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Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease

Men have a shorter life expectancy compared with women but the underlying factor(s) are not clear. Late-onset, sporadic Alzheimer disease (AD) is a common and lethal neurodegenerative disorder and many germline inherited variants have been found to influence the risk of developing AD. Our previous r...

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Autores principales: Dumanski, Jan P., Lambert, Jean-Charles, Rasi, Chiara, Giedraitis, Vilmantas, Davies, Hanna, Grenier-Boley, Benjamin, Lindgren, Cecilia M., Campion, Dominique, Dufouil, Carole, Pasquier, Florence, Amouyel, Philippe, Lannfelt, Lars, Ingelsson, Martin, Kilander, Lena, Lind, Lars, Forsberg, Lars A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908225/
https://www.ncbi.nlm.nih.gov/pubmed/27231129
http://dx.doi.org/10.1016/j.ajhg.2016.05.014
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author Dumanski, Jan P.
Lambert, Jean-Charles
Rasi, Chiara
Giedraitis, Vilmantas
Davies, Hanna
Grenier-Boley, Benjamin
Lindgren, Cecilia M.
Campion, Dominique
Dufouil, Carole
Pasquier, Florence
Amouyel, Philippe
Lannfelt, Lars
Ingelsson, Martin
Kilander, Lena
Lind, Lars
Forsberg, Lars A.
author_facet Dumanski, Jan P.
Lambert, Jean-Charles
Rasi, Chiara
Giedraitis, Vilmantas
Davies, Hanna
Grenier-Boley, Benjamin
Lindgren, Cecilia M.
Campion, Dominique
Dufouil, Carole
Pasquier, Florence
Amouyel, Philippe
Lannfelt, Lars
Ingelsson, Martin
Kilander, Lena
Lind, Lars
Forsberg, Lars A.
author_sort Dumanski, Jan P.
collection PubMed
description Men have a shorter life expectancy compared with women but the underlying factor(s) are not clear. Late-onset, sporadic Alzheimer disease (AD) is a common and lethal neurodegenerative disorder and many germline inherited variants have been found to influence the risk of developing AD. Our previous results show that a fundamentally different genetic variant, i.e., lifetime-acquired loss of chromosome Y (LOY) in blood cells, is associated with all-cause mortality and an increased risk of non-hematological tumors and that LOY could be induced by tobacco smoking. We tested here a hypothesis that men with LOY are more susceptible to AD and show that LOY is associated with AD in three independent studies of different types. In a case-control study, males with AD diagnosis had higher degree of LOY mosaicism (adjusted odds ratio = 2.80, p = 0.0184, AD events = 606). Furthermore, in two prospective studies, men with LOY at blood sampling had greater risk for incident AD diagnosis during follow-up time (hazard ratio [HR] = 6.80, 95% confidence interval [95% CI] = 2.16–21.43, AD events = 140, p = 0.0011). Thus, LOY in blood is associated with risks of both AD and cancer, suggesting a role of LOY in blood cells on disease processes in other tissues, possibly via defective immunosurveillance. As a male-specific risk factor, LOY might explain why males on average live shorter lives than females.
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spelling pubmed-49082252016-12-02 Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease Dumanski, Jan P. Lambert, Jean-Charles Rasi, Chiara Giedraitis, Vilmantas Davies, Hanna Grenier-Boley, Benjamin Lindgren, Cecilia M. Campion, Dominique Dufouil, Carole Pasquier, Florence Amouyel, Philippe Lannfelt, Lars Ingelsson, Martin Kilander, Lena Lind, Lars Forsberg, Lars A. Am J Hum Genet Article Men have a shorter life expectancy compared with women but the underlying factor(s) are not clear. Late-onset, sporadic Alzheimer disease (AD) is a common and lethal neurodegenerative disorder and many germline inherited variants have been found to influence the risk of developing AD. Our previous results show that a fundamentally different genetic variant, i.e., lifetime-acquired loss of chromosome Y (LOY) in blood cells, is associated with all-cause mortality and an increased risk of non-hematological tumors and that LOY could be induced by tobacco smoking. We tested here a hypothesis that men with LOY are more susceptible to AD and show that LOY is associated with AD in three independent studies of different types. In a case-control study, males with AD diagnosis had higher degree of LOY mosaicism (adjusted odds ratio = 2.80, p = 0.0184, AD events = 606). Furthermore, in two prospective studies, men with LOY at blood sampling had greater risk for incident AD diagnosis during follow-up time (hazard ratio [HR] = 6.80, 95% confidence interval [95% CI] = 2.16–21.43, AD events = 140, p = 0.0011). Thus, LOY in blood is associated with risks of both AD and cancer, suggesting a role of LOY in blood cells on disease processes in other tissues, possibly via defective immunosurveillance. As a male-specific risk factor, LOY might explain why males on average live shorter lives than females. Elsevier 2016-06-02 2016-05-23 /pmc/articles/PMC4908225/ /pubmed/27231129 http://dx.doi.org/10.1016/j.ajhg.2016.05.014 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Dumanski, Jan P.
Lambert, Jean-Charles
Rasi, Chiara
Giedraitis, Vilmantas
Davies, Hanna
Grenier-Boley, Benjamin
Lindgren, Cecilia M.
Campion, Dominique
Dufouil, Carole
Pasquier, Florence
Amouyel, Philippe
Lannfelt, Lars
Ingelsson, Martin
Kilander, Lena
Lind, Lars
Forsberg, Lars A.
Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title_full Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title_fullStr Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title_full_unstemmed Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title_short Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease
title_sort mosaic loss of chromosome y in blood is associated with alzheimer disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908225/
https://www.ncbi.nlm.nih.gov/pubmed/27231129
http://dx.doi.org/10.1016/j.ajhg.2016.05.014
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