Multivariate genetic analysis of high density lipoprotein particles

The aim of this study was to investigate the effect of genetic factors on three components of plasma high density lipoproteins, HDL-cholesterol (HDL-C), apolipoprotein A-I (apo A-I) and lipoprotein particle Lp A-I (Lp A-I), which contains apo A-I but not apo A-II. These analyses were carried out on...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Atherosclerosis 1992-02, Vol.92 (2), p.219-227
Hauptverfasser: Steinmetz, J., Boerwinkle, E., Gueguen, R., Visvikis, S., Henny, J., Siest, G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 227
container_issue 2
container_start_page 219
container_title Atherosclerosis
container_volume 92
creator Steinmetz, J.
Boerwinkle, E.
Gueguen, R.
Visvikis, S.
Henny, J.
Siest, G.
description The aim of this study was to investigate the effect of genetic factors on three components of plasma high density lipoproteins, HDL-cholesterol (HDL-C), apolipoprotein A-I (apo A-I) and lipoprotein particle Lp A-I (Lp A-I), which contains apo A-I but not apo A-II. These analyses were carried out on 106 nuclear families with one or more children (407 subjects) who volunteered for health screening at the Center for Preventive Medicine, Vandoeuvre, France. After adjustment by stepwise multiple linear regression analysis for age, gender, weight, height, ponderosity, alcohol consumption, smoking habits, and hormonal treatment in females, a multifactorial model (considering the effect of polygenes, individual, specific, environmental and common household factors) was fitted to each variable separately. The hypothesis of no common household effects was accepted for each of the traits. The contribution of genetic factors to inter-individual variance was larger than the contribution of environmental factors for apo A-1 ( h 2 = 0.81) and Lp A-I ( h 2 = 0.63) but not for HDL-C ( h 2 = 0.44). Bivariate analyses were carried out by parameterizing covariance components between traits. The genetic correlations were always significantly different from zero. They were estimated to be 0.73 between HDL-C and apo A-I, 0.40 between HDL-C and Lp A-I, 0.51 between apo A-I and Lp A-I. These results suggest that HDL-C, apo A-I and Lp A-I are only in part affected by the same genes and that the measurement of lipids as well as the apo A-I and Lp A-I gives complementary and different information on the metabolic and genetic aspects.
doi_str_mv 10.1016/0021-9150(92)90281-K
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73071503</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>002191509290281K</els_id><sourcerecordid>73071503</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-29811bdbfd8da8655edf0a6e467eadf87d9e3e7ae3dc10a9bc68ad3dfaca97963</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EKqXwByBlgRAsAnZetjdIqOKlFrGBtTWxJ61RmgQ7qdS_JyVV2bGaxT0zunMIOWf0llGW3VEasVCylF7L6EbSSLBwdkDGTHAZskQkh2S8R47JifdflNKEMzEiIxaLVKbpmEzfurK1a3AWWgwWWGFrdQAVlBtvfVAXwdIuloHBytt2E5S2qRtXt2iroAHXsyX6U3JUQOnxbDcn5PPp8WP6Es7fn1-nD_NQxyJrw0gKxnKTF0YYEFmaoikoZJhkHMEUghuJMXLA2GhGQeY6E2BiU4AGyWUWT8jVcLdv8N2hb9XKeo1lCRXWnVc8prz_Ne7BZAC1q713WKjG2RW4jWJUbd2prRi1FaNkpH7dqVm_drG73-UrNH9Lg6w-v9zl4DWUhYNKW7_H0pSJLOE9dj9g2LtYW3TKa4uVRmMd6laZ2v7f4wfKo4yL</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73071503</pqid></control><display><type>article</type><title>Multivariate genetic analysis of high density lipoprotein particles</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Steinmetz, J. ; Boerwinkle, E. ; Gueguen, R. ; Visvikis, S. ; Henny, J. ; Siest, G.</creator><creatorcontrib>Steinmetz, J. ; Boerwinkle, E. ; Gueguen, R. ; Visvikis, S. ; Henny, J. ; Siest, G.</creatorcontrib><description>The aim of this study was to investigate the effect of genetic factors on three components of plasma high density lipoproteins, HDL-cholesterol (HDL-C), apolipoprotein A-I (apo A-I) and lipoprotein particle Lp A-I (Lp A-I), which contains apo A-I but not apo A-II. These analyses were carried out on 106 nuclear families with one or more children (407 subjects) who volunteered for health screening at the Center for Preventive Medicine, Vandoeuvre, France. After adjustment by stepwise multiple linear regression analysis for age, gender, weight, height, ponderosity, alcohol consumption, smoking habits, and hormonal treatment in females, a multifactorial model (considering the effect of polygenes, individual, specific, environmental and common household factors) was fitted to each variable separately. The hypothesis of no common household effects was accepted for each of the traits. The contribution of genetic factors to inter-individual variance was larger than the contribution of environmental factors for apo A-1 ( h 2 = 0.81) and Lp A-I ( h 2 = 0.63) but not for HDL-C ( h 2 = 0.44). Bivariate analyses were carried out by parameterizing covariance components between traits. The genetic correlations were always significantly different from zero. They were estimated to be 0.73 between HDL-C and apo A-I, 0.40 between HDL-C and Lp A-I, 0.51 between apo A-I and Lp A-I. These results suggest that HDL-C, apo A-I and Lp A-I are only in part affected by the same genes and that the measurement of lipids as well as the apo A-I and Lp A-I gives complementary and different information on the metabolic and genetic aspects.</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/0021-9150(92)90281-K</identifier><identifier>PMID: 1385955</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ireland Ltd</publisher><subject>Adolescent ; Adult ; Apolipoprotein A-I - genetics ; Apolipoprotein A-I - metabolism ; Biological and medical sciences ; Cholesterol, HDL - blood ; Cholesterol, HDL - genetics ; Environment ; Female ; Fundamental and applied biological sciences. Psychology ; HDL-cholesterol, Apo A-I, Lp A-I particles ; Healthy families ; Heritability ; Humans ; Lipids. Glycolipids ; Lipoprotein(a) ; Lipoproteins - blood ; Lipoproteins - genetics ; Lipoproteins, HDL - blood ; Lipoproteins, HDL - genetics ; Male ; Metabolisms and neurohumoral controls ; Models, Genetic ; Multivariate Analysis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Atherosclerosis, 1992-02, Vol.92 (2), p.219-227</ispartof><rights>1992</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-29811bdbfd8da8655edf0a6e467eadf87d9e3e7ae3dc10a9bc68ad3dfaca97963</citedby><cites>FETCH-LOGICAL-c386t-29811bdbfd8da8655edf0a6e467eadf87d9e3e7ae3dc10a9bc68ad3dfaca97963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/002191509290281K$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=5518647$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1385955$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steinmetz, J.</creatorcontrib><creatorcontrib>Boerwinkle, E.</creatorcontrib><creatorcontrib>Gueguen, R.</creatorcontrib><creatorcontrib>Visvikis, S.</creatorcontrib><creatorcontrib>Henny, J.</creatorcontrib><creatorcontrib>Siest, G.</creatorcontrib><title>Multivariate genetic analysis of high density lipoprotein particles</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>The aim of this study was to investigate the effect of genetic factors on three components of plasma high density lipoproteins, HDL-cholesterol (HDL-C), apolipoprotein A-I (apo A-I) and lipoprotein particle Lp A-I (Lp A-I), which contains apo A-I but not apo A-II. These analyses were carried out on 106 nuclear families with one or more children (407 subjects) who volunteered for health screening at the Center for Preventive Medicine, Vandoeuvre, France. After adjustment by stepwise multiple linear regression analysis for age, gender, weight, height, ponderosity, alcohol consumption, smoking habits, and hormonal treatment in females, a multifactorial model (considering the effect of polygenes, individual, specific, environmental and common household factors) was fitted to each variable separately. The hypothesis of no common household effects was accepted for each of the traits. The contribution of genetic factors to inter-individual variance was larger than the contribution of environmental factors for apo A-1 ( h 2 = 0.81) and Lp A-I ( h 2 = 0.63) but not for HDL-C ( h 2 = 0.44). Bivariate analyses were carried out by parameterizing covariance components between traits. The genetic correlations were always significantly different from zero. They were estimated to be 0.73 between HDL-C and apo A-I, 0.40 between HDL-C and Lp A-I, 0.51 between apo A-I and Lp A-I. These results suggest that HDL-C, apo A-I and Lp A-I are only in part affected by the same genes and that the measurement of lipids as well as the apo A-I and Lp A-I gives complementary and different information on the metabolic and genetic aspects.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Apolipoprotein A-I - genetics</subject><subject>Apolipoprotein A-I - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cholesterol, HDL - blood</subject><subject>Cholesterol, HDL - genetics</subject><subject>Environment</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HDL-cholesterol, Apo A-I, Lp A-I particles</subject><subject>Healthy families</subject><subject>Heritability</subject><subject>Humans</subject><subject>Lipids. Glycolipids</subject><subject>Lipoprotein(a)</subject><subject>Lipoproteins - blood</subject><subject>Lipoproteins - genetics</subject><subject>Lipoproteins, HDL - blood</subject><subject>Lipoproteins, HDL - genetics</subject><subject>Male</subject><subject>Metabolisms and neurohumoral controls</subject><subject>Models, Genetic</subject><subject>Multivariate Analysis</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EKqXwByBlgRAsAnZetjdIqOKlFrGBtTWxJ61RmgQ7qdS_JyVV2bGaxT0zunMIOWf0llGW3VEasVCylF7L6EbSSLBwdkDGTHAZskQkh2S8R47JifdflNKEMzEiIxaLVKbpmEzfurK1a3AWWgwWWGFrdQAVlBtvfVAXwdIuloHBytt2E5S2qRtXt2iroAHXsyX6U3JUQOnxbDcn5PPp8WP6Es7fn1-nD_NQxyJrw0gKxnKTF0YYEFmaoikoZJhkHMEUghuJMXLA2GhGQeY6E2BiU4AGyWUWT8jVcLdv8N2hb9XKeo1lCRXWnVc8prz_Ne7BZAC1q713WKjG2RW4jWJUbd2prRi1FaNkpH7dqVm_drG73-UrNH9Lg6w-v9zl4DWUhYNKW7_H0pSJLOE9dj9g2LtYW3TKa4uVRmMd6laZ2v7f4wfKo4yL</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Steinmetz, J.</creator><creator>Boerwinkle, E.</creator><creator>Gueguen, R.</creator><creator>Visvikis, S.</creator><creator>Henny, J.</creator><creator>Siest, G.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>19920201</creationdate><title>Multivariate genetic analysis of high density lipoprotein particles</title><author>Steinmetz, J. ; Boerwinkle, E. ; Gueguen, R. ; Visvikis, S. ; Henny, J. ; Siest, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-29811bdbfd8da8655edf0a6e467eadf87d9e3e7ae3dc10a9bc68ad3dfaca97963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Apolipoprotein A-I - genetics</topic><topic>Apolipoprotein A-I - metabolism</topic><topic>Biological and medical sciences</topic><topic>Cholesterol, HDL - blood</topic><topic>Cholesterol, HDL - genetics</topic><topic>Environment</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HDL-cholesterol, Apo A-I, Lp A-I particles</topic><topic>Healthy families</topic><topic>Heritability</topic><topic>Humans</topic><topic>Lipids. Glycolipids</topic><topic>Lipoprotein(a)</topic><topic>Lipoproteins - blood</topic><topic>Lipoproteins - genetics</topic><topic>Lipoproteins, HDL - blood</topic><topic>Lipoproteins, HDL - genetics</topic><topic>Male</topic><topic>Metabolisms and neurohumoral controls</topic><topic>Models, Genetic</topic><topic>Multivariate Analysis</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steinmetz, J.</creatorcontrib><creatorcontrib>Boerwinkle, E.</creatorcontrib><creatorcontrib>Gueguen, R.</creatorcontrib><creatorcontrib>Visvikis, S.</creatorcontrib><creatorcontrib>Henny, J.</creatorcontrib><creatorcontrib>Siest, G.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steinmetz, J.</au><au>Boerwinkle, E.</au><au>Gueguen, R.</au><au>Visvikis, S.</au><au>Henny, J.</au><au>Siest, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multivariate genetic analysis of high density lipoprotein particles</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>92</volume><issue>2</issue><spage>219</spage><epage>227</epage><pages>219-227</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>The aim of this study was to investigate the effect of genetic factors on three components of plasma high density lipoproteins, HDL-cholesterol (HDL-C), apolipoprotein A-I (apo A-I) and lipoprotein particle Lp A-I (Lp A-I), which contains apo A-I but not apo A-II. These analyses were carried out on 106 nuclear families with one or more children (407 subjects) who volunteered for health screening at the Center for Preventive Medicine, Vandoeuvre, France. After adjustment by stepwise multiple linear regression analysis for age, gender, weight, height, ponderosity, alcohol consumption, smoking habits, and hormonal treatment in females, a multifactorial model (considering the effect of polygenes, individual, specific, environmental and common household factors) was fitted to each variable separately. The hypothesis of no common household effects was accepted for each of the traits. The contribution of genetic factors to inter-individual variance was larger than the contribution of environmental factors for apo A-1 ( h 2 = 0.81) and Lp A-I ( h 2 = 0.63) but not for HDL-C ( h 2 = 0.44). Bivariate analyses were carried out by parameterizing covariance components between traits. The genetic correlations were always significantly different from zero. They were estimated to be 0.73 between HDL-C and apo A-I, 0.40 between HDL-C and Lp A-I, 0.51 between apo A-I and Lp A-I. These results suggest that HDL-C, apo A-I and Lp A-I are only in part affected by the same genes and that the measurement of lipids as well as the apo A-I and Lp A-I gives complementary and different information on the metabolic and genetic aspects.</abstract><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>1385955</pmid><doi>10.1016/0021-9150(92)90281-K</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9150
ispartof Atherosclerosis, 1992-02, Vol.92 (2), p.219-227
issn 0021-9150
1879-1484
language eng
recordid cdi_proquest_miscellaneous_73071503
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adolescent
Adult
Apolipoprotein A-I - genetics
Apolipoprotein A-I - metabolism
Biological and medical sciences
Cholesterol, HDL - blood
Cholesterol, HDL - genetics
Environment
Female
Fundamental and applied biological sciences. Psychology
HDL-cholesterol, Apo A-I, Lp A-I particles
Healthy families
Heritability
Humans
Lipids. Glycolipids
Lipoprotein(a)
Lipoproteins - blood
Lipoproteins - genetics
Lipoproteins, HDL - blood
Lipoproteins, HDL - genetics
Male
Metabolisms and neurohumoral controls
Models, Genetic
Multivariate Analysis
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Multivariate genetic analysis of high density lipoprotein particles
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T00%3A34%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multivariate%20genetic%20analysis%20of%20high%20density%20lipoprotein%20particles&rft.jtitle=Atherosclerosis&rft.au=Steinmetz,%20J.&rft.date=1992-02-01&rft.volume=92&rft.issue=2&rft.spage=219&rft.epage=227&rft.pages=219-227&rft.issn=0021-9150&rft.eissn=1879-1484&rft_id=info:doi/10.1016/0021-9150(92)90281-K&rft_dat=%3Cproquest_cross%3E73071503%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73071503&rft_id=info:pmid/1385955&rft_els_id=002191509290281K&rfr_iscdi=true