. Rich, Stephen S. Mozaffarian, Dariush Steffen, Lyn Rimm, Eric B. Hu, Frank B. Ridker, Paul M. Fornage, Myriam Friedlander, Yechiel |
description | Very long-chain saturated fatty acids (VLSFAs) are saturated fatty acids with 20 or more carbons. In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influence circulating levels of VLSFAs is not known. We investigated the association of common genetic variation with plasma phospholipid/erythrocyte levels of three VLSFAs by performing genome-wide association studies in seven population-based cohorts comprising 10,129 subjects of European ancestry. We observed associations of circulating VLSFA concentrations with common variants in two genes, serine palmitoyl-transferase long-chain base subunit 3 (SPTLC3), a gene involved in the rate-limiting step of de novo sphingolipid synthesis, and ceramide synthase 4 (CERS4). The SPTLC3 variant at rs680379 was associated with higher arachidic acid (20:0 , P = 5.81 × 10−13). The CERS4 variant at rs2100944 was associated with higher levels of 20:0 (P = 2.65 × 10−40) and in analyses that adjusted for 20:0, with lower levels of behenic acid (P = 4.22 × 10−26) and lignoceric acid (P = 3.20 × 10−21). These novel associations suggest an inter-relationship of circulating VLSFAs and sphingolipid synthesis. |
doi_str_mv | 10.1194/jlr.M052456 |
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In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influence circulating levels of VLSFAs is not known. We investigated the association of common genetic variation with plasma phospholipid/erythrocyte levels of three VLSFAs by performing genome-wide association studies in seven population-based cohorts comprising 10,129 subjects of European ancestry. We observed associations of circulating VLSFA concentrations with common variants in two genes, serine palmitoyl-transferase long-chain base subunit 3 (SPTLC3), a gene involved in the rate-limiting step of de novo sphingolipid synthesis, and ceramide synthase 4 (CERS4). The SPTLC3 variant at rs680379 was associated with higher arachidic acid (20:0 , P = 5.81 × 10−13). The CERS4 variant at rs2100944 was associated with higher levels of 20:0 (P = 2.65 × 10−40) and in analyses that adjusted for 20:0, with lower levels of behenic acid (P = 4.22 × 10−26) and lignoceric acid (P = 3.20 × 10−21). These novel associations suggest an inter-relationship of circulating VLSFAs and sphingolipid synthesis.</description><identifier>ISSN: 0022-2275</identifier><identifier>EISSN: 1539-7262</identifier><identifier>DOI: 10.1194/jlr.M052456</identifier><identifier>PMID: 25378659</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>arachidic acid ; behenic acid ; Cohort Studies ; Fatty Acids - blood ; Genetic Loci ; Genetic Variation ; Genome-Wide Association Study - methods ; Humans ; lignoceric acid ; Patient-Oriented and Epidemiological Research ; sphingolipids</subject><ispartof>Journal of lipid research, 2015-01, Vol.56 (1), p.176-184</ispartof><rights>2015 © 2015 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>Copyright © 2015 by the American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>Copyright © 2015 by the American Society for Biochemistry and Molecular Biology, Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-4042894845f656ace720aa9f3094b403cfc7bb7cfba82d709d8c270caaa5c1373</citedby><cites>FETCH-LOGICAL-c493t-4042894845f656ace720aa9f3094b403cfc7bb7cfba82d709d8c270caaa5c1373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274065/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022227520356509$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3535,27903,27904,45759,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25378659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lemaitre, Rozenn N.</creatorcontrib><creatorcontrib>King, Irena B.</creatorcontrib><creatorcontrib>Kabagambe, Edmond K.</creatorcontrib><creatorcontrib>Wu, Jason H.Y.</creatorcontrib><creatorcontrib>McKnight, Barbara</creatorcontrib><creatorcontrib>Manichaikul, Ani</creatorcontrib><creatorcontrib>Guan, Weihua</creatorcontrib><creatorcontrib>Sun, Qi</creatorcontrib><creatorcontrib>Chasman, Daniel I.</creatorcontrib><creatorcontrib>Foy, Millennia</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Zhu, Jingwen</creatorcontrib><creatorcontrib>Siscovick, David S.</creatorcontrib><creatorcontrib>Tsai, Michael Y.</creatorcontrib><creatorcontrib>Arnett, Donna K.</creatorcontrib><creatorcontrib>Psaty, Bruce M.</creatorcontrib><creatorcontrib>Djousse, Luc</creatorcontrib><creatorcontrib>Chen, Yii-Der I.</creatorcontrib><creatorcontrib>Tang, Weihong</creatorcontrib><creatorcontrib>Weng, Lu-Chen</creatorcontrib><creatorcontrib>Wu, Hongyu</creatorcontrib><creatorcontrib>Jensen, Majken K.</creatorcontrib><creatorcontrib>Chu, Audrey Y.</creatorcontrib><creatorcontrib>Jacobs, David R.</creatorcontrib><creatorcontrib>Rich, Stephen S.</creatorcontrib><creatorcontrib>Mozaffarian, Dariush</creatorcontrib><creatorcontrib>Steffen, Lyn</creatorcontrib><creatorcontrib>Rimm, Eric B.</creatorcontrib><creatorcontrib>Hu, Frank B.</creatorcontrib><creatorcontrib>Ridker, Paul M.</creatorcontrib><creatorcontrib>Fornage, Myriam</creatorcontrib><creatorcontrib>Friedlander, Yechiel</creatorcontrib><title>Genetic loci associated with circulating levels of very long-chain saturated fatty acids[S]</title><title>Journal of lipid research</title><addtitle>J Lipid Res</addtitle><description>Very long-chain saturated fatty acids (VLSFAs) are saturated fatty acids with 20 or more carbons. In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influence circulating levels of VLSFAs is not known. We investigated the association of common genetic variation with plasma phospholipid/erythrocyte levels of three VLSFAs by performing genome-wide association studies in seven population-based cohorts comprising 10,129 subjects of European ancestry. We observed associations of circulating VLSFA concentrations with common variants in two genes, serine palmitoyl-transferase long-chain base subunit 3 (SPTLC3), a gene involved in the rate-limiting step of de novo sphingolipid synthesis, and ceramide synthase 4 (CERS4). The SPTLC3 variant at rs680379 was associated with higher arachidic acid (20:0 , P = 5.81 × 10−13). The CERS4 variant at rs2100944 was associated with higher levels of 20:0 (P = 2.65 × 10−40) and in analyses that adjusted for 20:0, with lower levels of behenic acid (P = 4.22 × 10−26) and lignoceric acid (P = 3.20 × 10−21). 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King, Irena B. ; Kabagambe, Edmond K. ; Wu, Jason H.Y. ; McKnight, Barbara ; Manichaikul, Ani ; Guan, Weihua ; Sun, Qi ; Chasman, Daniel I. ; Foy, Millennia ; Wang, Lu ; Zhu, Jingwen ; Siscovick, David S. ; Tsai, Michael Y. ; Arnett, Donna K. ; Psaty, Bruce M. ; Djousse, Luc ; Chen, Yii-Der I. ; Tang, Weihong ; Weng, Lu-Chen ; Wu, Hongyu ; Jensen, Majken K. ; Chu, Audrey Y. ; Jacobs, David R. ; Rich, Stephen S. ; Mozaffarian, Dariush ; Steffen, Lyn ; Rimm, Eric B. ; Hu, Frank B. ; Ridker, Paul M. ; Fornage, Myriam ; Friedlander, Yechiel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-4042894845f656ace720aa9f3094b403cfc7bb7cfba82d709d8c270caaa5c1373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>arachidic acid</topic><topic>behenic acid</topic><topic>Cohort Studies</topic><topic>Fatty Acids - blood</topic><topic>Genetic Loci</topic><topic>Genetic Variation</topic><topic>Genome-Wide Association Study - methods</topic><topic>Humans</topic><topic>lignoceric acid</topic><topic>Patient-Oriented and Epidemiological Research</topic><topic>sphingolipids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lemaitre, Rozenn N.</creatorcontrib><creatorcontrib>King, Irena B.</creatorcontrib><creatorcontrib>Kabagambe, Edmond K.</creatorcontrib><creatorcontrib>Wu, Jason H.Y.</creatorcontrib><creatorcontrib>McKnight, Barbara</creatorcontrib><creatorcontrib>Manichaikul, Ani</creatorcontrib><creatorcontrib>Guan, Weihua</creatorcontrib><creatorcontrib>Sun, Qi</creatorcontrib><creatorcontrib>Chasman, Daniel I.</creatorcontrib><creatorcontrib>Foy, Millennia</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Zhu, Jingwen</creatorcontrib><creatorcontrib>Siscovick, David S.</creatorcontrib><creatorcontrib>Tsai, Michael Y.</creatorcontrib><creatorcontrib>Arnett, Donna K.</creatorcontrib><creatorcontrib>Psaty, Bruce M.</creatorcontrib><creatorcontrib>Djousse, Luc</creatorcontrib><creatorcontrib>Chen, Yii-Der I.</creatorcontrib><creatorcontrib>Tang, Weihong</creatorcontrib><creatorcontrib>Weng, Lu-Chen</creatorcontrib><creatorcontrib>Wu, Hongyu</creatorcontrib><creatorcontrib>Jensen, Majken K.</creatorcontrib><creatorcontrib>Chu, Audrey Y.</creatorcontrib><creatorcontrib>Jacobs, David R.</creatorcontrib><creatorcontrib>Rich, Stephen S.</creatorcontrib><creatorcontrib>Mozaffarian, Dariush</creatorcontrib><creatorcontrib>Steffen, Lyn</creatorcontrib><creatorcontrib>Rimm, Eric B.</creatorcontrib><creatorcontrib>Hu, Frank B.</creatorcontrib><creatorcontrib>Ridker, Paul M.</creatorcontrib><creatorcontrib>Fornage, Myriam</creatorcontrib><creatorcontrib>Friedlander, Yechiel</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Journal of lipid research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lemaitre, Rozenn N.</au><au>King, Irena B.</au><au>Kabagambe, Edmond K.</au><au>Wu, Jason H.Y.</au><au>McKnight, Barbara</au><au>Manichaikul, Ani</au><au>Guan, Weihua</au><au>Sun, Qi</au><au>Chasman, Daniel I.</au><au>Foy, Millennia</au><au>Wang, Lu</au><au>Zhu, Jingwen</au><au>Siscovick, David S.</au><au>Tsai, Michael Y.</au><au>Arnett, Donna K.</au><au>Psaty, Bruce M.</au><au>Djousse, Luc</au><au>Chen, Yii-Der I.</au><au>Tang, Weihong</au><au>Weng, Lu-Chen</au><au>Wu, Hongyu</au><au>Jensen, Majken K.</au><au>Chu, Audrey Y.</au><au>Jacobs, David R.</au><au>Rich, Stephen S.</au><au>Mozaffarian, Dariush</au><au>Steffen, Lyn</au><au>Rimm, Eric B.</au><au>Hu, Frank B.</au><au>Ridker, Paul M.</au><au>Fornage, Myriam</au><au>Friedlander, Yechiel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic loci associated with circulating levels of very long-chain saturated fatty acids[S]</atitle><jtitle>Journal of lipid research</jtitle><addtitle>J Lipid Res</addtitle><date>2015-01</date><risdate>2015</risdate><volume>56</volume><issue>1</issue><spage>176</spage><epage>184</epage><pages>176-184</pages><issn>0022-2275</issn><eissn>1539-7262</eissn><abstract>Very long-chain saturated fatty acids (VLSFAs) are saturated fatty acids with 20 or more carbons. In contrast to the more abundant saturated fatty acids, such as palmitic acid, there is growing evidence that circulating VLSFAs may have beneficial biological properties. Whether genetic factors influence circulating levels of VLSFAs is not known. We investigated the association of common genetic variation with plasma phospholipid/erythrocyte levels of three VLSFAs by performing genome-wide association studies in seven population-based cohorts comprising 10,129 subjects of European ancestry. We observed associations of circulating VLSFA concentrations with common variants in two genes, serine palmitoyl-transferase long-chain base subunit 3 (SPTLC3), a gene involved in the rate-limiting step of de novo sphingolipid synthesis, and ceramide synthase 4 (CERS4). The SPTLC3 variant at rs680379 was associated with higher arachidic acid (20:0 , P = 5.81 × 10−13). The CERS4 variant at rs2100944 was associated with higher levels of 20:0 (P = 2.65 × 10−40) and in analyses that adjusted for 20:0, with lower levels of behenic acid (P = 4.22 × 10−26) and lignoceric acid (P = 3.20 × 10−21). These novel associations suggest an inter-relationship of circulating VLSFAs and sphingolipid synthesis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25378659</pmid><doi>10.1194/jlr.M052456</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | arachidic acid behenic acid Cohort Studies Fatty Acids - blood Genetic Loci Genetic Variation Genome-Wide Association Study - methods Humans lignoceric acid Patient-Oriented and Epidemiological Research sphingolipids |
title | Genetic loci associated with circulating levels of very long-chain saturated fatty acids[S] |
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