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Volumn 165, Issue 6, 2014, Pages 1154-1160.e1

Quantitative trait analysis of polymorphisms in two bilirubin metabolism enzymes to physiologic bilirubin levels in chinese newborns

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE; HEME OXYGENASE 1; UNCLASSIFIED DRUG; URIDINE DIPHOSPHATE GLUCURONOSYL TRANSFERASE 1A1; HMOX1 PROTEIN, HUMAN; UGT1A1 ENZYME;

EID: 84912126339     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2014.08.041     Document Type: Article
Times cited : (21)

References (39)
  • 1
    • 0025161908 scopus 로고
    • Laboratory evaluation of jaundice in newborns: Frequency, cost, and yield
    • T.B. Newman, M.J. Easterling, E.S. Goldman, and D.K. Stevenson Laboratory evaluation of jaundice in newborns: frequency, cost, and yield Am J Dis Child 144 1990 364 368
    • (1990) Am J Dis Child , vol.144 , pp. 364-368
    • Newman, T.B.1    Easterling, M.J.2    Goldman, E.S.3    Stevenson, D.K.4
  • 2
    • 0028086109 scopus 로고
    • Practice parameter: Management of hyperbilirubinemia in the healthy term newborn
    • Academy Of Pediatrics Provisional Committee For Quality Improvement And Subcommittee On Hyperbilirubinemia
    • American Academy of Pediatrics, Provisional Committee for Quality Improvement and Subcommittee on Hyperbilirubinemia Practice parameter: management of hyperbilirubinemia in the healthy term newborn Pediatrics 94 1994 558 565
    • (1994) Pediatrics , vol.94 , pp. 558-565
  • 3
    • 42949176762 scopus 로고    scopus 로고
    • Readmission for neonatal jaundice in California, 1991-2000: Trends and implications
    • A.E. Burgos, S.K. Schmitt, D.K. Stevenson, and C.S. Phibbs Readmission for neonatal jaundice in California, 1991-2000: trends and implications Pediatrics 121 2008 e864 e869
    • (2008) Pediatrics , vol.121 , pp. 864-e869
    • Burgos, A.E.1    Schmitt, S.K.2    Stevenson, D.K.3    Phibbs, C.S.4
  • 4
    • 0031949264 scopus 로고    scopus 로고
    • Gilbert syndrome accelerates development of neonatal jaundice
    • J.D. Bancroft, B. Kreamer, and G.R. Gourley Gilbert syndrome accelerates development of neonatal jaundice J Pediatr 132 1998 656 660
    • (1998) J Pediatr , vol.132 , pp. 656-660
    • Bancroft, J.D.1    Kreamer, B.2    Gourley, G.R.3
  • 5
    • 0033001454 scopus 로고    scopus 로고
    • Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism
    • Y. Maruo, K. Nishizawa, H. Sato, Y. Doida, and M. Shimada Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism Pediatrics 103 1999 1224 1227
    • (1999) Pediatrics , vol.103 , pp. 1224-1227
    • Maruo, Y.1    Nishizawa, K.2    Sato, H.3    Doida, Y.4    Shimada, M.5
  • 8
    • 70450223891 scopus 로고    scopus 로고
    • Common disorders are quantitative traits
    • R. Plomin, C.M. Haworth, and O.S. Davis Common disorders are quantitative traits Nat Rev Genet 10 2009 872 878
    • (2009) Nat Rev Genet , vol.10 , pp. 872-878
    • Plomin, R.1    Haworth, C.M.2    Davis, O.S.3
  • 9
    • 3042718933 scopus 로고    scopus 로고
    • Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation
    • Academy Of Pediatrics Subcommittee On Hyperbilirubinemia
    • American Academy of Pediatrics, Subcommittee on Hyperbilirubinemia Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation Pediatrics 114 2004 297 316
    • (2004) Pediatrics , vol.114 , pp. 297-316
  • 10
    • 0041004612 scopus 로고    scopus 로고
    • 2nd ed People's Medical Publishing House Beijing, China
    • H. Jin, D. Huang, and X. Guan Practical neonatology 2nd ed 1997 People's Medical Publishing House Beijing, China
    • (1997) Practical Neonatology
    • Jin, H.1    Huang, D.2    Guan, X.3
  • 11
    • 33745675471 scopus 로고    scopus 로고
    • 6th ed People's Medical Publishing House Beijing, China
    • Y. Hu, R. Wu, and Z. Jiang Practical pediatrics 6th ed 1996 People's Medical Publishing House Beijing, China
    • (1996) Practical Pediatrics
    • Hu, Y.1    Wu, R.2    Jiang, Z.3
  • 12
    • 0028904620 scopus 로고
    • Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
    • S. Aono, Y. Adachi, E. Uyama, Y. Yamada, H. Keino, and T. Nanno Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome Lancet 345 1995 958 959
    • (1995) Lancet , vol.345 , pp. 958-959
    • Aono, S.1    Adachi, Y.2    Uyama, E.3    Yamada, Y.4    Keino, H.5    Nanno, T.6
  • 13
    • 0028867826 scopus 로고
    • The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
    • P.J. Bosma, J.R. Chowdhury, C. Bakker, S. Gantla, A. de Boer, and B.A. Oostra The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome N Engl J Med 333 1995 1171 1175
    • (1995) N Engl J Med , vol.333 , pp. 1171-1175
    • Bosma, P.J.1    Chowdhury, J.R.2    Bakker, C.3    Gantla, S.4    De Boer, A.5    Oostra, B.A.6
  • 14
    • 0033925281 scopus 로고    scopus 로고
    • Microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with susceptibility to emphysema
    • N. Yamada, M. Yamaya, S. Okinaga, K. Nakayama, K. Sekizawa, and S. Shibahara Microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with susceptibility to emphysema Am J Hum Genet 66 2000 187 195
    • (2000) Am J Hum Genet , vol.66 , pp. 187-195
    • Yamada, N.1    Yamaya, M.2    Okinaga, S.3    Nakayama, K.4    Sekizawa, K.5    Shibahara, S.6
  • 15
    • 63849300402 scopus 로고    scopus 로고
    • Common variants of four bilirubin metabolism genes and their association with serum bilirubin and coronary artery disease in Chinese Han population
    • R. Lin, Y. Wang, W. Fu, D. Zhang, H. Zheng, and T. Yu Common variants of four bilirubin metabolism genes and their association with serum bilirubin and coronary artery disease in Chinese Han population Pharmacogenet Genom 19 2009 310 318
    • (2009) Pharmacogenet Genom , vol.19 , pp. 310-318
    • Lin, R.1    Wang, Y.2    Fu, W.3    Zhang, D.4    Zheng, H.5    Yu, T.6
  • 16
    • 84905472522 scopus 로고    scopus 로고
    • Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants
    • Y. Zhou, S.N. Wang, H. Li, W. Zha, X. Wang, and Y. Liu Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants PLoS One 9 2014 e104251
    • (2014) PLoS One , vol.9 , pp. 104251
    • Zhou, Y.1    Wang, S.N.2    Li, H.3    Zha, W.4    Wang, X.5    Liu, Y.6
  • 17
    • 0026689178 scopus 로고
    • Performing the exact test of Hardy-Weinberg proportion for multiple alleles
    • S.W. Guo, and E.A. Thompson Performing the exact test of Hardy-Weinberg proportion for multiple alleles Biometrics 48 1992 361 372
    • (1992) Biometrics , vol.48 , pp. 361-372
    • Guo, S.W.1    Thompson, E.A.2
  • 18
    • 0001677717 scopus 로고
    • Controlling the false discovery rate: A practical and powerful approach to multiple testing
    • Y. Benjamini, and Y. Hochberg Controlling the false discovery rate: a practical and powerful approach to multiple testing J R Stat Soc B 57 1995 289 300
    • (1995) J R Stat Soc B , vol.57 , pp. 289-300
    • Benjamini, Y.1    Hochberg, Y.2
  • 19
    • 0032493441 scopus 로고    scopus 로고
    • Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism
    • E. Beutler, T. Gelbart, and A. Demina Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism Proc Natl Acad Sci U S A 95 1998 8170 8174
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 8170-8174
    • Beutler, E.1    Gelbart, T.2    Demina, A.3
  • 20
    • 63749092727 scopus 로고    scopus 로고
    • Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations
    • R. Lin, X. Wang, Y. Wang, F. Zhang, W. Fu, and T. Yu Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations Hum Mutat 30 2009 609 615
    • (2009) Hum Mutat , vol.30 , pp. 609-615
    • Lin, R.1    Wang, X.2    Wang, Y.3    Zhang, F.4    Fu, W.5    Yu, T.6
  • 21
    • 33646340427 scopus 로고    scopus 로고
    • Transcutaneous bilirubin levels in the first 96 hours in a normal newborn population of > or = 35 weeks' gestation
    • M.J. Maisels, and E. Kring Transcutaneous bilirubin levels in the first 96 hours in a normal newborn population of > or = 35 weeks' gestation Pediatrics 117 2006 1169 1173
    • (2006) Pediatrics , vol.117 , pp. 1169-1173
    • Maisels, M.J.1    Kring, E.2
  • 22
    • 74049103705 scopus 로고    scopus 로고
    • Transcutaneous bilirubin levels for the first 120 postnatal hours in healthy neonates
    • S. Fouzas, L. Mantagou, E. Skylogianni, S. Mantagos, and A. Varvarigou Transcutaneous bilirubin levels for the first 120 postnatal hours in healthy neonates Pediatrics 125 2010 e52 e57
    • (2010) Pediatrics , vol.125 , pp. 52-e57
    • Fouzas, S.1    Mantagou, L.2    Skylogianni, E.3    Mantagos, S.4    Varvarigou, A.5
  • 23
    • 78951494992 scopus 로고    scopus 로고
    • Transcutaneous bilirubin nomogram for predicting neonatal hyperbilirubinemia in healthy term and late-preterm Chinese infants
    • Z.B. Yu, X.Y. Dong, S.P. Han, Y.L. Chen, Y.F. Qiu, and L. Sha Transcutaneous bilirubin nomogram for predicting neonatal hyperbilirubinemia in healthy term and late-preterm Chinese infants Eur J Pediatr 170 2011 185 191
    • (2011) Eur J Pediatr , vol.170 , pp. 185-191
    • Yu, Z.B.1    Dong, X.Y.2    Han, S.P.3    Chen, Y.L.4    Qiu, Y.F.5    Sha, L.6
  • 24
    • 0027739943 scopus 로고
    • Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II
    • S. Aono, Y. Yamada, H. Keino, N. Hanada, T. Nakagawa, and Y. Sasaoka Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II Biochem Biophys Res Commun 197 1993 1239 1244
    • (1993) Biochem Biophys Res Commun , vol.197 , pp. 1239-1244
    • Aono, S.1    Yamada, Y.2    Keino, H.3    Hanada, N.4    Nakagawa, T.5    Sasaoka, Y.6
  • 25
    • 79951635412 scopus 로고    scopus 로고
    • 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice
    • H.C. Chou, M.H. Chen, H.I. Yang, Y.N. Su, W.S. Hsieh, and C.Y. Chen 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice Pediatr Res 69 2011 170 174
    • (2011) Pediatr Res , vol.69 , pp. 170-174
    • Chou, H.C.1    Chen, M.H.2    Yang, H.I.3    Su, Y.N.4    Hsieh, W.S.5    Chen, C.Y.6
  • 26
    • 84880573155 scopus 로고    scopus 로고
    • UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia
    • J.M. Skierka, K.E. Kotzer, S.A. Lagerstedt, D.J. O'Kane, and L.M. Baudhuin UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia J Pediatr 162 2013 1146 1152
    • (2013) J Pediatr , vol.162 , pp. 1146-1152
    • Skierka, J.M.1    Kotzer, K.E.2    Lagerstedt, S.A.3    O'Kane, D.J.4    Baudhuin, L.M.5
  • 28
    • 67649851008 scopus 로고    scopus 로고
    • Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
    • S. Sanna, F. Busonero, A. Maschio, P.F. McArdle, G. Usala, and M. Dei Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia Hum Mol Genet 18 2009 2711 2718
    • (2009) Hum Mol Genet , vol.18 , pp. 2711-2718
    • Sanna, S.1    Busonero, F.2    Maschio, A.3    McArdle, P.F.4    Usala, G.5    Dei, M.6
  • 29
    • 77956154650 scopus 로고    scopus 로고
    • Genome-wide association of serum bilirubin levels in a Korean population
    • T.W. Kang, H.J. Kim, H. Ju, J.H. Kim, Y.J. Jeon, and H.C. Lee Genome-wide association of serum bilirubin levels in a Korean population Hum Mol Genet 19 2010 3672 3678
    • (2010) Hum Mol Genet , vol.19 , pp. 3672-3678
    • Kang, T.W.1    Kim, H.J.2    Ju, H.3    Kim, J.H.4    Jeon, Y.J.5    Lee, H.C.6
  • 31
    • 2942527225 scopus 로고    scopus 로고
    • UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer
    • K. Sai, M. Saeki, Y. Saito, S. Ozawa, N. Katori, and H. Jinno UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer Clin Pharmacol Ther 75 2004 501 515
    • (2004) Clin Pharmacol Ther , vol.75 , pp. 501-515
    • Sai, K.1    Saeki, M.2    Saito, Y.3    Ozawa, S.4    Katori, N.5    Jinno, H.6
  • 33
    • 0344083645 scopus 로고    scopus 로고
    • Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population
    • C.S. Ki, K.A. Lee, S.Y. Lee, H.J. Kim, S.S. Cho, and J.H. Park Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population Clin Chem 49 2003 2078 2081
    • (2003) Clin Chem , vol.49 , pp. 2078-2081
    • Ki, C.S.1    Lee, K.A.2    Lee, S.Y.3    Kim, H.J.4    Cho, S.S.5    Park, J.H.6
  • 34
    • 33749524440 scopus 로고    scopus 로고
    • Association between the UGT1A1∗28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study
    • J.P. Lin, C.J. O'Donnell, J.P. Schwaiger, L.A. Cupples, A. Lingenhel, and S.C. Hunt Association between the UGT1A1∗28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study Circulation 114 2006 1476 1481
    • (2006) Circulation , vol.114 , pp. 1476-1481
    • Lin, J.P.1    O'Donnell, C.J.2    Schwaiger, J.P.3    Cupples, L.A.4    Lingenhel, A.5    Hunt, S.C.6
  • 35
    • 0019860388 scopus 로고
    • The prenatal and postnatal development of UDP-glucuronyltransferase activity towards bilirubin and the effect of premature birth on this activity in the human liver
    • N. Kawade, and S. Onishi The prenatal and postnatal development of UDP-glucuronyltransferase activity towards bilirubin and the effect of premature birth on this activity in the human liver Biochem J 196 1981 257 260
    • (1981) Biochem J , vol.196 , pp. 257-260
    • Kawade, N.1    Onishi, S.2
  • 36
    • 0024272881 scopus 로고
    • The inadequacy of perinatal glucuronidation: Immunoblot analysis of the developmental expression of individual UDP-glucuronosyltransferase isoenzymes in rat and human liver microsomes
    • M.W. Coughtrie, B. Burchell, J.E. Leakey, and R. Hume The inadequacy of perinatal glucuronidation: immunoblot analysis of the developmental expression of individual UDP-glucuronosyltransferase isoenzymes in rat and human liver microsomes Mol Pharmacol 34 1988 729 735
    • (1988) Mol Pharmacol , vol.34 , pp. 729-735
    • Coughtrie, M.W.1    Burchell, B.2    Leakey, J.E.3    Hume, R.4
  • 37
    • 77950407754 scopus 로고    scopus 로고
    • Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus
    • R. Fujiwara, N. Nguyen, S. Chen, and R.H. Tukey Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus Proc Natl Acad Sci U S A 107 2010 5024 5029
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 5024-5029
    • Fujiwara, R.1    Nguyen, N.2    Chen, S.3    Tukey, R.H.4
  • 38
    • 77950294848 scopus 로고    scopus 로고
    • Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase-1 gene promoter polymorphism
    • O.G. Bozkaya, A. Kumral, D.C. Yesilirmak, A. Ulgenalp, N. Duman, and D. Ercal Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase-1 gene promoter polymorphism Acta Paediatr 99 2010 679 683
    • (2010) Acta Paediatr , vol.99 , pp. 679-683
    • Bozkaya, O.G.1    Kumral, A.2    Yesilirmak, D.C.3    Ulgenalp, A.4    Duman, N.5    Ercal, D.6


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