Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: The NHLBI Family Heart Study follow-up examination

S. J. Bielinski; J. S. Pankow; M. B. Miller; P. N. Hopkins; J. H. Eckfeldt; J. Hixson; Y. Liu; T. Register; R. H. Myers; D. K. Arnett

doi:10.1038/sj.gene.6364434

Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: The NHLBI Family Heart Study follow-up examination

S. J. Bielinski, J. S. Pankow, M. B. Miller, P. N. Hopkins, J. H. Eckfeldt, J. Hixson, Y. Liu, T. Register, R. H. Myers, D. K. Arnett

Producción científica: Article › revisión exhaustiva

18 Citas (Scopus)

Resumen

Atherogenesis is a chronic inflammatory process. Critical in the inflammation process is monocyte chemoattractant protein-1 (MCP-1). To locate genomic regions that affect circulating MCP-1 levels, a genome-wide linkage scan was conducted in a sample of whites and blacks. Phenotype and genetic marker data were available for 2501 white and 513 black participants in the National Heart Lung Blood Institute Family Heart Study follow-up examination. Heritability for MCP-1 was 0.37 in whites and 0.47 in blacks after adjusting for the effects of sex, age, age-sex interaction, smoking status, lifetime smoking exposure (pack-years) and field center. Significant linkage was observed for MCP-1 in a combined black and white sample on chromosome 3 (logarithm of the odds ratio (LOD)=3.5 at 78cM, P=0.0001) and suggestive linkage was observed in whites on chromosome 5 (LOD=1.8 at 128cM, P=0.002). Located under the linkage peak on chromosome 3 is the chemokine receptor gene cluster, including CCR2, the receptor for MCP-1. This study provides preliminary evidence linking genetic variation in a receptor to circulating levels of its ligand, as previously demonstrated for the low-density lipoprotein receptor. Further characterization of these chromosomal regions is needed to identify the functional mutations associated with circulating levels of MCP-1.

Idioma original	English
Páginas (desde-hasta)	684-690
Número de páginas	7
Publicación	Genes and Immunity
Volumen	8
N.º	8
DOI	https://doi.org/10.1038/sj.gene.6364434
Estado	Published - dic 2007

Nota bibliográfica

Funding Information:
We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (no. 5 T32 HL007972) and the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL 67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901 and U01 HL67902. Financial support was also partially provided by the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56566, U01 HL56567, U01 HL56568 and U01 HL56569. This report is presented on behalf of the investigators of the NHLBI FHS. The investigators thank the study participants and staff for their valuable contributions.

Financiación

We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (no. 5 T32 HL007972) and the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL 67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901 and U01 HL67902. Financial support was also partially provided by the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56566, U01 HL56567, U01 HL56568 and U01 HL56569. This report is presented on behalf of the investigators of the NHLBI FHS. The investigators thank the study participants and staff for their valuable contributions.

Financiadores	Número del financiador
National Institutes of Health (NIH)	5 T32 HL007972
National Heart, Lung, and Blood Institute (NHLBI)	U01 HL56569, U01HL056568, U01 HL 67893, U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56566, U01 HL56567, U01 HL67897, U01 HL67896, U01 HL67895, U01 HL67894, U01 HL67902, U01 HL67901, U01 HL67900, U01 HL67899, U01 HL67898
University of Minnesota, Minnesota Supercomputing Institute

ASJC Scopus subject areas

Immunology
Genetics
Genetics(clinical)

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10.1038/sj.gene.6364434

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Bielinski, S. J., Pankow, J. S., Miller, M. B., Hopkins, P. N., Eckfeldt, J. H., Hixson, J., Liu, Y., Register, T., Myers, R. H., & Arnett, D. K. (2007). Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: The NHLBI Family Heart Study follow-up examination. Genes and Immunity, 8(8), 684-690. https://doi.org/10.1038/sj.gene.6364434

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title = "Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: The NHLBI Family Heart Study follow-up examination",

abstract = "Atherogenesis is a chronic inflammatory process. Critical in the inflammation process is monocyte chemoattractant protein-1 (MCP-1). To locate genomic regions that affect circulating MCP-1 levels, a genome-wide linkage scan was conducted in a sample of whites and blacks. Phenotype and genetic marker data were available for 2501 white and 513 black participants in the National Heart Lung Blood Institute Family Heart Study follow-up examination. Heritability for MCP-1 was 0.37 in whites and 0.47 in blacks after adjusting for the effects of sex, age, age-sex interaction, smoking status, lifetime smoking exposure (pack-years) and field center. Significant linkage was observed for MCP-1 in a combined black and white sample on chromosome 3 (logarithm of the odds ratio (LOD)=3.5 at 78cM, P=0.0001) and suggestive linkage was observed in whites on chromosome 5 (LOD=1.8 at 128cM, P=0.002). Located under the linkage peak on chromosome 3 is the chemokine receptor gene cluster, including CCR2, the receptor for MCP-1. This study provides preliminary evidence linking genetic variation in a receptor to circulating levels of its ligand, as previously demonstrated for the low-density lipoprotein receptor. Further characterization of these chromosomal regions is needed to identify the functional mutations associated with circulating levels of MCP-1.",

author = "Bielinski, \{S. J.\} and Pankow, \{J. S.\} and Miller, \{M. B.\} and Hopkins, \{P. N.\} and Eckfeldt, \{J. H.\} and J. Hixson and Y. Liu and T. Register and Myers, \{R. H.\} and Arnett, \{D. K.\}",

note = "Funding Information: We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (no. 5 T32 HL007972) and the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL 67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901 and U01 HL67902. Financial support was also partially provided by the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56566, U01 HL56567, U01 HL56568 and U01 HL56569. This report is presented on behalf of the investigators of the NHLBI FHS. The investigators thank the study participants and staff for their valuable contributions.",

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doi = "10.1038/sj.gene.6364434",

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T1 - Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3

T2 - The NHLBI Family Heart Study follow-up examination

AU - Bielinski, S. J.

AU - Pankow, J. S.

AU - Miller, M. B.

AU - Hopkins, P. N.

AU - Eckfeldt, J. H.

AU - Hixson, J.

AU - Liu, Y.

AU - Register, T.

AU - Myers, R. H.

AU - Arnett, D. K.

N1 - Funding Information: We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (no. 5 T32 HL007972) and the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL 67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901 and U01 HL67902. Financial support was also partially provided by the National Heart, Lung and Blood Institute cooperative agreement Grants U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56566, U01 HL56567, U01 HL56568 and U01 HL56569. This report is presented on behalf of the investigators of the NHLBI FHS. The investigators thank the study participants and staff for their valuable contributions.

PY - 2007/12

Y1 - 2007/12

N2 - Atherogenesis is a chronic inflammatory process. Critical in the inflammation process is monocyte chemoattractant protein-1 (MCP-1). To locate genomic regions that affect circulating MCP-1 levels, a genome-wide linkage scan was conducted in a sample of whites and blacks. Phenotype and genetic marker data were available for 2501 white and 513 black participants in the National Heart Lung Blood Institute Family Heart Study follow-up examination. Heritability for MCP-1 was 0.37 in whites and 0.47 in blacks after adjusting for the effects of sex, age, age-sex interaction, smoking status, lifetime smoking exposure (pack-years) and field center. Significant linkage was observed for MCP-1 in a combined black and white sample on chromosome 3 (logarithm of the odds ratio (LOD)=3.5 at 78cM, P=0.0001) and suggestive linkage was observed in whites on chromosome 5 (LOD=1.8 at 128cM, P=0.002). Located under the linkage peak on chromosome 3 is the chemokine receptor gene cluster, including CCR2, the receptor for MCP-1. This study provides preliminary evidence linking genetic variation in a receptor to circulating levels of its ligand, as previously demonstrated for the low-density lipoprotein receptor. Further characterization of these chromosomal regions is needed to identify the functional mutations associated with circulating levels of MCP-1.

AB - Atherogenesis is a chronic inflammatory process. Critical in the inflammation process is monocyte chemoattractant protein-1 (MCP-1). To locate genomic regions that affect circulating MCP-1 levels, a genome-wide linkage scan was conducted in a sample of whites and blacks. Phenotype and genetic marker data were available for 2501 white and 513 black participants in the National Heart Lung Blood Institute Family Heart Study follow-up examination. Heritability for MCP-1 was 0.37 in whites and 0.47 in blacks after adjusting for the effects of sex, age, age-sex interaction, smoking status, lifetime smoking exposure (pack-years) and field center. Significant linkage was observed for MCP-1 in a combined black and white sample on chromosome 3 (logarithm of the odds ratio (LOD)=3.5 at 78cM, P=0.0001) and suggestive linkage was observed in whites on chromosome 5 (LOD=1.8 at 128cM, P=0.002). Located under the linkage peak on chromosome 3 is the chemokine receptor gene cluster, including CCR2, the receptor for MCP-1. This study provides preliminary evidence linking genetic variation in a receptor to circulating levels of its ligand, as previously demonstrated for the low-density lipoprotein receptor. Further characterization of these chromosomal regions is needed to identify the functional mutations associated with circulating levels of MCP-1.

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Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: The NHLBI Family Heart Study follow-up examination

Resumen

Nota bibliográfica

Financiación

ASJC Scopus subject areas

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