Paternal germ line aging: DNA methylation age prediction from human sperm
Abstract Background The 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...
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doaj-c58070fa31ea4fc9ab1487f52d896a4e2020-11-25T01:42:21ZengBMCBMC Genomics1471-21642018-10-0119111010.1186/s12864-018-5153-4Paternal germ line aging: DNA methylation age prediction from human spermTimothy G. Jenkins0Kenneth I. Aston1Bradley Cairns2Andrew Smith3Douglas T. Carrell4Andrology and IVF Laboratories, University of UtahAndrology and IVF Laboratories, University of UtahHuntsman Cancer InstituteUniversity of Southern CaliforniaAndrology and IVF Laboratories, University of UtahAbstract Background The 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. Results We 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 predicting age with an R2 of 0.89, a mean absolute error (MAE) of 2.04 years, and a mean absolute percent error (MAPE) of 6.28% in our data set. We additionally investigated the reproducibility of prediction with our model in an independent cohort where 6 technical replicates of 10 individual samples were tested on different arrays. We found very similar age prediction accuracy (MAE = 2.37 years; MAPE = 7.05%) with a high degree of precision between replicates (standard deviation of only 0.877 years). Additionally, we found that smokers trended toward increased age profiles when compared to ‘never smokers’ though this pattern was only striking in a portion of the samples screened. Conclusions The 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 suggest that the aging process in sperm may be impacted by environmental factors, though this effect appears to be quite subtle and future work is needed to establish this relationship.http://link.springer.com/article/10.1186/s12864-018-5153-4Sperm epigeneticsAgingDNA methylationAging calculator |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Timothy G. Jenkins Kenneth I. Aston Bradley Cairns Andrew Smith Douglas T. Carrell |
spellingShingle |
Timothy G. Jenkins Kenneth I. Aston Bradley Cairns Andrew Smith Douglas T. Carrell Paternal germ line aging: DNA methylation age prediction from human sperm BMC Genomics Sperm epigenetics Aging DNA methylation Aging calculator |
author_facet |
Timothy G. Jenkins Kenneth I. Aston Bradley Cairns Andrew Smith Douglas T. Carrell |
author_sort |
Timothy G. Jenkins |
title |
Paternal germ line aging: DNA methylation age prediction from human sperm |
title_short |
Paternal germ line aging: DNA methylation age prediction from human sperm |
title_full |
Paternal germ line aging: DNA methylation age prediction from human sperm |
title_fullStr |
Paternal germ line aging: DNA methylation age prediction from human sperm |
title_full_unstemmed |
Paternal germ line aging: DNA methylation age prediction from human sperm |
title_sort |
paternal germ line aging: dna methylation age prediction from human sperm |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2018-10-01 |
description |
Abstract Background The 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. Results We 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 predicting age with an R2 of 0.89, a mean absolute error (MAE) of 2.04 years, and a mean absolute percent error (MAPE) of 6.28% in our data set. We additionally investigated the reproducibility of prediction with our model in an independent cohort where 6 technical replicates of 10 individual samples were tested on different arrays. We found very similar age prediction accuracy (MAE = 2.37 years; MAPE = 7.05%) with a high degree of precision between replicates (standard deviation of only 0.877 years). Additionally, we found that smokers trended toward increased age profiles when compared to ‘never smokers’ though this pattern was only striking in a portion of the samples screened. Conclusions The 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 suggest that the aging process in sperm may be impacted by environmental factors, though this effect appears to be quite subtle and future work is needed to establish this relationship. |
topic |
Sperm epigenetics Aging DNA methylation Aging calculator |
url |
http://link.springer.com/article/10.1186/s12864-018-5153-4 |
work_keys_str_mv |
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