{"title":"A hexaplex droplet digital PCR assay for DNA methylation-based age prediction from blood samples targeting ELOVL2, FHL2, and TRIM59","authors":"Rita Fakhr , Un Na Koh , So Eun Lee , Si-Keun Lim","doi":"10.1016/j.fsigen.2025.103396","DOIUrl":null,"url":null,"abstract":"<div><div>DNA methylation analysis has emerged as a promising approach, offering valuable information in forensic investigations. This study presents the development of a hexaplex droplet digital PCR (ddPCR) assay for forensic age prediction based on three well-established age-associated markers: <em>ELOVL2</em>, <em>FHL2</em>, and <em>TRIM59</em>. The assay reliably distinguished methylation levels as low as 1 %, with no cross-reactivity or signal interference in the multiplex format. To evaluate the assay’s predictive performance, two statistical methods were used: hold-out cross-validation and 5-fold cross-validation. In both methods, all three markers showed strong correlations with chronological age. In the hold-out method, the model achieved a mean absolute error (MAE) of 2.80 years for the test set. Comparable performance was observed in 5-fold cross-validation, with an average MAE of 3.13 years. Prediction accuracy was higher in younger individuals and decreased with older age. The hexaplex assay allows all markers to be analyzed under identical experimental conditions, enhancing consistency, minimizing technical variability, and reducing reagent costs. Future work will include validation studies in accordance with the Scientific Working Group on DNA Analysis Methods (SWGDAM) guidelines and application to real forensic casework to further confirm the assay’s practical utility.</div></div>","PeriodicalId":50435,"journal":{"name":"Forensic Science International-Genetics","volume":"81 ","pages":"Article 103396"},"PeriodicalIF":3.6000,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Forensic Science International-Genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872497325001760","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
DNA methylation analysis has emerged as a promising approach, offering valuable information in forensic investigations. This study presents the development of a hexaplex droplet digital PCR (ddPCR) assay for forensic age prediction based on three well-established age-associated markers: ELOVL2, FHL2, and TRIM59. The assay reliably distinguished methylation levels as low as 1 %, with no cross-reactivity or signal interference in the multiplex format. To evaluate the assay’s predictive performance, two statistical methods were used: hold-out cross-validation and 5-fold cross-validation. In both methods, all three markers showed strong correlations with chronological age. In the hold-out method, the model achieved a mean absolute error (MAE) of 2.80 years for the test set. Comparable performance was observed in 5-fold cross-validation, with an average MAE of 3.13 years. Prediction accuracy was higher in younger individuals and decreased with older age. The hexaplex assay allows all markers to be analyzed under identical experimental conditions, enhancing consistency, minimizing technical variability, and reducing reagent costs. Future work will include validation studies in accordance with the Scientific Working Group on DNA Analysis Methods (SWGDAM) guidelines and application to real forensic casework to further confirm the assay’s practical utility.
期刊介绍:
Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.
The scope of the journal includes:
Forensic applications of human polymorphism.
Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies.
Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms.
Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications.
Non-human DNA polymorphisms for crime scene investigation.
Population genetics of human polymorphisms of forensic interest.
Population data, especially from DNA polymorphisms of interest for the solution of forensic problems.
DNA typing methodologies and strategies.
Biostatistical methods in forensic genetics.
Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches.
Standards in forensic genetics.
Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards.
Quality control.
Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies.
Criminal DNA databases.
Technical, legal and statistical issues.
General ethical and legal issues related to forensic genetics.