FP7Reintegration grant2010–2013

FETALPROJECT2010 · Documentation of lung growth after tracheal occlusion to reverse pulmonary hypoplasia in congenital diaphragmatic hernia. Experimental studies in the rat and clinical implications of fetal therapy

FP7 — People (Marie Curie Actions)

Duration
2010-11-01 → 2013-10-31
EU contribution
€45,000
Participants
1
Scheme
MC-ERG

Lines connect the coordinator with its partners.

Results in brief

Documentation of lung growth after tracheal occlusion to reverse pulmonary hypoplasia in congenital diaphragmatic hernia. Experimental studies in the rat and clinical implications of fetal therapy.

The primary research goal and objective of the “Fetalproject2010” was to advance existing knowledge in invasive fetal medicine. For this purpose we focused on pulmonary hypoplasia in the context of congenital diaphragmatic hernia (CDH) and its relatively new prenatal treatment option, tracheal occlusion (TO). We selected a number of different facets in this field to conduct research on which included the optimal timing of fetal surgery, potential drug side effects on lung development, the application of innovative technologies in fetal diagnostics and the psychosocial impact of fetal medicine on affected parents. The institutions that worked in close cooperation on these projects were the University of Tuebingen, Germany and the Katholieke Universiteit (KU) Leuven, Belgium. In summary our results so far are: (1) Increased lung proliferation is dependent on the length not the time-point of tracheal occlusion in the nitrofen rat model for pulmonary hypoplasia in congenital diaphragmatic hernia. (2) Maternal nifedipine administration does not impact fetal lung growth in the nitrofen rat model of congenital diaphragmatic hernia. (3) Pregnant women awaiting invasive prenatal diagnosis and fetal therapy face higher levels of state-anxiety than women undergoing noninvasive procedures. Traits of depression and high state-anxiety are found in at least one third of women undergoing fetal therapy. (4) High resolution 1H NMR spectroscopy successfully discriminates amniotic fluid of fetuses with congenital diaphragmatic hernia from healthy controls. These results will facilitate the planning and conducting of future studies in the field of fetal medicine. They identified new areas of interest and could weaken doubts about drug safety in the case of nifedipine tocolysis for mothers carrying an infant with pulmonary hypoplasia. The experienced researcher was after her trans-national mobility phase reintegrated in her home country. She successfully established her own working group, hence, transferring knowledge and skills from the old to the new host organization. This new working group comprises of doctoral students and multiple co-operations linking departments at the University of Tuebingen as well as the Katholieke Universiteit Leuven. The robust new research structure will support the ongoing career of the fellow further linking two big European research centers. Multiple publications have already been the result of this collaboration and more will follow.

Data: CORDIS, © European Union

Project objective

The objective of the “Fetalproject2010” is to advance our knowledge in fetal medicine. We focus on pulmonary hypoplasia (PH) in congenital diaphragmatic hernia (CDH) and its relatively new prenatal treatment option, tracheal occlusion (TO). TO prevents egress of pulmonary fluid, thus triggering lung growth. Yet, the procedure is invasive, with main risks premature rupture of membranes and preterm delivery. The question remains as to the optimal occlusion period. We aim to investigate the effects of TO at distinct phases of lung development in the nitrofen (NF) rat. Our results will provide a scientific basis for timing of TO in human CDH fetuses. Patients after fetal surgery are at high risk for tocolysis. One drug frequently used is nifedipine, which inhibits airway small muscle (ASM) contractions in vitro. ASM are believed to be crucial for lung development. We plan to study the impact of nifedipine application on hypoplastic lungs ±TO in the NF rat. Our results will demonstrate potential safety issues. Few centers, including the two host institutions, offer fetal surgery such as TO. We aim to investigate with questionnaires how couples are affected psychologically by interventions. Our results will help to identify the distinct needs of these parents and to tailor support. MRI-spectroscopy (MRS) and fetal magnetoencephalography (fMEG) offer new non-invasive methods to study fetal fluid composition, organ function and development. CDH is associated with altered levels of e. g. vitamin A and decreased cerebral perfusion, the functional impact of the latter is unknown. We aim to investigate the potential of MRS and fMEG in studying lung development as well as brain activity in fetuses with CDH. These results will help to define new markers and methods for diagnostic and prognostic purposes in fetuses with CDH. This grant will help to reintegrate an experienced researcher coming from KU Leuven, Belgium, into the new host organization, University Tübingen, Germany.

Original text from CORDIS.

Participants

  • EBERHARD KARLS UNIVERSITAET TUEBINGEN · TuebingenCoordinatorGermany

Links

Data: CORDIS, © European Union