Literature DB >> 12497247

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.

C L Beever1, M D Stephenson, M S Peñaherrera, R H Jiang, D K Kalousek, M Hayden, L Field, C J Brown, W P Robinson.   

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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Year:  2002        PMID: 12497247      PMCID: PMC379232          DOI: 10.1086/346119

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  40 in total

Review 1.  Skewed X inactivation and recurrent spontaneous abortion.

Authors:  W P Robinson; C Beever; C J Brown; M D Stephenson
Journal:  Semin Reprod Med       Date:  2001-06       Impact factor: 1.303

2.  Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns.

Authors:  Christy Beever; Betty P Y Lai; Sarah E L Baldry; Maria S Peñaherrera; Ruby Jiang; Wendy P Robinson; Carolyn J Brown
Journal:  Am J Med Genet A       Date:  2003-07-30       Impact factor: 2.802

3.  Reproductive outcome in patients with diminished ovarian reserve.

Authors:  A J Levi; M F Raynault; P A Bergh; M R Drews; B T Miller; R T Scott
Journal:  Fertil Steril       Date:  2001-10       Impact factor: 7.329

4.  A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.

Authors:  M C Lanasa; W A Hogge; C J Kubik; R B Ness; J Harger; T Nagel; T Prosen; N Markovic; E P Hoffman
Journal:  Am J Obstet Gynecol       Date:  2001-09       Impact factor: 8.661

5.  X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes.

Authors:  S Mumm; L Herrera; P W Waeltz; A Scardovi; R Nagaraja; T Esposito; D Schlessinger; M Rocchi; A Forabosco
Journal:  Genomics       Date:  2001-08       Impact factor: 5.736

6.  The origin of abnormalities in recurrent aneuploidy/polyploidy.

Authors:  W P Robinson; D E McFadden; M D Stephenson
Journal:  Am J Hum Genet       Date:  2001-10-23       Impact factor: 11.025

7.  Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation.

Authors:  Catherine L Anderson; Carolyn J Brown
Journal:  Hum Genet       Date:  2002-02-01       Impact factor: 4.132

8.  Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss.

Authors:  S Uehara; M Hashiyada; K Sato; Y Sato; K Fujimori; K Okamura
Journal:  Fertil Steril       Date:  2001-11       Impact factor: 7.329

Review 9.  To err (meiotically) is human: the genesis of human aneuploidy.

Authors:  T Hassold; P Hunt
Journal:  Nat Rev Genet       Date:  2001-04       Impact factor: 53.242

10.  Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos.

Authors:  P P Tam; M H Snow
Journal:  J Embryol Exp Morphol       Date:  1981-08
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  19 in total

1.  Trisomy recurrence: a reconsideration based on North American data.

Authors:  Dorothy Warburton; Louis Dallaire; Maya Thangavelu; Lori Ross; Bruce Levin; Jennie Kline
Journal:  Am J Hum Genet       Date:  2004-07-08       Impact factor: 11.025

2.  X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.

Authors:  James M Amos-Landgraf; Amy Cottle; Robert M Plenge; Mike Friez; Charles E Schwartz; John Longshore; Huntington F Willard
Journal:  Am J Hum Genet       Date:  2006-07-27       Impact factor: 11.025

Review 3.  X chromosome inactivation in clinical practice.

Authors:  Karen Helene Orstavik
Journal:  Hum Genet       Date:  2009-04-25       Impact factor: 4.132

4.  Skewed X chromosome inactivation and trisomic spontaneous abortion: no association.

Authors:  Dorothy Warburton; Jennie Kline; Ann Kinney; Chih-Yu Yu; Bruce Levin; Stephen Brown
Journal:  Am J Hum Genet       Date:  2009-07-30       Impact factor: 11.025

5.  Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype.

Authors:  Palma Finelli; Silvia Maria Sirchia; Maura Masciadri; Milena Crippa; Maria Paola Recalcati; Daniela Rusconi; Daniela Giardino; Laura Monti; Francesca Cogliati; Francesca Faravelli; Federica Natacci; Leonardo Zoccante; Bernardo Dalla Bernardina; Silvia Russo; Lidia Larizza
Journal:  Mol Cytogenet       Date:  2012-04-04       Impact factor: 2.009

6.  Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.

Authors:  Mercy Y Laurino; Robin L Bennett; Devki S Saraiya; Lisa Baumeister; Debra Lochner Doyle; Kathleen Leppig; Barbara Pettersen; Robert Resta; Larry Shields; Stefanie Uhrich; Elizabeth A Varga; Wendy H Raskind
Journal:  J Genet Couns       Date:  2005-06       Impact factor: 2.537

7.  FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.

Authors:  Karla L Bretherick; Margo R Fluker; Wendy P Robinson
Journal:  Hum Genet       Date:  2005-06-02       Impact factor: 4.132

8.  X-chromosome inactivation patterns in Korean women with idiopathic recurrent spontaneous abortion.

Authors:  Jin-Woo Kim; So-Yeon Park; Young-Mi Kim; Jin-Mee Kim; Jung-Yeol Han; Hyun-Mee Ryu
Journal:  J Korean Med Sci       Date:  2004-04       Impact factor: 2.153

9.  Role of progesterone receptor polymorphisms in the recurrent spontaneous abortions: Indian case.

Authors:  Meka Aruna; Theeya Nagaraja; Sadaranga Andal; Surapaneni Tarakeswari; Pisapati V S Sirisha; Alla G Reddy; Kumarasamy Thangaraj; Lalji Singh; B Mohan Reddy
Journal:  PLoS One       Date:  2010-01-14       Impact factor: 3.240

10.  Misbehaviour of XIST RNA in breast cancer cells.

Authors:  Silvia M Sirchia; Silvia Tabano; Laura Monti; Maria P Recalcati; Manuela Gariboldi; Francesca R Grati; Giovanni Porta; Palma Finelli; Paolo Radice; Monica Miozzo
Journal:  PLoS One       Date:  2009-05-15       Impact factor: 3.240

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