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Completed No phase listed Observational

Fatty Acid Binding Protein 2 (FABP2) Ancillary Proposal

ClinicalTrials.gov ID: NCT00256633

Public ClinicalTrials.gov record NCT00256633. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 5, 2026, 6:05 AM EST

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Official title

CSP #465C - Fatty Acid Binding Protein 2 (FABP2) Ancillary Proposal

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

TITLE: CSP 465-C, Fatty Acid Binding protein 2 (FABP2) ancillary proposal to CSP# 465 Glycemic Control and Complications in Diabetes Mellitus Type 2. Angeliki Georgopoulos, M.D. Carlos Abraira M.D. William Duckworth M.D. Fatty acid binding protein 2 (FABP2) is involved in the transport of long chain fatty acids across the intestinal epithelium. A common (40-45%) polymorphism of FABP2 gene (codon 54 Threonine for Alanine) results in increased intestinal fatty acid absorption and triglyceride secretion (Baier et al J Clin Invest 95:1281-87, 1995; Baier et al J Biol Chem 271: 10892-10896,1996). We have found (JCEM 85:3155-60, 2000) that in patients with type 2 diabetes, the codon 54 polymorphism of the FABP2 results in fasting and postprandial hypertriglyceridemia. Since hypertriglyceridemia is a risk factor for atherosclerosis in type 2 diabetes and it is part of the insulin resistance syndrome, the objective of this ancillary study would be to screen the participants of the CSP# 465 study for the polymorphism and assess a) whether those carrying the polymorphism respond differently to the various treatment modalities and b) whether they develop more cardiovascular events compared to the ones lacking the polymorphism. There is one study that suggests an association of the polymorphism with a history of parental stroke (JCEM 85:2801-4, 2000). The only additional request from the study participants will be to agree to the collection of a blood sample to be used for DNA isolation and screening for the polymorphism. No additional funds are requested. If this polymorphism proves to be a predictor of either the response to a specific treatment modality or of the risk to macro-vascular complications, it will be very easy to screen for it and target our treatment modalities appropriately.

Study identification

NCT ID
NCT00256633
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
874 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2007 (Type not available)
Primary completion
May 2008 (Actual)
Completion
May 2008 (Actual)
Last update posted
May 23, 2014

2007 – 2008

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Carl T. Hayden VA Medical Center Phoenix Arizona 85012 —
Southern Arizona VA Health Care System, Tucson Tucson Arizona 85723 —
VA Central California Health Care System, Fresno Fresno California 93703 —
VA San Diego Healthcare System, San Diego San Diego California 92161 —
VA Medical Center, Miami Miami Florida 33125 —
Edward Hines, Jr. VA Hospital Hines Illinois 60141-5000 —
Richard Roudebush VA Medical Center, Indianapolis Indianapolis Indiana 46202-2884 —
VA Medical Center, Lexington Lexington Kentucky 40502 —
VA Medical Center, Minneapolis Minneapolis Minnesota 55417 —
VA Medical Center, Omaha Omaha Nebraska 68105-1873 —
VA New Jersey Health Care System, East Orange East Orange New Jersey 07018 —
VA Pittsburgh Health Care System Pittsburgh Pennsylvania 15240 —
VA Medical Center Nashville Tennessee 37212-2637 —
VA South Texas Health Care System, San Antonio San Antonio Texas 78229 —
VA Medical Center, Salem VA Salem Virginia 24153 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00256633, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 23, 2014 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00256633 live on ClinicalTrials.gov.

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