학술논문

Developmental changes in polyunsaturated fetal plasma phospholipids and feto-maternal plasma phospholipid ratios and their association with bronchopulmonary dysplasia.
Document Type
Article
Source
European Journal of Nutrition. Oct2016, Vol. 55 Issue 7, p2265-2274. 10p. 1 Chart, 5 Graphs.
Subject
*BRONCHOPULMONARY dysplasia
*CLINICAL trials
*CORD blood
*PREMATURE infants
*LECITHIN
*PHOSPHOLIPIDS
*PROBABILITY theory
*REGRESSION analysis
*RESEARCH funding
*STATISTICS
*T-test (Statistics)
*UNSATURATED fatty acids
*DATA analysis
*FETAL development
*SEVERITY of illness index
*DATA analysis software
*DESCRIPTIVE statistics
*MANN Whitney U Test
*FETUS
*PREGNANCY
Language
ISSN
1436-6207
Abstract
Background: Docosahexaenoic (C22:6) and arachidonic acid (C20:4) are long-chain polyunsaturated fatty acids (LC-PUFA), essential to fetal development, and preferentially transported by plasma phospholipids. Objective: To characterize fetal and maternal plasma phospholipid changes during gestation, and to investigate whether LC-PUFA phospholipid profiles are associated with bronchopulmonary dysplasia (BPD). Design: Cord plasma and parturient serum from N = 108 pregnancies [24-42 week postmenstrual age (PMA)] were collected. Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) were analyzed with tandem mass spectrometry. PMA-associated changes were quantified, and break point analyses served to describe nonlinear changes during gestation. Results: PC and PE were lower in cord than in parturient samples. In parturients, PC decreased until 33 week PMA, but then re-increased, whereas in cord plasma, concentrations linearly decreased. Fetal PC and PC sub-group values correlated with maternal values. C20:4-PC was twofold higher in cord than in maternal samples throughout gestation. C22:6-PC values, however, exceeded maternal values only beyond 33 week PMA. Consequently, early preterm C20:4-PC-to-C22:6-PC ratio largely exceeded term infant values. In infants born before 28 week PMA, a low C20:4-PC-to-C22:6-PC ratio was associated with BPD severity. Conclusions: Fetal plasma LC-PUFA-PC composition correlates with maternal values. Fetal C20:4-PC exceeds maternal values throughout gestation, whereas C22:6-PC exceeds maternal values only beyond 33 week PMA, resulting in a low fetal C20:4-PC/C22:6-PC ratio only toward end gestation. A low C20:4-PC/C22:6-PC ratio before 28 week PMA is associated with BPD severity. These data point to a concept of PMA-adjusted ARA and DHA supplementation and, potentially, cord plasma phospholipid analysis for BPD prediction. [ABSTRACT FROM AUTHOR]