Clinical Trials Directory

Trials / Completed

CompletedNCT07264257

Choline and Brain Functioning in Postmenopausal Women

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
University of Vermont · Academic / Other
Sex
Female
Age
50 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study will use a randomized placebo-controlled trial to examine a single oral dose of 1650 mg choline influences brain functioning as measured by fMRI.

Detailed description

Choline is an essential nutrient that, in addition to its role in the brain, has a number of critical structural and physiologic roles throughout the body, including providing structural integrity and signaling function for cell membranes, facilitating lipid transport from the liver, and acting as the major source of methyl groups through diet. Aside from dietary intake, the only source of choline in the body is de novo synthesis of phosphatidylcholine, catalyzed by phosphatdylethanolamine-N-methyltransferase (PEMT). The PEMT gene has several estrogen-responsive components in its promoter region and is induced by estrogen. Post-menopausal (hypo-estrogenic) women with loss of function mutations in PEMT have been found to exhibit end-organ damage typical of choline deficiency. Choline is also involved in the synthesis of acetylcholine, a major neurotransmitter and the central and peripheral nervous systems. The relationship between brain effects of the normal functioning of the cholinergic system and hormone changes after menopause has been demonstrated in preclinical studies in rat models and in experimentally in human studies. While the preclinical and clinical experiment studies have many similar findings regarding the influence of estrogen on cholinergic functioning, what is not clear from this research is how individual differences arise in the effects of the hormone withdrawal after menopause on brain functioning in middle aged women. It is possible that the estrogen control of the transcription of the PEMT gene may influence the availability of choline. This study will examine the effects of a single oral dose of oral dose of 1650 mg choline versus placebo in 20 healthy postmenopausal women aged 50-65 years. Choline or placebo will be administered three hours before an MRI session where subjects undergo functional MRI scans.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCholineEach subject gets one 1650 mg oral choline dose or placebo on each of two study days.
DIETARY_SUPPLEMENTPlaceboEach subject gets one 1650 mg oral choline dose or placebo on each of two study days.

Timeline

Start date
2022-06-15
Primary completion
2022-12-20
Completion
2025-03-01
First posted
2025-12-04
Last updated
2025-12-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07264257. Inclusion in this directory is not an endorsement.