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Título
Genetic susceptibility to telomere shortening through the rs2293607 polymorphism is associated with a greater risk of alcohol use disorder
Autor(es)
Palabras clave
Genetic polymorphism
Telomere
Alcoholism
Alcohol use disorder
Telomerase
Clasificación UNESCO
2415 Biología Molecular
Fecha de publicación
2022
Editor
Elsevier
Citación
Llorente, H., Perez-Rivera, J.-A., Perez-Nieto, M., Cieza-Borrella, C., Pastor, I., Novo-Veleiro, I., Fernández-Mateos, J., Chamorro, A.-J., Crecente-Otero, P., Laso, F.-J., González-Sarmiento, R., & Marcos, M. (2022). Genetic susceptibility to telomere shortening through the rs2293607 polymorphism is associated with a greater risk of alcohol use disorder. Mechanisms of Ageing and Development, 206, 111693. https://doi.org/10.1016/j.mad.2022.111693
Resumen
[EN] Telomere shortening is usually considered a biomarker of ageing. Harmful alcohol use promotes accelerated
biological ageing and alcohol use disorders (AUDs) are associated with short telomere length (TL). This study was
conducted to examine the relationship of TL to AUD and determine whether single nucleotide polymorphisms
(SNPs) in TERC and TERT modulate this association. For this purpose, we genotyped TERC SNPs rs2293607,
rs12696304, and rs16847897 and TERT SNPs rs2735940, rs2736100, and rs2736098 in 308 male patients with
AUD and 255 sex-matched healthy controls and measured TL in a subset of 99 patients and 99 controls paired by
age and smoking status. Our results showed that the mean TL was shorter in patients with AUD than in controls.
The area under the ROC curve was 0.70 (P < 0.001). The GG genotype of TERC rs2293607 was more common
among patients with AUD than among controls (9.8% vs. 5.1%; P = 0.038). No difference was found for the other
SNPs. Carriers of the GG genotype of rs2293607 had shorter telomeres than did allele A carriers. In conclusion,
patients with AUD had shorter telomeres. Genetic susceptibility to telomere shortening through the rs2293607
SNP is associated with a greater risk of AUD.
URI
ISSN
0047-6374
DOI
10.1016/j.mad.2022.111693
Versión del editor
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Publicación en abierto financiada por la Universidad de Salamanca como participante en el Acuerdo Transformativo CRUE-CSIC con Elsevier, 2021-2024













