The incidence of preterm birth increases annually. Premature delivery has become the leading cause of neonatal illness and death. For the survived premature babies, the incidence of sequelae is also higher than the full-term babies, which brings a heavy burden to a family and society. Preterm birth has become the important factor affecting the quality of births. The occurrence of premature birth is the outcome of combined action of genetic and environmental factors. However, its etiology is not clear. Recent studies have shown that the risk of preterm birth is associated with dietary factors. Choline is an essential nutrient for human health and it plays an important role in the growth and development of fetuses and neonates. The investigators previously found that serum levels of free choline in preterm mothers were lower than those in normal mothers with full-term birth. Serum levels of free choline also reduced in preterms after receiving parenteral nutrition (PN). However, the relationships between choline and preterm birth is not clear. Therefore, this study is aimed to explore the effect of choline intake during pregnancy and genetic polymorphisms on the risk of preterm birth and on the clinical outcomes in preterms receiving total PN therapy. Healthy Chinese pregnant women with their healthy term infants will be recruited as the control group, while Chinese women with preterm delivery and their preterm infants will be recruited as the preterm group. Dietary choline intake during pregnancy will be evaluated by semi-quantitative food frequency questionnaire and 24-h dietary recall questionnaire. Gene polymorphisms in the key enzymes of choline metabolism will be identified among the participated women and neonates through Real-time polymerase chain reaction. Choline and its related metabolites will be assayed using high performance liquid chromatography combined with mass spectrometry among all mothers and preterms before and after 7-days PN treatment. The influence of genetic risk factors and metabolic changes of choline on the physical and mental development of preterms will be evaluated. The results of this study will contribute to a comprehensive understanding of the role of choline and the relative gene polymorphisms on the risk of preterm birth, which will be helpful for estimating the high risk in advance. The results will also provide the scientific evidences to establish the personalized amount of choline intake among women and infants, optimize nutrition support for pregnant women and preterms, and promote better prenatal and postnatal care.
Study Type
OBSERVATIONAL
Enrollment
400
No intervention
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, China
RECRUITINGDistribution of single nucleotide polymorphisms of the targeted genes
Time frame: June 2016 - December,2019
Plasma concentrations of choline
Time frame: 3 years
Plasma concentrations of betaine
Time frame: 3 years
Plasma concentrations of phosphocholine
Time frame: 3 years
Dietary questionnaire of choline intake during pregnancy
Time frame: through study completion, an average of 3 years
Serum alanine aminotransferase
Time frame: through study completion, an average of 3 years
Serum aspartate aminotransferase
Time frame: through study completion, an average of 3 years
Serum total bilirubin
Time frame: through study completion, an average of 3 years
Serum direct bilirubin
Time frame: through study completion, an average of 3 years
Serum bile acid
Time frame: through study completion, an average of 3 years
Serum gamma glutamyl transferase
Time frame: through study completion, an average of 3 years
Serum triglyceride
Time frame: through study completion, an average of 3 years
Mental developmental index
Time frame: through study completion, an average of 3 years
Psychomotor developmental index
Time frame: through study completion, an average of 3 years
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