Literature DB >> 28931225

Persistent Herpesvirus Infections and Telomere Attrition Over 3 Years in the Whitehall II Cohort.

Jennifer B Dowd1,2, Jos A Bosch3,4,5, Andrew Steptoe6, Bamini Jayabalasingham2, Jue Lin7, Robert Yolken8, Allison E Aiello9.   

Abstract

The determinants of telomere attrition, a potential marker of cellular aging, are not well understood. Persistent herpesvirus infections including cytomegalovirus (CMV) infection may be particularly important for telomere dynamics via mechanisms such as inflammation, oxidative stress, and their impact on peripheral blood lymphocyte composition. This study examined the association of 4 human herpesviruses (CMV, herpes simplex virus type 1, human herpesvirus type 6, and Epstein-Barr virus) with change in leukocyte telomere length (LTL) over 3 years in 400 healthy individuals (aged 53-76 years) from the Whitehall II cohort. CMV, herpes simplex virus type 1, and human herpesvirus 6 infection were independently associated with greater 3-year LTL attrition, with no association found for Epstein-Barr virus. The magnitudes of these associations were large, for example, the equivalent of almost 12 years of chronological age for those CMV seropositive. Seropositivity to more herpesviruses was additively associated with greater LTL attrition (3 herpesviruses vs none, β = -0.07 and P = .02; 4 infections vs none, β = -0.14 and P < .001). Higher immunoglobulin G antibody levels among those seropositive to CMV were also associated with shorter LTL at follow-up. These associations were robust to adjustment for age, sex, employment grade, body mass index, and smoking status. These results suggest that exposure to infectious agents should be an important consideration in future studies of telomere dynamics.
© The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Epstein-Barr virus; Whitehall II; cytomegalovirus; herpes simplex virus; telomeres

Mesh:

Substances:

Year:  2017        PMID: 28931225      PMCID: PMC5853283          DOI: 10.1093/infdis/jix255

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  50 in total

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5.  Loneliness and Telomere Length: Immune and Parasympathetic Function in Associations With Accelerated Aging.

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6.  Life Course Socioeconomic Disadvantage and the Aging Immune System: Findings From the Health and Retirement Study.

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