Literature DB >> 28567595

Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?

Laura Alencastro de Azevedo1, Joyce Bonazzoni1, Sandrine Comparsi Wagner2, Mariela Granero Farias3, Christina M Bittar3, Liane Daudt3, Simone Martins de Castro4.   

Abstract

BACKGROUND: Increased destruction of erythrocytes in patients with sickle cell disease results in chronic hyperbilirubinemia and leads to the formation of gallstones.
OBJECTIVES: The objective of this study was to determine the combined influence of alpha thalassemia, fetal hemoglobin, and the UGT1A1 polymorphism on serum bilirubin levels and cholelithiasis in patients with sickle cell disease.
METHODS: We analyzed 72 patients treated in the outpatient hematology unit of the Clinical Hospital of Porto Alegre. The alpha thalassemia trait was determined by multiplex polymerase chain reaction and the polymorphisms of UGT1A1 by capillary electrophoresis with tagged primers.
RESULTS: Total and indirect bilirubin levels differed significantly between genotypes TA7/TA7 and TA6/TA6 (p < 0.05). Bilirubin levels were influenced by the UGT1A1 polymorphism but not by alpha thalassemia and fetal hemoglobin. There was no association between cholelithiasis and any of the variables studied.
CONCLUSION: These preliminary findings suggest that the UGT1A1 gene can influence serum bilirubin levels in sickle cell anemia and serve as a tool to differentiate an acute hemolytic condition from a pre-existing condition of hyperbilirubinemia.

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Year:  2017        PMID: 28567595     DOI: 10.1007/s40291-017-0283-y

Source DB:  PubMed          Journal:  Mol Diagn Ther        ISSN: 1177-1062            Impact factor:   4.074


  26 in total

1.  Genome-wide association meta-analysis for total serum bilirubin levels.

Authors:  Andrew D Johnson; Maryam Kavousi; Albert V Smith; Ming-Huei Chen; Abbas Dehghan; Thor Aspelund; Jing-Ping Lin; Cornelia M van Duijn; Tamara B Harris; L Adrienne Cupples; Andre G Uitterlinden; Lenore Launer; Albert Hofman; Fernando Rivadeneira; Bruno Stricker; Qiong Yang; Christopher J O'Donnell; Vilmundur Gudnason; Jacqueline C Witteman
Journal:  Hum Mol Genet       Date:  2009-05-04       Impact factor: 6.150

2.  Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.

Authors:  Vicky Chaar; Lysiane Kéclard; Jean Pierre Diara; Claudine Leturdu; Jacques Elion; Rajagopal Krishnamoorthy; John Clayton; Marc Romana
Journal:  Haematologica       Date:  2005-02       Impact factor: 9.941

Review 3.  Family 1 uridine-5'-diphosphate glucuronosyltransferases (UGT1A): from Gilbert's syndrome to genetic organization and variability.

Authors:  Christian P Strassburg; Tim O Lankisch; Michael P Manns; Ursula Ehmer
Journal:  Arch Toxicol       Date:  2008-05-20       Impact factor: 5.153

4.  Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.

Authors:  Katarzyna Rawa; Anna Adamowicz-Salach; Michal Matysiak; Anna Trzemecka; Beata Burzynska
Journal:  J Clin Pathol       Date:  2012-05-03       Impact factor: 3.411

5.  Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations.

Authors:  Laura J Horsfall; David Zeitlyn; Ayele Tarekegn; Endashaw Bekele; Mark G Thomas; Neil Bradman; Dallas M Swallow
Journal:  Ann Hum Genet       Date:  2011-03       Impact factor: 1.670

6.  Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease.

Authors:  Vassiliki Kalotychou; Katerina Antonatou; Revekka Tzanetea; Evaggelos Terpos; Dimitris Loukopoulos; Yannis Rombos
Journal:  Blood Cells Mol Dis       Date:  2003 Jul-Aug       Impact factor: 3.039

7.  Polymorphic variants of UGT1A1 in neonatal jaundice in southern Brazil.

Authors:  Clarissa Gutiérrez Carvalho; Simone Martins Castro; Ana Paula Santin; Laura Alencastro de Azevedo; Maria Luiza Saraiva Pereira; Roberto Giugliani
Journal:  J Trop Pediatr       Date:  2010-01-08       Impact factor: 1.165

8.  A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

Authors:  Jacqueline N Milton; Paola Sebastiani; Nadia Solovieff; Stephen W Hartley; Pallav Bhatnagar; Dan E Arking; Daniel A Dworkis; James F Casella; Emily Barron-Casella; Christopher J Bean; W Craig Hooper; Michael R DeBaun; Melanie E Garrett; Karen Soldano; Marilyn J Telen; Allison Ashley-Koch; Mark T Gladwin; Clinton T Baldwin; Martin H Steinberg; Elizabeth S Klings
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

9.  Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and β(s) Haplotype: First Report on Comparison between Arab-Indian and African β(s) Genes.

Authors:  Said Y Alkindi; Anil Pathare; Shoaib Al Zadjali; Vinodhkumar Panjwani; Fauzia Wasim; Hammad Khan; Pradeep Chopra; Rajagopal Krishnamoorthy; Salam Alkindi
Journal:  Mediterr J Hematol Infect Dis       Date:  2015-11-01       Impact factor: 2.576

10.  The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.

Authors:  Nisha Vasavda; Stephan Menzel; Sheila Kondaveeti; Emma Maytham; Moji Awogbade; Sybil Bannister; Juliette Cunningham; Andrew Eichholz; Yvonne Daniel; Iheanyi Okpala; Tony Fulford; Swee Lay Thein
Journal:  Br J Haematol       Date:  2007-07       Impact factor: 6.998

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