4.6 Review

Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta-analysis

Journal

Publisher

WILEY
DOI: 10.1111/1471-0528.12382

Keywords

arrayCGH; CMA; karyotyping; microarray; miscarriage

Funding

  1. EME TABLET Trial
  2. Children's Charity SPARKS
  3. NIHR clinical lecturer fellowship
  4. Medical Research Council [G0700526] Funding Source: researchfish
  5. National Institute for Health Research [CL-2010-09-003] Funding Source: researchfish
  6. MRC [G0700526] Funding Source: UKRI

Ask authors/readers for more resources

BackgroundApproximately 50% of spontaneous miscarriages are associated with chromosome abnormalities. Identification of these karyotypic abnormalities helps to estimate recurrence risks in future pregnancies. Chromosomal microarray analysis (CMA) is transforming clinical cytogenetic practice with its ability to examine the human genome at increasingly high resolution. ObjectivesThe aim of this study was to determine whether CMA testing on the products of conception following miscarriage provides better diagnostic information compared with conventional karyotyping. Search strategyMEDLINE (from 1996 to December 2012), EMBASE (from 1974 to December 2012), and CINAHL (from 1996 to December 2012) databases were searched electronically. Selection criteriaStudies were selected if CMA was used on products of conception following miscarriage, alongside conventional karyotyping. Data collection and analysisNine papers were included in the systematic review and meta-analysis. All statistical analyses were performed using stata 11.0 (Stata Corp., College Station, TX, USA). Main resultsThere was agreement between CMA and karyotyping in 86.0% of cases (95%CI 77.0-96.0%). CMA detected 13% (95%CI 8.0-21.0) additional chromosome abnormalities over conventional full karyotyping. In addition, traditional, full karyotyping detected 3% (95%CI 1.0-10.0%) additional abnormalities over CMA. The incidence of a variant of unknown significance (VOUS) being detected was 2% (95%CI 1.0-10.0%). Author's conclusionsCompared with karyotyping, there appears to be an increased detection rate of chromosomal abnormalities when CMA is used to analyse the products of conception; however, some of these abnormalities are VOUS, and this information should be provided when counselling women following miscarriage and when taking consent for the analysis of miscarriage products by CMA.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available