Cell-free fetal DNA in maternal plasma during physiological single male pregnancies: methodology issues and kinetics
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu srovnávací studie, hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
18504375
DOI
10.1159/000132400
PII: 000132400
Knihovny.cz E-zdroje
- MeSH
- biochemická analýza krve metody MeSH
- biologické markery krev MeSH
- DNA krev MeSH
- druhý trimestr těhotenství krev MeSH
- kinetika MeSH
- lidé MeSH
- maternofetální výměna látek * MeSH
- plod MeSH
- první trimestr těhotenství krev MeSH
- těhotenství krev MeSH
- třetí trimestr těhotenství krev MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- těhotenství krev MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- biologické markery MeSH
- DNA MeSH
OBJECTIVE: To analyze methodological influences and characterize the concentrations of cell-free fetal DNA (cffDNA) circulating in maternal plasma at different gestational ages in physiological pregnancies. METHODS: We investigated 238 independent samples from single male-bearing pregnancies of different gestation age. In the other 50 pregnancies, the samples were collected three times during pregnancy (at all trimesters) to evaluate the kinetics of cffDNA. The manual and automated DNA extraction methods (Roche) were compared. cffDNA was amplified using real-time PCR method and Y-specific sequences SRY and DYS14. Total cell-free DNA circulating in maternal plasma was determined by the use of the GADPH sequence. RESULTS: The elevation in the concentration of cffDNA during pregnancy with the highest value in the third trimester was observed independently on the DNA extraction method and on the Y-specific amplified sequence. The same is documented for the percentage of fetal DNA in total cell-free DNA in maternal plasma. It increases also in successive trimesters (8.3, 10.7 and 23.2%). CONCLUSIONS: We discuss methodological problems and describe statistical parameters of cffDNA concentrations in maternal plasma during pregnancy as the basic information for comparison with pregnancies having a pathological outcome.
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