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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02938091
Other study ID # Study 2480
Secondary ID
Status Completed
Phase N/A
First received October 16, 2016
Last updated October 17, 2016
Start date January 2008
Est. completion date July 2012

Study information

Verified date October 2016
Source Tufts University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The investigators evaluated dietary modulation of LIPC rs1800588 (-514 C/T) for lipids and glucose using a randomized cross-over design comparing a high-fat Western diet and a low-fat traditional Hispanic diet in Caribbean Hispanics (n=42; 4 weeks/phase).


Description:

The LIPC -514 C/T single nucleotide polymorphism (SNP) has been inconsistently associated with high density lipoprotein cholesterol (HDL-C) in population studies, supporting the possibility of its modulation by dietary factors. To investigate the interaction between the common LIPC -514(C/T) SNP and dietary fat, the investigators compared changes in lipids and glucose in response to two levels of dietary total fat (20% energy intake vs. 39% energy intake) in a crossover, randomized dietary intervention study enrolling Caribbean Hispanics. Individuals were screened for LIPC rs1800588 genotype prior to enrollment, and genotype-associated differences in response to diet were evaluated.

The study was designed to test the following hypotheses:

1. Carriers of the T allele consuming a low fat (LF) diet will have decreased hepatic lipase activity as compared with subjects with the CC genotype at the -514(C/T) polymorphism. Conversely, in individuals consuming a high fat (HF) diet, T carriers will exhibit an impaired ability to down regulate hepatic lipase activity.

2. Based on differences in hepatic lipase activity, the investigators hypothesized that a significant and clinically relevant proportion of the individual variability in fasting plasma HDL-C responses to changes in dietary fat intake would be due to variability at the LIPC locus. Specifically, CC subjects will respond to increases in total dietary fat consumption with significant increases in HDL-C concentration. Conversely, increased fat consumption in T carrying subjects will result in decreased HDL-C concentration.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date July 2012
Est. primary completion date July 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Self-reported Caribbean Hispanics

Exclusion Criteria:

- diabetes

- uncontrolled hypertension

- self-reported liver disease; severe kidney dysfunction; angina; endocrine disease; preexisting cardiovascular disease or gallbladder disease, or pancreatitis within the past 12 months

- use of lipid-lowering or hypoglycemic medications

- BMI >34 kg/m2

- alcohol consumption (>2 drinks/day)

- smoking within the past 6 months or illegal drug use

- pregnancy or breastfeeding

- weight gain or loss of more than 9 kg within the past 6 months

- extreme levels of physical or athletic activity, strict vegetarians/vegans

- egg, wheat, milk, fish, or nut allergies

- unwillingness to discontinue fish oil or flaxseed supplements or drinking alcohol during the study

- travel plans precluding availability for the two 4-week study phases

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
High-fat diet
Typical Western diet
Low-fat diet
Traditional Caribbean Hispanic diet

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tufts University

Outcome

Type Measure Description Time frame Safety issue
Primary change in fasting high-density lipoprotein cholesterol From date of randomization until completion of each 4 week dietary intervention No
Secondary change in fasting plasma triglycerides From date of randomization until completion of the 4 week dietary intervention No
Secondary change in fasting plasma glucose From date of randomization until completion of the 4 week dietary intervention No
Secondary oral glucose tolerance test 2 hours post-oral glucose load No
Secondary post-prandial lipemia 4 hours 4 hours post-oral fat load No
Secondary post-prandial lipemia 8 hours 8 hours post-oral fat load No
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