Evidence map›Paper›PMID 41339892›Full record

ArticleBMC medicine2025

KoMethylNet: a novel epigenetic clock based on neural network analysis of DNA methylation data and epigenetic age acceleration in a Korean population.

Dabin Yun, Kwangyeon Oh, Yujin Kim, Yong Min Ahn, Hemang M Parikh, Xiaoxi Meng, Zhaoming Wang, Nan Song

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Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Dabin YunCollege of Pharmacy, Chungbuk National University, Cheongju, Chungbuk, Korea.
Kwangyeon OhDepartment of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN, USA.
Yujin KimDepartment of Digital Health, Samsung Advanced Institute for Health Sciences and Technology (SAIHST), Samsung Medical Center, Sungkyunkwan University, Seoul, Korea.
Yong Min AhnDepartment of Psychiatry, Seoul National University College of Medicine, Seoul, Korea.
Hemang M ParikhHealth Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Xiaoxi MengDepartment of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN, USA.
Zhaoming WangHealth Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Nan SongCollege of Pharmacy, Chungbuk National University, Cheongju, Chungbuk, Korea. nan.song@chungbuk.ac.kr.

Funding

Ministry of Science and ICT, South Korea RS-2024-00358322, RS-2024-00440787
6 · The paper itself

Abstract

backgroundEpigenetic clocks have been extensively investigated in individuals of European ancestry and may be suboptimal in East Asians. We developed a novel epigenetic clock (KoMethylNet) using neural network analysis of DNA methylation (DNAm) data from the Korean population to predict chronological ages.

methodsDNAm data (367,785 CpG sites) from 2,747 participants (Infinium Human Methylation 450 K BeadChip: N = 397; Infinium MethylationEPIC BeadChip: N = 2,350) in the Korean Genome and Epidemiology Study (KoGES) were used to train the neural network on chronological ages. SHapley Additive exPlanation analysis was used to select the optimal number of CpG sites. KoMethylNet-epigenetic age acceleration (EAA)-phenotype analysis was conducted with linear regression, to identify aging-related phenotypes in the Korean population.

resultsKoMethylNet, which uses 300 CpG sites, achieved a mean absolute error (MAE) of 2.82 years, a mean squared error (MSE) of 12.68 years, and a Pearson's correlation coefficient (R) of 0.90 with chronological age. In the external validation using healthy Korean individuals, KoMethylNet achieved the highest performance (MAE = 2.74, MSE = 12.29, R = 0.94). Seven phenotypes, including diabetes-related traits (diabetes, HbA1c, and urine glucose), were positively associated with KoMethylNet-EAA.

conclusionsWe developed a neural network-based DNAm aging clock using Korean population data that enables precise age prediction and offers potential opportunities for advancing aging-related research in Korea.

Indexed as

AgingDNA MethylationEpigenesis, GeneticNeural Networks, ComputerAdultAgedCpG IslandsEast Asian PeopleFemaleHumansMaleMiddle AgedRepublic of KoreaDeep learningDNA methylation aging clockEpigenetic age acceleration

Identifiers

PMID41339892
PMCPMC12781313

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.