Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population

Pediatrics & Neonatology - Tập 61 - Trang 318-324 - 2020
Wei Shen1, Penghao Kuang2, Bin Wang3, Qiyi Zeng3, Chao Chen1,4, Xinzhu Lin1
1Neonatology Department, Women and Children's Hospital, Xiamen University, Xiamen, Fujian 361003, China
2General Surgery Department, Zhongshan Hospital, Xiamen University, Xiamen, Fujian 361004, China
3Center of Pediatrics, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, China
4Neonatology Department, Children's Hospital of Fudan University, Shanghai 201102, China

Tài liệu tham khảo

Hallman, 2002, Surfactant proteins and genetic predisposition to respiratory distress syndrome, Semin Perinatol, 26, 450, 10.1053/sper.2002.37314 Hallman, 2012, Premature birth and diseases in premature infants: common genetic background?, J Matern Fetal Neonatal Med, 25, 21, 10.3109/14767058.2012.667600 Jobe, 1993, Pulmonary surfactant therapy, N Engl J Med, 328, 861, 10.1056/NEJM199303253281208 Agassandian, 2013, Surfactant phospholipid metabolism, Biochim Biophys Acta, 1831, 612, 10.1016/j.bbalip.2012.09.010 Nakanishi, 2006, Cloning and characterization of mouse lung-type acyl-CoA:lysophosphatidylcholine acyltransferase 1 (LPCAT1). Expression in alveolar type II cells and possible involvement in surfactant production, J Biol Chem, 281, 20140, 10.1074/jbc.M600225200 Lin, 2015, Lysophosphatidylcholine acyltransferase 1 (LPCAT1) specifically interacts with phospholipid transfer protein starD10 to facilitate surfactant phospholipid trafficking in alveolar type II cells, J Biol Chem, 290, 18559, 10.1074/jbc.M115.666701 Chatterjee, 2009, Role of 5'- and 3'-untranslated regions of mRNAs in human diseases, Biol Cell, 101, 251, 10.1042/BC20080104 Kaya, 2017, Association of Rho-kinase gene polymorphisms with respiratory distress syndrome in preterm neonates, Pediatr Neonatol, 58, 36, 10.1016/j.pedneo.2015.12.006 Shen, 2014, Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population, Ital J Pediatr, 40, 27, 10.1186/1824-7288-40-27 Gortner, 2018, Review demonstrates that less invasive surfactant administration in preterm neonates leads to fewer complications, Acta Paediatr, 107, 736, 10.1111/apa.14161 Rutkowska, 2019, Severe bronchopulmonary dysplasia - incidence and predictive factors in a prospective, multicenter study in very preterm infants with respiratory distress syndrome, J Matern Fetal Neonatal Med, 32, 1958, 10.1080/14767058.2017.1422711 Wambach, 2016, Functional characterization of ATP-binding cassette transporter A3 mutations from infants with respiratory distress syndrome, Am J Respir Cell Mol Biol, 55, 716, 10.1165/rcmb.2016-0008OC Somaschini, 2018, Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome, J Perinatol, 38, 337, 10.1038/s41372-017-0018-2 Rämet, 2000, Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population, Am J Hum Genet, 66, 1569, 10.1086/302906 Chang, 2016, Genetic polymorphisms of SP-A, SP-B, and SP-D and risk of respiratory distress syndrome in preterm neonates, Med Sci Monit, 22, 5091, 10.12659/MSM.898553 Fatahi, 2018, Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS, J Matern Fetal Neonatal Med, 31, 2965, 10.1080/14767058.2017.1359829 Fatahi, 2017, Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS, J Matern Fetal Neonatal Med, 30, 2585, 10.1080/14767058.2016.1256994 Karjalainen, 2008, Haplotype analysis of ABCA3: association with respiratory distress in very premature infants, Ann Med, 40, 56, 10.1080/07853890701611094 Tian, 2016, The haplotype TGGAG in the ABCA3 gene increases the risk of respiratory distress syndrome in preterm infants in southern China, Pediatr Neonatol, 57, 188, 10.1016/j.pedneo.2015.09.002 Lyra, 2011, Surfactant protein B gene polymorphism in preterm babies with respiratory distress syndrome, Braz J Med Biol Res, 44, 66, 10.1590/S0100-879X2010007500147 Harayama, 2009, Biosynthesis of phosphatidylcholine by human lysophosphatidylcholine acyltransferase 1, J Lipid Res, 50, 1824, 10.1194/jlr.M800500-JLR200 Moessinger, 2014, Two different pathways of phosphatidylcholine synthesis, the Kennedy Pathway and the Lands Cycle, differentially regulate cellular triacylglycerol storage, BMC Cell Biol, 15, 43, 10.1186/s12860-014-0043-3 Wambach, 2012, Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome, Pediatrics, 130, e1575, 10.1542/peds.2012-0918 Bridges, 2010, LPCAT1 regulates surfactant phospholipid synthesis and is required for transitioning to air breathing in mice, J Clin Invest, 120, 1736, 10.1172/JCI38061 Wittke-Thompson, 2005, Rational inferences about departures from Hardy-Weinberg equilibrium, Am J Hum Genet, 76, 967, 10.1086/430507 Chen, 2006, Identification and characterization of a lysophosphatidylcholine acyltransferase in alveolar type II cells, Proc Natl Acad Sci USA, 103, 11724, 10.1073/pnas.0604946103 Welch, 2016, Amniotic fluid LPCAT1 mRNA correlates with the lamellar body count, J Perinat Med, 44, 531, 10.1515/jpm-2015-0008 Welch, 2018, Maternal plasma LPCAT 1 mRNA correlates with lamellar body count, J Perinat Med, 46, 429, 10.1515/jpm-2017-0057