The Potential of Carnosine Supplementation in Reducing the Cardiometabolic Risk

NCT ID: NCT02686996

Last Updated: 2018-03-22

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 84 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-02-13
• Study Completion Date: 2020-06-12

Brief Summary

The aim of this study is to determine whether carnosine supplementation in overweight/obese individuals can improve insulin secretion and/or insulin resistance by decreasing sub clinical inflammation.

The investigators hypothesise that carnosine supplementation will reduce type 2 diabetes and cardiovascular risk factors by lowering chronic low-grade inflammation (CLI), oxidative stress, advanced glycation end products (AGEs), and advanced lipoxidation end products (ALEs).

Aim :To determine the capacity of carnosine supplementation to decrease major risk factors for type 2 diabetes and cardiovascular disease and identify metabolic pathways involved, specifically by:

1. Reducing diabetes risk (insulin sensitivity; secretory function and glucose tolerance)

2. Improving cardiovascular risk factors (lipids; arterial (aortic) stiffness; central blood pressure (cBP); endothelial function).

3. Decreasing the CLI, oxidative stress, AGEs, and ALEs, and increase detoxification of reactive carbonyl species (RCSs).

Detailed Description

Cardiovascular risk factors including type 2 diabetes underpin a major threat to the globe and result in a heavy health and financial burden across the healthcare system. Treating type 2 diabetes and cardiovascular disease is expensive and often unsatisfactory. Current medications bring unwanted side effects, and often merely delay rather than prevent type 2 diabetes complications and cardiovascular disease. As a further concern, the micro- and macrovascular complications of type 2 diabetes often start developing before actual diagnosis. Diabetes prevention and treatment through weight loss and exercise programs is a difficult and costly public health measure, leaving the tidal wave of type 2 diabetes to swell even more. An alternative is urgently needed: a low-cost safe approach, easy to implement at population level.

Could carnosine be that alternative? The evidence suggests carnosine has significant metabolic impact and presents such an alternative. A naturally occurring dipeptide, carnosine is already emerging as a human therapy in exercise physiology, heart failure, cataract prevention and treatment, neurology, and psychiatry. A promising further use may derive from its effect on cardiovascular risk factors. Metabolic research, though confined to animal studies, strongly suggests that carnosine supplementation aids the prevention and treatment of obesity, type 2 diabetes, and cardiovascular disease - by virtue of its anti-inflammatory, antioxidative, and anti-glycating effects. The investigators conducted the first pilot data in human and demonstrate relationships among carnosine, obesity, insulin resistance, and dyslipidemia. Put briefly, the pilot weighs strongly in favour of carnosine as a means of reducing cardiovascular risk in humans.

Too good to be true? Apart from its excellent side-effect profile, carnosine is inexpensive and seemingly safe (available as an over-the-counter food additive), making it prima facie ideal for population use. In this setting research is now urgently needed - to test the significant metabolic potential of carnosine to address a major health problem.

The investigators propose a comprehensive double-blind placebo-controlled human trial to investigate the effects of carnosine supplementation on cardiovascular risk factors. If the investigators demonstrate a role in reducing risk factors for type 2 diabetes and cardiovascular disease in overweight and obese non-diabetic humans, the public health implications will be revolutionary, offering the world a genuine low cost, accessible, intervention to curtail the advance of obesity, type 2 diabetes, and cardiovascular disease.

Conditions

Insulin Sensitivity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: QUADRUPLE

Study Groups

Intervention

Each participant will be given a daily oral dose 2 g of carnosine (2 tablets twice daily) for 14 weeks

Group Type: ACTIVE_COMPARATOR

carnosine

Intervention Type: DIETARY_SUPPLEMENT

Carnosine capsules (2g) twice per day for 14 weeks

Control

Each participant will be given a daily oral dose 2 g of identical placebo tablets ( 2 tablets twice daily) for 14 weeks

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo (methylcellulose) capsules for control group identical to intervention capsules and dose

Interventions

carnosine

Carnosine capsules (2g) twice per day for 14 weeks

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Placebo (methylcellulose) capsules for control group identical to intervention capsules and dose

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Age >18 or <60 years,
• Weight change < 5 kg in last 12 months
• BMI >25kg/m2 but weight <159kg due to DEXA scan restrictions
• Non-diabetic, no allergy, non-smoker, no high alcohol use
• No current intake of medications including vitamin supplements
• No kidney, cardiovascular, haematological, respiratory, gastrointestinal, endocrine or central nervous system disease, as well as no psychiatric disorders, no active cancer within the last five years; no presence of acute inflammation (by history, physical or laboratory examination)
• Not pregnant or lactating

Exclusion Criteria

• Age <18 or > 60 years
• Weight change > 5 kg in last 12 months
• Diabetes (diagnosed or oral glucose tolerance test (OGTT), allergy
• Current smoking habit, high alcohol use
• Current intake of medications including vitamin supplements
• Kidney, cardiovascular, haematological, respiratory, gastrointestinal, endocrine or central nervous system disease, as well as psychiatric disorder, active cancer within the last five years; presence of acute inflammation (by history, physical or laboratory examination)
• pregnancy or lactation

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Monash University

OTHER

Sponsor Role: lead

Responsible Party

Barbora de Courten

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Barbora de courten, MD,PHD,MPH

Role: PRINCIPAL_INVESTIGATOR

Monash University

Locations

Monash Centre for Health Research and Implementation

Melbourne, Victoria, Australia

Site Status: RECRUITING

Countries

Australia

Central Contacts

Barbora de Courten, MD,PHD,MPH

Role: CONTACT

barbora.decourten@monash.edu

+61 385722651

Facility Contacts

Barbora de Courten, MD,PHD,MPH

Role: primary

barbora.decourten@monash.edu

+61 3 9594 7086

References

Menon K, Cameron JD, de Courten M, de Courten B. Use of carnosine in the prevention of cardiometabolic risk factors in overweight and obese individuals: study protocol for a randomised, double-blind placebo-controlled trial. BMJ Open. 2021 May 13;11(5):e043680. doi: 10.1136/bmjopen-2020-043680.

Reference Type: DERIVED

PMID: 33986049 (View on PubMed)

Other Identifiers

16061A

Identifier Type: -

Identifier Source: org_study_id