Literature DB >> 1142378

Population studies on Gilbert's syndrome.

D Owens, J Evans.   

Abstract

Total serum bilirubin concentration was measured by an Autoanalyzer technique in 197 normal males and 102 normal females. The mean bilirubin concentration was significantly lower in the females than in the males. Total bilirubin concentration in the males showed a bimodal distribution with an antimode at 24 mumol/1 (1.4 mg/100ml). Individuals with bilirubin concentration above this value had unconjugated hyperbilirubinaemia and probable Gilbert's syndrome. Total bilirubin concentration in the females again showed a bimodal distribution with an antimode at 12 mumol/1 (0.7 mg/100ml). It is conceivable that females with bilirubin levels above this also have Gilbert's syndrome. This suggests that the population incidence of Gilbert's syndrome could be as high as 6% and that the sex incidence is approximately equal.

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Year:  1975        PMID: 1142378      PMCID: PMC1013257          DOI: 10.1136/jmg.12.2.152

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  13 in total

1.  DEFECTS IN HEPATIC TRANSPORT OF BILIRUBIN IN CONGENITAL HYPERBILIRUBINAEMIA: AN ANALYSIS OF PLASMA BILIRUBIN DISAPPEARANCE CURVES.

Authors:  B H BILLING; R WILLIAMS; T G RICHARDS
Journal:  Clin Sci       Date:  1964-10       Impact factor: 6.124

2.  PLASMA BILIRUBIN DETERMINATION IN THE NEWBORN INFANT. A METHODOLOGICAL STUDY WITH SPECIAL REFERENCE TO THE INFLUENCE OF HEMOLYSIS.

Authors:  M MICHAUELSSON; B NOSSLIN; S SJOELIN
Journal:  Pediatrics       Date:  1965-06       Impact factor: 7.124

3.  Constitutional hepatic dysfunction (Gilbert's disease): its natural history and related syndromes.

Authors:  W T FOULK; H R BUTT; C A OWEN; F F WHITCOMB; H L MASON
Journal:  Medicine (Baltimore)       Date:  1959-02       Impact factor: 1.889

4.  LATENT LIVER DISEASE IN PERSONS RECOVERED FROM CATARRHAL JAUNDICE AND IN OTHERWISE NORMAL MEDICAL STUDENTS AS REVEALED BY THE BILIRUBIN EXCRETION TEST.

Authors:  A Kornberg
Journal:  J Clin Invest       Date:  1942-05       Impact factor: 14.808

5.  Treatment of Gilbert's syndrome with phenobarbitone.

Authors:  M Black; S Sherlock
Journal:  Lancet       Date:  1970-06-27       Impact factor: 79.321

6.  Diagnosis of Gilbert's syndrome: role of reduced caloric intake test.

Authors:  D Owens; S Sherlock
Journal:  Br Med J       Date:  1973-09-15

7.  Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin.

Authors:  P D Berk; J R Bloomer; R B Howe; N I Berlin
Journal:  Am J Med       Date:  1970-09       Impact factor: 4.965

8.  Hepatic bilirubin udp-glucuronyl transferase activity in liver disease and gilbert's syndrome.

Authors:  M Black; B H Billing
Journal:  N Engl J Med       Date:  1969-06-05       Impact factor: 91.245

9.  Studies of bilirubin kinetics in normal adults.

Authors:  P D Berk; R B Howe; J R Bloomer; N I Berlin
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

10.  Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome).

Authors:  P D Berk; T F Blaschke; J G Waggoner
Journal:  Gastroenterology       Date:  1972-09       Impact factor: 22.682

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  31 in total

1.  Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.

Authors:  Shabana Farheen; Sanghamitra Sengupta; Amal Santra; Suparna Pal; Gopal Krishna Dhali; Meenakshi Chakravorty; Partha P Majumder; Abhijit Chowdhury
Journal:  World J Gastroenterol       Date:  2006-04-14       Impact factor: 5.742

2.  Proton magnetic resonance spectroscopy of the anterior cingulate gyrus, insular cortex and thalamus in schizophrenia associated with idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome).

Authors:  Rei Yasukawa; Tsuyoshi Miyaoka; Shoichi Mizuno; Takuji Inagaki; Jun Horiguchi; Kazushige Oda; Hajime Kitagaki
Journal:  J Psychiatry Neurosci       Date:  2005-11       Impact factor: 6.186

3.  Effect of dietary composition on the unconjugated hyperbilirubinaemia of Gilbert's syndrome.

Authors:  J L Gollan; C Bateman; B H Billing
Journal:  Gut       Date:  1976-05       Impact factor: 23.059

4.  Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Authors:  Yoshihiro Maruo; Yoriko Morioka; Hiroshi Fujito; Sayuri Nakahara; Takahide Yanagi; Katsuyuki Matsui; Asami Mori; Hiroshi Sato; Robert H Tukey; Yoshihiro Takeuchi
Journal:  J Pediatr       Date:  2014-03-17       Impact factor: 4.406

5.  Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.

Authors:  Akitaka Nomura; Yoshihiro Maruo; Takashi Taga; Yoshihiro Takeuchi
Journal:  Pediatr Res       Date:  2016-04-08       Impact factor: 3.756

6.  Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.

Authors:  Shigeo Iijima; Takehiko Ohzeki; Yoshihiro Maruo
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759

7.  Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans.

Authors:  Leonie C Jacobs; Andreas Wollstein; Oscar Lao; Albert Hofman; Caroline C Klaver; André G Uitterlinden; Tamar Nijsten; Manfred Kayser; Fan Liu
Journal:  Hum Genet       Date:  2012-10-11       Impact factor: 4.132

8.  Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

Authors:  Jae Hee Lee; Kyung Rye Moon
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

Review 9.  Pharmacogenetics: a tool for individualizing antineoplastic therapy.

Authors:  F Innocenti; L Iyer; M J Ratain
Journal:  Clin Pharmacokinet       Date:  2000-11       Impact factor: 6.447

10.  Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.

Authors:  Katsuyuki Matsui; Yoshihiro Maruo; Hiroshi Sato; Yoshihiro Takeuchi
Journal:  BMC Gastroenterol       Date:  2010-06-08       Impact factor: 3.067

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