HIV-1 Infection Accelerates Age According to the Epigenetic Clock.

TitleHIV-1 Infection Accelerates Age According to the Epigenetic Clock.
Publication TypeJournal Article
Year of Publication2015
AuthorsHorvath, S, Levine, AJ
JournalJ Infect Dis
Volume212
Issue10
Pagination1563-73
Date Published2015 Nov 15
ISSN1537-6613
KeywordsAdolescent, Adult, Aged, Aging, Blood Cells, Brain, DNA, Epigenesis, Genetic, HIV Infections, HIV-1, Humans, Internal, Male, Methylation, Middle Aged, Young Adult
Abstract

BACKGROUND: Infection with human immunodeficiency virus type 1 (HIV) is associated with clinical symptoms of accelerated aging, as evidenced by the increased incidence and diversity of age-related illnesses at relatively young ages and supporting findings of organ and cellular pathologic analyses. But it has been difficult to detect an accelerated aging effect at a molecular level.METHODS: Here, we used an epigenetic biomarker of aging based on host DNA methylation levels to study accelerated aging effects due to HIV infection. DNA from brain and blood tissue was assayed via the Illumina Infinium Methylation 450 K platform.RESULTS: Using 6 novel DNA methylation data sets, we show that HIV infection leads to an increase in epigenetic age both in brain tissue (7.4 years) and blood (5.2 years). While the observed accelerated aging effects in blood may reflect changes in blood cell composition (notably exhausted cytotoxic T cells), it is less clear what explains the observed accelerated aging effects in brain tissue.CONCLUSIONS: Overall, our results demonstrate that the epigenetic clock is a useful biomarker for detecting accelerated aging effects due to HIV infection. This tool can be used to accurately determine the extent of age acceleration in individual tissues and cells.

DOI10.1093/infdis/jiv277
Alternate JournalJ Infect Dis
PubMed ID25969563
PubMed Central IDPMC4621253
Grant ListR24-NS38841 / NS / NINDS NIH HHS / United States
U24 MH100929 / MH / NIMH NIH HHS / United States
U01 MH083507 / MH / NIMH NIH HHS / United States
R24 MH059724 / MH / NIMH NIH HHS / United States
UL1TR000124 / TR / NCATS NIH HHS / United States
U01-MH083501 / MH / NIMH NIH HHS / United States
R21 AG046954 / AG / NIA NIH HHS / United States
U01 MH083500 / MH / NIMH NIH HHS / United States
AI28697 / AI / NIAID NIH HHS / United States
R24 NS045491 / NS / NINDS NIH HHS / United States
U24 MH100928 / MH / NIMH NIH HHS / United States
R24-NS45491 / NS / NINDS NIH HHS / United States
R24 MH059745 / MH / NIMH NIH HHS / United States
UL1 TR000124 / TR / NCATS NIH HHS / United States
R24 NS038841 / NS / NINDS NIH HHS / United States
R01 DA030913 / DA / NIDA NIH HHS / United States
R24-MH59745 / MH / NIMH NIH HHS / United States
R24-MH59724 / MH / NIMH NIH HHS / United States
UM1 AI035043 / AI / NIAID NIH HHS / United States
P30 AI028697 / AI / NIAID NIH HHS / United States
U01 MH083501 / MH / NIMH NIH HHS / United States
U01-AI-35040 / AI / NIAID NIH HHS / United States
U01 MH083506 / MH / NIMH NIH HHS / United States
5R01AG042511-02 / AG / NIA NIH HHS / United States
U01-MH08021 / MH / NIMH NIH HHS / United States
U01-MH083506 / MH / NIMH NIH HHS / United States
U01 AI035040 / AI / NIAID NIH HHS / United States
U01-MH083507 / MH / NIMH NIH HHS / United States
R01 AG042511 / AG / NIA NIH HHS / United States
R01DA030913 / DA / NIDA NIH HHS / United States