{Reference Type}: Journal Article
{Title}: Non-invasive cell-free DNA-based approach for the diagnosis of clinical miscarriage: A retrospective study.
{Author}: Balaguer N;Rodrigo L;Mateu-Brull E;Campos-Galindo I;Castellón JA;Al-Asmar N;Rubio C;Milán M;
{Journal}: BJOG
{Volume}: 131
{Issue}: 2
{Year}: 2024 Jan 2
{Factor}: 7.331
{DOI}: 10.1111/1471-0528.17629
{Abstract}: <B>OBJECTIVE: </B>To evaluate cell-free DNA (cfDNA) testing as a non-invasive approach to detecting aneuploidies in clinical miscarriages.<BR><B>METHODS: </B>A retrospective cohort study of women with pregnancy loss.<BR><B>METHODS: </B>Hospitals and genetic analysis laboratories.<BR><B>METHODS: </B>Pregnancy losses in the period 2021-2022.<BR><B>METHODS: </B>Results derived from non-invasive cfDNA testing (Veriseq NIPT Solution V2) of maternal blood and invasive analysis of products of conception (POC) (Ion ReproSeq) compared in 120 women who suffered a miscarriage.<BR><B>METHODS: </B>Concordance rate results, cfDNA testing performance, non-informative rate (NIR) and fetal fraction (FF).<BR><B>RESULTS: </B>We found no significant differences in the NIR between invasive (iPOC) and non-invasive (niPOC) analysis of POC (10.0% [12/120] versus 16.7% [20/120]). Of 120 samples, 90 provided an informative result in iPOC and niPOC groups (75%). cfDNA analysis correctly identified 74/87 (85.1%) samples (excluding triploidies). Sensitivity and specificity were 79.4% and 100%, respectively; all discordant cases were female. A binomial logistic model suggested fetal sex as the only variable influencing the concordance rate (P = 0.035). A Y-chromosome-based FF estimate allowed the optimal reclassification of cfDNA of non-informative male fetuses and a more accurate evaluation of cfDNA testing performance. The difference between the two FF estimates (native algorithm and Y-chromosome-based) suggests that female non-concordant cases may represent non-informative cases.<BR><B>CONCLUSIONS: </B>Cell-free DNA-based testing provides a non-invasive approach to determining the genetic cause of clinical miscarriage.