Official Title
Evaluation of the Relationship Between Vaginal, Placental and Neonatal Mycobiota and Microbiome With Preterm Birth in Women With Short Cervical Length
Brief Title
Vaginal, Placental and Neonatal Buccal Mycobiota and Microbiome in Preterm Birth
Protocol ID
NCT04165252
Lead Sponsor
Koç University
Brief Summary
Microbiota contributes to the immunological, hormonal and metabolic homeostasis of the
host. As in all natural orifices in the body, there is also a microbiota and mycobiota
specific to the vagina.
On the other hand, the sonographic short cervix in the second trimester of pregnancy is
associated with preterm delivery, which may be an important cause of mortality and
morbidity in the neonatal period. American Society of Obstetricians and Gynecologists
(ACOG), British Royal Society of Obstetricians and Gynecologists (RCOG) and the American
Society of Maternal Fetal Medicine (SMFM) suggest that the measurement of transvaginal
sonographic cervical length at 20-24 gestational weeks for the screening of preterm
birth. The aforementioned associations also recommend the use of progesterone in the
treatment of women who diagnosed with short cervix by transvaginal ultrasonography due to
the fact that progesterone is an effective medication in the prevention of preterm birth
(Grade B).
Previous vaginal microbiota studies have shown that some bacterial species such as
Lactobacillus insers cause a predisposition to premature labor in women with a short
cervix. However, the prominent lack in these studies is that the eukaryotic fungi in
abundant vaginal flora have not been evaluated.
On the other hand, it was already shown that progesterone treatment is able to prevent
only 45% preterm birth in women with short cervical length. This observational
prospective study thus aims to evaluate the variety of microbiota and/or mycobiota in
pregnancies resulting in preterm birth and those who give birth at term. Although women
with short cervical length receive progesterone regularly from the second trimester, the
preterm birth may occur. In this study, the investigators also aim to evaluate the
patterns of microbiota and mycobiota from vaginal swabs of women who had preterm birth
with short cervical length and postpartum swabs of the placenta and fetal oral cavity.
Detailed Description
Preterm birth is responsible for more than 70% of all neonatal and infant deaths. In
addition, the risk of cerebral palsy among children born preterm is 10 times than those
born at term. The risk of preterm birth is inversely related to cervical length at
midgestation. Randomized-controlled trials involving singleton pregnancies with a short
cervical length ( less than 25 mm) have shown that the prophylactic use of progesterone
significantly decrease the rate of preterm delivery and neonatal death. The relation of
vaginal micobiota with preterm birth has been documented. Yet, impact of short cervical
lenght and progesteron treatment on vaginal, neonatal and placental microbiota and
mycobiota has not been evaluated. The objectives of present study are to adress the
following points;
1. Longitudinal maternal (vaginal), fetal (oral) and placental (basal plate and
parenchyma) 16S-based and 18S-based metagenomic profiling with inferred metagenomics
will reveal distinct microbial communities in association with preterm birth.
2. Comparison of vaginal, neonatal (buccal) and placental (basal plate and parenchyma)
16s rRNA with bacteria and 18s rRNA with fungi in pregnant women with a short
cervical length with those with normal cervical length;
2. Comparison of maternal (vaginal), neonatal(oral) and placental (basal plate and
parenchyma)16s rRNA with bacteria and 18s rRNA with fungi in pregnant women with short
cervical length who gave a preterm birth with those who gave birth at term; 3. The effect
of progesterone on maternal (vaginal), neonatal (buccal) and placental (basal plate and
parenchyma)16s rRNA with bacteria and 18s rRNA with fungi.
The measurements of cervical length will be performed in two different periods of
pregnancy (11-14 and 18-22 weeks of gestation) in singleton pregnancies. Firstly, the
vaginal swabs will be collected from women who accept to participate in the study at
11-14th weeks of gestation just before the measurement of cervical length. Also, the
vaginal swabs will be done again at 18-22 weeks of gestation as explained above.
Micronized progesterone will be started in women with a cervical length equal or less
than 25 mm (smaller than 3rd percentile) at 18-22 weeks of gestation. The medication
(progesterone 200mg) will be administered intravaginally every night before bedtime and
will continue until 36th gestational week unless the patient gives birth. Measurement of
cervical length will be repeated transvaginally at 28th and 32nd gestational weeks, and
samples will be obtained with a cervical swab before these measurements. In order to
evaluate the presence of placental mycobiota and microbiota, 1 cm x 1 cm x 1 cm of the
tissue sample from the placenta that is 3 cm lateral of the cord insertion will be taken
under sterile conditions after birth. In order to evaluate the amniotic compartment, a
buccal mucosal swab will be collected from the neonates immediately after birth. All
samples will be delivered to our Research Laboratory immediately and stored in -80 ℃
cabinet until the evaluation. The V3-V4 regions by the 16s ribosomal RNA sequencing
method will be sequenced with the Illumina MiSeq device and the data will be analyzed
according to the protocols standardized in the Human Microbiome Project.
DNA samples that will be ranked from the data to be sequenced in accordance with the ITS1
region metabiota protocol will be evaluated within the Human Microbiome Project.
Pseudomonas, Escherichia, Neisseria, Streptococcus, Lactobacillus, Candida, Actinomyces
will be used as positive controls and, V3-V4 and ITS regions will be matched for
bacterial microbiota and Fungal microbiota. After the "Operational taxonomic units" of
the amplicons are configured with the VSEARCH program, the analyzes will be carried out
with GENBANK microbiota and micobiota data.
Study Period
-
Enrollment Count
92 participants
Eligibility Criteria
Inclusion Criteria:
- Singleton pregnancies
- The subject has voluntarily signed the Informed Consent Form and associated forms
after having the contents explained
Exclusion Criteria:
- Multiple pregnancies
- The presence of a major fetal anomaly or known chromosomal abnormality
- Finding the intrauterine mort de fetus
- Antibiotic and/or antifungal use within two weeks at the collection of samples
- Pregnant women under 18 years of age
- Women with previous cervical surgery
- Women who do not accept to participate to be in the study
- The presence of a uterine anomaly
- Women with vaginal bleeding at the time of cervical swabs taken
Filters
Preterm Birth
Microbial Colonization
UNKNOWN
ADULT