Human Requirements for the Nutrient Choline

NCT ID: NCT00065546

Last Updated: 2012-01-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

43 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2012-01-31

Brief Summary

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The purpose of this study is to increase our understanding of how much choline humans need to get from their diet. Choline is an essential nutrient found in many foods, including eggs and milk. In addition to dietary sources, choline can be made in the liver. Choline is important in making membranes or wrappers for all the cells in the body and for making chemicals that allow nerve cells to work properly. In a previous study we found that the dietary requirement for choline varies greatly from person to person. This was caused, in part, by how much estrogen a person has and their genetic makeup. We are conducting this study to explore how estrogen levels and specific differences in genes influence choline requirements so that we can refine the dietary recommendations for this nutrient.

Detailed Description

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Choline is an essential nutrient essential used for the structural integrity and signaling functions of cell membranes, cholinergic neurotransmission, and lipid transport/metabolism. Choline is obtained from the diet and from endogenous biosynthesis catalyzed by the enzyme phosphatidylethanolamine N-methyltransferase (PEMT). The major premise for this proposal is that humans require a dietary source of choline and that this requirement has significant individual variation and is modulated by estrogen and common genetic polymorphisms. The promoter of the PEMT gene is estrogen responsive, and we hypothesize that estrogen status influences the dietary requirement for choline. We identified other common single nucleotide polymorphisms (SNPs) that increase or decrease the likelihood that a human will develop organ dysfunction when fed a low choline diet. Experiments are proposed that will refine our understanding of estrogen-mediated induction of the PEMT promoter; determine whether postmenopausal women treated with estrogen have a decreased susceptibility to developing organ dysfunction associated with choline deficiency; determine the prevalence of SNPs that increase susceptibility to choline deficiency in the population and examine dietary choline requirements in humans with these SNPs.

Conditions

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Postmenopausal Women

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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1

Post-menopausal women randomized to receive estrogen replacement therapy.

Group Type ACTIVE_COMPARATOR

Estrogen plus choline depletion diet

Intervention Type OTHER

Post-menopausal subjects receive estrogen and are then challenged with a low choline diet to determine if estrogen protects them from induction of choline deficiency.

2

Post-menopausal women randomized to receive a placebo.

Group Type PLACEBO_COMPARATOR

Placebo plus choline depletion diet

Intervention Type OTHER

Post-menopausal women are randomized to receive a placebo and are then subjected to a low choline diet to determine if clinical signs of choline deficiency can be induced.

3

Pre-menopausal women with specific genetic variants.

Group Type EXPERIMENTAL

Pre-menopausal women with SNPs given a low choline diet

Intervention Type OTHER

Pre-menopausal women with specific genetic polymorphisms in genes related to choline metabolism are placed on a choline depletion diet to determine if the SNPs increase or decrease the risk of diet-induced choline deficiency.

Interventions

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Estrogen plus choline depletion diet

Post-menopausal subjects receive estrogen and are then challenged with a low choline diet to determine if estrogen protects them from induction of choline deficiency.

Intervention Type OTHER

Placebo plus choline depletion diet

Post-menopausal women are randomized to receive a placebo and are then subjected to a low choline diet to determine if clinical signs of choline deficiency can be induced.

Intervention Type OTHER

Pre-menopausal women with SNPs given a low choline diet

Pre-menopausal women with specific genetic polymorphisms in genes related to choline metabolism are placed on a choline depletion diet to determine if the SNPs increase or decrease the risk of diet-induced choline deficiency.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy
* Non-smoker
* BMI between 18 and 34
* Normal mammogram in last 12 months (post-menopausal women only)

Exclusion Criteria

* Hormone or estrogen therapy
* Allergic to soy, eggs, wheat
* History of breast, uterine, or other estrogen-dependent cancer
* Liver or kidney problems
* History of circulation, bleeding, or blood-clotting disorder
* Anemia or evidence of iron overload
* Hyperthyroidism, neurological disorder, or autoimmune disease
* Diabetes controlled by insulin
* Positive serology for HIV or Hepatitis B or C
* Alcohol or illegal drug misuse/abuse
* Pacemaker, aneurysm clip, cardiac heart valve, mechanical devices/implants
* Other metal in body (i.e. injured by a BB, shrapnel, or metallic object)
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role collaborator

University of North Carolina, Chapel Hill

OTHER

Sponsor Role lead

Responsible Party

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Steven Zeisel

Professor of Nutrition and Pediatrics, Director, UNC Nutrition Research Institute

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Steven H Zeisel, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of North Carolina, Chapel Hill

Leslie M Fischer, PhD, MPH, RD

Role: STUDY_DIRECTOR

University of North Carolina, Chapel Hill

Locations

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University of North Carolina

Chapel Hill, North Carolina, United States

Site Status

Countries

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United States

References

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da Costa KA, Corbin KD, Niculescu MD, Galanko JA, Zeisel SH. Identification of new genetic polymorphisms that alter the dietary requirement for choline and vary in their distribution across ethnic and racial groups. FASEB J. 2014 Jul;28(7):2970-8. doi: 10.1096/fj.14-249557. Epub 2014 Mar 26.

Reference Type DERIVED
PMID: 24671709 (View on PubMed)

da Costa KA, Sanders LM, Fischer LM, Zeisel SH. Docosahexaenoic acid in plasma phosphatidylcholine may be a potential marker for in vivo phosphatidylethanolamine N-methyltransferase activity in humans. Am J Clin Nutr. 2011 May;93(5):968-74. doi: 10.3945/ajcn.110.011064. Epub 2011 Mar 16.

Reference Type DERIVED
PMID: 21411618 (View on PubMed)

Fischer LM, da Costa KA, Kwock L, Galanko J, Zeisel SH. Dietary choline requirements of women: effects of estrogen and genetic variation. Am J Clin Nutr. 2010 Nov;92(5):1113-9. doi: 10.3945/ajcn.2010.30064. Epub 2010 Sep 22.

Reference Type DERIVED
PMID: 20861172 (View on PubMed)

Other Identifiers

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R01DK055865

Identifier Type: NIH

Identifier Source: secondary_id

View Link

DK55865

Identifier Type: -

Identifier Source: org_study_id

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