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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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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. |
format | Online Article Text |
id | pubmed-4908225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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