Evaluation of Fructose Ingestion and the Renin Angiotensin System in Humans

NCT ID: NCT01407627

Last Updated: 2022-05-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 64 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-07-31
• Study Completion Date: 2021-05-31

Brief Summary

Fructose is an ingredient that is added to many of our foods. It is a cheaper, sweeter additive that can be found in everything from soda pop to yogurt to granola bars. In the last few years a significant number of studies have been published linking consumption of fructose with obesity, hypertension and more recently, kidney and cardiovascular disease.

Animal studies show a strong link between excessive ingestion of fructose and the development of kidney and cardiovascular disease mediated by the renin angiotensin system, a hormonal system whose activation is detrimental to both the kidney and the heart. There has been very little research done on the potentially pathophysiological relationship between a high fructose diet and kidney and cardiovascular disease in humans.

The investigators hypothesize that ingestion of fructose will result in upregulation of the renin angiotensin system in humans.

Cardiovascular disease in women is a significant risk factor. By having women participate who are on the birth control pill and as well as women who use non oral forms of birth control or no birth control, kidney function and cardiovascular health can be examined as it relates to in the influence oral hormones might play. How the kidney responds to the influence of sugar and fructose while a woman is on an oral birth control pill, may reveal mechanisms that could help us understand cardiovascular disease in women.

Detailed Description

PRIMARY AIM: To examine whether the physiologic and molecular responses to Angiotensin II (AngII) challenge differ in response to fructose intake as assessed by two independent means:

1. The renal and mean arterial pressure (MAP) response to an AngII challenge.

2. Reactive changes in circulating levels of renin and aldosterone with graded AngII challenge.

PRIMARY HYPOTHESES: Ingestion of fructose in healthy subjects will result in:

1. A decrease in renal and systemic sensitivity to infused AngII.

2. A decrease in the reactive changes in renin and aldosterone with graded AngII challenge.

Conditions

Chronic Kidney Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: TRIPLE

Study Groups

Fructose First

1. Study Day 1 - measurement of renal hemodynamics and blood pressure

2. Subjects will ingest fructose 200g daily x 14d

3. Study Day 2 - measurement of renal hemodynamics

4. Minimum 1 week "washout" period

5. Subjects will ingest dextrose 200g daily x 14d

6. Study Day 3 - measurement of renal hemodynamics and blood pressure

Group Type: EXPERIMENTAL

Fructose

Intervention Type: DIETARY_SUPPLEMENT

Subjects will be randomized to one of 2 sequences:

Sequence 1: Fructose (intervention) 200g daily x 14d followed by Dextrose (control) 200g daily x 14d Sequence 2: Dextrose (control) 200g daily x 14d followed by Fructose (intervention) 200g daily x 14d

Dextrose First

1. Study Day 1 - measurement of renal hemodynamics and blood pressure

2. Subjects will ingest dextrose 200g daily x 14d

3. Study Day 2 - measurement of renal hemodynamics

4. Minimum 1 week "washout" period

5. Subjects will ingest fructose 200g daily x 14d

6. Study Day 3 - measurement of renal hemodynamics and blood pressure

Group Type: ACTIVE_COMPARATOR

Fructose

Intervention Type: DIETARY_SUPPLEMENT

Subjects will be randomized to one of 2 sequences:

Sequence 1: Fructose (intervention) 200g daily x 14d followed by Dextrose (control) 200g daily x 14d Sequence 2: Dextrose (control) 200g daily x 14d followed by Fructose (intervention) 200g daily x 14d

Interventions

Fructose

Subjects will be randomized to one of 2 sequences:

Sequence 1: Fructose (intervention) 200g daily x 14d followed by Dextrose (control) 200g daily x 14d Sequence 2: Dextrose (control) 200g daily x 14d followed by Fructose (intervention) 200g daily x 14d

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• age≥18 years,
• able to comprehend study and comply with high-salt diet
• kidney disease (on the approval of their nephrologist)
• on an oral birth control pill and non oral birth control and those not on birth control

Exclusion Criteria

• cardiovascular disease (symptoms consistent with myocardial ischemia, previously documented myocardial ischemia, cardiac arrhythmias or valve abnormalities, or abnormal ECG at screening)
• cerebrovascular disease (transient ischemic attacks or stroke)
• hypertension (BP>140/90 or use of antihypertensive medications)
• diabetes mellitus (defined by history, use of hypoglycemic agents or a fasting glucose >7mmol/L)
• hyperlipidemia (LDL >4.5mmol/L or use of lipid-lowering agents)
• pregnancy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Calgary

OTHER

Sponsor Role: lead

Responsible Party

Sofia Ahmed

Dr. Sofia Ahmed

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sofia B Ahmed, MD MMSc

Role: PRINCIPAL_INVESTIGATOR

University of Calgary

Locations

University of Calgary

Calgary, Alberta, Canada

Countries

Canada

Other Identifiers

AIHS

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

University of Calgary

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

UCalgary Sugar Study

Identifier Type: -

Identifier Source: org_study_id