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The Effect of Antecedent Hypoglycaemia on β2-Adrenergic Sensitivity
This study is ongoing, but not recruiting participants.
Sponsored by: Radboud University
Information provided by: Radboud University
ClinicalTrials.gov Identifier: NCT00160056
  Purpose

Hypoglycaemia unawareness is a common complication in patients with type 1 diabetes and with insulin-treated type 2 diabetes of long duration. The loss of autonomic symptoms to hypoglycemia does not solely depend on loss of adrenaline responses.Differences in sensitivity to catecholamines may also be involved.

Reconciling the data on β2-adrenergic receptor polymorphism to those on loss of β-adrenergic sensitivity in diabetic patients with hypoglycemia unawareness, we hypothesize that hypoglycemia unawareness is at least partly the result of desensitization of the β2-adrenergic receptor and that patients who are homozygous for arginine at codon 16 are particularly susceptible for this desensitization process, whereas patients who are homozygous for glycine at codon 16 are resistant for desensitization.

Objectives

  1. To determine whether, and if so to what extent, antecedent hypoglycemia reduces β2-adrenergic sensitivity in healthy subjects with Arg16 homozygosity.
  2. To investigate whether or not healthy subjects with Gly16 homozygosity are resistant to desensitization
  3. To confirm that antecedent hypoglycemia reduces the heart rate response to isoproterenol and to assess to what extent this reduced response is mediated by impairments in baroreflex sensitivity.

Condition Intervention
Diabetes
Hypoglycemia Unawareness
Procedure: Hypoglycemia

MedlinePlus related topics: Diabetes Hypoglycemia
Drug Information available for: Albuterol sulfate Albuterol Levalbuterol hydrochloride Levalbuterol tartrate Epinephrine Epinephrine bitartrate
U.S. FDA Resources
Study Type: Interventional
Study Design: Diagnostic, Randomized, Single Blind, Placebo Control, Crossover Assignment
Official Title: The Effect of Antecedent Hypoglycaemia on β2-Adrenergic Sensitivity in Subjects With Homozygous Arg16 and gly16 Polymorphism of the β2-Adrenergic Receptor

Further study details as provided by Radboud University:

Estimated Enrollment: 20
Study Start Date: April 2005
Estimated Study Completion Date: February 2007
  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Informed consent
  • Homozygous for Arginine at codon 16 or homozygous Gly at codon 16
  • No regular usage of medication other than oral contraceptives

Exclusion Criteria:

  • History of cerebrovascular, cardiovascular, or peripheral vascular disease
  • Smoking
  • Alcohol usage of more than 10 units per week
  • Inability to abstain from xanthine-derivatives (coffee, tea, cola, chocolate, cacao) or alcohol for 2 days
  • BMI above 30 kg/m2
  • Participation to any other trial in the preceding 3 months
  • Ongoing disease of any kind
  • Pregnancy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00160056

Locations
Netherlands, Gelderland
Radboud University Nijmegen Medical Centre
Nijmegen, Gelderland, Netherlands, 6500HB
Sponsors and Collaborators
Radboud University
Investigators
Principal Investigator: Paul Smits, PhD, MD Radboud University
  More Information

Study ID Numbers: HB2-001
Study First Received: September 9, 2005
Last Updated: February 28, 2007
ClinicalTrials.gov Identifier: NCT00160056  
Health Authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by Radboud University:
Hypoglycemia unawareness
Diabetes
adrenal receptor
adrenerg respons
adrenergic beta-agonists
salbutamol

Study placed in the following topic categories:
Metabolic Diseases
Albuterol
Diabetes Mellitus
Epinephrine
Metabolic disorder
Glucose Metabolism Disorders
Hypoglycemia

ClinicalTrials.gov processed this record on January 16, 2009