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Pathogen burden and leukocyte telomere length in the United States

BACKGROUND: Prior studies in humans have suggested that telomere shortening may be accelerated by infection, but research on multiple pathogens and use of large population-based study samples has been limited. We estimated cross-sectional associations between seropositivity to five persistent pathog...

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Autores principales: Noppert, Grace A., Feinstein, Lydia, Dowd, Jennifer B., Stebbins, Rebecca C., Zang, Emma, Needham, Belinda L., Meier, Helen C. S., Simanek, Amanda, Aiello, Allison E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677839/
https://www.ncbi.nlm.nih.gov/pubmed/33292353
http://dx.doi.org/10.1186/s12979-020-00206-9
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author Noppert, Grace A.
Feinstein, Lydia
Dowd, Jennifer B.
Stebbins, Rebecca C.
Zang, Emma
Needham, Belinda L.
Meier, Helen C. S.
Simanek, Amanda
Aiello, Allison E.
author_facet Noppert, Grace A.
Feinstein, Lydia
Dowd, Jennifer B.
Stebbins, Rebecca C.
Zang, Emma
Needham, Belinda L.
Meier, Helen C. S.
Simanek, Amanda
Aiello, Allison E.
author_sort Noppert, Grace A.
collection PubMed
description BACKGROUND: Prior studies in humans have suggested that telomere shortening may be accelerated by infection, but research on multiple pathogens and use of large population-based study samples has been limited. We estimated cross-sectional associations between seropositivity to five persistent pathogens (Herpes Simplex Virus Type-1 (HSV-1), Herpes Simplex Virus Type-2 (HSV-2), cytomegalovirus (CMV), Helicobacter pylori (H.pylori), and Hepatitis B) as well as total pathogen burden and leukocyte telomere length. Data were derived from the National Health and Nutrition Examination Survey (1999–2000) for individuals 20–49 years of age, N = 1708. We analyzed the influence of each pathogen separately, a pathogen count score and a latent class model of pathogen burden on log telomere length using linear regression models, adjusted for covariates. RESULTS: Individuals in a latent pathogen burden class characterized by high probabilities of infection with HSV-1, CMV, and H. pylori, had significantly decreased log telomere length (− 0.30 [95% CI: − 0.36, − 0.24]) compared to those in a latent class characterized by low probabilities of all five infections. There were limited significant associations using other pathogen measures. CONCLUSIONS: These results suggest that infection with specific combinations of pathogens may be one mechanism contributing to accelerated cellular senescence with possible origins early in the life course. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-020-00206-9.
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spelling pubmed-76778392020-11-20 Pathogen burden and leukocyte telomere length in the United States Noppert, Grace A. Feinstein, Lydia Dowd, Jennifer B. Stebbins, Rebecca C. Zang, Emma Needham, Belinda L. Meier, Helen C. S. Simanek, Amanda Aiello, Allison E. Immun Ageing Research BACKGROUND: Prior studies in humans have suggested that telomere shortening may be accelerated by infection, but research on multiple pathogens and use of large population-based study samples has been limited. We estimated cross-sectional associations between seropositivity to five persistent pathogens (Herpes Simplex Virus Type-1 (HSV-1), Herpes Simplex Virus Type-2 (HSV-2), cytomegalovirus (CMV), Helicobacter pylori (H.pylori), and Hepatitis B) as well as total pathogen burden and leukocyte telomere length. Data were derived from the National Health and Nutrition Examination Survey (1999–2000) for individuals 20–49 years of age, N = 1708. We analyzed the influence of each pathogen separately, a pathogen count score and a latent class model of pathogen burden on log telomere length using linear regression models, adjusted for covariates. RESULTS: Individuals in a latent pathogen burden class characterized by high probabilities of infection with HSV-1, CMV, and H. pylori, had significantly decreased log telomere length (− 0.30 [95% CI: − 0.36, − 0.24]) compared to those in a latent class characterized by low probabilities of all five infections. There were limited significant associations using other pathogen measures. CONCLUSIONS: These results suggest that infection with specific combinations of pathogens may be one mechanism contributing to accelerated cellular senescence with possible origins early in the life course. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-020-00206-9. BioMed Central 2020-11-19 /pmc/articles/PMC7677839/ /pubmed/33292353 http://dx.doi.org/10.1186/s12979-020-00206-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Noppert, Grace A.
Feinstein, Lydia
Dowd, Jennifer B.
Stebbins, Rebecca C.
Zang, Emma
Needham, Belinda L.
Meier, Helen C. S.
Simanek, Amanda
Aiello, Allison E.
Pathogen burden and leukocyte telomere length in the United States
title Pathogen burden and leukocyte telomere length in the United States
title_full Pathogen burden and leukocyte telomere length in the United States
title_fullStr Pathogen burden and leukocyte telomere length in the United States
title_full_unstemmed Pathogen burden and leukocyte telomere length in the United States
title_short Pathogen burden and leukocyte telomere length in the United States
title_sort pathogen burden and leukocyte telomere length in the united states
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677839/
https://www.ncbi.nlm.nih.gov/pubmed/33292353
http://dx.doi.org/10.1186/s12979-020-00206-9
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