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The Effect of Antecedent Hypoglycaemia on β2-Adrenergic Sensitivity - Article


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Hypoglycemia

Low Blood Sugar


Clinical Trial: The Effect of Antecedent Hypoglycaemia on β2-Adrenergic Sensitivity

This study is currently recruiting patients.
Verified by Radboud University September 2005

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

Study Type: Interventional
Study Design: 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: 

Expected Total Enrollment:  20

Study start: April 2005

Eligibility

Ages Eligible for Study:  18 Years   -   40 Years,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

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

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00160056

Bas JJW Schouwenberg, MD      +312417449    b.schouwenberg@aig.umcn.nl
Bastiaan E de Galan, PhD MD       b.degalan@aig.umcn.nl

Netherlands, Gelderland
      Radboud University Nijmegen Medical Centre, Nijmegen,  Gelderland,  6500HB,  Netherlands; Recruiting
Bas Schouwenberg, MD  +312417449    b.schouwenberg@aig.umcn.nl 
Bas Schouwenberg, MD,  Principal Investigator

Study chairs or principal investigators

Paul Smits, PhD, MD,  Principal Investigator,  Radboud University   

More Information

Study ID Numbers:  HB2-001
Last Updated:  September 11, 2005
Record first received:  September 9, 2005
ClinicalTrials.gov Identifier:  NCT00160056
Health Authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
ClinicalTrials.gov processed this record on 2005-09-13


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Page Updated: December 9, 2005
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