Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination

Suzette J. Bielinski; James S. Pankow; Catherine Leiendecker Foster; Michael B. Miller; Paul N. Hopkins; John H. Eckfeldt; Jim Hixson; Yongmei Liu; Tom Register; Richard H. Myers; Donna K. Arnett

doi:10.1016/j.atherosclerosis.2007.10.006

Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination

Suzette J. Bielinski, James S. Pankow, Catherine Leiendecker Foster, Michael B. Miller, Paul N. Hopkins, John H. Eckfeldt, Jim Hixson, Yongmei Liu, Tom Register, Richard H. Myers, Donna K. Arnett

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Atherogenesis is a chronic inflammatory process in which intercellular adhesion molecule 1 (ICAM-1) plays a critical role. Circulating soluble ICAM-1 (sICAM-1) is thought to be the result of cleavage of membrane-bound ICAM-1 and its concentration in serum/plasma has been shown to be heritable. Genome-wide linkage scans were conducted for quantitative trait loci influencing sICAM-1. Phenotype and genetic marker data were available for 2617 white and 531 black individuals in the NHLBI Family Heart Study follow-up examination. Heritability for sICAM-1 was 0.39 in whites and 0.59 in blacks. Significant linkage was observed on chromosome 19 (LOD = 4.0 at 14 cM) in whites near the ICAM gene cluster that includes the structural gene for ICAM-1. The T-allele of ICAM-1 SNP rs5491 has been strongly associated with the specific sICAM-1 assay we used in our study. Through additional genotyping we were able to rule out rs5491 as the cause of the linkage finding. This study provides preliminary evidence linking genetic variation in the ICAM1 structural gene to circulating sICAM-1 levels.

Original language	English
Pages (from-to)	172-178
Number of pages	7
Journal	Atherosclerosis
Volume	199
Issue number	1
DOIs	https://doi.org/10.1016/j.atherosclerosis.2007.10.006
State	Published - Jul 2008

Bibliographical note

Funding Information:
We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (#5 T32 HL007972). Support was provided by the National Heart, Lung, and Blood Institute cooperative agreement grants U01 HL67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901, U01 HL67902. 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, U01 HL56569. This report is presented on behalf of the investigators of the NHLBI Family Heart Study. The investigators thank the study participants and staff for their valuable contributions.

Funding

We are grateful for resources from the University of Minnesota Supercomputing Institute, the NIH Training Grant in Cardiovascular Disease Genetic Epidemiology (#5 T32 HL007972). Support was provided by the National Heart, Lung, and Blood Institute cooperative agreement grants U01 HL67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901, U01 HL67902. 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, U01 HL56569. This report is presented on behalf of the investigators of the NHLBI Family Heart Study. The investigators thank the study participants and staff for their valuable contributions.

Funders	Funder number
National Institutes of Health (NIH)	5 T32 HL007972
National Heart, Lung, and Blood Institute (NHLBI)	U01 HL56568, U01 HL56569, U01 HL56563, U01 HL56564, U01 HL56565, U01 HL56567, U01 HL67897, U01 HL67896, U01 HL67895, U01 HL67894, U01 HL67893, U01HL056566, U01 HL67902, U01 HL67901, U01 HL67900, U01 HL67899, U01 HL67898
University of Minnesota, Minnesota Supercomputing Institute

Keywords

Atherosclerosis
ICAM gene cluster
Inflammation
Intercellular adhesion molecule-1
Linkage (genetics)

ASJC Scopus subject areas

Cardiology and Cardiovascular Medicine

Access to Document

10.1016/j.atherosclerosis.2007.10.006

Cite this

Bielinski, S. J., Pankow, J. S., Foster, C. L., Miller, M. B., Hopkins, P. N., Eckfeldt, J. H., Hixson, J., Liu, Y., Register, T., Myers, R. H., & Arnett, D. K. (2008). Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination. Atherosclerosis, 199(1), 172-178. https://doi.org/10.1016/j.atherosclerosis.2007.10.006

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title = "Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination",

abstract = "Atherogenesis is a chronic inflammatory process in which intercellular adhesion molecule 1 (ICAM-1) plays a critical role. Circulating soluble ICAM-1 (sICAM-1) is thought to be the result of cleavage of membrane-bound ICAM-1 and its concentration in serum/plasma has been shown to be heritable. Genome-wide linkage scans were conducted for quantitative trait loci influencing sICAM-1. Phenotype and genetic marker data were available for 2617 white and 531 black individuals in the NHLBI Family Heart Study follow-up examination. Heritability for sICAM-1 was 0.39 in whites and 0.59 in blacks. Significant linkage was observed on chromosome 19 (LOD = 4.0 at 14 cM) in whites near the ICAM gene cluster that includes the structural gene for ICAM-1. The T-allele of ICAM-1 SNP rs5491 has been strongly associated with the specific sICAM-1 assay we used in our study. Through additional genotyping we were able to rule out rs5491 as the cause of the linkage finding. This study provides preliminary evidence linking genetic variation in the ICAM1 structural gene to circulating sICAM-1 levels.",

keywords = "Atherosclerosis, ICAM gene cluster, Inflammation, Intercellular adhesion molecule-1, Linkage (genetics)",

author = "Bielinski, {Suzette J.} and Pankow, {James S.} and Foster, {Catherine Leiendecker} and Miller, {Michael B.} and Hopkins, {Paul N.} and Eckfeldt, {John H.} and Jim Hixson and Yongmei Liu and Tom Register and Myers, {Richard H.} and Arnett, {Donna 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 (#5 T32 HL007972). Support was provided by the National Heart, Lung, and Blood Institute cooperative agreement grants U01 HL67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901, U01 HL67902. 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, U01 HL56569. This report is presented on behalf of the investigators of the NHLBI Family Heart Study. The investigators thank the study participants and staff for their valuable contributions.",

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doi = "10.1016/j.atherosclerosis.2007.10.006",

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Bielinski, SJ, Pankow, JS, Foster, CL, Miller, MB, Hopkins, PN, Eckfeldt, JH, Hixson, J, Liu, Y, Register, T, Myers, RH & Arnett, DK 2008, 'Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination', Atherosclerosis, vol. 199, no. 1, pp. 172-178. https://doi.org/10.1016/j.atherosclerosis.2007.10.006

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T1 - Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19

T2 - The NHLBI Family Heart Study follow-up examination

AU - Bielinski, Suzette J.

AU - Pankow, James S.

AU - Foster, Catherine Leiendecker

AU - Miller, Michael B.

AU - Hopkins, Paul N.

AU - Eckfeldt, John H.

AU - Hixson, Jim

AU - Liu, Yongmei

AU - Register, Tom

AU - Myers, Richard H.

AU - Arnett, Donna 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 (#5 T32 HL007972). Support was provided by the National Heart, Lung, and Blood Institute cooperative agreement grants U01 HL67893, U01 HL67894, U01 HL67895, U01 HL67896, U01 HL67897, U01 HL67898, U01 HL67899, U01 HL67900, U01 HL67901, U01 HL67902. 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, U01 HL56569. This report is presented on behalf of the investigators of the NHLBI Family Heart Study. The investigators thank the study participants and staff for their valuable contributions.

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N2 - Atherogenesis is a chronic inflammatory process in which intercellular adhesion molecule 1 (ICAM-1) plays a critical role. Circulating soluble ICAM-1 (sICAM-1) is thought to be the result of cleavage of membrane-bound ICAM-1 and its concentration in serum/plasma has been shown to be heritable. Genome-wide linkage scans were conducted for quantitative trait loci influencing sICAM-1. Phenotype and genetic marker data were available for 2617 white and 531 black individuals in the NHLBI Family Heart Study follow-up examination. Heritability for sICAM-1 was 0.39 in whites and 0.59 in blacks. Significant linkage was observed on chromosome 19 (LOD = 4.0 at 14 cM) in whites near the ICAM gene cluster that includes the structural gene for ICAM-1. The T-allele of ICAM-1 SNP rs5491 has been strongly associated with the specific sICAM-1 assay we used in our study. Through additional genotyping we were able to rule out rs5491 as the cause of the linkage finding. This study provides preliminary evidence linking genetic variation in the ICAM1 structural gene to circulating sICAM-1 levels.

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KW - ICAM gene cluster

KW - Inflammation

KW - Intercellular adhesion molecule-1

KW - Linkage (genetics)

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Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: The NHLBI Family Heart Study follow-up examination

Abstract

Bibliographical note

Funding

Keywords

ASJC Scopus subject areas

Access to Document

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