Metabolomic profiling of intrauterine growth-restricted preterm infants: a matched case-control study

被引:5
作者
Priante, Elena [1 ]
Verlato, Giovanna [1 ]
Stocchero, Matteo [2 ]
Giordano, Giuseppe [2 ]
Pirillo, Paola [2 ]
Bonadies, Luca [1 ]
Visentin, Silvia [3 ]
Moschino, Laura [1 ]
Baraldi, Eugenio [1 ,2 ]
机构
[1] Univ Hosp Padua, Dept Womens & Childrens Hlth, Neonatal Intens Care Unit, Padua, Italy
[2] Citta Speranza, Inst Pediat Res, Lab Mass Spectrometry & Metabol, Padua, Italy
[3] Univ Hosp Padua, Dept Womens & Childrens Hlth, Unit Gynecol & Obstet, Padua, Italy
关键词
ONE-CARBON METABOLISM; FOR-GESTATIONAL-AGE; FETAL-GROWTH; TRYPTOPHAN; BIRTH; CARNOSINE; STRESS; DAMAGE;
D O I
10.1038/s41390-022-02292-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: The biochemical variations occurring in intrauterine growth restriction (IUGR), when a fetus is unable to achieve its genetically determined potential, are not fully understood. The aim of this study is to compare the urinary metabolomic profile between IUGR and non-IUGR very preterm infants to investigate the biochemical adaptations of neonates affected by early-onset-restricted intrauterine growth. METHODS: Neonates born <32 weeks of gestation admitted to neonatal intensive care unit (NICU) were enrolled in this prospective matched case-control study. IUGR was diagnosed by an obstetric ultra-sonographer and all relevant clinical data during NICU stay were captured. For each subject, a urine sample was collected within 48 h of life and underwent untargeted metabolomic analysis using mass spectrometry ultra-performance liquid chromatography. Data were analyzed using multivariate and univariate statistical analyses. RESULTS: Among 83 enrolled infants, 15 IUGR neonates were matched with 19 non-IUGR controls. Untargeted metabolomic revealed evident clustering of IUGR neonates versus controls showing derangements of pathways related to tryptophan and histidine metabolism and aminoacyl-tRNA and steroid hormones biosynthesis. CONCLUSIONS: Neonates with IUGR showed a distinctive urinary metabolic profile at birth. Although results are preliminary, metabolomics is proving to be a promising tool to explore biochemical pathways involved in this disease.
引用
收藏
页码:1599 / 1608
页数:10
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