ArticleAmerican journal of human genetics2003
Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.
Article in American journal of human genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.
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22 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.
- Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.Journal of genetic counseling · 2005Guideline
- Case report: Variability in clinical manifestations within a family with incontinentia pigmenti.Frontiers in medicine · 2024Article
- Chromosomal abnormalities in recurrent pregnancy loss and its association with clinical characteristics.Journal of assisted reproduction and genetics · 2023Article
- Investigation of the role of X chromosome inactivation and androgen receptor CAG repeat polymorphisms in patients with recurrent pregnancy loss: a prospective case-control study.BMC pregnancy and childbirth · 2022Article
- Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti.Molecular genetics & genomic medicine · 2020Article
- Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation.Human reproduction (Oxford, England) · 2012Article
- Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype.Molecular cytogenetics · 2012Article
- Copy number changes on the X chromosome in women with and without highly skewed X-chromosome inactivation.Cytogenetic and genome research · 2012Article
- High-resolution methylation polymerase chain reaction for fragile X analysis: evidence for novel FMR1 methylation patterns undetected in Southern blot analyses.Genetics in medicine : official journal of the American College of Medical Genetics · 2011Article
- Article
- Skewed X inactivation and IVF-conceived infants.Reproductive biomedicine online · 2010Article
- Role of progesterone receptor polymorphisms in the recurrent spontaneous abortions: Indian case.PloS one · 2010Article
- X chromosome inactivation in clinical practice.Human genetics · 2009Review
- Skewed X chromosome inactivation and trisomic spontaneous abortion: no association.American journal of human genetics · 2009Article
- Misbehaviour of XIST RNA in breast cancer cells.PloS one · 2009Article
- MECP2 promoter methylation and X chromosome inactivation in autism.Autism research : official journal of the International Society for Autism Research · 2008Article
- X-chromosome inactivation patterns in females with Prader-Willi syndrome.American journal of medical genetics. Part A · 2007Article
- X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.American journal of human genetics · 2006Article
- Skewed X chromosome inactivation and early-onset breast cancer.Journal of medical genetics · 2006Article
- FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.Human genetics · 2005Article
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Authors and funding
9 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An increase in extremely skewed X-chromosome inactivation (XCI) (> or = 90%) among women who experienced recurrent spontaneous abortion (RSA) has been previously reported. To further delineate the etiology of this association, we have evaluated XCI status in 207 women who experience RSA. A significant excess of trisomic losses was observed among the women who had RSA with skewed XCI versus those without skewed XCI (P=.02). There was also a significant excess of boys among live births in this group (P=.04), which is contrary to expectations if the cause of skewed XCI was only that these women carried X-linked lethal mutations. To confirm the association between skewed XCI and the risk of trisomy, an independent group of 53 women, ascertained on the basis of a prenatal diagnosis of trisomy mosaicism, were investigated. Only cases for which the trisomy was shown to be of maternal meiotic origin were included. The results show a significantly higher level of extreme skewing (> or = 90%) in women whose pregnancies involved placental trisomy mosaicism (17%) than in either of two separate control populations (n=102 and 99) (P=.02 compared with total control subjects). An additional 11 cases were ascertained on the basis of one or more trisomic-pregnancy losses. When all women in the present study with a trisomic pregnancy (n=103) were considered together, skewed XCI was identified in 18%, as compared with 7% in all controls (n=201) (P=.005). This difference was more pronounced when a cutoff of extreme skewing of 95% was used (10% vs. 1.5% skewed; P=.002). Maternal age was not associated with skewing in either the patient or control populations and therefore cannot account for the association with trisomy. Previous studies have shown that a reduced ovarian reserve is associated with increased risk of trisomic pregnancies. We hypothesize that the association between skewed XCI and trisomic pregnancies is produced by a common mechanism that underlies both and that involves a reduction of the size of the follicular pool.
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