Association between the PPARA L162V polymorphism and plasma lipid levels: The Framingham Offspring study
Peroxisome proliferator activated receptor (PPAR) alpha is a member of the nuclear receptor superfamily that regulates key proteins involved in fatty acid oxidation, extracellular lipid metabolism, hemostasis, and inflammation. A L162V polymorphism at the PPARA locus has been associated with alterat...
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Veröffentlicht in: | Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2002-05, Vol.22 (5), p.805-810 |
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description | Peroxisome proliferator activated receptor (PPAR) alpha is a member of the nuclear receptor superfamily that regulates key proteins involved in fatty acid oxidation, extracellular lipid metabolism, hemostasis, and inflammation. A L162V polymorphism at the PPARA locus has been associated with alterations in lipid and apolipoprotein concentrations. We studied the association among lipids, lipoproteins, and apolipoproteins and the presence of the L162V polymorphism in 2373 participants (1128 men and 1244 women) in the Framingham Offspring Study. The frequency of the less common allele (V162) was 0.069. The V162 allele was associated with increased serum concentrations of total and LDL cholesterol in men (P=0.0012 and P=0.0004, respectively) and apolipoprotein B in men (P=0.009) and women (P=0.03 after adjustment for age, body mass index, smoking, and use of beta-blockers, diuretics or estrogens). Apolipoprotein (apo) C-III concentrations were higher in carriers of the V162 allele. The association of the L162V polymorphism on LDL cholesterol concentration was greatest in those who also carried the E2 allele at the APOE locus and the G allele at the APOC3 3238C>G polymorphism. This suggests that alterations in triglyceride-rich lipoprotein metabolism may be involved in the generation of the increase in LDL cholesterol observed with the L162V PPARA polymorphism. |
doi_str_mv | 10.1161/01.ATV.0000012302.11991.42 |
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S ; DEMISSIE, S ; CUPPLES, L. A ; CORELLA, D ; WILSON, P. W ; SCHAEFER, E. J ; ORDOVAS, J. M</creator><creatorcontrib>TAI, E. S ; DEMISSIE, S ; CUPPLES, L. A ; CORELLA, D ; WILSON, P. W ; SCHAEFER, E. J ; ORDOVAS, J. M</creatorcontrib><description>Peroxisome proliferator activated receptor (PPAR) alpha is a member of the nuclear receptor superfamily that regulates key proteins involved in fatty acid oxidation, extracellular lipid metabolism, hemostasis, and inflammation. A L162V polymorphism at the PPARA locus has been associated with alterations in lipid and apolipoprotein concentrations. We studied the association among lipids, lipoproteins, and apolipoproteins and the presence of the L162V polymorphism in 2373 participants (1128 men and 1244 women) in the Framingham Offspring Study. The frequency of the less common allele (V162) was 0.069. The V162 allele was associated with increased serum concentrations of total and LDL cholesterol in men (P=0.0012 and P=0.0004, respectively) and apolipoprotein B in men (P=0.009) and women (P=0.03 after adjustment for age, body mass index, smoking, and use of beta-blockers, diuretics or estrogens). Apolipoprotein (apo) C-III concentrations were higher in carriers of the V162 allele. The association of the L162V polymorphism on LDL cholesterol concentration was greatest in those who also carried the E2 allele at the APOE locus and the G allele at the APOC3 3238C>G polymorphism. This suggests that alterations in triglyceride-rich lipoprotein metabolism may be involved in the generation of the increase in LDL cholesterol observed with the L162V PPARA polymorphism.</description><identifier>ISSN: 1079-5642</identifier><identifier>EISSN: 1524-4636</identifier><identifier>DOI: 10.1161/01.ATV.0000012302.11991.42</identifier><identifier>PMID: 12006394</identifier><identifier>CODEN: ATVBFA</identifier><language>eng</language><publisher>Philadelphia, PA: Lippincott</publisher><subject>Amino Acid Substitution - genetics ; Analytical, structural and metabolic biochemistry ; Apolipoprotein C-III ; Apolipoproteins B - blood ; Apolipoproteins B - genetics ; Apolipoproteins C - blood ; Apolipoproteins C - genetics ; Biological and medical sciences ; Cardiovascular Diseases - genetics ; Cholesterol, LDL - blood ; Cholesterol, LDL - genetics ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Leucine - genetics ; Lipids ; Lipids - blood ; Lipids - genetics ; Male ; Middle Aged ; Miscellaneous ; Other biological molecules ; Polymorphism, Genetic - genetics ; Receptors, Cytoplasmic and Nuclear - genetics ; Transcription Factors - genetics ; Valine - genetics</subject><ispartof>Arteriosclerosis, thrombosis, and vascular biology, 2002-05, Vol.22 (5), p.805-810</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. 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A</creatorcontrib><creatorcontrib>CORELLA, D</creatorcontrib><creatorcontrib>WILSON, P. W</creatorcontrib><creatorcontrib>SCHAEFER, E. J</creatorcontrib><creatorcontrib>ORDOVAS, J. M</creatorcontrib><title>Association between the PPARA L162V polymorphism and plasma lipid levels: The Framingham Offspring study</title><title>Arteriosclerosis, thrombosis, and vascular biology</title><addtitle>Arterioscler Thromb Vasc Biol</addtitle><description>Peroxisome proliferator activated receptor (PPAR) alpha is a member of the nuclear receptor superfamily that regulates key proteins involved in fatty acid oxidation, extracellular lipid metabolism, hemostasis, and inflammation. A L162V polymorphism at the PPARA locus has been associated with alterations in lipid and apolipoprotein concentrations. We studied the association among lipids, lipoproteins, and apolipoproteins and the presence of the L162V polymorphism in 2373 participants (1128 men and 1244 women) in the Framingham Offspring Study. The frequency of the less common allele (V162) was 0.069. The V162 allele was associated with increased serum concentrations of total and LDL cholesterol in men (P=0.0012 and P=0.0004, respectively) and apolipoprotein B in men (P=0.009) and women (P=0.03 after adjustment for age, body mass index, smoking, and use of beta-blockers, diuretics or estrogens). Apolipoprotein (apo) C-III concentrations were higher in carriers of the V162 allele. The association of the L162V polymorphism on LDL cholesterol concentration was greatest in those who also carried the E2 allele at the APOE locus and the G allele at the APOC3 3238C>G polymorphism. This suggests that alterations in triglyceride-rich lipoprotein metabolism may be involved in the generation of the increase in LDL cholesterol observed with the L162V PPARA polymorphism.</description><subject>Amino Acid Substitution - genetics</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Apolipoprotein C-III</subject><subject>Apolipoproteins B - blood</subject><subject>Apolipoproteins B - genetics</subject><subject>Apolipoproteins C - blood</subject><subject>Apolipoproteins C - genetics</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular Diseases - genetics</subject><subject>Cholesterol, LDL - blood</subject><subject>Cholesterol, LDL - genetics</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Leucine - genetics</subject><subject>Lipids</subject><subject>Lipids - blood</subject><subject>Lipids - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Other biological molecules</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Receptors, Cytoplasmic and Nuclear - genetics</subject><subject>Transcription Factors - genetics</subject><subject>Valine - genetics</subject><issn>1079-5642</issn><issn>1524-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkV1rFDEUhoMotlb_goSC3s2ak6_J9G4otgoLLbL2NpzJZNwpmQ-TGWX_fVO7sGBukhOe93y9hFwC2wBo-MJgU-8eNuz5ABeM5--qgo3kr8g5KC4LqYV-nd-srAqlJT8j71J6zLjknL0lZ8AZ06KS52RfpzS5Hpd-Gmnjl7_ej3TZe3p_X_-o6RY0f6DzFA7DFOd9nwaKY0vngGlAGvq5b2nwf3xIV3SXVTcRh378tceB3nVdmmMOaFrW9vCevOkwJP_heF-Qnzdfd9ffiu3d7ffrels4ydRSGFG1WoDjjRPcKOO1g0Y4j0q5CrgD1ZQoKy1RGQOulN502HRa6Vah4SguyOeXvHOcfq8-LXbok_Mh4OinNdkSdGm4lBm8_A98nNY45t4sz3symmuWoasXyMUppeg7m0caMB4sMPtshmVgsxn2ZIb9Z4aVPIs_HiuszeDbk_S4_Qx8OgKYHIYu4uj6dOKELjVoI54AB5WRfQ</recordid><startdate>20020501</startdate><enddate>20020501</enddate><creator>TAI, E. S</creator><creator>DEMISSIE, S</creator><creator>CUPPLES, L. A</creator><creator>CORELLA, D</creator><creator>WILSON, P. W</creator><creator>SCHAEFER, E. J</creator><creator>ORDOVAS, J. M</creator><general>Lippincott</general><general>American Heart Association, Inc</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20020501</creationdate><title>Association between the PPARA L162V polymorphism and plasma lipid levels: The Framingham Offspring study</title><author>TAI, E. S ; DEMISSIE, S ; CUPPLES, L. A ; CORELLA, D ; WILSON, P. W ; SCHAEFER, E. J ; ORDOVAS, J. 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Psychology</topic><topic>Humans</topic><topic>Leucine - genetics</topic><topic>Lipids</topic><topic>Lipids - blood</topic><topic>Lipids - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Other biological molecules</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Transcription Factors - genetics</topic><topic>Valine - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAI, E. S</creatorcontrib><creatorcontrib>DEMISSIE, S</creatorcontrib><creatorcontrib>CUPPLES, L. A</creatorcontrib><creatorcontrib>CORELLA, D</creatorcontrib><creatorcontrib>WILSON, P. W</creatorcontrib><creatorcontrib>SCHAEFER, E. J</creatorcontrib><creatorcontrib>ORDOVAS, J. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between the PPARA L162V polymorphism and plasma lipid levels: The Framingham Offspring study</atitle><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle><addtitle>Arterioscler Thromb Vasc Biol</addtitle><date>2002-05-01</date><risdate>2002</risdate><volume>22</volume><issue>5</issue><spage>805</spage><epage>810</epage><pages>805-810</pages><issn>1079-5642</issn><eissn>1524-4636</eissn><coden>ATVBFA</coden><abstract>Peroxisome proliferator activated receptor (PPAR) alpha is a member of the nuclear receptor superfamily that regulates key proteins involved in fatty acid oxidation, extracellular lipid metabolism, hemostasis, and inflammation. A L162V polymorphism at the PPARA locus has been associated with alterations in lipid and apolipoprotein concentrations. We studied the association among lipids, lipoproteins, and apolipoproteins and the presence of the L162V polymorphism in 2373 participants (1128 men and 1244 women) in the Framingham Offspring Study. The frequency of the less common allele (V162) was 0.069. The V162 allele was associated with increased serum concentrations of total and LDL cholesterol in men (P=0.0012 and P=0.0004, respectively) and apolipoprotein B in men (P=0.009) and women (P=0.03 after adjustment for age, body mass index, smoking, and use of beta-blockers, diuretics or estrogens). Apolipoprotein (apo) C-III concentrations were higher in carriers of the V162 allele. The association of the L162V polymorphism on LDL cholesterol concentration was greatest in those who also carried the E2 allele at the APOE locus and the G allele at the APOC3 3238C>G polymorphism. This suggests that alterations in triglyceride-rich lipoprotein metabolism may be involved in the generation of the increase in LDL cholesterol observed with the L162V PPARA polymorphism.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>12006394</pmid><doi>10.1161/01.ATV.0000012302.11991.42</doi><tpages>6</tpages></addata></record> |
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subjects | Amino Acid Substitution - genetics Analytical, structural and metabolic biochemistry Apolipoprotein C-III Apolipoproteins B - blood Apolipoproteins B - genetics Apolipoproteins C - blood Apolipoproteins C - genetics Biological and medical sciences Cardiovascular Diseases - genetics Cholesterol, LDL - blood Cholesterol, LDL - genetics Female Fundamental and applied biological sciences. Psychology Humans Leucine - genetics Lipids Lipids - blood Lipids - genetics Male Middle Aged Miscellaneous Other biological molecules Polymorphism, Genetic - genetics Receptors, Cytoplasmic and Nuclear - genetics Transcription Factors - genetics Valine - genetics |
title | Association between the PPARA L162V polymorphism and plasma lipid levels: The Framingham Offspring study |
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