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

被引:6
作者
de Azevedo, Laura Alencastro [1 ]
Bonazzoni, Joyce [1 ]
Wagner, Sandrine Comparsi [2 ]
Farias, Mariela Granero [3 ]
Bittar, Christina M. [3 ]
Daudt, Liane [3 ]
de Castro, Simone Martins [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Fac Farm, Av Ipiranga 2752, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Fed Ciencias Saude Porto Alegre, Porto Alegre, RS, Brazil
[3] Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
关键词
GILBERTS-SYNDROME; SOUTHERN BRAZIL; ANEMIA; PROMOTER; GENE; PREVALENCE; ASSOCIATION; CHILDREN; METAANALYSIS;
D O I
10.1007/s40291-017-0283-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:437 / 442
页数:6
相关论文
共 26 条
[1]   Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and βs Haplotype: First Report on Comparison between Arab-Indian and African βs Genes [J].
Alkindi, Said Y. ;
Pathare, Anil ;
Al Zadjali, Shoaib ;
Panjwani, Vinodhkumar ;
Wasim, Fauzia ;
Khan, Hammad ;
Chopra, Pradeep ;
Krishnamoorthy, Rajagopal ;
Alkindi, Salam .
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES, 2015, 7
[2]   GENETIC INHERITANCE OF GILBERTS-SYNDROME [J].
BOSMA, PJ ;
CHOWDHURY, JR ;
JANSEN, PHM .
LANCET, 1995, 346 (8970) :314-315
[3]   Molecular genetic basis of Gilbert's syndrome [J].
Burchell, B ;
Hume, R .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1999, 14 (10) :960-966
[4]   Polymorphic Variants of UGT1A1 in Neonatal Jaundice in Southern Brazil [J].
Carvalho, Clarissa Gutierrez ;
Castro, Simone Martins ;
Santin, Ana Paula ;
de Azevedo, Laura Alencastro ;
Saraiva Pereira, Maria Luiza ;
Giugliani, Roberto .
JOURNAL OF TROPICAL PEDIATRICS, 2010, 56 (05) :366-367
[5]  
Chaar V, 2005, HAEMATOLOGICA, V90, P188
[6]   Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene [J].
Chaouch, Leila ;
Talbi, Emna ;
Moumni, Imen ;
Ben Chaabene, Arij ;
Kalai, Miniar ;
Chaouachi, Dorra ;
Mallouli, Fethi ;
Ghanem, Abderraouf ;
Abbes, Salem .
DISEASE MARKERS, 2013, 2013 :67-72
[7]   Prevalence of UGT1A1 Gene Polymorphism in Patients with Hemolytic Anemia in Southern Brazil [J].
de Azevedo, Laura Alencastro ;
Santin, Ana Paula ;
Wagner, Sandrine Comparsi ;
Zaleski, Carina da Fontoura ;
Bock, Hugo ;
Saraiva-Pereira, Maria Luiza ;
de Castro, Simone Martins .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2011, 15 (1-2) :107-110
[8]   Fetal Hemoglobin Levels in African American and Hispanic Children With Sickle Cell Disease at Baseline and in Response to Hydroxyurea [J].
Ender, Katherine L. ;
Lee, Margaret T. ;
Sheth, Sujit ;
Licursi, Maureen ;
Crotty, Jennifer ;
Barral, Sandra ;
Green, Nancy S. .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2011, 33 (07) :496-499
[9]   UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia [J].
Fertrin, KY ;
Melo, MB ;
Assis, AM ;
Saad, STO ;
Costa, FF .
CLINICAL GENETICS, 2003, 64 (02) :160-162
[10]   DIRECT IDENTIFICATION OF SICKLE-CELL-ANEMIA BY BLOT HYBRIDIZATION [J].
GEEVER, RF ;
WILSON, LB ;
NALLASETH, FS ;
MILNER, PF ;
BITTNER, M ;
WILSON, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (08) :5081-5085