Literature DB >> 30159247

Chromosomal instability in first trimester miscarriage: a common cause of pregnancy loss?

Philip John Hardy1, Kathy Hardy1.   

Abstract

BACKGROUND: First trimester miscarriage without underlying medical conditions is most commonly caused by chromosomal abnormalities reported to occur in 50% or more of cases. These chromosomal changes in early losses include both numerical abnormalities and structural alterations that result in gain and/or loss of genetic information. Structural alterations are much less common than numerical changes. Jumping translocations (JTs) are considered extremely rare with only four cases previously reported.
METHODS: We report 12 examples of chromosome instability seen in the fetal material of spontaneous first trimester miscarriages in a single study population.
RESULTS: In these examples, we observed different cell lines with related chromosomal alterations. Some may be considered to be JT, where a single donor site was observed with different recipients. Others involved more than one site on the "donor" chromosome. One reported miscarriage involved multiple aneuploidy. All alterations resulted in partial trisomies and monosomies which predisposed the pregnancy to chromosomal imbalance and subsequent demise. Patient demographic data did not indicate possible causes of the errors observed.
CONCLUSIONS: This is the first report of such a large cohort and is believed to be the result of increased knowledge and depth of analysis in this area, rather than a representation of confounding factors in this population. It is therefore proposed that identifying these chromosomal changes must be incorporated into the system of testing within the clinical environment. We must also recognize that some routine laboratory techniques will fail to detect such genetic changes.

Entities:  

Keywords:  Chromosomal instability (CIN); chromosomes; jumping translocations (JTs); miscarriage; structural alterations

Year:  2018        PMID: 30159247      PMCID: PMC6087828          DOI: 10.21037/tp.2018.03.02

Source DB:  PubMed          Journal:  Transl Pediatr        ISSN: 2224-4336


  26 in total

1.  Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation.

Authors:  G Lefort; P Blanchet; A M Chaze; A Girardet; P Sarda; J Demaille; F Pellestor
Journal:  J Med Genet       Date:  2001-01       Impact factor: 6.318

2.  "Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis.

Authors:  G Gimelli; E Porro; F Santi; S Scappaticci; O Zuffardi
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

Review 3.  The conundrum of a jumping translocation (JT) in CVS from twins and review of JTs.

Authors:  Kavita S Reddy
Journal:  Am J Med Genet A       Date:  2010-11       Impact factor: 2.802

4.  The presence of interstitial telomeric sequences in constitutional chromosome abnormalities.

Authors:  V M Park; K M Gustashaw; T M Wathen
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

5.  Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.

Authors:  Halil Aslan; Birsen Karaman; Gokhan Yildirim; Yavuz Ceylan
Journal:  Prenat Diagn       Date:  2005-11       Impact factor: 3.050

Review 6.  Jumping translocation with partial duplications and triplications of chromosomes 7 and 15.

Authors:  T Jewett; D Marnane; W Stewart; R Hayworth-Hodge; L Finklea; K Klinepeter; P N Rao; M J Pettenati
Journal:  Clin Genet       Date:  1998-05       Impact factor: 4.438

7.  Molecular and genetic characterization of a radiation-induced structural rearrangement in mouse chromosome 2 causing mutations at the limb deformity and agouti loci.

Authors:  R P Woychik; W M Generoso; L B Russell; K T Cain; N L Cacheiro; S J Bultman; P B Selby; M E Dickinson; B L Hogan; J C Rutledge
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

8.  Interstitial telomeric sequences at the junction site of a jumping translocation.

Authors:  J R Vermeesch; P Petit; F Speleman; K Devriendt; J P Fryns; P Marynen
Journal:  Hum Genet       Date:  1997-06       Impact factor: 4.132

Review 9.  Centrosome amplification in tumorigenesis.

Authors:  Simon J Anderhub; Alwin Krämer; Bettina Maier
Journal:  Cancer Lett       Date:  2012-02-14       Impact factor: 8.679

Review 10.  Defining 'chromosomal instability'.

Authors:  Jochen B Geigl; Anna C Obenauf; Thomas Schwarzbraun; Michael R Speicher
Journal:  Trends Genet       Date:  2008-01-14       Impact factor: 11.639

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  4 in total

1.  Prevalence of chromosome anomalies in a deer farm with fertility decline in Malaysia.

Authors:  Muhammad Sanusi Yahaya; Mohd Shahrom Salisi; Nur Mahiza Md Isa; Goh Yong Meng; Abdwahid Haron
Journal:  Future Sci OA       Date:  2020-06-02

2.  Cross-sectional study of chromosomal aberrations and immunologic factors in Iraqi couples with recurrent pregnancy loss.

Authors:  Doaa A Khamees; Mushtak T S Al-Ouqaili
Journal:  PeerJ       Date:  2022-02-07       Impact factor: 2.984

3.  Altered Thermal Behavior of Blood Plasma Proteome Related to Inflammatory Cytokines in Early Pregnancy Loss.

Authors:  Regina Komsa-Penkova; Avgustina Danailova; Sashka Krumova; Galya Georgieva; Ina Giosheva; Lidia Gartcheva; Ivan Iliev; Emil Gartchev; Kameliya Kercheva; Alexey Savov; Svetla Todinova
Journal:  Int J Mol Sci       Date:  2022-08-06       Impact factor: 6.208

4.  The effects of DICER1 and DROSHA polymorphisms on susceptibility to recurrent spontaneous abortion.

Authors:  Marzieh Ghasemi; Mahnaz Rezaei; Atefeh Yazdi; Narjes Keikha; Rostam Maruei-Milan; Mina Asadi-Tarani; Saeedeh Salimi
Journal:  J Clin Lab Anal       Date:  2019-10-28       Impact factor: 2.352

  4 in total

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