CClinicalTrials.gg
Status unknownNCT01771042Updated Jan 18, 2013

The Effects of Weight Loss on Neuroadrenergic Function

An interventional study of Dietary weight loss at 25% energy deficit in Obesity, Type 2 Diabetes and Metabolic Syndrome, sponsored by Baker Heart Research Institute. Status unknown at 1 site in Australia. Open to participants aged 45 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-01-18.

Sponsored by Baker Heart Research Institute · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2013), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Non-randomized
Ages
45 Years to 65 Years
Sex
All
01

Study summary

Elevated subconscious nervous system activity is a characteristic of the obese state and contributes importantly to the risk of heart disease and diabetes. This project will compare sympathetic nervous system activity and function in a group of obese persons with differing levels of sugar tolerance (normal, impaired and type 2 diabetic). Inter-relationships with insulin action, blood pressure, heart and kidney function will be determined before and after a 4-month weight loss and 3-month weight loss maintenance program.

It is hypothesized that the transition from normal sugar tolerance to impaired sugar tolerance to type 2 diabetes will be accompanied by escalating sympathetic nervous system dysfunction. Furthermore, that weight loss will favorably improve sympathetic function, with greatest benefits occurring in those subjects who are insulin resistant with high blood insulin concentration.

Read the detailed description

The twin epidemics of obesity and diabetes represent a major public health problem worldwide. There is a growing body of evidence to suggest that autonomic dysfunction, comprising elevated sympathetic nervous system (SNS) activity and blunted sympathetic neural responsiveness plays a role in both the pathogenesis and target organ complications of obesity and diabetes. The proposed project will undertake a detailed comparative analysis of neuroadrenergic function along the diabetes continuum, its inter-relationship with insulin sensitivity and secretion, and target organ function, and the benefits of active weight loss and weight loss maintenance within different strata of metabolic risk.

02

Conditions studied

  • Obesity
  • Type 2 Diabetes
  • Metabolic Syndrome

Keywords

  • weight loss
  • metabolic syndrome
  • sympathetic nervous system
  • insulin resistance
  • glucose tolerance
03

In context

Metabolic Syndrome

1,964 studies on the registry are indexed under Metabolic Syndrome; 330 are open to participants now.

This study's planned enrollment of 120 is above the median of 60 across 1,460 interventional studies indexed under Metabolic Syndrome.

Browse Metabolic Syndrome studies →

Lead sponsor

Baker Heart Research Institute is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Men and postmenopausal women (n=120), untreated, weight-stable, non-smoking, aged 45-65 years, BMI 27-45 kg/m2, will be recruited. Glucose tolerance status will be determined by a 75-g oral glucose tolerance test (OGTT), using WHO criteria (53): normal glucose tolerance, fasting plasma glucose \< 7.0 mmol/L and 2-h plasma glucose \< 7.8 mmol/L; IGT, fasting plasma glucose \< 7.0 mmol/L and 2-h plasma glucose > 7.8 and \< 11.1 mmol/L; T2D, fasting plasma glucose > 7.0 mmol/L or 2-h plasma glucose > 11.1 mmol/L. Hyper-insulinemia will be defined as an insulin area under the curve during OGTT > 8000 mU/L ∙ min-1 and hypo-insulinemia as \< 8000 mU/L ∙ min-1.

Exclusion criteria

Exclusion Criteria:

Prior history of cardiovascular disease (previous myocardial infarction, angina, stroke, heart failure, secondary hypertension), renal (serum creatinine >0.12 mmol/L or estimated GFR \<60 ml/min/1.73 m2) or hepatic disease or diseases which may affect measured parameters (e.g. thyroid disease); severe hypertension; a history of surgical weight loss; CPAP therapy; and >4 alcoholic drinks/day. T2D individuals with moderate hyperglycemia (HbA1c >9%) will be excluded so that hypoglycaemic pharmacotherapy may be instituted (54). Participants will be sought through newspaper advertising and poster displays in primary health care centres (General Practices). Newly diagnosed T2D subjects

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Normal glucose tolerant

    Weight loss attained by 25% caloric restriction. This arm will be both a glycemic and time control. Initially they will undergo a 4-month weight maintenance phase (acting as time control), followed by 4 month weight loss.

    Other: Dietary weight loss at 25% energy deficit

  • Experimental
    Impaired glucose tolerant

    Weight loss using 25% caloric restriction. Impaired glucose tolerant subjects will undergo 4 months weight loss (25% caloric deficit) followed by 3 months weight loss maintenance

    Other: Dietary weight loss at 25% energy deficit

  • Experimental
    Type 2 diabetic hyperinsulinemic

    Weight loss using 25% caloric restriction. This group will undergo 4 months weight loss (25% caloric deficit) followed by 3 months weight loss maintenance

    Other: Dietary weight loss at 25% energy deficit

  • Experimental
    Type 2 diabetic hypoinsulinemic

    Weight loss via 25% caloric restriction. This group will undergo 4 months weight loss (25% caloric deficit) followed by 3 months weight loss maintenance

    Other: Dietary weight loss at 25% energy deficit

Interventions

  • OtherDietary weight loss at 25% energy deficit

    Dietary weight loss at 25% energy deficit. Dietary macronutrient content will comprise 25% protein, 30% fat and 45% carbohydrate.

06

What researchers measure

Primary outcomes

  1. Change in whole-body norepinephrine kinetics

    The study will examine the dynamic processes of norepinephrine spillover into and removal from the central plasma compartment using the isotope dilution technique.Measurements will be made at baseline, after 4 months active weight loss, and again after 3 months weight loss maintenance. The weight loss maintenance phase will permit differentiation of the effects of active weight loss (incorporating both negative energy balance and weight loss per se) and stable lower body weight on sympathetic neural parameters.

    Time frame: 4 months and 7 months

Secondary outcomes

  1. Change in muscle sympathetic nerve activity

    Muscle sympathetic nerve firing will be quantified by the technique of mirconeurography at baseline and after 4 months active weight loss and 3 months weight loss maintenance. The weight loss maintenance phase will permit differentiation of the effects of active weight loss (incorporating both negative energy balance and weight loss per se) and stable lower body weight on sympathetic nerve firing and pattern.

    Time frame: 4 months and 7 months

Other outcomes

  1. Change in insulin sensitivity

    Insulin sensitivity will be assessed by the gold standard euglycemic hyperinsulinemic clamp method at baseline and after 4 months active weight loss and 3 months weight loss maintenance. The weight loss maintenance phase will permit differentiation of the effects of active weight loss (incorporating both negative energy balance and weight loss per se) and stable lower body weight on insulin sensitivity.

    Time frame: 4 months and 7 months

07

Study locations

1 site
  • Baker IDI Heart & Diabetes Institute
    Melbourne, Victoria 8008, Australia
08

References and documents

Publications

  • Straznicky NE, Grima MT, Sari CI, Lambert EA, Phillips SE, Eikelis N, Kobayashi D, Hering D, Mariani JA, Dixon JB, Nestel PJ, Karapanagiotidis S, Schlaich MP, Lambert GW. Reduction in peripheral vascular resistance predicts improvement in insulin clearance following weight loss. Cardiovasc Diabetol. 2015 Aug 22;14:113. doi: 10.1186/s12933-015-0276-2. PubMed 26297500 ↗
  • Straznicky NE, Grima MT, Lambert EA, Sari CI, Eikelis N, Nestel PJ, Phillips SE, Hering D, Karapanagiotidis S, Dixon JB, Schlaich MP, Lambert GW. Arterial norepinephrine concentration is inversely and independently associated with insulin clearance in obese individuals with metabolic syndrome. J Clin Endocrinol Metab. 2015 Apr;100(4):1544-50. doi: 10.1210/jc.2014-3796. Epub 2015 Jan 15. PubMed 25590214 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 18, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01771042
Lead sponsor
Baker Heart Research Institute
Responsible party
Nora E. Straznicky (Group Leader/Senior Research Officer, Baker Heart Research Institute) — Principal investigator
First posted
Jan 18, 2013
Start date
Apr 2013
Primary completion
Apr 2017 (estimated)
Completion
Apr 2017 (estimated)
Last update
Jan 18, 2013

Study contacts

Dr Nora E Straznicky, PhD MPH
Contact
nora.straznicky@bakeridi.edu.au
61 3 8532 1371
Ms Mariee T Grima, BNutr MDiet
Contact
mariee.grima@bakeridi.edu.au
61 3 8532 1523
Dr Nora E Straznicky, PhD MPH
principal investigator · Baker IDI Heart & Diabetes Institute

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.

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