Loading…
Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study
Increased serum levels of C-reactive protein (CRP), an important component of the innate immune response, are associated with increased risk of cardiovascular disease (CVD). Multiple single nucleotide polymorphisms (SNP) have been identified which are associated with CRP levels, and Mendelian random...
Saved in:
Published in: | PloS one 2019-10, Vol.14 (10), p.e0223574 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3 |
---|---|
cites | cdi_FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3 |
container_end_page | |
container_issue | 10 |
container_start_page | e0223574 |
container_title | PloS one |
container_volume | 14 |
creator | Best, Lyle G Balakrishnan, Poojitha Cole, Shelley A Haack, Karin Kocarnik, Jonathan M Pankratz, Nathan Anderson, Matthew Z Franceschini, Nora Howard, Barbara V Lee, Elisa T North, Kari E Umans, Jason G Yracheta, Joseph M Navas-Acien, Ana Voruganti, V Saroja |
description | Increased serum levels of C-reactive protein (CRP), an important component of the innate immune response, are associated with increased risk of cardiovascular disease (CVD). Multiple single nucleotide polymorphisms (SNP) have been identified which are associated with CRP levels, and Mendelian randomization studies have shown a positive association between SNPs increasing CRP expression and risk of colon cancer (but thus far not CVD). The effects of individual genetic variants often interact with the genetic background of a population and hence we sought to resolve the genetic determinants of serum CRP in a number of American Indian populations.
The Strong Heart Family Study (SHFS) has serum CRP measurements from 2428 tribal members, recruited as large families from three regions of the United States. Microsatellite markers and MetaboChip defined SNP genotypes were incorporated into variance components, decomposition-based linkage and association analyses.
CRP levels exhibited significant heritability (h2 = 0.33 ± 0.05, p |
doi_str_mv | 10.1371/journal.pone.0223574 |
format | article |
fullrecord | <record><control><sourceid>proquest_plos_</sourceid><recordid>TN_cdi_plos_journals_2306485733</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_f81e2a867967410f85431cd789fa8f34</doaj_id><sourcerecordid>2306485733</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3</originalsourceid><addsrcrecordid>eNp1kc1uEzEUhS0EoqXwBggssU6wfcc_wwKpimgbKRIIytryjO3E0cQO9qRS3h6XTKt2wcrW9TnfPfJB6D0lcwqSft6mQ45mmO9TdHPCGHDZvEDntAU2E4zAyyf3M_SmlC0hHJQQr9EZUFENsj1Hq2sX3Rh6bCrrWELByeNNWfz8gUPElzuXQ28iXkYbTCxf8O3G4V9jTnGNb5zJI74yuzAc6-xgj2_RK2-G4t5N5wX6ffXtdnEzW32_Xi4uV7OeMzHOWt5y7pw1RCkvO1pTMUW4aKSHxkPHCFcNs95y3lILHsB03HgloOsU63u4QB9P3P2Qip4-omgGRDSKS4CqWJ4UNpmt3uewM_mokwn63yDlta7hQz847RV1zCghWyEbSrziDdDeStV6o2qgyvo6bTt0O2d7F8dshmfQ5y8xbPQ63emKlJTxCvg0AXL6c3Bl_E_k5qTqcyolO_-4gRJ93_iDS983rqfGq-3D03SPpoeK4S_zDqgH</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2306485733</pqid></control><display><type>article</type><title>Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study</title><source>PubMed (Medline)</source><source>Publicly Available Content Database</source><creator>Best, Lyle G ; Balakrishnan, Poojitha ; Cole, Shelley A ; Haack, Karin ; Kocarnik, Jonathan M ; Pankratz, Nathan ; Anderson, Matthew Z ; Franceschini, Nora ; Howard, Barbara V ; Lee, Elisa T ; North, Kari E ; Umans, Jason G ; Yracheta, Joseph M ; Navas-Acien, Ana ; Voruganti, V Saroja</creator><contributor>Wang, Heming</contributor><creatorcontrib>Best, Lyle G ; Balakrishnan, Poojitha ; Cole, Shelley A ; Haack, Karin ; Kocarnik, Jonathan M ; Pankratz, Nathan ; Anderson, Matthew Z ; Franceschini, Nora ; Howard, Barbara V ; Lee, Elisa T ; North, Kari E ; Umans, Jason G ; Yracheta, Joseph M ; Navas-Acien, Ana ; Voruganti, V Saroja ; Wang, Heming</creatorcontrib><description>Increased serum levels of C-reactive protein (CRP), an important component of the innate immune response, are associated with increased risk of cardiovascular disease (CVD). Multiple single nucleotide polymorphisms (SNP) have been identified which are associated with CRP levels, and Mendelian randomization studies have shown a positive association between SNPs increasing CRP expression and risk of colon cancer (but thus far not CVD). The effects of individual genetic variants often interact with the genetic background of a population and hence we sought to resolve the genetic determinants of serum CRP in a number of American Indian populations.
The Strong Heart Family Study (SHFS) has serum CRP measurements from 2428 tribal members, recruited as large families from three regions of the United States. Microsatellite markers and MetaboChip defined SNP genotypes were incorporated into variance components, decomposition-based linkage and association analyses.
CRP levels exhibited significant heritability (h2 = 0.33 ± 0.05, p<1.3 X 10-20). A locus on chromosome (chr) 6, near marker D6S281 (approximately at 169.6 Mb, GRCh38/hg38) showed suggestive linkage (LOD = 1.9) to CRP levels. No individual SNPs were found associated with CRP levels after Bonferroni adjustment for multiple testing (threshold <7.77 x 10-7), however, we found nominal associations, many of which replicate previous findings at the CRP, HNF1A and 7 other loci. In addition, we report association of 46 SNPs located at 7 novel loci on chromosomes 2, 5, 6(2 loci), 9, 10 and 17, with an average of 15.3 Kb between SNPs and all with p-values less than 7.2 X 10-4.
In agreement with evidence from other populations, these data show CRP serum levels are under considerable genetic influence; and include loci, such as near CRP and other genes, that replicate results from other ethnic groups. These findings also suggest possible novel loci on chr 6 and other chromosomes that warrant further investigation.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0223574</identifier><identifier>PMID: 31622379</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>African Americans ; Alleles ; Biology and Life Sciences ; Biomarkers - blood ; Biomedical research ; C-reactive protein ; C-Reactive Protein - genetics ; Cancer ; Cardiovascular diseases ; Chromosomes ; Colon ; Colon cancer ; Diabetes ; Environmental health ; Family studies ; Female ; Gene loci ; Genetic analysis ; Genetic diversity ; Genetic Linkage ; Genetic markers ; Genetic Predisposition to Disease ; Genetic variance ; Genetic Variation ; Genetics, Population ; Genome-Wide Association Study ; Genomes ; Genomics ; Genotype ; Genotypes ; Health risks ; Health sciences ; Heart diseases ; Heritability ; Humans ; Immune response ; Indians, North American - genetics ; Influence ; Innate immunity ; Male ; Markers ; Medical research ; Medicine and Health Sciences ; Metabolism ; Microsatellites ; Minority & ethnic groups ; Native Americans ; Nucleotides ; Nutrition research ; Obesity ; Polymorphism, Single Nucleotide ; Population genetics ; Populations ; Proteins ; Public health ; Serum levels ; Single-nucleotide polymorphism ; Studies</subject><ispartof>PloS one, 2019-10, Vol.14 (10), p.e0223574</ispartof><rights>2019 Best et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Best et al 2019 Best et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3</citedby><cites>FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3</cites><orcidid>0000-0003-1683-2170 ; 0000-0002-7813-0724 ; 0000-0002-2746-3350</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2306485733/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2306485733?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,25740,27911,27912,36999,44577,53778,53780,74881</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31622379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Wang, Heming</contributor><creatorcontrib>Best, Lyle G</creatorcontrib><creatorcontrib>Balakrishnan, Poojitha</creatorcontrib><creatorcontrib>Cole, Shelley A</creatorcontrib><creatorcontrib>Haack, Karin</creatorcontrib><creatorcontrib>Kocarnik, Jonathan M</creatorcontrib><creatorcontrib>Pankratz, Nathan</creatorcontrib><creatorcontrib>Anderson, Matthew Z</creatorcontrib><creatorcontrib>Franceschini, Nora</creatorcontrib><creatorcontrib>Howard, Barbara V</creatorcontrib><creatorcontrib>Lee, Elisa T</creatorcontrib><creatorcontrib>North, Kari E</creatorcontrib><creatorcontrib>Umans, Jason G</creatorcontrib><creatorcontrib>Yracheta, Joseph M</creatorcontrib><creatorcontrib>Navas-Acien, Ana</creatorcontrib><creatorcontrib>Voruganti, V Saroja</creatorcontrib><title>Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Increased serum levels of C-reactive protein (CRP), an important component of the innate immune response, are associated with increased risk of cardiovascular disease (CVD). Multiple single nucleotide polymorphisms (SNP) have been identified which are associated with CRP levels, and Mendelian randomization studies have shown a positive association between SNPs increasing CRP expression and risk of colon cancer (but thus far not CVD). The effects of individual genetic variants often interact with the genetic background of a population and hence we sought to resolve the genetic determinants of serum CRP in a number of American Indian populations.
The Strong Heart Family Study (SHFS) has serum CRP measurements from 2428 tribal members, recruited as large families from three regions of the United States. Microsatellite markers and MetaboChip defined SNP genotypes were incorporated into variance components, decomposition-based linkage and association analyses.
CRP levels exhibited significant heritability (h2 = 0.33 ± 0.05, p<1.3 X 10-20). A locus on chromosome (chr) 6, near marker D6S281 (approximately at 169.6 Mb, GRCh38/hg38) showed suggestive linkage (LOD = 1.9) to CRP levels. No individual SNPs were found associated with CRP levels after Bonferroni adjustment for multiple testing (threshold <7.77 x 10-7), however, we found nominal associations, many of which replicate previous findings at the CRP, HNF1A and 7 other loci. In addition, we report association of 46 SNPs located at 7 novel loci on chromosomes 2, 5, 6(2 loci), 9, 10 and 17, with an average of 15.3 Kb between SNPs and all with p-values less than 7.2 X 10-4.
In agreement with evidence from other populations, these data show CRP serum levels are under considerable genetic influence; and include loci, such as near CRP and other genes, that replicate results from other ethnic groups. These findings also suggest possible novel loci on chr 6 and other chromosomes that warrant further investigation.</description><subject>African Americans</subject><subject>Alleles</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers - blood</subject><subject>Biomedical research</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - genetics</subject><subject>Cancer</subject><subject>Cardiovascular diseases</subject><subject>Chromosomes</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Diabetes</subject><subject>Environmental health</subject><subject>Family studies</subject><subject>Female</subject><subject>Gene loci</subject><subject>Genetic analysis</subject><subject>Genetic diversity</subject><subject>Genetic Linkage</subject><subject>Genetic markers</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetic variance</subject><subject>Genetic Variation</subject><subject>Genetics, Population</subject><subject>Genome-Wide Association Study</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Health risks</subject><subject>Health sciences</subject><subject>Heart diseases</subject><subject>Heritability</subject><subject>Humans</subject><subject>Immune response</subject><subject>Indians, North American - genetics</subject><subject>Influence</subject><subject>Innate immunity</subject><subject>Male</subject><subject>Markers</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Metabolism</subject><subject>Microsatellites</subject><subject>Minority & ethnic groups</subject><subject>Native Americans</subject><subject>Nucleotides</subject><subject>Nutrition research</subject><subject>Obesity</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Proteins</subject><subject>Public health</subject><subject>Serum levels</subject><subject>Single-nucleotide polymorphism</subject><subject>Studies</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kc1uEzEUhS0EoqXwBggssU6wfcc_wwKpimgbKRIIytryjO3E0cQO9qRS3h6XTKt2wcrW9TnfPfJB6D0lcwqSft6mQ45mmO9TdHPCGHDZvEDntAU2E4zAyyf3M_SmlC0hHJQQr9EZUFENsj1Hq2sX3Rh6bCrrWELByeNNWfz8gUPElzuXQ28iXkYbTCxf8O3G4V9jTnGNb5zJI74yuzAc6-xgj2_RK2-G4t5N5wX6ffXtdnEzW32_Xi4uV7OeMzHOWt5y7pw1RCkvO1pTMUW4aKSHxkPHCFcNs95y3lILHsB03HgloOsU63u4QB9P3P2Qip4-omgGRDSKS4CqWJ4UNpmt3uewM_mokwn63yDlta7hQz847RV1zCghWyEbSrziDdDeStV6o2qgyvo6bTt0O2d7F8dshmfQ5y8xbPQ63emKlJTxCvg0AXL6c3Bl_E_k5qTqcyolO_-4gRJ93_iDS983rqfGq-3D03SPpoeK4S_zDqgH</recordid><startdate>20191017</startdate><enddate>20191017</enddate><creator>Best, Lyle G</creator><creator>Balakrishnan, Poojitha</creator><creator>Cole, Shelley A</creator><creator>Haack, Karin</creator><creator>Kocarnik, Jonathan M</creator><creator>Pankratz, Nathan</creator><creator>Anderson, Matthew Z</creator><creator>Franceschini, Nora</creator><creator>Howard, Barbara V</creator><creator>Lee, Elisa T</creator><creator>North, Kari E</creator><creator>Umans, Jason G</creator><creator>Yracheta, Joseph M</creator><creator>Navas-Acien, Ana</creator><creator>Voruganti, V Saroja</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1683-2170</orcidid><orcidid>https://orcid.org/0000-0002-7813-0724</orcidid><orcidid>https://orcid.org/0000-0002-2746-3350</orcidid></search><sort><creationdate>20191017</creationdate><title>Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study</title><author>Best, Lyle G ; Balakrishnan, Poojitha ; Cole, Shelley A ; Haack, Karin ; Kocarnik, Jonathan M ; Pankratz, Nathan ; Anderson, Matthew Z ; Franceschini, Nora ; Howard, Barbara V ; Lee, Elisa T ; North, Kari E ; Umans, Jason G ; Yracheta, Joseph M ; Navas-Acien, Ana ; Voruganti, V Saroja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>African Americans</topic><topic>Alleles</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers - blood</topic><topic>Biomedical research</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - genetics</topic><topic>Cancer</topic><topic>Cardiovascular diseases</topic><topic>Chromosomes</topic><topic>Colon</topic><topic>Colon cancer</topic><topic>Diabetes</topic><topic>Environmental health</topic><topic>Family studies</topic><topic>Female</topic><topic>Gene loci</topic><topic>Genetic analysis</topic><topic>Genetic diversity</topic><topic>Genetic Linkage</topic><topic>Genetic markers</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetic variance</topic><topic>Genetic Variation</topic><topic>Genetics, Population</topic><topic>Genome-Wide Association Study</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Health risks</topic><topic>Health sciences</topic><topic>Heart diseases</topic><topic>Heritability</topic><topic>Humans</topic><topic>Immune response</topic><topic>Indians, North American - genetics</topic><topic>Influence</topic><topic>Innate immunity</topic><topic>Male</topic><topic>Markers</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Metabolism</topic><topic>Microsatellites</topic><topic>Minority & ethnic groups</topic><topic>Native Americans</topic><topic>Nucleotides</topic><topic>Nutrition research</topic><topic>Obesity</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Population genetics</topic><topic>Populations</topic><topic>Proteins</topic><topic>Public health</topic><topic>Serum levels</topic><topic>Single-nucleotide polymorphism</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Best, Lyle G</creatorcontrib><creatorcontrib>Balakrishnan, Poojitha</creatorcontrib><creatorcontrib>Cole, Shelley A</creatorcontrib><creatorcontrib>Haack, Karin</creatorcontrib><creatorcontrib>Kocarnik, Jonathan M</creatorcontrib><creatorcontrib>Pankratz, Nathan</creatorcontrib><creatorcontrib>Anderson, Matthew Z</creatorcontrib><creatorcontrib>Franceschini, Nora</creatorcontrib><creatorcontrib>Howard, Barbara V</creatorcontrib><creatorcontrib>Lee, Elisa T</creatorcontrib><creatorcontrib>North, Kari E</creatorcontrib><creatorcontrib>Umans, Jason G</creatorcontrib><creatorcontrib>Yracheta, Joseph M</creatorcontrib><creatorcontrib>Navas-Acien, Ana</creatorcontrib><creatorcontrib>Voruganti, V Saroja</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 Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Databases</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Best, Lyle G</au><au>Balakrishnan, Poojitha</au><au>Cole, Shelley A</au><au>Haack, Karin</au><au>Kocarnik, Jonathan M</au><au>Pankratz, Nathan</au><au>Anderson, Matthew Z</au><au>Franceschini, Nora</au><au>Howard, Barbara V</au><au>Lee, Elisa T</au><au>North, Kari E</au><au>Umans, Jason G</au><au>Yracheta, Joseph M</au><au>Navas-Acien, Ana</au><au>Voruganti, V Saroja</au><au>Wang, Heming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2019-10-17</date><risdate>2019</risdate><volume>14</volume><issue>10</issue><spage>e0223574</spage><pages>e0223574-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Increased serum levels of C-reactive protein (CRP), an important component of the innate immune response, are associated with increased risk of cardiovascular disease (CVD). Multiple single nucleotide polymorphisms (SNP) have been identified which are associated with CRP levels, and Mendelian randomization studies have shown a positive association between SNPs increasing CRP expression and risk of colon cancer (but thus far not CVD). The effects of individual genetic variants often interact with the genetic background of a population and hence we sought to resolve the genetic determinants of serum CRP in a number of American Indian populations.
The Strong Heart Family Study (SHFS) has serum CRP measurements from 2428 tribal members, recruited as large families from three regions of the United States. Microsatellite markers and MetaboChip defined SNP genotypes were incorporated into variance components, decomposition-based linkage and association analyses.
CRP levels exhibited significant heritability (h2 = 0.33 ± 0.05, p<1.3 X 10-20). A locus on chromosome (chr) 6, near marker D6S281 (approximately at 169.6 Mb, GRCh38/hg38) showed suggestive linkage (LOD = 1.9) to CRP levels. No individual SNPs were found associated with CRP levels after Bonferroni adjustment for multiple testing (threshold <7.77 x 10-7), however, we found nominal associations, many of which replicate previous findings at the CRP, HNF1A and 7 other loci. In addition, we report association of 46 SNPs located at 7 novel loci on chromosomes 2, 5, 6(2 loci), 9, 10 and 17, with an average of 15.3 Kb between SNPs and all with p-values less than 7.2 X 10-4.
In agreement with evidence from other populations, these data show CRP serum levels are under considerable genetic influence; and include loci, such as near CRP and other genes, that replicate results from other ethnic groups. These findings also suggest possible novel loci on chr 6 and other chromosomes that warrant further investigation.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31622379</pmid><doi>10.1371/journal.pone.0223574</doi><orcidid>https://orcid.org/0000-0003-1683-2170</orcidid><orcidid>https://orcid.org/0000-0002-7813-0724</orcidid><orcidid>https://orcid.org/0000-0002-2746-3350</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2019-10, Vol.14 (10), p.e0223574 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2306485733 |
source | PubMed (Medline); Publicly Available Content Database |
subjects | African Americans Alleles Biology and Life Sciences Biomarkers - blood Biomedical research C-reactive protein C-Reactive Protein - genetics Cancer Cardiovascular diseases Chromosomes Colon Colon cancer Diabetes Environmental health Family studies Female Gene loci Genetic analysis Genetic diversity Genetic Linkage Genetic markers Genetic Predisposition to Disease Genetic variance Genetic Variation Genetics, Population Genome-Wide Association Study Genomes Genomics Genotype Genotypes Health risks Health sciences Heart diseases Heritability Humans Immune response Indians, North American - genetics Influence Innate immunity Male Markers Medical research Medicine and Health Sciences Metabolism Microsatellites Minority & ethnic groups Native Americans Nucleotides Nutrition research Obesity Polymorphism, Single Nucleotide Population genetics Populations Proteins Public health Serum levels Single-nucleotide polymorphism Studies |
title | Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T23%3A36%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20analysis%20of%20hsCRP%20in%20American%20Indians:%20The%20Strong%20Heart%20Family%20Study&rft.jtitle=PloS%20one&rft.au=Best,%20Lyle%20G&rft.date=2019-10-17&rft.volume=14&rft.issue=10&rft.spage=e0223574&rft.pages=e0223574-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0223574&rft_dat=%3Cproquest_plos_%3E2306485733%3C/proquest_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c526t-95955eeda088f7b15382805647f34f3b205842dfd5591d3f33ab5af863bb82cc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2306485733&rft_id=info:pmid/31622379&rfr_iscdi=true |