Duarte galactose-1-phosphate uridyl transferase genotypes are not associated with ovarian cancer risk

Capsule:
This study suggests that Duarte1 and Duarte2 genotypes do not appear to play a role in the association from galactose intake, possible ovarian dysfunction, and the link with ovarian cancer.

Authors:
Melissa A. Merritt, Ph.D., Joanne Kotsopoulos, Ph.D., Daniel W. Cramer, M.D., Sc.D., Susan E. Hankinson, Sc.D., Kathryn L. Terry, Sc.D., Shelley S. Tworoger, Ph.D.

Volume 98, Issue 3, Pages 687-691, September 2012

Abstract:

Objective:
To investigate whether Galactose-1-phosphate uridyl transferase (GALT) variant genotypes were associated with epithelial ovarian cancer risk and to determine if this association was modified by lactose intake.

Design:
Two prospective cohort studies and a case-control study.

Setting:
Academic institution.

Patient(s):
992 cases and 1,050 population-based controls from a New England case-control study and 240 cases and 900 controls from the Nurses’ Health Studies.

Intervention(s):
None.

Main Outcome Measure(s):
Genotyping of the N314D variant and the 4-bp deletion (-119delGTCA) of GALT using the Taqman 5’ nuclease assay. Duarte1 (D1) genotype individuals have a missense mutation (N314D) associated with normal GALT activity unless it occurs together with an associated 4-bp deletion leading to reduced GALT activity (Duarte2 or D2).

Result(s):
Logistic regression analysis identified no association between D1/D2 genotypes and ovarian cancer risk (pooled RR, 1.1 (95% CI, 0.8-1.5) for D1 and 1.0 (95% CI, 0.7-1.4) for D2). We did not observe a significant interaction between D1 and D2 genotypes in analyses stratified by level of lactose intake (Pinteraction ≥ 0.3).

Conclusion(s):
D1 and D2 genotypes do not appear to play a role in the association between galactose intake, possible ovarian dysfunction and the link with ovarian cancer.

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