Genetic Basis for Prediction of Non-responders to Dietary Plant Sterol Intervention

Cardiovascular Disease Clinical Trial

— GenePredict-PS  

Official title:

Genetic Basis for Prediction of Non-responders to Dietary Plant Sterol Intervention

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02765516
• Other study ID #: MITACS Converge MC00009
• Status: Terminated
• Phase: N/A
• Start date: July 5, 2017
• Est. completion date: December 31, 2019

Study information

• Verified date: May 2020
• Source: University of Manitoba
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to utilize information on associations between genetic predisposition pertaining to multiple single nucleotide polymorphisms (SNPs) and the degree of responsiveness of low-density lipoprotein cholesterol (LDL-C) lowering to plant sterols (PS). The predictive potential of SNPs associated with PS responsiveness will be evaluated using a randomized human intervention trial examining responsiveness of lowering blood LDL-C levels to PS intervention.

Description:

On average plant sterol (PS) consumption of 2-3 grams a day leads to a ~10% decrease in low-density lipoprotein cholesterol (LDL-C). However, inter-individual response to PS consumption varies, with some individuals showing low or no reductions in LDL-C levels, while some even showing an increase in levels. Determining factors that predict the direction of response of LDL-C to PS would be helpful in identifying individuals who should consume PS and individuals who should seek another method of treating hypercholesterolemia. The objective of this research proposal is to test the a priori predictive potential of a combination of three single nucleotide polymorphisms (SNPs), i.e., genosets, previously associated with response to PS in a post-hoc manner. A clinical trial with a priori recruitment of participants based on genoset which will test LDL-C response to PS consumption using a randomized, double blind, placebo controlled crossover design is proposed.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 43
• Est. completion date: December 31, 2019
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Fasting LDL-C concentration >3.0 and <4.9 mmol/L

• Fasting glucose concentration <6.1 mmol/L

• Fasting triglyceride concentration <4.52 mmol/L

• Genoset required: ; ApoE e3/e3 CYP7A1 rs3808607 T/T (n=20); ApoE e3/e3 CYP7A1 rs3808607 G/- (n=22); ApoE e4/- CYP7A1 rs3808607 -/- (n=22)

Exclusion Criteria:

• Consuming, or have consumed in the last 3 months, medications or nutritional supplements which are known to affect lipid metabolism (such as cholestyramine, colestipol, niacin, clofibrate, gemfibrozil, probucol, HMG-CoA R inhibitors, methotrexate, high dose dietary supplements, fish oil capsules or plant sterol or stanol), or have any dietary restrictions which would prevent them from consuming the trial treatments

• BMI >40

• Must not have self-reported weight gain or loss greater than 3 kg in the past three months

• Phytosterolemic

• History of active cardiovascular disease including stroke, congestive heart failure, myocardial infarction, unstable angina pectoris, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, temporal ischemic attacks, anemia, abnormal electrolytes, proteinuria, and abnormal liver, kidney or thyroid function

• Type 1 or type 2 diabetes, a history of cancer or malignancy in the last 5 years, or any metabolic disease, gastrointestinal disorder or other clinically significant disease/disorder which could interfere with the results of the study or the safety of the participant.

• Uncontrolled hypertension having systolic blood pressure >160mm Hg or diastolic blood pressure >100mm Hg

• Smoker, tobacco/snuff/nicotine users, recreational drug users

• Consume more than 14 alcoholic beverages a week

• Participants who are pregnant or plan to become pregnant during the trial period or lactating mothers

• Participants will be excluded if they have clinically significant biochemistry defined as: LDL-C <3.0mmol/L or >4.9 mmol/L; TC > 6.2 mmol/L; fasting glucose: > 6.1 mmol/ l, fasting TG >4.52 mmol/L; AST >100 U/L; ALT >100 U/L or or any other clinically significant abnormality in hematology and/or biochemistry at the investigator's discretion

• Patients with unstable or serious illness, for example, dementia, terminal illness, recent bereavement, recent significant medical diagnosis will also be excluded

Related Conditions & MeSH terms

• Cardiovascular Disease
• Cardiovascular Diseases
• Hypercholesterolemia

Intervention

Other:
• Plant sterols
2.0g/day of plant sterols incorporated into margarine to be consumed for 28 days
• Placebo
Identical margarine without additional plant sterols to be consumed for 28 days

Locations

Country	Name	City	State
Canada	Department of Human Nutritional sciences, University of Manitoba	Winnipeg	Manitoba

Sponsors (4)

Lead Sponsor	Collaborator
University of Manitoba	Mitacs, Nutritional Fundamentals for Health, Unilever R&D

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in fasting low-density lipoprotein cholesterol (LDL-C) levels between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in fasting total cholesterol (TC) levels between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in fasting high-density lipoprotein cholesterol levels between placebo and treatment endpoints		Endpoint (Days 28,29) of each treatment period
Secondary	Change in fasting triglyceride (TG) levels between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in body weight between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in body mass index (BMI) between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in waist circumference between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in blood pressure between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in arterial stiffness-Pulse wave velocity between placebo and treatment endpoints (in a crossover design)	Pulse wave velocity will be determined using an automated oscillometric measurement device (Mobil-O-Graph, IEM, Stolberg, Germany).	Endpoint (Days 28,29) of each treatment period
Secondary	Change in arterial stiffness-augmentation index between placebo and treatment endpoints (in a crossover design)	Augmentation index will be determined using an automated oscillometric measurement device (Mobil-O-Graph, IEM, Stolberg, Germany).	Endpoint (Days 28,29) of each treatment period
Secondary	Change in fasting glucose levels between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in blood sterols and sterol precursors (non-cholesterol sterols) levels between placebo and treatment endpoints (in a crossover design)		Endpoint (Days 28,29) of each treatment period
Secondary	Change in fractional cholesterol synthesis between placebo and treatment endpoints (in a crossover design)	A fasted blood sample will be taken on day 28 of each study period prior to deuterium oxide administration, as well as fasting samples on day 29. The change in deuterium enrichment within red blood cell (RBC) free cholesterol we be determined as an index of synthesis over days 28 and 29.	Endpoint (Day 28,29) of each treatment period