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Methylome-wide Analysis of Chronic HIV Infection Reveals Five-Year Increase in Biological Age and Epigenetic Targeting of HLA.
- Source :
-
Molecular cell [Mol Cell] 2016 Apr 21; Vol. 62 (2), pp. 157-168. - Publication Year :
- 2016
-
Abstract
- HIV-infected individuals are living longer on antiretroviral therapy, but many patients display signs that in some ways resemble premature aging. To investigate and quantify the impact of chronic HIV infection on aging, we report a global analysis of the whole-blood DNA methylomes of 137 HIV+ individuals under sustained therapy along with 44 matched HIV- individuals. First, we develop and validate epigenetic models of aging that are independent of blood cell composition. Using these models, we find that both chronic and recent HIV infection lead to an average aging advancement of 4.9 years, increasing expected mortality risk by 19%. In addition, sustained infection results in global deregulation of the methylome across >80,000 CpGs and specific hypomethylation of the region encoding the human leukocyte antigen locus (HLA). We find that decreased HLA methylation is predictive of lower CD4 / CD8 T cell ratio, linking molecular aging, epigenetic regulation, and disease progression.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Aging immunology
Anti-HIV Agents therapeutic use
CD4-CD8 Ratio
Case-Control Studies
Chronic Disease
CpG Islands
Disease Progression
Gene Expression Profiling
Genome-Wide Association Study
Genotype
HIV Infections diagnosis
HIV Infections drug therapy
HIV Infections immunology
HIV Infections mortality
HLA Antigens immunology
Humans
Models, Genetic
Phenotype
Risk Factors
Time Factors
Treatment Outcome
Aging genetics
DNA Methylation
Epigenesis, Genetic
HIV Infections genetics
HLA Antigens genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 62
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 27105112
- Full Text :
- https://doi.org/10.1016/j.molcel.2016.03.019