Genetic Susceptibility for Bronchopulmonary Dysplasia in Preterm Infants

NCT ID: NCT00904774

Last Updated: 2009-05-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

800 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-05-31

Brief Summary

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Despite considerable obstetric and neonatal advances in the care of very low birth weight (VLBW) neonates, bronchopulmonary dysplasia (BPD) continues to occur among 20 to 40% of surviving infants, and new ways for combatting this disease must be found. BPD appears to result from arrested lung development, but its etiology has not yet been fully established. Besides the role of the exposure of the immature lung to injurious factors in the development of BPD, a genetic susceptibility for BPD in preterm infants was recently evidenced. Taking advantage of new genomic technologies, the objective of the investigators' project is to identify predisposing human genetic variants through:

1. a genome-wide association (GWA) study in VLBW neonates,
2. a candidate-gene association study, including selection of single nucleotide polymorphisms (SNPs) found in (a) and
3. functional studies of any SNP found to be convincingly associated with BPD in (a) and (b).

Detailed Description

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Conditions

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Bronchopulmonary Dysplasia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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premature neonates

gestational age less than 28 weeks

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Gestational age \< 28 weeks
* Inborn birth
* Prophylactic administration of surfactant in the delivery room
* Written informed consent obtained from parents

Exclusion Criteria

* Gestational age of 28 weeks or more
* Outborn birth
* No prophylactic administration of surfactant in the delivery room
* Congenital malformation
* Absence of written informed consent obtained from parents
Maximum Eligible Age

8 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Intercommunal Creteil

OTHER

Sponsor Role lead

Responsible Party

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INSERM U955

Locations

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Centre Hospitalier Intercommunal

Créteil, , France

Site Status

Countries

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France

References

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Hadchouel A, Decobert F, Franco-Montoya ML, Halphen I, Jarreau PH, Boucherat O, Martin E, Benachi A, Amselem S, Bourbon J, Danan C, Delacourt C. Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung development. PLoS One. 2008 Sep 11;3(9):e3188. doi: 10.1371/journal.pone.0003188.

Reference Type BACKGROUND
PMID: 18784838 (View on PubMed)

Related Links

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http://www.premup.org/

The french PremUp Foundation is dedicated to pregnancy and the newborn

Other Identifiers

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AOR 07 018

Identifier Type: -

Identifier Source: org_study_id

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