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An association between the N314D polymorphism of galactose-1-phosphate uridyl transferase and endometriosis has recently been reported in a North American population. To determine whether such an association exists in the UK population, we genotyped 148 women with sporadic (n = 91) or familial (n = 57) endometriosis, a control population of 95 male blood donors and a control group of 53 women with a normal pelvis at hysterectomy. Heterozygosity for the polymorphism was found in 14.9% (22/148) of affected women, 13.7% (13/95) of male blood donors and 11.3% (6/53) of women with a normal pelvis. There was no statistically significant difference in the frequency of the polymorphism between cases and controls in the UK population, even when the cases were divided into groups of moderate-severe disease, sporadic cases or familial cases. We conclude that the galactose-1-phosphate uridyl transferase N314D polymorphism is unlikely to be associated with endometriosis in the UK population.

More information Original publication

DOI

10.1093/molehr/5.10.990

Type

Journal article

Publication Date

1999-10-01T00:00:00+00:00

Volume

5

Pages

990 - 993

Total pages

3

Keywords

Adult, Amino Acid Substitution, Case-Control Studies, Endometriosis, Female, Gene Frequency, Genotype, Heterozygote, Humans, Male, Middle Aged, Polymorphism, Genetic, UDPglucose-Hexose-1-Phosphate Uridylyltransferase, United Kingdom