Accelerated epigenetic aging in adolescents living with HIV is associated with altered development of brain structures.

Journal: Journal of neurovirology

Volume: 28

Issue: 2

Year of Publication: 2022

Affiliated Institutions:  Department of Psychiatry and Mental Health, SA MRC Unit On Risk & Resilience in Mental Disorders, University of Cape Town, Groote Schuur Hospital, Observatory, Cape Town, , South Africa. hoare.jax@gmail.com. Department of Psychiatry and Mental Health, SA MRC Unit On Risk & Resilience in Mental Disorders, University of Cape Town, Groote Schuur Hospital, Observatory, Cape Town, , South Africa. Department of Statistics, University of Cape Town, Rondebosch, Cape Town, South Africa. Centre for Infectious Disease Epidemiology and Research, School of Public Health & Family Medicine, University of Cape Town, Cape Town, South Africa. Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, SA Medical Research Council Unit On Child and Adolescent Health, Cape Town, South Africa. Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, , USA. Department of Neurology, David Geffen School of Medicine, at the University of California, Los Angeles, CA, USA.

Abstract summary 

We recently demonstrated that adolescents perinatally infected with HIV-1 (PHIV+) have accelerated aging as measured by a highly accurate epigenetic biomarker of aging known as the epigenetic clock. However, whether epigenetic age acceleration in PHIV+ impacts brain development at the macro- and microstructural levels of brain anatomy has not been studied. We report on a cross-sectional study of PHIV+ enrolled in the Cape Town Adolescent Antiretroviral Cohort (CTAAC). The Illumina Infinium Methylation EPIC array was used to generate DNA methylation data from the blood samples of 180 PHIV+ aged 9 to 12 years. The epigenetic clock software and method was used to estimate two measures, epigenetic age acceleration (AgeAccelerationResidual) and extrinsic epigenetic age acceleration (EEAA). Each participant underwent T1 structural magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI). In order to investigate the associations of chronological age, sex, epigenetic age acceleration and treatment variables (CNS penetration effectiveness score (CPE)) of antiretroviral regimen on brain structure in PHIV+, we developed stepwise multiple regression models in R (version 3.4.3, 2017) including grey and white matter volumes, cortical thickness, cortical surface area and DTI measures of white matter microstructural integrity. The mean DNAm age (16.01 years) of the participants was higher than their mean chronological age (10.77 years). Epigenetic age acceleration contributed more to regional alterations of brain volumes, cortical thickness, cortical surface areas and neuronal microstructure than chronological age, in a range of regions. CPE positively contributed to volume of the brain stem. Understanding the drivers of epigenetic age acceleration could lead to valuable insights into structural brain alterations, and the persistence of neurocognitive disorders in seen in PHIV+ .

Authors & Co-authors:  Hoare Jacqueline J Stein Dan J DJ Heany Sarah J SJ Fouche Jean-Paul JP Phillips Nicole N Er Sebnem S Myer Landon L Zar Heather J HJ Horvath Steve S Levine Andrew J AJ

Study Outcome 

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Statistics
Citations :  Ackermann C, Andronikou S, Saleh MG, et al. (2016) Early Antiretroviral Therapy in HIV-Infected Children Is Associated with Diffuse White Matter Structural Abnormality and Corpus Callosum Sparing. American Journal of Neuroradiology 37:2363–2369. doi: 10.3174/ajnr.A4921
Authors :  10
Identifiers
Doi : 10.1007/s13365-021-00947-3
SSN : 1538-2443
Study Population
Male,Female
Mesh Terms
Adolescent
Other Terms
Brain imaging;DNA methylation;DTI;Epigenetic clock;HIV;MRI;Perinatal HIV
Study Design
Cohort Study,Cross Sectional Study
Study Approach
Country of Study
Publication Country
United States