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Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury
Background: Human cytomegalovirus (HCMV) infects ~50% of adults in the United States. HCMV infections may cause vascular inflammation leading to cardiovascular disease, but the existing evidence is inconsistent. Objective: We investigated demographic predictors of HCMV infection and explored associa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363776/ https://www.ncbi.nlm.nih.gov/pubmed/32733818 http://dx.doi.org/10.3389/fcimb.2020.00334 |
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author | Styles, Jennifer N. Converse, Reagan R. Griffin, Shannon M. Wade, Timothy J. Klein, Elizabeth Nylander-French, Leena A. Stewart, Jill R. Sams, Elizabeth Hudgens, Edward Egorov, Andrey I. |
author_facet | Styles, Jennifer N. Converse, Reagan R. Griffin, Shannon M. Wade, Timothy J. Klein, Elizabeth Nylander-French, Leena A. Stewart, Jill R. Sams, Elizabeth Hudgens, Edward Egorov, Andrey I. |
author_sort | Styles, Jennifer N. |
collection | PubMed |
description | Background: Human cytomegalovirus (HCMV) infects ~50% of adults in the United States. HCMV infections may cause vascular inflammation leading to cardiovascular disease, but the existing evidence is inconsistent. Objective: We investigated demographic predictors of HCMV infection and explored associations between HCMV infection status, the intensity of anti-HCMV Immunoglobulin G (IgG) antibody response, and biomarkers of inflammation and endothelial function which are known predictors of cardiovascular disease. Methods: We conducted a cross-sectional study of 694 adults residing in the Raleigh-Durham-Chapel Hill, NC metropolitan area. Serum samples were tested for IgG antibody response to HCMV, and for biomarkers of vascular injury including soluble intercellular adhesion molecule 1 (sICAM-1), soluble vascular cell adhesion molecule 1 (sVCAM-1), C-reactive protein (CRP), and serum amyloid A (SAA). Associations between HCMV and biomarker levels were analyzed using two approaches with HCMV serostatus modeled as a binary variable and as an ordinal variable with five categories comprised of seronegative individuals and quartiles of anti-HCMV antibody responses in seropositive individuals. Results: HCMV seroprevalence in the study population was 56%. Increased body mass index, increased age, female gender, racial/ethnic minority status, and current smoking were significantly associated with HCMV seropositivity in a multivariate regression analysis. HCMV seropositivity was also associated with 9% (95% confidence interval 4–15%) and 20% (0.3–44%) increases in median levels of sICAM-1 and CRP, respectively, after adjusting for covariates. The association between HCMV seropositivity and median levels of sVCAM-1 and SAA were positive but not statistically significant. Significant positive associations were observed between the intensity of anti-HCMV IgG responses and levels of sICAM-1 and sVCAM-1 (p-values 0.0008 and 0.04 for linear trend, respectively). To our knowledge, this is the first epidemiological study to show a relationship between anti-HCMV IgG responses and vascular injury biomarkers sICAM-1 and sVCAM-1 in the general population. Conclusion: HCMV infections are associated with vascular injury and inflammation biomarkers in adult residents of North Carolina. |
format | Online Article Text |
id | pubmed-7363776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73637762020-07-29 Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury Styles, Jennifer N. Converse, Reagan R. Griffin, Shannon M. Wade, Timothy J. Klein, Elizabeth Nylander-French, Leena A. Stewart, Jill R. Sams, Elizabeth Hudgens, Edward Egorov, Andrey I. Front Cell Infect Microbiol Cellular and Infection Microbiology Background: Human cytomegalovirus (HCMV) infects ~50% of adults in the United States. HCMV infections may cause vascular inflammation leading to cardiovascular disease, but the existing evidence is inconsistent. Objective: We investigated demographic predictors of HCMV infection and explored associations between HCMV infection status, the intensity of anti-HCMV Immunoglobulin G (IgG) antibody response, and biomarkers of inflammation and endothelial function which are known predictors of cardiovascular disease. Methods: We conducted a cross-sectional study of 694 adults residing in the Raleigh-Durham-Chapel Hill, NC metropolitan area. Serum samples were tested for IgG antibody response to HCMV, and for biomarkers of vascular injury including soluble intercellular adhesion molecule 1 (sICAM-1), soluble vascular cell adhesion molecule 1 (sVCAM-1), C-reactive protein (CRP), and serum amyloid A (SAA). Associations between HCMV and biomarker levels were analyzed using two approaches with HCMV serostatus modeled as a binary variable and as an ordinal variable with five categories comprised of seronegative individuals and quartiles of anti-HCMV antibody responses in seropositive individuals. Results: HCMV seroprevalence in the study population was 56%. Increased body mass index, increased age, female gender, racial/ethnic minority status, and current smoking were significantly associated with HCMV seropositivity in a multivariate regression analysis. HCMV seropositivity was also associated with 9% (95% confidence interval 4–15%) and 20% (0.3–44%) increases in median levels of sICAM-1 and CRP, respectively, after adjusting for covariates. The association between HCMV seropositivity and median levels of sVCAM-1 and SAA were positive but not statistically significant. Significant positive associations were observed between the intensity of anti-HCMV IgG responses and levels of sICAM-1 and sVCAM-1 (p-values 0.0008 and 0.04 for linear trend, respectively). To our knowledge, this is the first epidemiological study to show a relationship between anti-HCMV IgG responses and vascular injury biomarkers sICAM-1 and sVCAM-1 in the general population. Conclusion: HCMV infections are associated with vascular injury and inflammation biomarkers in adult residents of North Carolina. Frontiers Media S.A. 2020-07-09 /pmc/articles/PMC7363776/ /pubmed/32733818 http://dx.doi.org/10.3389/fcimb.2020.00334 Text en Copyright © 2020 Styles, Converse, Griffin, Wade, Klein, Nylander-French, Stewart, Sams, Hudgens and Egorov. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Styles, Jennifer N. Converse, Reagan R. Griffin, Shannon M. Wade, Timothy J. Klein, Elizabeth Nylander-French, Leena A. Stewart, Jill R. Sams, Elizabeth Hudgens, Edward Egorov, Andrey I. Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title | Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title_full | Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title_fullStr | Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title_full_unstemmed | Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title_short | Human Cytomegalovirus Infections Are Associated With Elevated Biomarkers of Vascular Injury |
title_sort | human cytomegalovirus infections are associated with elevated biomarkers of vascular injury |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363776/ https://www.ncbi.nlm.nih.gov/pubmed/32733818 http://dx.doi.org/10.3389/fcimb.2020.00334 |
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