Exploring the Health Benefits Associated With Daily Pulse Consumption in Individuals With Peripheral Arterial Disease

NCT ID: NCT00755677

Last Updated: 2012-03-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-03-31
• Study Completion Date: 2008-07-31

Brief Summary

This is a single site, open registration, dietary proof of concept, food substance study designed to explore the health benefits associated with daily pulse consumption in individuals with peripheral arterial disease. The investigators hypothesis that a diet containing at least one serving of pulse crops (dried beans, peas, lentil, chickpeas) per day provides flavonoid compounds that improve cardiovascular health by increasing the levels of serum adiponectin is based on evidence from the literature that indicates flavonoids present in these foods are capable of improving arterial stiffness and reducing hypercholesterolemia.

Detailed Description

Objectives:

• Correlate serum adiponectin levels with daily intake of pulses in individuals with peripheral arterial disease
• Monitor changes in arterial stiffness and endothelial dysfunction in individuals with early stage cardiovascular disease
• Determine the tolerability of daily consumption of pulses in the targeted population
• Identify changes in the expression profile of white blood cells.

Study Duration: 12 months

Study Design:

• This is a single site, open registration, dietary proof of concept, food substance study designed to explore the health benefits associated with daily pulse consumption in individuals with arterial disease
• Each subject will undergo a 7-day adaptation period consisting of a consumption of ¼ cup of pulses per serving daily, followed by a minimum of ½ cup of pulses per serving daily
• Total duration of subject participation is 8 weeks;
• Subjects will be asked to attend 3 in-person clinic visits over the duration of their participation in the study for screening, registration/baseline and end of study assessments
• Telephone follow-up to subjects will occur at weeks 1,2,4, and 6
• Both clinical assessment and subject-based data will be collected at various points of the study schedule
• Subjects will be asked to complete a food frequency questionnaire at the outset, maintain a 3-day food record at two separate occasions, and undergo a brief semi-structured interview during the telephone follow-up assessments of the study

Assessments:

1. Screening Visit: Informed consent; inclusion/exclusion criteria assessment; medical history; physical exam; food frequency questionnaire; 3-day food record

2. Registration/Baseline: Registration; assess for changes to medical history (including medication profile) and physical condition; urine sample; fasting blood sample; assessment of arterial stiffness and ankle-brachial index; begin adaptation period (7 days)with food items containing ¼ c of pulses per serving

3. Visits 1,2,4 & 6: Telephone follow-up to assess adverse events and tolerability with semi-structured subject interview; distribution (weekly) of food items containing a minimum of ½ cup pulses per serving; 3-day food record repeated at week 6

4. Visit 8 (final): Assess for adverse events and changes to medical history and physical exam; urine sample; fasting blood sample collection; assessment of arterial stiffness and and ankle-brachial index

Outcomes:

• Descriptive analysis of clinical data: Demographics, medical history, physical findings, concomitant medications and adverse events
• Identification of changes in endothelial function (determined by measuring pulse wave velocity (PWV), ankle-brachial index, soluble adhesion molecule levels and coagulation status) in response to dietary modification
• Correlation of serum adiponectin levels, including adiponectin multimers and truncated form (globular adiponectin) with endothelial function
• Correlation of changes in endothelial cell function with serum isoflavone levels
• Qualitative analysis of data collected from semi-structured subject interviews to assess parameters associated with tolerability of diet and to identify favoured recipes
• Profile cohort using 55,000 gene microarray to identify potential biomarkers and changes in gene expression (phenotype mapping) induced by diet
• Use microarrays to examine gene methylation and single nucleotide polymorphisms (SNP) in DNA samples to determine if changes in expression profile are due to epigenetic modification (global) or allelic (individual) variation in the study cohort in response to a pulse-enriched diet
• Serum and urinary eicosanoids will be analyzed by a multi-step procedure utilizing liquid chromatography, derivitization steps, thin-layer chromatography and gas chromatography-mass spectrometry
• Serum will also be analyzed for fatty acid composition using thin-layer chromatography and gas chromatography

Conditions

Peripheral Arterial Disease

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

pulses

Interventional. Participants are registered sequentially to undergo daily consumption of pulses for eight weeks

Group Type: OTHER

Pulses

Intervention Type: OTHER

subjects consume 1 pulse food daily for eight weeks

Interventions

Pulses

subjects consume 1 pulse food daily for eight weeks

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Presence of peripheral arterial disease including those with claudication as defined by an ankle brachial index of ≤ 0.90 and asymptomatic carotid stenosis lesion of > 50%
• Male or female (> 40 years of age)
• Willing to comply with the protocol requirements
• Willing to provide informed consent
• Stable medication profile with no changes anticipated for the duration of the proposed study schedule (8 weeks)

Exclusion Criteria

• Renal failure requiring dialysis
• Currently smoking
• Hormone replacement therapy
• Inability to adhere to a regular diet
• Additional intake of pulses outside the planned daily requirements outlined in the study
• History of gastrointestinal reactions or allergies to pulses

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 82 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Manitoba

OTHER

Sponsor Role: collaborator

St. Boniface Hospital

OTHER

Sponsor Role: lead

Responsible Party

Dr.Peter Zahradka

Professor, Department of Physiology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Peter Zahradka, PhD

Role: PRINCIPAL_INVESTIGATOR

St. Boniface Hospital

Locations

St. Boniface General Hospital

Winnipeg, Manitoba, Canada

Countries

Canada

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Other Identifiers

Pulse Study

Identifier Type: -

Identifier Source: org_study_id