Back

Diminished sex hormone levels influence the risk of skewed X chromosome inactivation

Roberts, A. L.; Osterdahl, M. F.; Sahoo, A.; Pickles, J.; Franklin-Cheung, C.; Wadge, S.; Mohamoud, N. A.; Morea, A.; Amar, A.; Morris, D. L.; Vyse, T. J.; Steves, C. J.; Small, K. S.

2026-04-22 genetic and genomic medicine
10.64898/2026.04.20.26351303 medRxiv
Show abstract

BackgroundX chromosome inactivation (XCI) is the mechanism which randomly silences one X chromosome to equalise gene expression between 46, XX females and 46, XY males. Though XCI is expected to result in a random pattern of mosaicism across tissues, some females display a significantly unbalanced ratio in immune cells, termed XCI-skew, in which [&ge;]75% of cells have the same X inactivated. XCI-skew is associated with adverse health outcomes and its prevalence increases with age - particularly after midlife - yet the specific risk factors have yet to be identified. The menopausal transition, which is driven by profound shifts in sex hormone levels, has significant impact on chronic disease risk yet the molecular and cellular effects are incompletely understood. We hypothesised that the menopausal transition may impact XCI-skew. MethodsUsing XCI data measured in blood-derived DNA from 1,395 females from the TwinsUK population cohort, along with questionnaires, genetic data, and sex hormone measures, we carried out a cross-sectional study to assess the impact of the menopausal transition and sex hormones on XCI-skew. ResultsWe demonstrate that early menopause (<45yrs) is associated with increased risk of XCI-skew. In subset analyses across those who had a surgically induced or natural menopause, we find the association restricted to those who underwent a surgical menopause. We next identify a low polygenic score (PGS) for testosterone levels is significantly associated with XCI-skew, which we replicate in an independent dataset (n=149), while a PGS for age at natural menopause is not associated. Finally, using longitudinal measures across two time points spanning [~]18 years we show XCI-skew is a stable cellular phenotype that typically increases over time. DiscussionThese data represent the first environmental and genetic risk factors of XCI-skew, both of which implicate endogenous sex hormone levels, particularly testosterone. We propose XCI-skew may have clinical relevance in postmenopausal females.

Matching journals

The top 8 journals account for 50% of the predicted probability mass.

1
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 5%
10.3%
2
Clinical Epigenetics
53 papers in training set
Top 0.1%
8.6%
3
The Journal of Clinical Endocrinology & Metabolism
35 papers in training set
Top 0.2%
7.0%
4
Nature Communications
4913 papers in training set
Top 28%
6.5%
5
Human Reproduction
18 papers in training set
Top 0.1%
6.5%
6
Scientific Reports
3102 papers in training set
Top 30%
4.0%
7
Cancers
200 papers in training set
Top 2%
3.7%
8
BMC Medicine
163 papers in training set
Top 1%
3.7%
50% of probability mass above
9
iScience
1063 papers in training set
Top 7%
2.8%
10
PLOS Genetics
756 papers in training set
Top 6%
2.7%
11
Aging
69 papers in training set
Top 0.9%
2.4%
12
PLOS ONE
4510 papers in training set
Top 47%
2.1%
13
Frontiers in Genetics
197 papers in training set
Top 4%
1.8%
14
Science Advances
1098 papers in training set
Top 15%
1.8%
15
Frontiers in Cell and Developmental Biology
218 papers in training set
Top 4%
1.7%
16
eLife
5422 papers in training set
Top 41%
1.7%
17
Bioinformatics
1061 papers in training set
Top 7%
1.5%
18
Aging Cell
144 papers in training set
Top 2%
1.4%
19
International Journal of Molecular Sciences
453 papers in training set
Top 10%
1.2%
20
Frontiers in Immunology
586 papers in training set
Top 6%
1.0%
21
The American Journal of Human Genetics
206 papers in training set
Top 3%
1.0%
22
Human Molecular Genetics
130 papers in training set
Top 3%
0.8%
23
Biology of Sex Differences
29 papers in training set
Top 0.6%
0.8%
24
Human Genetics and Genomics Advances
70 papers in training set
Top 0.7%
0.8%
25
Epigenomics
10 papers in training set
Top 0.1%
0.8%
26
Genes
126 papers in training set
Top 3%
0.8%
27
Endocrinology
38 papers in training set
Top 0.6%
0.7%
28
Molecular Psychiatry
242 papers in training set
Top 4%
0.7%
29
The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences
22 papers in training set
Top 0.4%
0.7%
30
Neuropsychopharmacology
134 papers in training set
Top 3%
0.7%