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Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men

Mosaic loss of Y chromosome (mLOY) is the most frequently detected somatic copy number alteration in leukocytes of men. In this study, we investigate blood cell counts as a potential mechanism linking mLOY to disease risk in 206,353 UK males. Associations between mLOY, detected by genotyping arrays,...

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Autores principales: Lin, Shu-Hong, Loftfield, Erikka, Sampson, Josh N., Zhou, Weiyin, Yeager, Meredith, Freedman, Neal D., Chanock, Stephen J., Machiela, Mitchell J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046668/
https://www.ncbi.nlm.nih.gov/pubmed/32108144
http://dx.doi.org/10.1038/s41598-020-59963-8
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author Lin, Shu-Hong
Loftfield, Erikka
Sampson, Josh N.
Zhou, Weiyin
Yeager, Meredith
Freedman, Neal D.
Chanock, Stephen J.
Machiela, Mitchell J.
author_facet Lin, Shu-Hong
Loftfield, Erikka
Sampson, Josh N.
Zhou, Weiyin
Yeager, Meredith
Freedman, Neal D.
Chanock, Stephen J.
Machiela, Mitchell J.
author_sort Lin, Shu-Hong
collection PubMed
description Mosaic loss of Y chromosome (mLOY) is the most frequently detected somatic copy number alteration in leukocytes of men. In this study, we investigate blood cell counts as a potential mechanism linking mLOY to disease risk in 206,353 UK males. Associations between mLOY, detected by genotyping arrays, and blood cell counts were assessed by multivariable linear models adjusted for relevant risk factors. Among the participants, mLOY was detected in 39,809 men. We observed associations between mLOY and reduced erythrocyte count (−0.009 [−0.014, −0.005] × 10(12) cells/L, p = 2.75 × 10(−5)) and elevated thrombocyte count (5.523 [4.862, 6.183] × 10(9) cells/L, p = 2.32 × 10(−60)) and leukocyte count (0.218 [0.198, 0.239] × 10(9) cells/L, p = 9.22 × 10(−95)), particularly for neutrophil count (0.174 × [0.158, 0.190]10(9) cells/L, p = 1.24 × 10(−99)) and monocyte count (0.021 [0.018 to 0.024] × 10(9) cells/L, p = 6.93 × 10(−57)), but lymphocyte count was less consistent (0.016 [0.007, 0.025] × 10(9) cells/L, p = 8.52 × 10(−4)). Stratified analyses indicate these associations are independent of the effects of aging and smoking. Our findings provide population-based evidence for associations between mLOY and blood cell counts that should stimulate investigation of the underlying biological mechanisms linking mLOY to cancer and chronic disease risk.
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spelling pubmed-70466682020-03-05 Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men Lin, Shu-Hong Loftfield, Erikka Sampson, Josh N. Zhou, Weiyin Yeager, Meredith Freedman, Neal D. Chanock, Stephen J. Machiela, Mitchell J. Sci Rep Article Mosaic loss of Y chromosome (mLOY) is the most frequently detected somatic copy number alteration in leukocytes of men. In this study, we investigate blood cell counts as a potential mechanism linking mLOY to disease risk in 206,353 UK males. Associations between mLOY, detected by genotyping arrays, and blood cell counts were assessed by multivariable linear models adjusted for relevant risk factors. Among the participants, mLOY was detected in 39,809 men. We observed associations between mLOY and reduced erythrocyte count (−0.009 [−0.014, −0.005] × 10(12) cells/L, p = 2.75 × 10(−5)) and elevated thrombocyte count (5.523 [4.862, 6.183] × 10(9) cells/L, p = 2.32 × 10(−60)) and leukocyte count (0.218 [0.198, 0.239] × 10(9) cells/L, p = 9.22 × 10(−95)), particularly for neutrophil count (0.174 × [0.158, 0.190]10(9) cells/L, p = 1.24 × 10(−99)) and monocyte count (0.021 [0.018 to 0.024] × 10(9) cells/L, p = 6.93 × 10(−57)), but lymphocyte count was less consistent (0.016 [0.007, 0.025] × 10(9) cells/L, p = 8.52 × 10(−4)). Stratified analyses indicate these associations are independent of the effects of aging and smoking. Our findings provide population-based evidence for associations between mLOY and blood cell counts that should stimulate investigation of the underlying biological mechanisms linking mLOY to cancer and chronic disease risk. Nature Publishing Group UK 2020-02-27 /pmc/articles/PMC7046668/ /pubmed/32108144 http://dx.doi.org/10.1038/s41598-020-59963-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Shu-Hong
Loftfield, Erikka
Sampson, Josh N.
Zhou, Weiyin
Yeager, Meredith
Freedman, Neal D.
Chanock, Stephen J.
Machiela, Mitchell J.
Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title_full Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title_fullStr Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title_full_unstemmed Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title_short Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men
title_sort mosaic chromosome y loss is associated with alterations in blood cell counts in uk biobank men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046668/
https://www.ncbi.nlm.nih.gov/pubmed/32108144
http://dx.doi.org/10.1038/s41598-020-59963-8
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