DNA methylation signatures of bilateral hippocampal volume, asymmetry and atrophy: a cross-omics analysis in the general population

BACKGROUND: Left-right hippocampal volumetric asymmetry and atrophy are implicated in neurodegenerative and neuropsychiatric disorders, yet their molecular basis in healthy adults remains poorly understood. METHODS: We conducted a meta-analysis of epigenome-wide association studies across six population-based cohorts (n = 8156; 53% women; mean age = 60.7 years) to identify DNA methylation signatures associated with left and right hippocampal volumes (LHCV, RHCV) and hippocampal asymmetry (i.e, differences between left and right volumes divided by their sums). FINDINGS: We identified five CpGs and 262 differentially methylated regions associated with LHCV, nine CpGs and 246 regions with RHCV, one CpG and 16 regions with asymmetry. Cross-omics integration uncovered 15 LHCV-related and 13 RHCV-related methylation-gene expression pairs, with five overlapping genes primarily involved in immune regulation. LHCV-specific genes were involved in cellular signalling, and Mendelian randomisation (MR) analyses supported a potential causal association between brain expression of DIP2C and increased risk of major depressive disorder. RHCV-specific genes were involved in neuronal differentiation pathways, with MR analyses suggesting that brain-tissue expression of BAIAP2, MACF1, SLC16A5, and CORO1B was associated with neuropsychiatric disorders. We also identified sex-specific patterns with hippocampal asymmetry. Notably, baseline methylation at these sites predicted hippocampal atrophy rates, explaining >10% of the variation. Associations with multiple healthy dietary patterns suggest modifiable influences on hippocampal structure. INTERPRETATION: These findings highlight distinct methylation profiles as potential biomarkers or therapeutic targets for neuropsychiatric and neurodegenerative conditions. FUNDING: Institutional funds, Federal Ministry of Education and Research of Germany, Alzheimer's Association.

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Journal
EBioMedicine
Published
2026-05-11
DOI
https://doi.org/10.1016/j.ebiom.2026.106289
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00

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article

DNA methylation signatures of bilateral hippocampal volume, asymmetry and atrophy: a cross-omics analysis in the general population

Karen A. Mather, Dina Vojinović, Santiago Estrada, Monique M.B. Breteler et al.
EBioMedicine
Epigenetics and DNA Methylation
article

DNA methylation signatures of bilateral hippocampal volume, asymmetry and atrophy: a cross-omics analysis in the general population

Karen A. Mather, Dina Vojinović, Santiago Estrada, Monique M.B. Breteler, Nicola J. Armstrong, Katharina Wittfeld, Natalie A. Royle, Valentina Talevi, Konstantinos Melas, Hans Jörgen Grabe, Joanna M. Wardlaw, Mohammed A. Imtiaz, Juliana Petri Tavares, Dan Liu, Marian Beekman, Henry Völzke, Simon R. Cox, Ruiqi Wang, Qiong Yang, Alexander Teumer, Perminder S. Sachdev, Robert F. Hillary, N. Ahmad Aziz, P. Eline Slagboom, Robin Bülow, Wei Wen
article en

Abstract

BACKGROUND: Left-right hippocampal volumetric asymmetry and atrophy are implicated in neurodegenerative and neuropsychiatric disorders, yet their molecular basis in healthy adults remains poorly understood. METHODS: We conducted a meta-analysis of epigenome-wide association studies across six population-based cohorts (n = 8156; 53% women; mean age = 60.7 years) to identify DNA methylation signatures associated with left and right hippocampal volumes (LHCV, RHCV) and hippocampal asymmetry (i.e, differences between left and right volumes divided by their sums). FINDINGS: We identified five CpGs and 262 differentially methylated regions associated with LHCV, nine CpGs and 246 regions with RHCV, one CpG and 16 regions with asymmetry. Cross-omics integration uncovered 15 LHCV-related and 13 RHCV-related methylation-gene expression pairs, with five overlapping genes primarily involved in immune regulation. LHCV-specific genes were involved in cellular signalling, and Mendelian randomisation (MR) analyses supported a potential causal association between brain expression of DIP2C and increased risk of major depressive disorder. RHCV-specific genes were involved in neuronal differentiation pathways, with MR analyses suggesting that brain-tissue expression of BAIAP2, MACF1, SLC16A5, and CORO1B was associated with neuropsychiatric disorders. We also identified sex-specific patterns with hippocampal asymmetry. Notably, baseline methylation at these sites predicted hippocampal atrophy rates, explaining >10% of the variation. Associations with multiple healthy dietary patterns suggest modifiable influences on hippocampal structure. INTERPRETATION: These findings highlight distinct methylation profiles as potential biomarkers or therapeutic targets for neuropsychiatric and neurodegenerative conditions. FUNDING: Institutional funds, Federal Ministry of Education and Research of Germany, Alzheimer's Association.

EBioMedicineVol. 128
Boston University (US), New South Wales Department of Health (AU), NHS Lothian (GB), Curtin University (AU), Universitätsmedizin Greifswald (DE), Leiden University Medical Center (NL), German Center for Neurodegenerative Diseases (DE), UNSW Sydney (AU), Framingham Heart Study (US), Max Planck Institute for Biology of Ageing (DE), University of Edinburgh (GB)
Alzheimer's Association, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung
Zero hunger
Openalex Percentile: Top 10%
Epigenetics and DNA Methylation
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