Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits

Copy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of CNVs in coronary heart disease (CHD) traits has been limited. We examined the use of the cnvHap algorithm for CNV detection, using data for...

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Published in:Circulation. Cardiovascular genetics Vol. 5; no. 5; p. 555
Main Authors: Costelloe, Seán J, El-Sayed Moustafa, Julia S, Drenos, Fotios, Palmen, Jutta, Li, Qiao, Qiao, Li, Whiting, Stephen, Thomas, Michael, Kivimaki, Mika, Kumari, Meena, Hingorani, Aroon D, Tzoulaki, Ioanna, Järvelin, Marjo-Riitta, Marjo-Riitta, Järvelin, Ruokonen, Aimo, Aimo, Ruokonen, Hartikainen, Anna-Liisa, Pouta, Anneli, Walters, Robin G, Blakemore, Alexandra I F, Humphries, Steve E, Coin, Lachlan J M, Talmud, Philippa J
Format: Journal Article
Language:English
Published: United States 01.10.2012
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ISSN:1942-3268, 1942-3268
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Abstract Copy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of CNVs in coronary heart disease (CHD) traits has been limited. We examined the use of the cnvHap algorithm for CNV detection, using data for 2500 men from the Second Northwick Park Heart Study (NPHS-II). An Illumina custom chip, including 722 single-nucleotide polymorphisms covering 76 coronary heart disease-trait genes, was used. Common CNVs were significantly associated (at P<0.05, after correction) with coronary heart disease phenotypes in 5 genes. Novel associations of CNVs in toll-like receptor-4 with apolipoprotein AI were replicated (P<0.05) in the Whitehall II cohort (4887 subjects), whereas newly described associations of CNVs in sterol regulatory element-binding protein with apolipoprotein AI and associations of interleukin-6 signal transducer with apolipoprotein B were replicated in the data from 3546 subjects from the North Finnish Birth Cohort 1966 (P<0.05). This study supports the use of CNV detection algorithms such as cnvHap as potential tools for the identification of novel CNVs, some of which show significant association and replication with coronary heart disease risk phenotypes. However, the functional basis for these associations requires further substantiation.
AbstractList Copy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of CNVs in coronary heart disease (CHD) traits has been limited. We examined the use of the cnvHap algorithm for CNV detection, using data for 2500 men from the Second Northwick Park Heart Study (NPHS-II). An Illumina custom chip, including 722 single-nucleotide polymorphisms covering 76 coronary heart disease-trait genes, was used. Common CNVs were significantly associated (at P<0.05, after correction) with coronary heart disease phenotypes in 5 genes. Novel associations of CNVs in toll-like receptor-4 with apolipoprotein AI were replicated (P<0.05) in the Whitehall II cohort (4887 subjects), whereas newly described associations of CNVs in sterol regulatory element-binding protein with apolipoprotein AI and associations of interleukin-6 signal transducer with apolipoprotein B were replicated in the data from 3546 subjects from the North Finnish Birth Cohort 1966 (P<0.05). This study supports the use of CNV detection algorithms such as cnvHap as potential tools for the identification of novel CNVs, some of which show significant association and replication with coronary heart disease risk phenotypes. However, the functional basis for these associations requires further substantiation.
Copy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of CNVs in coronary heart disease (CHD) traits has been limited.BACKGROUNDCopy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of CNVs in coronary heart disease (CHD) traits has been limited.We examined the use of the cnvHap algorithm for CNV detection, using data for 2500 men from the Second Northwick Park Heart Study (NPHS-II). An Illumina custom chip, including 722 single-nucleotide polymorphisms covering 76 coronary heart disease-trait genes, was used. Common CNVs were significantly associated (at P<0.05, after correction) with coronary heart disease phenotypes in 5 genes. Novel associations of CNVs in toll-like receptor-4 with apolipoprotein AI were replicated (P<0.05) in the Whitehall II cohort (4887 subjects), whereas newly described associations of CNVs in sterol regulatory element-binding protein with apolipoprotein AI and associations of interleukin-6 signal transducer with apolipoprotein B were replicated in the data from 3546 subjects from the North Finnish Birth Cohort 1966 (P<0.05).METHODS AND RESULTSWe examined the use of the cnvHap algorithm for CNV detection, using data for 2500 men from the Second Northwick Park Heart Study (NPHS-II). An Illumina custom chip, including 722 single-nucleotide polymorphisms covering 76 coronary heart disease-trait genes, was used. Common CNVs were significantly associated (at P<0.05, after correction) with coronary heart disease phenotypes in 5 genes. Novel associations of CNVs in toll-like receptor-4 with apolipoprotein AI were replicated (P<0.05) in the Whitehall II cohort (4887 subjects), whereas newly described associations of CNVs in sterol regulatory element-binding protein with apolipoprotein AI and associations of interleukin-6 signal transducer with apolipoprotein B were replicated in the data from 3546 subjects from the North Finnish Birth Cohort 1966 (P<0.05).This study supports the use of CNV detection algorithms such as cnvHap as potential tools for the identification of novel CNVs, some of which show significant association and replication with coronary heart disease risk phenotypes. However, the functional basis for these associations requires further substantiation.CONCLUSIONSThis study supports the use of CNV detection algorithms such as cnvHap as potential tools for the identification of novel CNVs, some of which show significant association and replication with coronary heart disease risk phenotypes. However, the functional basis for these associations requires further substantiation.
Author Ruokonen, Aimo
Kumari, Meena
Pouta, Anneli
Costelloe, Seán J
Drenos, Fotios
Thomas, Michael
Järvelin, Marjo-Riitta
Aimo, Ruokonen
Kivimaki, Mika
Talmud, Philippa J
Walters, Robin G
Li, Qiao
Marjo-Riitta, Järvelin
Qiao, Li
Tzoulaki, Ioanna
Hartikainen, Anna-Liisa
Whiting, Stephen
Humphries, Steve E
El-Sayed Moustafa, Julia S
Hingorani, Aroon D
Coin, Lachlan J M
Palmen, Jutta
Blakemore, Alexandra I F
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crossref_primary_10_1161_CIRCULATIONAHA_113_002997
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Snippet Copy number variants (CNVs) are a major form of genomic variation, which may be implicated in complex disease phenotypes. However, investigation of the role of...
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SubjectTerms Algorithms
Apolipoprotein A-I - genetics
Apolipoprotein A-I - metabolism
Apolipoproteins B - genetics
Apolipoproteins B - metabolism
Cohort Studies
Coronary Disease - genetics
DNA Copy Number Variations
Genome, Human
Genotype
Humans
Interleukin-6 - genetics
Interleukin-6 - metabolism
Phenotype
Polymorphism, Single Nucleotide
Sterol Regulatory Element Binding Protein 1 - genetics
Sterol Regulatory Element Binding Protein 1 - metabolism
Toll-Like Receptor 4 - genetics
Toll-Like Receptor 4 - metabolism
Title Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits
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