Congenital pulmonary malformations: metabolomic profile of lung phenotype in infants

J Matern Fetal Neonatal Med. 2016;29(1):143-7. doi: 10.3109/14767058.2014.991708. Epub 2014 Dec 23.

Abstract

Background: The main hydrosoluble metabolites in three different human congenital pulmonary malformations are described by nuclear magnetic resonance (NMR) spectroscopy.

Methods: Bronchogenic cyst (BC), congenital lobar emphysema (CLE) and intrapulmonary sequestration (IPS), were analyzed with respect to a control sample. The extracted metabolites were submitted to high-resolution (1)H NMR-spectroscopy.

Results: Congenital lung malformations showed free choline, phosphocoline and myoinositol high levels. IPS and CLE were found increased in lactic acid/glucose ratio. Lactic acid and glucose values resulted to be more elevated in control sample.

Conclusions: Congenital lung lesions showed different metabolomic profiles useful for early diagnosis.

Keywords: Congenital lung malformations; metabolomic; translational research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Infant
  • Infant, Newborn
  • Lung / metabolism*
  • Male
  • Metabolome
  • Phenotype
  • Respiratory System Abnormalities / metabolism*