The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis
Tài liệu tham khảo
Lauer, 2011, Hyperbilirubinemia in the newborn, Pediatr Rev., 32, 341, 10.1542/pir.32-8-341
Hameed, 2011, Severe neonatal hyperbilirubinemia and adverse short-term consequences in Baghdad, Iraq, Neonatology., 100, 57, 10.1159/000321990
Subspecialty Group of Neonatology; Society of Pediatrics; Chinese Medical Association. Clinical characteristics of bilirubin encephalopathy in Chinese newborn infants – a national multicenter survey. Zhonghua Er Ke Za Zhi. 2012;50:331-5.
Maisels, 2011, Risk assessment and follow-up are the keys to preventing severe hyperbilirubinemia, J Pediatr (Rio J)., 87, 275, 10.2223/JPED.2120
Gamaleldin, 2011, Risk factors for neurotoxicity in newborns with severe neonatal hyperbilirubinemia, Pediatrics., 128, e925, 10.1542/peds.2011-0206
Vitek, 2009, Bilirubin chemistry and metabolism; harmful and protective aspects, Curr Pharm Des., 15, 2869, 10.2174/138161209789058237
Long, 2011, Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence, Acta Paediatr., 100, 966, 10.1111/j.1651-2227.2011.02176.x
Watchko, 2010, Exploring the genetic architecture of neonatal hyperbilirubinemia, Semin Fetal Neonatal Med., 15, 169, 10.1016/j.siny.2009.11.003
Tirona, 2001, Polymorphisms in OATP-C: identification of multiple allelic variants associated with altered transport activity among European- and African- Americans, J Biol Chem., 276, 35669, 10.1074/jbc.M103792200
Setia, 2002, Neonatal jaundice in Asian, white, and mixed-race infants, Arch Pediatr Adolesc Med., 156, 276, 10.1001/archpedi.156.3.276
Chang, 2011, Risk of hyperbilirubinemia in breast-fed infants, J Pediatr., 159, 561, 10.1016/j.jpeds.2011.03.042
Zhang, 2010, OATP 1B1 T521C/A388G is an important polymorphism gene related to neonatal hyperbilirubinemia, Chin J Pediatr., 48, 650
Tian, 2007, The association of mutations of UDP-glucuronosyl transferase 1A1 gene and organic anion transporter 2 gene with neonatal jaundice, Chin J Neonatology., 22, 193
Jiang, 2012, UGT1A1 and OATP2 gene mutations in neonates from northern China with hyperbilirubinemia, Chin J Neonatology., 27, 369
Huang, 2004, Risk factors for severe hyperbilirubinemia in neonates, Pediatr Res., 56, 682, 10.1203/01.PDR.0000141846.37253.AF
Wong, 2009, Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia, Malays J Pathol., 31, 99
Prachukthum, 2009, Genetic polymorphisms in Thai neonates with hyperbilirubinemia, Acta Paediatr., 98, 1106, 10.1111/j.1651-2227.2009.01275.x
Watchko, 2009, Complex multifactorial nature of significant hyperbilirubinemia in neonates, Pediatrics., 124, e868, 10.1542/peds.2009-0460
Büyükkale, 2011, Neonatal hyperbilirubinemia and organic anion transporting polypeptide-2 gene mutations, Am J Perinatol., 28, 619, 10.1055/s-0031-1276736
Alencastro de Azevedo, 2012, UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?, Pediatr Res., 72, 169, 10.1038/pr.2012.60
Kameyama, 2005, Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007G, by using transient expression systems of HeLa and HEK293 cells, Pharmacogenet Genomics., 15, 513, 10.1097/01.fpc.0000170913.73780.5f
Campbell, 2004, Inhibition of human organic anion transporting polypeptide OATP 1B1 as a mechanism of drug-induced hyperbilirubinemia, Chem Biol Interact., 150, 179, 10.1016/j.cbi.2004.08.008
Zhang, 2007, OATP1B1 polymorphism is a major determinant of serum bilirubin level but not associated with rifampicin-mediated bilirubin elevation, Clin Exp Pharmacol Physiol., 34, 1240, 10.1111/j.1440-1681.2007.04798.x
Michalski, 2002, A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter, J Biol Chem., 277, 43058, 10.1074/jbc.M207735200
