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Pvu II intron 15 polymorphism at the LDL receptor gene is associated with differences in serum lipid concentrations in subjects with low and high risk for coronary artery disease from Brazil
Coronary artery disease (CAD) has a high prevalence in the Brazilian population. Nevertheless, studies of genetic risk factors for CAD in this country have not been sufficiently conducted. We used the Pvu II polymorphism (intron 15) at the low-density lipoprotein receptor (LDLR) gene to study the ef...
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Published in: | Clinica chimica acta 2000-03, Vol.293 (1), p.75-88 |
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creator | Salazar, Luis A Hirata, Mario H Forti, Neusa Diament, Jayme Giannini, Sérgio D Issa, Jaqueline S Hirata, Rosario D.C |
description | Coronary artery disease (CAD) has a high prevalence in the Brazilian population. Nevertheless, studies of genetic risk factors for CAD in this country have not been sufficiently conducted. We used the
Pvu II polymorphism (intron 15) at the low-density lipoprotein receptor (LDLR) gene to study the effect of variation at this locus in determining plasma lipid concentrations in 128 white subjects presenting a lipid profile suggesting high risk for CAD (HRG) and 100 white normolipidemic individuals (controls, CG). The
Pvu II polymorphism was detected by PCR–RFLP. The P1P1 genotype for
Pvu II polymorphism (homozygous for absence of restriction site) was greater in HRG individuals than in CG subjects (57% vs. 38%,
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doi_str_mv | 10.1016/S0009-8981(99)00218-1 |
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Pvu II polymorphism (intron 15) at the low-density lipoprotein receptor (LDLR) gene to study the effect of variation at this locus in determining plasma lipid concentrations in 128 white subjects presenting a lipid profile suggesting high risk for CAD (HRG) and 100 white normolipidemic individuals (controls, CG). The
Pvu II polymorphism was detected by PCR–RFLP. The P1P1 genotype for
Pvu II polymorphism (homozygous for absence of restriction site) was greater in HRG individuals than in CG subjects (57% vs. 38%,
P<0.05). Moreover, the P1P1 genotype was strongly associated with high concentrations of total cholesterol (
P=0.0001), triglycerides (
P=0.0295), LDL-C (
P=0.0001), and VLDL-C concentrations (
P=0.0280) and lower HDL-C concentrations (
P=0.0051) in HRG subjects. Similarly, the CG individuals with P1P1 genotype presented high concentrations of total cholesterol and LDL-C compared to other genotypes (
P=0.0001). This study demonstrates the influence of
Pvu II polymorphism of the LDLR on serum lipid concentrations of individuals with low and high risk for CAD from Brazil.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/S0009-8981(99)00218-1</identifier><identifier>PMID: 10699424</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Aged ; Alleles ; Brazil ; Cholesterol concentrations ; Coronary artery disease ; Coronary Disease - blood ; Coronary Disease - genetics ; Deoxyribonucleases, Type II Site-Specific - genetics ; DNA - genetics ; DNA - isolation & purification ; Female ; Genetics ; Genotype ; Humans ; Introns - genetics ; Lipids - blood ; Low-density lipoprotein receptor gene ; Male ; Middle Aged ; Polymerase Chain Reaction ; Polymorphism, Genetic - genetics ; Polymorphism, Restriction Fragment Length ; Pvu II polymorphism ; Receptors, LDL - genetics ; Risk ; Sex Characteristics</subject><ispartof>Clinica chimica acta, 2000-03, Vol.293 (1), p.75-88</ispartof><rights>2000 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-31e2c01e5ffcc1d87a8c0f2a2531f3615200efd7cb460013b2f7acb9497a535c3</citedby><cites>FETCH-LOGICAL-c361t-31e2c01e5ffcc1d87a8c0f2a2531f3615200efd7cb460013b2f7acb9497a535c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10699424$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salazar, Luis A</creatorcontrib><creatorcontrib>Hirata, Mario H</creatorcontrib><creatorcontrib>Forti, Neusa</creatorcontrib><creatorcontrib>Diament, Jayme</creatorcontrib><creatorcontrib>Giannini, Sérgio D</creatorcontrib><creatorcontrib>Issa, Jaqueline S</creatorcontrib><creatorcontrib>Hirata, Rosario D.C</creatorcontrib><title>Pvu II intron 15 polymorphism at the LDL receptor gene is associated with differences in serum lipid concentrations in subjects with low and high risk for coronary artery disease from Brazil</title><title>Clinica chimica acta</title><addtitle>Clin Chim Acta</addtitle><description>Coronary artery disease (CAD) has a high prevalence in the Brazilian population. Nevertheless, studies of genetic risk factors for CAD in this country have not been sufficiently conducted. We used the
Pvu II polymorphism (intron 15) at the low-density lipoprotein receptor (LDLR) gene to study the effect of variation at this locus in determining plasma lipid concentrations in 128 white subjects presenting a lipid profile suggesting high risk for CAD (HRG) and 100 white normolipidemic individuals (controls, CG). The
Pvu II polymorphism was detected by PCR–RFLP. The P1P1 genotype for
Pvu II polymorphism (homozygous for absence of restriction site) was greater in HRG individuals than in CG subjects (57% vs. 38%,
P<0.05). Moreover, the P1P1 genotype was strongly associated with high concentrations of total cholesterol (
P=0.0001), triglycerides (
P=0.0295), LDL-C (
P=0.0001), and VLDL-C concentrations (
P=0.0280) and lower HDL-C concentrations (
P=0.0051) in HRG subjects. Similarly, the CG individuals with P1P1 genotype presented high concentrations of total cholesterol and LDL-C compared to other genotypes (
P=0.0001). This study demonstrates the influence of
Pvu II polymorphism of the LDLR on serum lipid concentrations of individuals with low and high risk for CAD from Brazil.</description><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Brazil</subject><subject>Cholesterol concentrations</subject><subject>Coronary artery disease</subject><subject>Coronary Disease - blood</subject><subject>Coronary Disease - genetics</subject><subject>Deoxyribonucleases, Type II Site-Specific - genetics</subject><subject>DNA - genetics</subject><subject>DNA - isolation & purification</subject><subject>Female</subject><subject>Genetics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Introns - genetics</subject><subject>Lipids - blood</subject><subject>Low-density lipoprotein receptor gene</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Pvu II polymorphism</subject><subject>Receptors, LDL - genetics</subject><subject>Risk</subject><subject>Sex Characteristics</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1TAQhS0EopfCI4BmhWARsJ1frxCUvytdCSRgbTn2uHFJ4tR2WpWH49nwbSrEjtXI9jlzPPMR8pTRV4yy5vU3SqkoOtGxF0K8pJSzrmD3yI51bVmUleD3ye6v5IQ8ivEiHyvasIfkhNFGiIpXO_L769UK-z24OQU_A6th8ePN5MMyuDiBSpAGhMP7AwTUuCQf4BxnBBdBxei1UwkNXLs0gHHWYsBZY8ztIGJYJxjd4gxon29zgkrOz9vr2l-gTnGzjv4a1GxgcOcDBBd_gs1B2ucvqXADKiTMxbiIKiLY4Cd4F9QvNz4mD6waIz65q6fkx8cP388-F4cvn_Znbw-FLhuWipIh15Rhba3WzHSt6jS1XPG6ZDYrak4pWtPqvmooZWXPbat0LyrRqrqsdXlKnm99l-AvV4xJTi5qHEc1o1-jbGleJ-NdFtabUAcfY0Arl-CmPIRkVB7ByVtw8khFCiFvwUmWfc_uAtZ-QvOPayOVBW82AeYxrxwGGbU7Ltu4TCZJ491_Iv4Aplur9w</recordid><startdate>20000301</startdate><enddate>20000301</enddate><creator>Salazar, Luis A</creator><creator>Hirata, Mario H</creator><creator>Forti, Neusa</creator><creator>Diament, Jayme</creator><creator>Giannini, Sérgio D</creator><creator>Issa, Jaqueline S</creator><creator>Hirata, Rosario D.C</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>20000301</creationdate><title>Pvu II intron 15 polymorphism at the LDL receptor gene is associated with differences in serum lipid concentrations in subjects with low and high risk for coronary artery disease from Brazil</title><author>Salazar, Luis A ; Hirata, Mario H ; Forti, Neusa ; Diament, Jayme ; Giannini, Sérgio D ; Issa, Jaqueline S ; Hirata, Rosario D.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-31e2c01e5ffcc1d87a8c0f2a2531f3615200efd7cb460013b2f7acb9497a535c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alleles</topic><topic>Brazil</topic><topic>Cholesterol concentrations</topic><topic>Coronary artery disease</topic><topic>Coronary Disease - blood</topic><topic>Coronary Disease - genetics</topic><topic>Deoxyribonucleases, Type II Site-Specific - genetics</topic><topic>DNA - genetics</topic><topic>DNA - isolation & purification</topic><topic>Female</topic><topic>Genetics</topic><topic>Genotype</topic><topic>Humans</topic><topic>Introns - genetics</topic><topic>Lipids - blood</topic><topic>Low-density lipoprotein receptor gene</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Pvu II polymorphism</topic><topic>Receptors, LDL - genetics</topic><topic>Risk</topic><topic>Sex Characteristics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salazar, Luis A</creatorcontrib><creatorcontrib>Hirata, Mario H</creatorcontrib><creatorcontrib>Forti, Neusa</creatorcontrib><creatorcontrib>Diament, Jayme</creatorcontrib><creatorcontrib>Giannini, Sérgio D</creatorcontrib><creatorcontrib>Issa, Jaqueline S</creatorcontrib><creatorcontrib>Hirata, Rosario D.C</creatorcontrib><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>Clinica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salazar, Luis A</au><au>Hirata, Mario H</au><au>Forti, Neusa</au><au>Diament, Jayme</au><au>Giannini, Sérgio D</au><au>Issa, Jaqueline S</au><au>Hirata, Rosario D.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pvu II intron 15 polymorphism at the LDL receptor gene is associated with differences in serum lipid concentrations in subjects with low and high risk for coronary artery disease from Brazil</atitle><jtitle>Clinica chimica acta</jtitle><addtitle>Clin Chim Acta</addtitle><date>2000-03-01</date><risdate>2000</risdate><volume>293</volume><issue>1</issue><spage>75</spage><epage>88</epage><pages>75-88</pages><issn>0009-8981</issn><eissn>1873-3492</eissn><abstract>Coronary artery disease (CAD) has a high prevalence in the Brazilian population. Nevertheless, studies of genetic risk factors for CAD in this country have not been sufficiently conducted. We used the
Pvu II polymorphism (intron 15) at the low-density lipoprotein receptor (LDLR) gene to study the effect of variation at this locus in determining plasma lipid concentrations in 128 white subjects presenting a lipid profile suggesting high risk for CAD (HRG) and 100 white normolipidemic individuals (controls, CG). The
Pvu II polymorphism was detected by PCR–RFLP. The P1P1 genotype for
Pvu II polymorphism (homozygous for absence of restriction site) was greater in HRG individuals than in CG subjects (57% vs. 38%,
P<0.05). Moreover, the P1P1 genotype was strongly associated with high concentrations of total cholesterol (
P=0.0001), triglycerides (
P=0.0295), LDL-C (
P=0.0001), and VLDL-C concentrations (
P=0.0280) and lower HDL-C concentrations (
P=0.0051) in HRG subjects. Similarly, the CG individuals with P1P1 genotype presented high concentrations of total cholesterol and LDL-C compared to other genotypes (
P=0.0001). This study demonstrates the influence of
Pvu II polymorphism of the LDLR on serum lipid concentrations of individuals with low and high risk for CAD from Brazil.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>10699424</pmid><doi>10.1016/S0009-8981(99)00218-1</doi><tpages>14</tpages></addata></record> |
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subjects | Adult Aged Alleles Brazil Cholesterol concentrations Coronary artery disease Coronary Disease - blood Coronary Disease - genetics Deoxyribonucleases, Type II Site-Specific - genetics DNA - genetics DNA - isolation & purification Female Genetics Genotype Humans Introns - genetics Lipids - blood Low-density lipoprotein receptor gene Male Middle Aged Polymerase Chain Reaction Polymorphism, Genetic - genetics Polymorphism, Restriction Fragment Length Pvu II polymorphism Receptors, LDL - genetics Risk Sex Characteristics |
title | Pvu II intron 15 polymorphism at the LDL receptor gene is associated with differences in serum lipid concentrations in subjects with low and high risk for coronary artery disease from Brazil |
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