Status:

COMPLETED

DHFR 19 bp Deletion Polymorphism and Folic Acid Utilization

Lead Sponsor:

Tufts University

Conditions:

Characterize rs70991108 Polymorphism of DHFR Gene

Eligibility:

FEMALE

21-45 years

Brief Summary

A genetic variation in the gene for the protein dihydrofolate reductase (DHFR) that is necessary to utilize folic acid (a synthetic form of the B vitamin folate found in supplements and fortified food...

Detailed Description

A 19bp deletion polymorphism of intron 1 of dihydrofolate reductase (DHFR 19bpdel) increases the risk for breast cancer, and retinoblastoma of the offspring, in folic acid supplement users. Folic acid...

Eligibility Criteria

Inclusion

  • Adult premenopausal women aged 21-45 in general good health, non-pregnant, minimum weight of 110 pounds.

Exclusion

  • Smoking, a terminal illness, any known chronic illness, rheumatoid arthritis, heart, kidney, liver or gastrointestinal disease requiring treatment, antifolate medications, metformin use.
  • More than 2 drinks a day.
  • Pregnant women have different metabolism when compared to other adults hence they will not be included in the study.
  • Non-English speaking subjects will be excluded since the study involves a computer based diet history questionnaire in English. The budget for this project does not include the cost of an interpreter.

Key Trial Info

Start Date :

February 1 2013

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2015

Estimated Enrollment :

117 Patients enrolled

Trial Details

Trial ID

NCT03319979

Start Date

February 1 2013

End Date

March 1 2015

Last Update

October 24 2017

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DHFR 19 bp Deletion Polymorphism and Folic Acid Utilization | DecenTrialz