EpiAge: a next-generation sequencing-based ELOVL2 epigenetic clock for biological age assessment in saliva and blood across health and disease

This study introduces EpiAgePublic, a new method to estimate biological age using only three specific sites on the gene <i>ELOVL2,</i> known for its connection to aging. Unlike traditional methods that require complex and extensive data, our model uses a simpler approach that is well-suited for next-generation sequencing technology, which is a more advanced method of analyzing DNA methylation. This new model overcomes some of the common challenges found in older methods, such as errors due to sample quality and processing variations. We tested EpiAgePublic with a large and varied group of over 4,600 people to ensure its accuracy. It performed on par with, and sometimes better than, more complicated models that use much more data for age estimation. We examined its effectiveness in understanding how factors like HIV infection and stress affect aging, confirming its usefulness in real-world clinical settings. Our results prove that our simple yet effective model, EpiAgePublic, can capture the subtle signs of aging with high accuracy. We also used this model in a study involving patients with Alzheimer's Disease, demonstrating the practical benefits of next-generation sequencing in making precise age-related assessments. This study lays the groundwork for future research on aging mechanisms and assessing how different interventions might impact the aging process using this clock.

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Publication Details

Journal
Aging
Published
2025-01-22
DOI
https://doi.org/10.18632/aging.206188
Citations
5
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
4.03
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article

EpiAge: a next-generation sequencing-based ELOVL2 epigenetic clock for biological age assessment in saliva and blood across health and disease

Moshe Szyf, A. Claudio Cuello, Sonia Do Carmo, Margherita Grasso et al.
5 citations
Aging
Epigenetics and DNA Methylation
4.03
article

EpiAge: a next-generation sequencing-based ELOVL2 epigenetic clock for biological age assessment in saliva and blood across health and disease

Moshe Szyf, A. Claudio Cuello, Sonia Do Carmo, Margherita Grasso, David Cheishvili, Filippo Caraci
article en
5 citations

Abstract

This study introduces EpiAgePublic, a new method to estimate biological age using only three specific sites on the gene <i>ELOVL2,</i> known for its connection to aging. Unlike traditional methods that require complex and extensive data, our model uses a simpler approach that is well-suited for next-generation sequencing technology, which is a more advanced method of analyzing DNA methylation. This new model overcomes some of the common challenges found in older methods, such as errors due to sample quality and processing variations. We tested EpiAgePublic with a large and varied group of over 4,600 people to ensure its accuracy. It performed on par with, and sometimes better than, more complicated models that use much more data for age estimation. We examined its effectiveness in understanding how factors like HIV infection and stress affect aging, confirming its usefulness in real-world clinical settings. Our results prove that our simple yet effective model, EpiAgePublic, can capture the subtle signs of aging with high accuracy. We also used this model in a study involving patients with Alzheimer's Disease, demonstrating the practical benefits of next-generation sequencing in making precise age-related assessments. This study lays the groundwork for future research on aging mechanisms and assessing how different interventions might impact the aging process using this clock.

AgingVol. 17(1)
University of Catania (IT), University of Oxford (GB), Oasi Maria SS (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), McGill University (CA)
Zero hunger
Openalex Percentile: Top 7%
Epigenetics and DNA Methylation
4.03
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