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Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans

BACKGROUND: Ageing is a heterogenous process characterised by cellular and molecular hallmarks, including changes to haematopoietic stem cells and is a primary risk factor for chronic diseases. X chromosome inactivation (XCI) randomly transcriptionally silences either the maternal or paternal X in e...

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Autores principales: Roberts, Amy L, Morea, Alessandro, Amar, Ariella, Zito, Antonino, El-Sayed Moustafa, Julia S, Tomlinson, Max, Bowyer, Ruth CE, Zhang, Xinyuan, Christiansen, Colette, Costeira, Ricardo, Steves, Claire J, Mangino, Massimo, Bell, Jordana T, Wong, Chloe CY, Vyse, Timothy J, Small, Kerrin S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681199/
https://www.ncbi.nlm.nih.gov/pubmed/36412098
http://dx.doi.org/10.7554/eLife.78263
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author Roberts, Amy L
Morea, Alessandro
Amar, Ariella
Zito, Antonino
El-Sayed Moustafa, Julia S
Tomlinson, Max
Bowyer, Ruth CE
Zhang, Xinyuan
Christiansen, Colette
Costeira, Ricardo
Steves, Claire J
Mangino, Massimo
Bell, Jordana T
Wong, Chloe CY
Vyse, Timothy J
Small, Kerrin S
author_facet Roberts, Amy L
Morea, Alessandro
Amar, Ariella
Zito, Antonino
El-Sayed Moustafa, Julia S
Tomlinson, Max
Bowyer, Ruth CE
Zhang, Xinyuan
Christiansen, Colette
Costeira, Ricardo
Steves, Claire J
Mangino, Massimo
Bell, Jordana T
Wong, Chloe CY
Vyse, Timothy J
Small, Kerrin S
author_sort Roberts, Amy L
collection PubMed
description BACKGROUND: Ageing is a heterogenous process characterised by cellular and molecular hallmarks, including changes to haematopoietic stem cells and is a primary risk factor for chronic diseases. X chromosome inactivation (XCI) randomly transcriptionally silences either the maternal or paternal X in each cell of 46, XX females to balance the gene expression with 46, XY males. Age acquired XCI-skew describes the preferential selection of cells across a tissue resulting in an imbalance of XCI, which is particularly prevalent in blood tissues of ageing females, and yet its clinical consequences are unknown. METHODS: We assayed XCI in 1575 females from the TwinsUK population cohort using DNA extracted from whole blood. We employed prospective, cross-sectional, and intra-twin study designs to characterise the relationship of XCI-skew with molecular and cellular measures of ageing, cardiovascular disease risk, and cancer diagnosis. RESULTS: We demonstrate that XCI-skew is independent of traditional markers of biological ageing and is associated with a haematopoietic bias towards the myeloid lineage. Using an atherosclerotic cardiovascular disease risk score, which captures traditional risk factors, XCI-skew is associated with an increased cardiovascular disease risk both cross-sectionally and within XCI-skew discordant twin pairs. In a prospective 10 year follow-up study, XCI-skew is predictive of future cancer incidence. CONCLUSIONS: Our study demonstrates that age acquired XCI-skew captures changes to the haematopoietic stem cell population and has clinical potential as a unique biomarker of chronic disease risk. FUNDING: KSS acknowledges funding from the Medical Research Council [MR/M004422/1 and MR/R023131/1]. JTB acknowledges funding from the ESRC [ES/N000404/1]. MM acknowledges funding from the National Institute for Health Research (NIHR)-funded BioResource, Clinical Research Facility and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London. TwinsUK is funded by the Wellcome Trust, Medical Research Council, European Union, Chronic Disease Research Foundation (CDRF), Zoe Global Ltd and the National Institute for Health Research (NIHR)-funded BioResource, Clinical Research Facility and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London.
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spelling pubmed-96811992022-11-23 Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans Roberts, Amy L Morea, Alessandro Amar, Ariella Zito, Antonino El-Sayed Moustafa, Julia S Tomlinson, Max Bowyer, Ruth CE Zhang, Xinyuan Christiansen, Colette Costeira, Ricardo Steves, Claire J Mangino, Massimo Bell, Jordana T Wong, Chloe CY Vyse, Timothy J Small, Kerrin S eLife Epidemiology and Global Health BACKGROUND: Ageing is a heterogenous process characterised by cellular and molecular hallmarks, including changes to haematopoietic stem cells and is a primary risk factor for chronic diseases. X chromosome inactivation (XCI) randomly transcriptionally silences either the maternal or paternal X in each cell of 46, XX females to balance the gene expression with 46, XY males. Age acquired XCI-skew describes the preferential selection of cells across a tissue resulting in an imbalance of XCI, which is particularly prevalent in blood tissues of ageing females, and yet its clinical consequences are unknown. METHODS: We assayed XCI in 1575 females from the TwinsUK population cohort using DNA extracted from whole blood. We employed prospective, cross-sectional, and intra-twin study designs to characterise the relationship of XCI-skew with molecular and cellular measures of ageing, cardiovascular disease risk, and cancer diagnosis. RESULTS: We demonstrate that XCI-skew is independent of traditional markers of biological ageing and is associated with a haematopoietic bias towards the myeloid lineage. Using an atherosclerotic cardiovascular disease risk score, which captures traditional risk factors, XCI-skew is associated with an increased cardiovascular disease risk both cross-sectionally and within XCI-skew discordant twin pairs. In a prospective 10 year follow-up study, XCI-skew is predictive of future cancer incidence. CONCLUSIONS: Our study demonstrates that age acquired XCI-skew captures changes to the haematopoietic stem cell population and has clinical potential as a unique biomarker of chronic disease risk. FUNDING: KSS acknowledges funding from the Medical Research Council [MR/M004422/1 and MR/R023131/1]. JTB acknowledges funding from the ESRC [ES/N000404/1]. MM acknowledges funding from the National Institute for Health Research (NIHR)-funded BioResource, Clinical Research Facility and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London. TwinsUK is funded by the Wellcome Trust, Medical Research Council, European Union, Chronic Disease Research Foundation (CDRF), Zoe Global Ltd and the National Institute for Health Research (NIHR)-funded BioResource, Clinical Research Facility and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London. eLife Sciences Publications, Ltd 2022-11-22 /pmc/articles/PMC9681199/ /pubmed/36412098 http://dx.doi.org/10.7554/eLife.78263 Text en © 2022, Roberts et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Epidemiology and Global Health
Roberts, Amy L
Morea, Alessandro
Amar, Ariella
Zito, Antonino
El-Sayed Moustafa, Julia S
Tomlinson, Max
Bowyer, Ruth CE
Zhang, Xinyuan
Christiansen, Colette
Costeira, Ricardo
Steves, Claire J
Mangino, Massimo
Bell, Jordana T
Wong, Chloe CY
Vyse, Timothy J
Small, Kerrin S
Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title_full Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title_fullStr Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title_full_unstemmed Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title_short Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans
title_sort age acquired skewed x chromosome inactivation is associated with adverse health outcomes in humans
topic Epidemiology and Global Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681199/
https://www.ncbi.nlm.nih.gov/pubmed/36412098
http://dx.doi.org/10.7554/eLife.78263
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