Triiodothyronine Exerts a Major Pleiotropic Effect on Reverse Cholesterol Transport Phenotypes
The thyroid hormone triiodothyronine (T3) is known to be a potent mediator of APOA1 gene expression. With the use of multivariate quantitative genetic analysis, we have assessed the magnitude of shared effects of T3 on plasma concentrations of apolipoprotein AI (apo AI) and three related phenotypesH...
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Veröffentlicht in: | Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 1996-02, Vol.16 (2), p.289-293 |
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creator | Comuzzie, Anthony G Blangero, J Mahaney, Michael C Sharp, R. Mark VandeBerg, John L Stern, Michael P MacCluer, Jean W |
description | The thyroid hormone triiodothyronine (T3) is known to be a potent mediator of APOA1 gene expression. With the use of multivariate quantitative genetic analysis, we have assessed the magnitude of shared effects of T3 on plasma concentrations of apolipoprotein AI (apo AI) and three related phenotypesHDL-C, apo AII, and LpAI (which is a concentration of apo AI that contains HDL particles). Maximum likelihood techniques were used to simultaneously estimate mean effects and variance components in large, extended Mexican American families living in San Antonio, Tex. We found that T3 accounted for 16%, 23%, 21%, and 37% of the additive genetic variance in HDL-C, apo AI, apo AII, and LpAI, respectively, while explaining virtually none of the random environmental variance in these phenotypes. T3 also has a pronounced effect on the pairwise genetic correlations among the four phenotypesAfter the pleiotropic effects of T3 concentrations are controlled for, the genetic correlations are reduced by 6% in the case of HDL-C and apo AI and 97% for apo AII and LpAI. Thus, genes that influence T3 have a significant effect on HDL-C, apo AI, apo AII, and LpAI and also on the correlations among these phenotypes. (Arterioscler Thromb Vasc Biol. 1996;16:289-293.) |
doi_str_mv | 10.1161/01.ATV.16.2.289 |
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Mark ; VandeBerg, John L ; Stern, Michael P ; MacCluer, Jean W</creator><creatorcontrib>Comuzzie, Anthony G ; Blangero, J ; Mahaney, Michael C ; Sharp, R. Mark ; VandeBerg, John L ; Stern, Michael P ; MacCluer, Jean W</creatorcontrib><description>The thyroid hormone triiodothyronine (T3) is known to be a potent mediator of APOA1 gene expression. With the use of multivariate quantitative genetic analysis, we have assessed the magnitude of shared effects of T3 on plasma concentrations of apolipoprotein AI (apo AI) and three related phenotypesHDL-C, apo AII, and LpAI (which is a concentration of apo AI that contains HDL particles). Maximum likelihood techniques were used to simultaneously estimate mean effects and variance components in large, extended Mexican American families living in San Antonio, Tex. We found that T3 accounted for 16%, 23%, 21%, and 37% of the additive genetic variance in HDL-C, apo AI, apo AII, and LpAI, respectively, while explaining virtually none of the random environmental variance in these phenotypes. T3 also has a pronounced effect on the pairwise genetic correlations among the four phenotypesAfter the pleiotropic effects of T3 concentrations are controlled for, the genetic correlations are reduced by 6% in the case of HDL-C and apo AI and 97% for apo AII and LpAI. Thus, genes that influence T3 have a significant effect on HDL-C, apo AI, apo AII, and LpAI and also on the correlations among these phenotypes. (Arterioscler Thromb Vasc Biol. 1996;16:289-293.)</description><identifier>ISSN: 1079-5642</identifier><identifier>EISSN: 1524-4636</identifier><identifier>DOI: 10.1161/01.ATV.16.2.289</identifier><identifier>PMID: 8620345</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Apolipoprotein A-I - blood ; Apolipoprotein A-II - blood ; Biological Transport ; Cholesterol - genetics ; Cholesterol - metabolism ; Cholesterol, HDL - blood ; Female ; Humans ; Lipoprotein(a) - analogs & derivatives ; Lipoprotein(a) - blood ; Male ; Middle Aged ; Multivariate Analysis ; Osmolar Concentration ; Phenotype ; Sex Characteristics ; Triiodothyronine - pharmacology</subject><ispartof>Arteriosclerosis, thrombosis, and vascular biology, 1996-02, Vol.16 (2), p.289-293</ispartof><rights>1996 American Heart Association, Inc.</rights><rights>Copyright American Heart Association, Inc. Feb 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3975-1da71872508647af2d6d482b76ff318925793e3f04298e6164ba89162eaa11293</citedby><cites>FETCH-LOGICAL-c3975-1da71872508647af2d6d482b76ff318925793e3f04298e6164ba89162eaa11293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8620345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Comuzzie, Anthony G</creatorcontrib><creatorcontrib>Blangero, J</creatorcontrib><creatorcontrib>Mahaney, Michael C</creatorcontrib><creatorcontrib>Sharp, R. Mark</creatorcontrib><creatorcontrib>VandeBerg, John L</creatorcontrib><creatorcontrib>Stern, Michael P</creatorcontrib><creatorcontrib>MacCluer, Jean W</creatorcontrib><title>Triiodothyronine Exerts a Major Pleiotropic Effect on Reverse Cholesterol Transport Phenotypes</title><title>Arteriosclerosis, thrombosis, and vascular biology</title><addtitle>Arterioscler Thromb Vasc Biol</addtitle><description>The thyroid hormone triiodothyronine (T3) is known to be a potent mediator of APOA1 gene expression. With the use of multivariate quantitative genetic analysis, we have assessed the magnitude of shared effects of T3 on plasma concentrations of apolipoprotein AI (apo AI) and three related phenotypesHDL-C, apo AII, and LpAI (which is a concentration of apo AI that contains HDL particles). Maximum likelihood techniques were used to simultaneously estimate mean effects and variance components in large, extended Mexican American families living in San Antonio, Tex. We found that T3 accounted for 16%, 23%, 21%, and 37% of the additive genetic variance in HDL-C, apo AI, apo AII, and LpAI, respectively, while explaining virtually none of the random environmental variance in these phenotypes. T3 also has a pronounced effect on the pairwise genetic correlations among the four phenotypesAfter the pleiotropic effects of T3 concentrations are controlled for, the genetic correlations are reduced by 6% in the case of HDL-C and apo AI and 97% for apo AII and LpAI. Thus, genes that influence T3 have a significant effect on HDL-C, apo AI, apo AII, and LpAI and also on the correlations among these phenotypes. (Arterioscler Thromb Vasc Biol. 1996;16:289-293.)</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Apolipoprotein A-I - blood</subject><subject>Apolipoprotein A-II - blood</subject><subject>Biological Transport</subject><subject>Cholesterol - genetics</subject><subject>Cholesterol - metabolism</subject><subject>Cholesterol, HDL - blood</subject><subject>Female</subject><subject>Humans</subject><subject>Lipoprotein(a) - analogs & derivatives</subject><subject>Lipoprotein(a) - blood</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Osmolar Concentration</subject><subject>Phenotype</subject><subject>Sex Characteristics</subject><subject>Triiodothyronine - pharmacology</subject><issn>1079-5642</issn><issn>1524-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAURSNEVdrCmhWSxYJdUj_b8ceyGg0tUhFVNbDE8iQvSgZPHOyEMv--rmbEgoVlW-_46uq4KN4DrQAkXFOobjY_KpAVq5g2r4oLqJkoheTydT5TZcpaCvamuExpRykVjNHz4lxLRrmoL4qfmzgMoQ1zf4hhHEYk678Y50Qc-ep2IZIHj0OYY5iGhqy7DpuZhJE84h-MCcmqDx7TjDF4soluTFOIM3nocQzzYcL0tjjrnE_47rRfFd8_rzeru_L-2-2X1c192XCj6hJap0ArVlMthXIda2UrNNsq2XUctGG1Mhx5l-sbjRKk2DptQDJ0DoAZflV8OuZOMfxeciO7H1KD3rsRw5KsUkZzqiCDH_8Dd2GJY-5mWU7XQkuaoesj1MSQUsTOTnHYu3iwQO2LdkvBZu0WpGU2a88vPpxil-0e23_8yXOei-P8KfhsK_3yyxNG26Pzc29f_oVLmj0YIynL1zIvqPkzUEKMYw</recordid><startdate>199602</startdate><enddate>199602</enddate><creator>Comuzzie, Anthony G</creator><creator>Blangero, J</creator><creator>Mahaney, Michael C</creator><creator>Sharp, R. Mark</creator><creator>VandeBerg, John L</creator><creator>Stern, Michael P</creator><creator>MacCluer, Jean W</creator><general>American Heart Association, Inc</general><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>199602</creationdate><title>Triiodothyronine Exerts a Major Pleiotropic Effect on Reverse Cholesterol Transport Phenotypes</title><author>Comuzzie, Anthony G ; Blangero, J ; Mahaney, Michael C ; Sharp, R. Mark ; VandeBerg, John L ; Stern, Michael P ; MacCluer, Jean W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3975-1da71872508647af2d6d482b76ff318925793e3f04298e6164ba89162eaa11293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Apolipoprotein A-I - blood</topic><topic>Apolipoprotein A-II - blood</topic><topic>Biological Transport</topic><topic>Cholesterol - genetics</topic><topic>Cholesterol - metabolism</topic><topic>Cholesterol, HDL - blood</topic><topic>Female</topic><topic>Humans</topic><topic>Lipoprotein(a) - analogs & derivatives</topic><topic>Lipoprotein(a) - blood</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Osmolar Concentration</topic><topic>Phenotype</topic><topic>Sex Characteristics</topic><topic>Triiodothyronine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Comuzzie, Anthony G</creatorcontrib><creatorcontrib>Blangero, J</creatorcontrib><creatorcontrib>Mahaney, Michael C</creatorcontrib><creatorcontrib>Sharp, R. Mark</creatorcontrib><creatorcontrib>VandeBerg, John L</creatorcontrib><creatorcontrib>Stern, Michael P</creatorcontrib><creatorcontrib>MacCluer, Jean W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Comuzzie, Anthony G</au><au>Blangero, J</au><au>Mahaney, Michael C</au><au>Sharp, R. Mark</au><au>VandeBerg, John L</au><au>Stern, Michael P</au><au>MacCluer, Jean W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Triiodothyronine Exerts a Major Pleiotropic Effect on Reverse Cholesterol Transport Phenotypes</atitle><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle><addtitle>Arterioscler Thromb Vasc Biol</addtitle><date>1996-02</date><risdate>1996</risdate><volume>16</volume><issue>2</issue><spage>289</spage><epage>293</epage><pages>289-293</pages><issn>1079-5642</issn><eissn>1524-4636</eissn><abstract>The thyroid hormone triiodothyronine (T3) is known to be a potent mediator of APOA1 gene expression. With the use of multivariate quantitative genetic analysis, we have assessed the magnitude of shared effects of T3 on plasma concentrations of apolipoprotein AI (apo AI) and three related phenotypesHDL-C, apo AII, and LpAI (which is a concentration of apo AI that contains HDL particles). Maximum likelihood techniques were used to simultaneously estimate mean effects and variance components in large, extended Mexican American families living in San Antonio, Tex. We found that T3 accounted for 16%, 23%, 21%, and 37% of the additive genetic variance in HDL-C, apo AI, apo AII, and LpAI, respectively, while explaining virtually none of the random environmental variance in these phenotypes. T3 also has a pronounced effect on the pairwise genetic correlations among the four phenotypesAfter the pleiotropic effects of T3 concentrations are controlled for, the genetic correlations are reduced by 6% in the case of HDL-C and apo AI and 97% for apo AII and LpAI. Thus, genes that influence T3 have a significant effect on HDL-C, apo AI, apo AII, and LpAI and also on the correlations among these phenotypes. (Arterioscler Thromb Vasc Biol. 1996;16:289-293.)</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>8620345</pmid><doi>10.1161/01.ATV.16.2.289</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Apolipoprotein A-I - blood Apolipoprotein A-II - blood Biological Transport Cholesterol - genetics Cholesterol - metabolism Cholesterol, HDL - blood Female Humans Lipoprotein(a) - analogs & derivatives Lipoprotein(a) - blood Male Middle Aged Multivariate Analysis Osmolar Concentration Phenotype Sex Characteristics Triiodothyronine - pharmacology |
title | Triiodothyronine Exerts a Major Pleiotropic Effect on Reverse Cholesterol Transport Phenotypes |
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