Skip to main content

Table 2 Summary of DNA methylation aging studies in PWH

From: Epigenome-wide epidemiologic studies of human immunodeficiency virus infection, treatment, and disease progression

Outcomes

Study design and characteristics of the study population

Platform

Key findings

Epigenetic aging based on DNAm markers of aging [69]

Case control study

8 data sets, brain specimens and blood specimens of PWH and matched HIV negative controls

450 K and 27 K

Increased epigenetic aging in brain tissue (7.4 years) and in blood (5.2 years) of PWH compared to HIV negative controls

Epigenetic aging based on DNAm markers of aging [70]

Case control study

137 HIV+ individuals compared to 44 HIV negative controls

450 K

4.9-year aging advancement in HIV+ individuals compared to HIV-negative controls. Increased expected mortality of 19% in PWH

Epigenetic aging based on DNAm and other markers of epigenetic aging [71]

Case control study

12 HIV+ individuals and 12 HIV- controls

450 K

Age advancement of 14 years in in HIV+ individuals compared to HIV- controls

Epigenetic aging based on DNAm and epigenetic clock [72]

Case control study

378 ART naïve HIV+ individuals with CD4 counts > 500 compared to 34 HIV- controls

850 K

Accelerated aging advancement occurs in PWH with preserved immune function compared to HIV- controls

Epigenetic aging based on DNAm and other epigenetic markers of age acceleration [26]

Case control study

Pediatric cohort

HIV+, HIV-exposed uninfected (HEU) and HIV unexposed, uninfected (HUU) children

N = 178

450 K

No differences in age acceleration between the three groups. However, significantly shorter telomere length in HIV+ children compared to HEU and HUU groups

Epigenetic aging based on DNAm markers of aging [25]

Case control study

31 perinatally infected HIV+ individuals compared to 30 HIV-negative controls

850 K

Differences in epigenetic age acceleration and extrinsic epigenetic age acceleration between HIV+ and HIV-negative groups. No difference in intrinsic epigenetic aging between groups

Epigenetic aging based on DNAm markers of aging [74]

Longitudinal cohort study

19 HIV+ individuals compared to 19 HIV-negative controls

450 K

Baseline DNAm age of PWH prior to ART initiation 11.2 years greater than HIV-negative controls

Epigenetic aging based on DNAm based markers of aging and epigenetic clock [75]

Prospective cohort study

4-year follow up period

63 aviremic HIV+ individuals on ART

850 K

No acceleration of epigenetic aging in the cohort over the follow-up period

Epigenetic aging based on DNAm markers of aging and epigenetic clocks [78]

Longitudinal cohort study

168 HIV+ individuals before ART initiation and 2 years after ART initiation compared to 44 HIV-negative controls with similar age and sex distribution

850 K

Epigenetic age acceleration in HIV+ individuals compared to HIV-negative controls. Reversal in epigenetic aging after 2 years of ART

Inflammation related single nucleotide polymorphisms as risk factors for age [80] acceleration and NADCs

Post-mortem cohort

HIV+ individuals

N = 155

450 K

Epigenetic aging significantly greater in IL-6 CC carriers and IL-10 CC homozygotes compared to other genotype groups

Association between DNAm markers of aging with measures of cognitive function in PWH [24]

Case control study

69 HIV+ individuals and 38 HIV-negative controls. Cohort > 60 years

850 K

Significant negative correlations between intrinsic epigenetic aging and executive function, attention and working memory and PhenoAge and attention

  1. IL interleukin, HIV human immunodeficiency virus, ART antiretroviral therapy, EWAS epigenome-wide association study, NADC non-AIDS related disease conditions