Literature DB >> 30638594

Genetic abnormalities and pregnancy loss.

Nathan R Blue1, Jessica M Page2, Robert M Silver3.   

Abstract

Genetic abnormalities, whether occurring in the conceptus or the parents, can predispose to sporadic or recurrent pregnancy loss (RPL). Abnormalities in the conceptus include aneuploidy, copy number changes, skewed X inactivation, and single gene disorders or mutations. Among parents who suffer RPL, the best studied genetic cause is balanced chromosomal translocations. For evaluation of genetic abnormalities in cases of pregnancy loss, chromosomal microarray is more likely to yield interpretable results than karyotype due to cell culture failure. For parents, karyotype remains the standard since microarray may not detect truly balanced translocations. For those with an identified underlying genetic abnormality, preimplantation genetic testing has been proposed to optimize the live birth rate. This approach shows promise, but currently lacks supporting evidence. In summary, various genetic causes for recurrent pregnancy loss are known, but when such a cause is identified, the implications for management remain unclear.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  aneuploidy; genetic; karyotype; microarray; miscarriage; preimplantation genetic testing; recurrent pregnancy loss

Mesh:

Year:  2018        PMID: 30638594      PMCID: PMC8272960          DOI: 10.1053/j.semperi.2018.12.002

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  52 in total

1.  Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestation.

Authors:  Jennifer E Warren; David K Turok; Teresa M Maxwell; Arthur R Brothman; Robert M Silver
Journal:  Obstet Gynecol       Date:  2009-11       Impact factor: 7.661

Review 2.  Pregnancy outcome after preimplantation genetic screening or natural conception in couples with unexplained recurrent miscarriage: a systematic review of the best available evidence.

Authors:  Anna M Musters; Sjoerd Repping; Johanna C Korevaar; Sebastiaan Mastenbroek; Jacqueline Limpens; Fulco van der Veen; Mariëtte Goddijn
Journal:  Fertil Steril       Date:  2011-01-08       Impact factor: 7.329

3.  Increased chromosome 16 disomy rates in human spermatozoa and recurrent spontaneous abortions.

Authors:  Michaela Neusser; Nina Rogenhofer; Stephanie Dürl; Robert Ochsenkühn; Matthias Trottmann; Vindi Jurinovic; Ortrud Steinlein; Viktoria von Schönfeldt; Stefan Müller; Christian J Thaler
Journal:  Fertil Steril       Date:  2015-08-25       Impact factor: 7.329

4.  Antepartum dalteparin versus no antepartum dalteparin for the prevention of pregnancy complications in pregnant women with thrombophilia (TIPPS): a multinational open-label randomised trial.

Authors:  Marc A Rodger; William M Hague; John Kingdom; Susan R Kahn; Alan Karovitch; Mathew Sermer; Anne Marie Clement; Suzette Coat; Wee Shian Chan; Joanne Said; Evelyne Rey; Sue Robinson; Rshmi Khurana; Christine Demers; Michael J Kovacs; Susan Solymoss; Kim Hinshaw; James Dwyer; Graeme Smith; Sarah McDonald; Jill Newstead-Angel; Anne McLeod; Meena Khandelwal; Robert M Silver; Gregoire Le Gal; Ian A Greer; Erin Keely; Karen Rosene-Montella; Mark Walker; Philip S Wells
Journal:  Lancet       Date:  2014-07-24       Impact factor: 79.321

5.  Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.

Authors:  Brynn Levy; Styrmir Sigurjonsson; Barbara Pettersen; Melissa K Maisenbacher; Megan P Hall; Zachary Demko; Ruth B Lathi; Rosina Tao; Vimla Aggarwal; Matthew Rabinowitz
Journal:  Obstet Gynecol       Date:  2014-08       Impact factor: 7.661

6.  Fluorescence in situ hybridization detects increased sperm aneuploidy in men with recurrent pregnancy loss.

Authors:  Ranjith Ramasamy; Jason M Scovell; Jason R Kovac; Peter J Cook; Dolores J Lamb; Larry I Lipshultz
Journal:  Fertil Steril       Date:  2015-02-20       Impact factor: 7.329

7.  Karyotype versus microarray testing for genetic abnormalities after stillbirth.

Authors:  Uma M Reddy; Grier P Page; George R Saade; Robert M Silver; Vanessa R Thorsten; Corette B Parker; Halit Pinar; Marian Willinger; Barbara J Stoll; Josefine Heim-Hall; Michael W Varner; Robert L Goldenberg; Radek Bukowski; Ronald J Wapner; Carolyn D Drews-Botsch; Barbara M O'Brien; Donald J Dudley; Brynn Levy
Journal:  N Engl J Med       Date:  2012-12-06       Impact factor: 91.245

8.  Genetic counseling in Robertsonian translocations der(13;14): frequencies of reproductive outcomes and infertility in 101 pedigrees.

Authors:  Hartmut Engels; Thomas Eggermann; Almut Caliebe; Anna Jelska; Regine Schubert; Herdit M Schüler; Barbara Panasiuk; Jacek Zaremba; Anna Latos-Bieleńska; Lucjusz Jakubowski; Klaus P Zerres; Gesa Schwanitz; Alina T Midro
Journal:  Am J Med Genet A       Date:  2008-10-15       Impact factor: 2.802

9.  Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations.

Authors:  Mayumi Sugiura-Ogasawara; Yasuhiko Ozaki; Takeshi Sato; Nobuhiro Suzumori; Kaoru Suzumori
Journal:  Fertil Steril       Date:  2004-02       Impact factor: 7.329

10.  Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.

Authors:  Trilochan Sahoo; Natasa Dzidic; Michelle N Strecker; Sara Commander; Mary K Travis; Charles Doherty; R Weslie Tyson; Arturo E Mendoza; Mary Stephenson; Craig A Dise; Carlos W Benito; Mandolin S Ziadie; Karine Hovanes
Journal:  Genet Med       Date:  2016-06-23       Impact factor: 8.822

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  6 in total

1.  A systematic review to guide future efforts in the determination of genetic causes of pregnancy loss.

Authors:  Andrew Z Carey; Nathan R Blue; Michael W Varner; Jessica M Page; Nathorn Chaiyakunapruk; Aaron R Quinlan; D Ware Branch; Robert M Silver; Tsegaselassie Workalemahu
Journal:  Front Reprod Health       Date:  2021-12-15

2.  Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population.

Authors:  Jianlong Zhuang; Chunnuan Chen; Rongfu Huang; Qi Luo; Yuying Jiang; Shuhong Zeng; Yuanbai Wang; Yingjun Xie
Journal:  Mol Cytogenet       Date:  2022-06-07       Impact factor: 1.904

3.  Blastocyst conversion rate and ploidy in patients with structural rearrangements.

Authors:  Iris G Insogna; A Lanes; L Dobson; E S Ginsburg; C Racowsky; E Yanushpolsky
Journal:  J Assist Reprod Genet       Date:  2021-03-03       Impact factor: 3.412

Review 4.  Endometrial Decidualization: The Primary Driver of Pregnancy Health.

Authors:  Shu-Wing Ng; Gabriella A Norwitz; Mihaela Pavlicev; Tamara Tilburgs; Carlos Simón; Errol R Norwitz
Journal:  Int J Mol Sci       Date:  2020-06-08       Impact factor: 5.923

5.  Prenatal Diagnosis Nomograms: A Novel Tool to Predict Fetal Chromosomal Abnormalities in High-Risk Patients.

Authors:  Yangzi Zhou; Zixuan Song; Lu Sun; Yuting Wang; Xiting Lin; Dandan Zhang
Journal:  Risk Manag Healthc Policy       Date:  2021-11-04

Review 6.  Genetic Testing for Aneuploidy in Patients Who Have Had Multiple Miscarriages: A Review of Current Literature.

Authors:  Ralph S Papas; William H Kutteh
Journal:  Appl Clin Genet       Date:  2021-07-23
  6 in total

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