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Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study
BACKGROUND: High-density lipoprotein cholesterol (HDL-C) exerts many anti-atherogenic properties including its role in reverse cholesterol transport (RCT). Scavenger receptor class B member 1 (SCARB1) plays a key role in RCT by selective uptake of HDL cholesteryl esters. We aimed to explore the gene...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643515/ https://www.ncbi.nlm.nih.gov/pubmed/26563154 http://dx.doi.org/10.1186/s12881-015-0250-6 |
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author | Niemsiri, Vipavee Wang, Xingbin Pirim, Dilek Radwan, Zaheda H. Bunker, Clareann H. Barmada, M. Michael Kamboh, M. Ilyas Demirci, F. Yesim |
author_facet | Niemsiri, Vipavee Wang, Xingbin Pirim, Dilek Radwan, Zaheda H. Bunker, Clareann H. Barmada, M. Michael Kamboh, M. Ilyas Demirci, F. Yesim |
author_sort | Niemsiri, Vipavee |
collection | PubMed |
description | BACKGROUND: High-density lipoprotein cholesterol (HDL-C) exerts many anti-atherogenic properties including its role in reverse cholesterol transport (RCT). Scavenger receptor class B member 1 (SCARB1) plays a key role in RCT by selective uptake of HDL cholesteryl esters. We aimed to explore the genetic contribution of SCARB1 to affecting lipid levels in African Blacks from Nigeria. METHODS: We resequenced 13 exons and exon-intron boundaries of SCARB1 in 95 individuals with extreme HDL-C levels using Sanger method. Then, we genotyped 147 selected variants (78 sequence variants, 69 HapMap tagSNPs, and 2 previously reported relevant variants) in the entire sample of 788 African Blacks using either the iPLEX Gold or TaqMan methods. A total of 137 successfully genotyped variants were further evaluated for association with major lipid traits. RESULTS: The initial gene-based analysis demonstrated evidence of association with HDL-C and apolipoprotein A-I (ApoA-I). The follow-up single-site analysis revealed nominal evidence of novel associations of nine common variants with HDL-C and/or ApoA-I (P < 0.05). The strongest association was between rs11057851 and HDL-C (P = 0.0043), which remained significant after controlling for multiple testing using false discovery rate. Rare variant association testing revealed a group of 23 rare variants (frequencies ≤1 %) associated with HDL-C (P = 0.0478). Haplotype analysis identified four SCARB1 regions associated with HDL-C (global P < 0.05). CONCLUSIONS: To our knowledge, this is the first report of a comprehensive association study of SCARB1 variations with lipid traits in an African Black population. Our results showed the consistent association of SCARB1 variants with HDL-C across various association analyses, supporting the role of SCARB1 in lipoprotein-lipid regulatory mechanism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-015-0250-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4643515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46435152015-11-14 Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study Niemsiri, Vipavee Wang, Xingbin Pirim, Dilek Radwan, Zaheda H. Bunker, Clareann H. Barmada, M. Michael Kamboh, M. Ilyas Demirci, F. Yesim BMC Med Genet Research Article BACKGROUND: High-density lipoprotein cholesterol (HDL-C) exerts many anti-atherogenic properties including its role in reverse cholesterol transport (RCT). Scavenger receptor class B member 1 (SCARB1) plays a key role in RCT by selective uptake of HDL cholesteryl esters. We aimed to explore the genetic contribution of SCARB1 to affecting lipid levels in African Blacks from Nigeria. METHODS: We resequenced 13 exons and exon-intron boundaries of SCARB1 in 95 individuals with extreme HDL-C levels using Sanger method. Then, we genotyped 147 selected variants (78 sequence variants, 69 HapMap tagSNPs, and 2 previously reported relevant variants) in the entire sample of 788 African Blacks using either the iPLEX Gold or TaqMan methods. A total of 137 successfully genotyped variants were further evaluated for association with major lipid traits. RESULTS: The initial gene-based analysis demonstrated evidence of association with HDL-C and apolipoprotein A-I (ApoA-I). The follow-up single-site analysis revealed nominal evidence of novel associations of nine common variants with HDL-C and/or ApoA-I (P < 0.05). The strongest association was between rs11057851 and HDL-C (P = 0.0043), which remained significant after controlling for multiple testing using false discovery rate. Rare variant association testing revealed a group of 23 rare variants (frequencies ≤1 %) associated with HDL-C (P = 0.0478). Haplotype analysis identified four SCARB1 regions associated with HDL-C (global P < 0.05). CONCLUSIONS: To our knowledge, this is the first report of a comprehensive association study of SCARB1 variations with lipid traits in an African Black population. Our results showed the consistent association of SCARB1 variants with HDL-C across various association analyses, supporting the role of SCARB1 in lipoprotein-lipid regulatory mechanism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-015-0250-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-12 /pmc/articles/PMC4643515/ /pubmed/26563154 http://dx.doi.org/10.1186/s12881-015-0250-6 Text en © Niemsiri et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Niemsiri, Vipavee Wang, Xingbin Pirim, Dilek Radwan, Zaheda H. Bunker, Clareann H. Barmada, M. Michael Kamboh, M. Ilyas Demirci, F. Yesim Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title | Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title_full | Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title_fullStr | Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title_full_unstemmed | Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title_short | Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study |
title_sort | genetic contribution of scarb1 variants to lipid traits in african blacks: a candidate gene association study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643515/ https://www.ncbi.nlm.nih.gov/pubmed/26563154 http://dx.doi.org/10.1186/s12881-015-0250-6 |
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