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...
Gespeichert in:
Veröffentlicht in: | Atherosclerosis 1992-02, Vol.92 (2), p.219-227 |
---|---|
Hauptverfasser: | , , , , , |
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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5518647$$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 |