Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia

被引:55
作者
Premawardhena, A
Fisher, CA
Fathiu, F
de Silva, S
Perera, W
Peto, TEA
Olivieri, NF
Weatherall, DJ [1 ]
机构
[1] Univ Oxford, Weatherall Inst Mol Med, Oxford, England
[2] Gen Hosp, Thalassaemia Unit, Kurunegala, Sri Lanka
[3] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[4] Toronto Gen Hosp, Toronto, ON, Canada
基金
英国惠康基金;
关键词
D O I
10.1016/S0140-6736(00)05082-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic hyperbilirubinaemia, gallstone formation, and bladder disease are unusually common in people with haemoglobin E beta thalassaemia in Sri Lanka. To determine whether this has a genetic basis we compared the bilirubin levels and frequency of gallstones in patients with different alleles of the UGT*1 gene. There was a significantly higher bilirubin level in those with the 7/7 genotypes compared with 6/6 and 6/7 genotype (p=0.032 and 0.0015 respectively), who also appeared more prone to gallstone formation. These results suggest that the UGT*1 genotpe is of importance in the genesis of gallstones in this population of patients.
引用
收藏
页码:1945 / 1946
页数:2
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