Cited by 87Prenatal Screening and DiagnosticsGenomic variations and chromosomal abnormalitiesReproductive System and Pregnancy

Reliability of 46,XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimens

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Lathi, Ruth B., Gustin, Stephanie L.F., Keller, Jennifer, Maisenbacher, Melissa K., Sigurjonsson, Styrmir, Tao, Rosina, Demko, Zach·2014·Fertility and Sterility

Abstract

Objective To examine the rate of maternal contamination in miscarriage specimens.Design Retrospective review of 1,222 miscarriage specimens submitted for chromosome testing with detection of maternal cell contamination (MCC).Setting Referral centers requesting genetic testing of miscarriage specimens at a single reference laboratory.Patient(s) Women with pregnancy loss who desire complete chromosome analysis of the pregnancy tissue.Intervention(s) Analysis of miscarriage specimens using single-nucleotide polymorphism (SNP) microarray technology with bioinformatics program to detect maternal cell contamination.Main outcome measure(s) Chromosome content of miscarriages and incidence of 46,XX results due to MCC.Result(s) Of the 1,222 samples analyzed, 592 had numeric chromosomal abnormalities, and 630 were normal 46,XX or 46,XY (456 and 187, respectively). In 269 of the 46,XX specimens, MCC with no embryonic component was found. With the exclusion of maternal 46,XX results, the chromosomal abnormality rate increased from 48% to 62%, and the ratio for XX to XY results dropped from 2.6 to 1.0.Conclusion(s) Over half of the normal 46,XX results in miscarriage specimens were due to MCC. The use of SNPs in MCC testing allows for precise identification of chromosomal abnormalities in miscarriage as well as MCC, improving the accuracy of products of conception testing.

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Research works printed but not linked: 2

  1. Griffin DK, Millie EA, Redline RW, Hassold TJ, Zaragoza MV. Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicism. Am J Med Genet 1997;72:297-301.
  2. Philipp T, Kalousek DK. Transcervical embryoscopy in missed abortion. J Assist Reprod Genet 2001;18:285-90.

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Authors
Lathi, R. B., Gustin, S. L. F., Keller, J., Maisenbacher, M. K., Sigurjonsson, S., Tao, R., & Demko, Z.
Affiliations
  • Stanford Health Care (US)
  • Natera (United States) (US)
Corresponding author
Lathi, Ruth B.
Venue
Fertility and Sterility
Publisher
Elsevier BV
Published
2014-01
Volume
101
Issue
1
Pages
178-182
ISSN
0015-0282 (ISSN-L)
OpenAlex
W2090421719
Cited by
87
References
18
Citations by year
2026: 1 · 2025: 3 · 2024: 3 · 2023: 7 · 2022: 9 · 2021: 11 · 2020: 10 · 2019: 5 · 2018: 7 · 2017: 9 · 2016: 7 · 2015: 6 · 2014: 8
FWCI
6.51
Type
journal article
Language
en
Open access
Locations
  • Fertility and Sterility (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Screening and Diagnostics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
  • Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
Keywords
miscarriage, maternal cell contamination, early pregnancy loss, SNP array, chromosomal abnormalities, test reliability, sex chromosome aneuploidy
MeSH terms
Abortion, Spontaneous, Adult, Female, Humans, Pregnancy, Pregnancy Trimester, First, Retrospective Studies, Reproducibility of Results, 46, XX Disorders of Sex Development

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