Evidence map›Paper›PMID 36412098›Full record

ArticleeLife2022

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

Amy L Roberts, Alessandro Morea, Ariella Amar, Antonino Zito, Julia S El-Sayed Moustafa, Max Tomlinson, Ruth C E Bowyer, Xinyuan Zhang, Colette Christiansen, Ricardo Costeira and 6 more

Abstract readTwin Study
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Amy L RobertsDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0002-5704-9249
Alessandro MoreaDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0002-7919-1932
Ariella AmarDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Antonino ZitoDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0003-1931-984X
Julia S El-Sayed MoustafaDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Max TomlinsonDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Ruth C E BowyerDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Xinyuan ZhangDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Colette ChristiansenDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Ricardo CosteiraDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Claire J StevesDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0002-4910-0489
Massimo ManginoDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0002-2167-7470
Jordana T BellDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.
Chloe C Y WongSocial, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Timothy J VyseDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0003-1123-1464
Kerrin S SmallDepartment of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.ORCID 0000-0003-4566-0005

Funding

Medical Research Council MR/M004422/1Medical Research Council MR/R023131/1Wellcome Trust
6 · The paper itself

Abstract

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.

Indexed as

Cardiovascular DiseasesX Chromosome InactivationCross-Sectional StudiesFemaleFollow-Up StudiesHumansMaleOutcome Assessment, Health CareProspective Studiescancercardiovascular diseaseepidemiologygeneticsgenomicsglobal healthhaematopoiesishumanX chromosome inactivation

Identifiers

PMID36412098
PMCPMC9681199

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.