Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia

Chronic hyperbilirubinaemia, gallstone formation, and gall bladder disease are unusually common in people with haemoglobin E βmathfrak halassaemia in Sri Lanka. To determine whether this has a genetic basis we compared the bilirubin levels and frequency of gallstones in patients with different allel...

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Veröffentlicht in:The Lancet (British edition) 2001-06, Vol.357 (9272), p.1945-1946
Hauptverfasser: Premawardhena, A, Fisher, CA, Fathiu, F, de Silva, S, Perera, W, Peto, TEA, Olivieri, NF, Weatherall, DJ
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Sprache:eng
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Zusammenfassung:Chronic hyperbilirubinaemia, gallstone formation, and gall bladder disease are unusually common in people with haemoglobin E βmathfrak halassaemia 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.
ISSN:0140-6736
1474-547X
DOI:10.1016/S0140-6736(00)05082-0