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Por favor, use este identificador para citar o enlazar este documento: https://ria.asturias.es/RIA/handle/123456789/14891
Título : Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19
Autor : Gonzalez-Fernandez, Mar
Vazquez-Coto, Daniel
Albaiceta, Guillermo M.
(Amado-Rodriguez, Laura
Clemente, Marta G.
Velazquez-Cuervo, Lucinda
Garcia-Lago, Claudia
Gomez, Juan
Coto, Eliecer
Palabras clave : Chromosome-Y
Haplogroups
COVID-19
Hypertension
Fecha de publicación : dic-2024
Editorial : Springer
Citación : - González Fernandez, M; Vázquez Coto, D; Albaiceta, GM; Amado Rodríguez, L; Clemente, MG; Velázquez Cuervo, L; García Lago, C; Gómez, J; Coto, E. Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19. Mol Genet Genomics. 2024. 299. (1). 49. DOI: 10.1007/s00438-024-02143-4.
Resumen : The main objective of this study was to determine whether the common Y-haplogroups were be associated with the risk of developing severe COVID-19 in Spanish male. We studied 479 patients who required hospitalization due to COVID-19 and 285 population controls from the region of Asturias (northern Spain), They were genotyped for several polymorphisms that define the common European Y-haplogroups. We compared the frequencies between patients and controls aged <= 65 and >65 years. There were no different haplogroup frequencies between the two age groups of controls. Haplogroup R1b was less common in patients aged <= 65 years. Haplogroup I was more common in the two patients groups compared to controls (p = 0.02). Haplogroup R1b was significantly more frequent among hypertensive patients, without difference between the hypertensive and normotensive controls. This suggested that R1b could increase the risk for severe COVID-19 among male with pre-existing hypertension. In conclusion, we described the Y-haplogroup structure among Asturians. We found an increased risk of severe COVID-19 among haplogroup I carriers, and a significantly higher frequency of R1b among hypertensive patients. These results indicate that Y-chromosome variants could serve as markers to define the risk of developing a severe form of COVID-19.
URI : https://ria.asturias.es/RIA/handle/123456789/14891
ISSN : 1617-4623
Aparece en las colecciones: Sanidad

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