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Volumn 134, Issue 4, 1999, Pages 441-446

Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn

Author keywords

[No Author keywords available]

Indexed keywords

ADULTHOOD; ALLELE; ARTICLE; BLOOD SAMPLING; DNA POLYMORPHISM; DNA SEQUENCE; GENE MUTATION; GENETIC PREDISPOSITION; GILBERT DISEASE; HUMAN; HYPERBILIRUBINEMIA; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN JAUNDICE; PEDIGREE; PRIORITY JOURNAL; PROMOTER REGION; TATA BOX;

EID: 0033510908     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(99)70201-5     Document Type: Article
Times cited : (139)

References (26)
  • 1
    • 0001747399 scopus 로고
    • Hereditary jaundice and disorders of bilirubin metabolism
    • Scriver CR, Beaudet AI, Sly WS, Valle D, editors. New York: McGraw-Hill
    • 1. Roy Chowdhury J, Wolkoff A, Roy Chowdhury N, Arias IM. Hereditary jaundice and disorders of bilirubin metabolism. In: Scriver CR, Beaudet AI, Sly WS, Valle D, editors. The metabolic basis of inherited disease. 7th ed. New York: McGraw-Hill; 1995. p. 2161-208.
    • (1995) The Metabolic Basis of Inherited Disease. 7th Ed. , pp. 2161-2208
    • Roy Chowdhury, J.1    Wolkoff, A.2    Roy Chowdhury, N.3    Arias, I.M.4
  • 2
    • 0018574014 scopus 로고
    • Postnatal development or uridine diphosphate glucuronosyltransferase activity towards bilirubin and 2-aminophenol in human liver
    • 2. Onishi S, Kawade N, Itoh S, Isobe K, Sugiama S. Postnatal development or uridine diphosphate glucuronosyltransferase activity towards bilirubin and 2-aminophenol in human liver. Biochem J 1979;184:705-7.
    • (1979) Biochem J , vol.184 , pp. 705-707
    • Onishi, S.1    Kawade, N.2    Itoh, S.3    Isobe, K.4    Sugiama, S.5
  • 3
    • 0000621679 scopus 로고
    • Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α 20β-diol, in maternal milk that inhibits glucuronide formation in vitro
    • 3. Arias IM, Gartner L, Seifter S, Furman M. Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α 20β-diol, in maternal milk that inhibits glucuronide formation in vitro. J Clin Invest 1964;43: 2037-47.
    • (1964) J Clin Invest , vol.43 , pp. 2037-2047
    • Arias, I.M.1    Gartner, L.2    Seifter, S.3    Furman, M.4
  • 4
    • 0017861029 scopus 로고
    • Clinical study of prolonged jaundice in breast-and bottle-fed babies
    • 4. Winfield CR, MacFaul R. Clinical study of prolonged jaundice in breast-and bottle-fed babies. Arch Dis Child 1978;53:506-7.
    • (1978) Arch Dis Child , vol.53 , pp. 506-507
    • Winfield, C.R.1    MacFaul, R.2
  • 5
  • 6
    • 0023936363 scopus 로고
    • Jaundice in the healthy newborn infant: A new approach to an old problem
    • 6. Maisels MJ, Gifford K, Antle CE, Leib GR. Jaundice in the healthy newborn infant: a new approach to an old problem. Pediatrics 1988;81:505-11.
    • (1988) Pediatrics , vol.81 , pp. 505-511
    • Maisels, M.J.1    Gifford, K.2    Antle, C.E.3    Leib, G.R.4
  • 7
    • 0020639259 scopus 로고
    • Neonatal jaundice in full-term infants: Role of breast-feeding and other causes
    • 7. Maisels MJ, Gifford K. Neonatal jaundice in full-term infants: role of breast-feeding and other causes. Am J Dis Child 1983;137:561-2.
    • (1983) Am J Dis Child , vol.137 , pp. 561-562
    • Maisels, M.J.1    Gifford, K.2
  • 8
    • 0028867826 scopus 로고
    • The genetic basis of reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
    • 8. Bosma PJ, Roy Chowdhury J, Bakker C, Gantla S, de Boer A, Oostra BA, et al. The genetic basis of reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. N Engl J Med 1995;333:1171-5.
    • (1995) N Engl J Med , vol.333 , pp. 1171-1175
    • Bosma, P.J.1    Roy Chowdhury, J.2    Bakker, C.3    Gantla, S.4    De Boer, A.5    Oostra, B.A.6
  • 9
    • 0030030762 scopus 로고    scopus 로고
    • Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
    • 9. Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996;347:578-81.
    • (1996) Lancet , vol.347 , pp. 578-581
    • Monaghan, G.1    Ryan, M.2    Seddon, R.3    Hume, R.4    Burchell, B.5
  • 11
    • 0030053274 scopus 로고    scopus 로고
    • The genetic basis of Gilbert's syndrome
    • 11. Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert's syndrome. Lancet 1996;347:557-8.
    • (1996) Lancet , vol.347 , pp. 557-558
    • Sato, H.1    Adachi, Y.2    Koiwai, O.3
  • 12
    • 0018611018 scopus 로고
    • Improved method for accurate quantitation of total and conjugated bilirubin in serum
    • 12. Novros JS, Koch TR, Knoblock EC. Improved method for accurate quantitation of total and conjugated bilirubin in serum. Clin Chem 1979;25:1891-9.
    • (1979) Clin Chem , vol.25 , pp. 1891-1899
    • Novros, J.S.1    Koch, T.R.2    Knoblock, E.C.3
  • 13
    • 0030728222 scopus 로고    scopus 로고
    • Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias
    • 13. Clarke DJ, Moghrabi N, Monaghan G, Cassidy A, Boxer B, Hume R, et al. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias. Clin Chim Acta 1998;266:63-74.
    • (1998) Clin Chim Acta , vol.266 , pp. 63-74
    • Clarke, D.J.1    Moghrabi, N.2    Monaghan, G.3    Cassidy, A.4    Boxer, B.5    Hume, R.6
  • 14
    • 0028904620 scopus 로고
    • Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
    • 14. Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, et al. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. Lancet 1995;345:958-9.
    • (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
  • 15
    • 0003902055 scopus 로고    scopus 로고
    • Infant feeding 1995
    • Foster K, Lader D, Cheesbrough S, editors. (Office for National Statistics). London: Government Statistical Service, The Stationery Office
    • 15. Foster K, Lader D, Cheesbrough S. Infant feeding 1995. In: Foster K, Lader D, Cheesbrough S, editors. (Office for National Statistics). Infant feeding 1995. London: Government Statistical Service, The Stationery Office; 1997. p. 1-8.
    • (1997) Infant Feeding 1995 , pp. 1-8
    • Foster, K.1    Lader, D.2    Cheesbrough, S.3
  • 16
    • 0024602667 scopus 로고
    • The effect of saccharolactone on rat intestinal absorption of bilirubin in the presence of human breast milk
    • 16. Gourley GR, Gourley MF, Arend R, Palta M. The effect of saccharolactone on rat intestinal absorption of bilirubin in the presence of human breast milk. Pediatr Res 1989;25:234-8.
    • (1989) Pediatr Res , vol.25 , pp. 234-238
    • Gourley, G.R.1    Gourley, M.F.2    Arend, R.3    Palta, M.4
  • 17
    • 0030691028 scopus 로고    scopus 로고
    • Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency. A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
    • 17. Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency. A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia. Proc Natl Acad Sci USA 1997;94: 12128-32.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 12128-12132
    • Kaplan, M.1    Renbaum, P.2    Levy-Lahad, E.3    Hammerman, C.4    Lahad, A.5    Beutler, E.6
  • 18
    • 0032005254 scopus 로고    scopus 로고
    • UGT promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis
    • 18. Iolascon A, Faienza MF, Moretti A, Perotta S, Miraglia del Giudice E. UGT promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. Blood 1998;91:1093.
    • (1998) Blood , vol.91 , pp. 1093
    • Iolascon, A.1    Faienza, M.F.2    Moretti, A.3    Perotta, S.4    Miraglia Del Giudice, E.5
  • 19
    • 0030663191 scopus 로고    scopus 로고
    • The expression of UDP-glucuronosyltransferase is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
    • 19. Sanpietro M, Lupica L, Perrero L, Comino A, Martinez DI, Mantemuros F, et al. The expression of UDP-glucuronosyltransferase is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 1997;99:437-9.
    • (1997) Br J Haematol , vol.99 , pp. 437-439
    • Sanpietro, M.1    Lupica, L.2    Perrero, L.3    Comino, A.4    Martinez, D.I.5    Mantemuros, F.6
  • 21
    • 0032493441 scopus 로고    scopus 로고
    • Racial variability in the UDP-glucuronosyltransferase 1 (UGTIAI) promoter: A balanced polymorphism for regulation of bilirubin metabolism
    • 21. Beutler E, Gelbert T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGTIAI) promoter: a balanced polymorphism for regulation of bilirubin metabolism. Proc Natl Acad Sci USA 1998;95: 8170-4.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 8170-8174
    • Beutler, E.1    Gelbert, T.2    Demina, A.3
  • 22
    • 0031719562 scopus 로고    scopus 로고
    • Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
    • 22. Akaba K, Kimura T, Sasaki A, Tanabe S, Ikogami T, Hashimoto M, et al. Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese. Biochem Mol Biol Int 1998;46:21-6.
    • (1998) Biochem Mol Biol Int , vol.46 , pp. 21-26
    • Akaba, K.1    Kimura, T.2    Sasaki, A.3    Tanabe, S.4    Ikogami, T.5    Hashimoto, M.6
  • 23
    • 0016242097 scopus 로고
    • Navajo jaundice: A variant of neonatal hyperbilirubinemia associated with breast-feeding
    • 23. Saland J, McNamara H, Cohen MI. Navajo jaundice: a variant of neonatal hyperbilirubinemia associated with breast-feeding. J Pediatr 1974;85:271-5.
    • (1974) J Pediatr , vol.85 , pp. 271-275
    • Saland, J.1    McNamara, H.2    Cohen, M.I.3
  • 24
    • 0018216093 scopus 로고
    • Jaundice and breast-feeding among Alaska Eskimo newborns
    • 24. Fisher Q, Cohen MI, Curda L. Jaundice and breast-feeding among Alaska Eskimo newborns. Am J Dis Child 1978;132:859-63.
    • (1978) Am J Dis Child , vol.132 , pp. 859-863
    • Fisher, Q.1    Cohen, M.I.2    Curda, L.3
  • 25
    • 0027085807 scopus 로고
    • Jaundice in Navajo neonates
    • 25. Johnson JD. Jaundice in Navajo neonates. Clin Pediatr (Phila) 1992; 12:716-8.
    • (1992) Clin Pediatr (Phila) , vol.12 , pp. 716-718
    • Johnson, J.D.1
  • 26
    • 0031949264 scopus 로고    scopus 로고
    • Gilbert syndrome accelerates development of neonatal jaundice
    • 26. Bancroft JD, Kreamer B, Gourley GR. Gilbert syndrome accelerates development of neonatal jaundice. J Pediatr 1998;132:656-60.
    • (1998) J Pediatr , vol.132 , pp. 656-660
    • Bancroft, J.D.1    Kreamer, B.2    Gourley, G.R.3


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