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Association between low fetal fraction in cellāfree DNA testing and adverse pregnancy outcome: A systematic review
- Source :
- Prenatal Diagnosis. 41:1287-1295
- Publication Year :
- 2021
- Publisher :
- Wiley, 2021.
-
Abstract
- Objective: Low fetal fraction (LFF) in prenatal cell-free DNA (cfDNA) testing is an important cause of test failure and no-call results. LFF might reflect early abnormal placentation and therefore be associated with adverse pregnancy outcome. Here, we review the available literature on the relationship between LFF in cfDNA testing and adverse pregnancy outcome. Method: A systematic literature search was conducted in MEDLINE and EMBASE up to November 1, 2020. Results: Five studies met the criteria for inclusion; all were retrospective observational cohort studies. The cohort sizes ranged from 370 to 6375 pregnancies, with all tests performed in the first trimester or early second trimester. A 4% cutoff for LFF was used in two studies, two studies used the 5th and 25th percentiles, respectively, and one study used a variety of cutoff values for LFF. LFF in prenatal cfDNA testing was observed to be associated with hypertensive disease of pregnancy, small for gestational age neonates, and preterm birth. Conflicting results were found regarding the association between LFF and gestational diabetes mellitus. Conclusions: LFF in cfDNA testing is associated with adverse pregnancy outcome,specifically pregnancy-related hypertensive disorders, preterm birth, and impaired fetal growth related to placental dysfunction. Since the available evidence is limited, a large prospective cohort study on the relationship between fetal fraction and pregnancy outcomes is needed.
- Subjects :
- Adult
medicine.medical_specialty
Fetus
Pregnancy
Obstetrics
business.industry
Noninvasive Prenatal Testing
Pregnancy Outcome
Obstetrics and Gynecology
medicine.disease
Gestational diabetes
Cohort
medicine
Hypertensive disease of pregnancy
Humans
Small for gestational age
Female
Prospective cohort study
business
Cell-Free Nucleic Acids
Genetics (clinical)
Cohort study
Subjects
Details
- ISSN :
- 10970223 and 01973851
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Prenatal Diagnosis
- Accession number :
- edsair.doi.dedup.....6f2a67378d3865125eadee79db0b8ee9