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Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort

Adverse conditions in early life, including environmental, biological and social influences, are risk factors for ill-health during aging and the onset of age-related disorders. In this context, the recent field of social epigenetics offers a valuable method for establishing the relationships among...

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Autores principales: Gomez-Verjan, Juan Carlos, Esparza-Aguilar, Marcelino, Martín-Martín, Verónica, Salazar-Perez, Cecilia, Cadena-Trejo, Cinthya, Gutierrez-Robledo, Luis Miguel, Martínez-Magaña, José Jaime, Nicolini, Humberto, Arroyo, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469534/
https://www.ncbi.nlm.nih.gov/pubmed/34573390
http://dx.doi.org/10.3390/genes12091408
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author Gomez-Verjan, Juan Carlos
Esparza-Aguilar, Marcelino
Martín-Martín, Verónica
Salazar-Perez, Cecilia
Cadena-Trejo, Cinthya
Gutierrez-Robledo, Luis Miguel
Martínez-Magaña, José Jaime
Nicolini, Humberto
Arroyo, Pedro
author_facet Gomez-Verjan, Juan Carlos
Esparza-Aguilar, Marcelino
Martín-Martín, Verónica
Salazar-Perez, Cecilia
Cadena-Trejo, Cinthya
Gutierrez-Robledo, Luis Miguel
Martínez-Magaña, José Jaime
Nicolini, Humberto
Arroyo, Pedro
author_sort Gomez-Verjan, Juan Carlos
collection PubMed
description Adverse conditions in early life, including environmental, biological and social influences, are risk factors for ill-health during aging and the onset of age-related disorders. In this context, the recent field of social epigenetics offers a valuable method for establishing the relationships among them However, current clinical studies on environmental changes and lifespan disorders are limited. In this sense, the Tlaltizapan (Mexico) cohort, who 52 years ago was exposed to infant malnutrition, low income and poor hygiene conditions, represents a vital source for exploring such factors. Therefore, in the present study, 52 years later, we aimed to explore differences in clinical/biochemical/anthropometric and epigenetic (DNA methylation) variables between individuals from such a cohort, in comparison with an urban-raised sample. Interestingly, only cholesterol levels showed significant differences between the cohorts. On the other hand, individuals from the Tlaltizapan cohort with more years of schooling had a lower epigenetic age in the Horvath (p-value = 0.0225) and PhenoAge (p-value = 0.0353) clocks, compared to those with lower-level schooling. Our analysis indicates 12 differentially methylated sites associated with the PI3-Akt signaling pathway and galactose metabolism in individuals with different durations of schooling. In conclusion, our results suggest that longer durations of schooling could promote DNA methylation changes that may reduce epigenetic age; nevertheless, further studies are needed.
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spelling pubmed-84695342021-09-27 Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort Gomez-Verjan, Juan Carlos Esparza-Aguilar, Marcelino Martín-Martín, Verónica Salazar-Perez, Cecilia Cadena-Trejo, Cinthya Gutierrez-Robledo, Luis Miguel Martínez-Magaña, José Jaime Nicolini, Humberto Arroyo, Pedro Genes (Basel) Article Adverse conditions in early life, including environmental, biological and social influences, are risk factors for ill-health during aging and the onset of age-related disorders. In this context, the recent field of social epigenetics offers a valuable method for establishing the relationships among them However, current clinical studies on environmental changes and lifespan disorders are limited. In this sense, the Tlaltizapan (Mexico) cohort, who 52 years ago was exposed to infant malnutrition, low income and poor hygiene conditions, represents a vital source for exploring such factors. Therefore, in the present study, 52 years later, we aimed to explore differences in clinical/biochemical/anthropometric and epigenetic (DNA methylation) variables between individuals from such a cohort, in comparison with an urban-raised sample. Interestingly, only cholesterol levels showed significant differences between the cohorts. On the other hand, individuals from the Tlaltizapan cohort with more years of schooling had a lower epigenetic age in the Horvath (p-value = 0.0225) and PhenoAge (p-value = 0.0353) clocks, compared to those with lower-level schooling. Our analysis indicates 12 differentially methylated sites associated with the PI3-Akt signaling pathway and galactose metabolism in individuals with different durations of schooling. In conclusion, our results suggest that longer durations of schooling could promote DNA methylation changes that may reduce epigenetic age; nevertheless, further studies are needed. MDPI 2021-09-13 /pmc/articles/PMC8469534/ /pubmed/34573390 http://dx.doi.org/10.3390/genes12091408 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gomez-Verjan, Juan Carlos
Esparza-Aguilar, Marcelino
Martín-Martín, Verónica
Salazar-Perez, Cecilia
Cadena-Trejo, Cinthya
Gutierrez-Robledo, Luis Miguel
Martínez-Magaña, José Jaime
Nicolini, Humberto
Arroyo, Pedro
Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title_full Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title_fullStr Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title_full_unstemmed Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title_short Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort
title_sort years of schooling could reduce epigenetic aging: a study of a mexican cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469534/
https://www.ncbi.nlm.nih.gov/pubmed/34573390
http://dx.doi.org/10.3390/genes12091408
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