scholarly journals Chronological age prediction based on DNA methylation: Massive parallel sequencing and random forest regression

2017 ◽  
Vol 31 ◽  
pp. 19-28 ◽  
Author(s):  
Jana Naue ◽  
Huub C.J. Hoefsloot ◽  
Olaf R.F. Mook ◽  
Laura Rijlaarsdam-Hoekstra ◽  
Marloes C.H. van der Zwalm ◽  
...  
Rechtsmedizin ◽  
2021 ◽  
Author(s):  
Jana Naue ◽  
Julia Winkelmann ◽  
Ulrike Schmidt ◽  
Sabine Lutz-Bonengel

AbstractThe analysis of age-dependent DNA methylation changes is a valuable tool in epigenetic research and forensic genetics. With some exceptions, most studies in the past concentrated on the analysis of blood, buccal, and saliva samples. Another important sample type in forensic investigations is hair, where age-dependent DNA methylation has not been investigated so far. In this pilot study a deeper look was taken at the possibilities and challenges of DNA methylation analysis in hair. The DNA methylation of selected age-dependent 5’-C-phosphate-G‑3’ (CpG) sites were characterized for their potential use as a biomarker for age prediction using plucked hair samples and massive parallel sequencing. Plucked hair roots of 49 individuals were included in the study. The DNA methylation of 31 hairs was successfully analyzed. The DNA methylation pattern of 10 loci, including ELOVL2, F5, KLF14, and TRIM59, was determined by amplicon-based massive parallel sequencing. Age-dependent changes were found for several markers. The results demonstrate the possible use of already established age-dependent markers but at the same time they have tissue/cell type-specific characteristics. Special challenges such as low amounts of DNA and degraded DNA as well as the possible heterogeneous cellular composition of plucked hair samples, have to be considered.


2020 ◽  
Author(s):  
Junyan Wang ◽  
Chunyan Wang ◽  
Lihong Fu ◽  
Qian Wang ◽  
Guangping Fu ◽  
...  

AbstractIn forensic science, accurate estimation of the age of a victim or suspect can facilitate the investigators to narrow a search and aid in solving a crime. Aging is a complex process associated with various molecular regulation on DNA or RNA levels. Recent studies have shown that circular RNAs (circRNAs) upregulate globally during aging in multiple organisms such as mice and elegans because of their ability to resist degradation by exoribonucleases. In the current study, we attempted to investigate circRNAs’ potential capability of age prediction. Here, we identified more than 40,000 circRNAs in the blood of thirteen Chinese unrelated healthy individuals with ages of 20-62 years according to their circRNA-seq profiles. Three methods were applied to select age-related circRNAs candidates including false discovery rate, lasso regression, and support vector machine. The analysis uncovered a strong bias for circRNA upregulation during aging in human blood. A total of 28 circRNAs were chosen for further validation in 50 healthy unrelated subjects aged between 19 and 72 years by RT-qPCR and finally, 7 age-related circRNAs were chosen for final age prediction models. Several different algorithms including multivariate linear regression (MLR), regression tree, bagging regression, random forest regression (RFR), and support vector regression (SVR) were compared based on root mean square error (RMSE) and mean average error (MAE) values. Among five modeling methods, random forest regression (RFR) performed better than the others with an RMSE value of 5.072 years and an MAE value of 4.065 years (R2 = 0.902). In this preliminary study, we firstly used circRNAs as additional novel age-related biomarkers for developing forensic age estimation models. We propose that the use of circRNAs to obtain additional clues for forensic investigations and serve as aging indicators for age prediction would become a promising field of interest.Author summaryIn forensic investigations, estimation of the age of biological evidence recovered from crime scenes can provide additional information such as chronological age or the appearance of a culprit, which could give valuable investigative leads especially when there is no eyewitness available. Hence, generating an accurate model for age prediction using body fluids such as blood commonly seen at a crime scene can be of vital importance. Various molecular changes on DNA or RNA levels were discovered that they upregulated or downregulated during a person’s lifetime. Although some biomarkers have been proved to be associated with aging and used to predict age, several disadvantages such as low sensitivity, prediction accuracy, instability and susceptibility of diseases or immune states, thus limiting their applicability in the field of age estimation. Here, we utilized a novel biomarker namely circular RNA (circRNA) to generate highly accurate age prediction models. We propose that circRNA is more suitable for forensic degradation samples because of its unique molecular structure. This preliminary research offers a new thought for exploring potential biomarker for age prediction.


Author(s):  
V. A. Lemesh ◽  
V. N. Kipen ◽  
M. V. Bahdanava ◽  
A. A. Burakova ◽  
A. A. Bulgak ◽  
...  

Based on the bioinformatic and statistical analysis of the GEO-projects to determine the genome-wide profile of human DNA methylation, a list of 27 CpG dinucleotides with a high predictive potential was formed to create models for prediction of the human age from blood samples. The methylation level was determined for 245 samples of individuals from the Republic of Belarus. The correlation coefficients R were calculated, and the mathematical models for determining the age of an individual were constructed. The average accuracy value of the age prediction from blood samples using 12 CpG-dinucleotides was 3.4 years (for men – 3.3, for women – 3.5). The results obtained will be used as a basis for development of calculators for predicting the age of an individual based on the biological traces for forensic experts.


2017 ◽  
Author(s):  
Timothy G Jenkins ◽  
Kenneth I Aston ◽  
Andrew Smith ◽  
Douglas T Carrell

AbstractBackgroundThe relationship between aging and epigenetic profiles has been highlighted in many recent studies. Models using somatic cell methylomes to predict age have been successfully constructed. However, gamete aging is quite distinct and as such age prediction using sperm methylomes is ineffective with current techniques.ResultsWe have produced a model that utilizes human sperm DNA methylation signatures to predict chronological age by utilizing methylation array data from a total of 329 samples. The dataset used for model construction includes infertile patients, sperm donors, and individuals from the general population. Our model is capable of accurately predicting age with an R2 of 0.928 in our test data set. We additionally investigated the repeatability of prediction by processing the same sample on 6 different arrays and found very robust age prediction with an average standard deviation of only 0.877 years. Additionally, we found that smokers have approximately 5% increased age profiles compared to ‘never smokers.’ConclusionsThe predictive model described herein was built to offer researchers the ability to assess “germ line age” by accessing sperm DNA methylation signatures at genomic regions affected by age. Our data suggest that this model can predict an individual’s chronological age with a high degree of accuracy regardless of fertility status and with a high degree of repeatability. Additionally, our data appear to show age acceleration patterns as a result of smoking suggesting that the aging process in sperm may be impacted by environmental factors, though this effect appears to be quite subtle.


2021 ◽  
Author(s):  
Kristina Fokias ◽  
Lotte Dierckx ◽  
Wim Van de Voorde ◽  
Bram Bekaert

Over the past decade, age prediction based on DNA methylation has become a vastly investigated topic; many age prediction models have been developed based on different DNAm markers and using various tissues. However, the potential of using nails to this end has not yet been explored. Their inherent resistance to decay and ease of sampling would offer an advantage in cases where post-mortem degradation poses challenges concerning sample collection and DNA-extraction. In the current study, clippings from both fingernails and toenails were collected from 108 living test subjects (age range: 0 – 96 years). The methylation status of 15 CpGs located in 4 previously established age-related markers (ASPA, EDARADD, PDE4C, ELOVL2) was investigated through pyrosequencing of bisulphite converted DNA. Significant dissimilarities in methylation levels were observed between all four limbs, hence limb-specific age prediction models were developed using ordinary least squares, weighted least squares and quantile regression analysis. When applied to their respective test sets, these models yielded a mean absolute deviation between predicted and chronological age ranging from 6.71 to 8.48 years. In addition, the assay was tested on methylation data derived from 5 nail samples collected from deceased individuals, demonstrating its feasibility for application in post-mortem cases. In conclusion, this study provides the first proof that chronological age can be assessed through DNA methylation patterns in nails.


2018 ◽  
Vol 36 ◽  
pp. 152-159 ◽  
Author(s):  
Jana Naue ◽  
Timo Sänger ◽  
Huub C.J. Hoefsloot ◽  
Sabine Lutz-Bonengel ◽  
Ate D. Kloosterman ◽  
...  

2020 ◽  
Vol 140 (1) ◽  
Author(s):  
Chiara Turchi ◽  
Filomena Melchionda ◽  
Mauro Pesaresi ◽  
Eleonora Ciarimboli ◽  
Carla Bini ◽  
...  

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