Blood-based sex-differential DNA methylation in Alzheimer’s disease

Aim: We aim to explore the blood-based sex-differential DNA methylation profiles in patients with Alzheimer’s disease (AD). Methods: The same analytical pipeline and meta-analysis procedure were applied to 254 patients with AD and 261 matched healthy controls (HC) from four blood-based datasets to identify sex-differentially methylated positions (sex-DMPs) and their biological functions. We further reviewed brain-based sex-DMPs previously reported in AD and intersected with blood-based sex-DMPs. Results: We identified 134 sex-DMPs in AD, 88 were unique to AD, and 46 were shared with HC. Eleven novel sex-DMPs and 28 sex-DMPs consistent across blood and brain were recognized for the first time. Differentially methylated genes, such as COL25A1 , MSUT2 , ELAVL4 , SLC17A7 , EPHA4 , and PPP2CB , were closely related to the pathogenesis of AD. In addition, immune-related processes were enriched in the enrichment analysis. Conclusion: Sex-differential DNA methylation in blood provides potential biomarkers for AD pathogenesis, and also points to potential drug targets for precision medicine.

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Publication Details

Journal
Ageing and Neurodegenerative Diseases
Published
2024-12-13
DOI
https://doi.org/10.20517/and.2024.28
Citations
2
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.47

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article

Blood-based sex-differential DNA methylation in Alzheimer’s disease

Tianmi Yang, Yi Xiao, Huifang Shang, Chunyu Li et al.
2 citations
Ageing and Neurodegenerative Diseases
Epigenetics and DNA Methylation
0.47
article

Blood-based sex-differential DNA methylation in Alzheimer’s disease

Tianmi Yang, Yi Xiao, Huifang Shang, Chunyu Li, Qianqian Wei, Yangfan Cheng
article en
2 citations

Abstract

Aim: We aim to explore the blood-based sex-differential DNA methylation profiles in patients with Alzheimer’s disease (AD). Methods: The same analytical pipeline and meta-analysis procedure were applied to 254 patients with AD and 261 matched healthy controls (HC) from four blood-based datasets to identify sex-differentially methylated positions (sex-DMPs) and their biological functions. We further reviewed brain-based sex-DMPs previously reported in AD and intersected with blood-based sex-DMPs. Results: We identified 134 sex-DMPs in AD, 88 were unique to AD, and 46 were shared with HC. Eleven novel sex-DMPs and 28 sex-DMPs consistent across blood and brain were recognized for the first time. Differentially methylated genes, such as COL25A1 , MSUT2 , ELAVL4 , SLC17A7 , EPHA4 , and PPP2CB , were closely related to the pathogenesis of AD. In addition, immune-related processes were enriched in the enrichment analysis. Conclusion: Sex-differential DNA methylation in blood provides potential biomarkers for AD pathogenesis, and also points to potential drug targets for precision medicine.

Ageing and Neurodegenerative DiseasesVol. 4(4)
Sichuan University (CN), West China Hospital of Sichuan University (CN)
University of Exeter, National Natural Science Foundation of China, Universidade de Macau, University of California, Los Angeles
Good health and well-being
Openalex Percentile: Top 34%
Epigenetics and DNA Methylation
0.47
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