Endothelial Dysfunction and Diabetes

Completed

• Conditions: Type 1 Diabetes Mellitus
• Interventions: Drug: Trinitrin; Drug: Neosynephrine 10% collyrium; Drug: Iontophoresis with acetylcholine delivery; Device: Dynamic Vessel Analyzer

• Registration Number: NCT01097551
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

The aim of the study is to progress in the understanding of the early retinal vascular and neural abnormalities in patients with diabetes, using a new device, the Dynamic Vessel Analyzer. The Dynamic Vessel Analyzer allows to measure the diameter of the retinal vessels and to assess how it varies in presence of various stimuli. Then, we will be able to assess if a vascular and/or a neural dysfunction is present early in patient with diabetes.

Detailed Description

Twenty patients with type 1 diabetes without diabetic retinopathy and without arterial hypertension will be compared with 20 sex and aged-matched healthy control subjects. To assess the presence of retinal endothelial dysfunction, the variations of the diameters of the retinal vessels will be assessed using the Dynamic Vessel Analyzer, before and after flicker light stimulation, sublingual nitroglycerin, neosynephrine eyedrops, and isometric contraction. To assess the presence of peripheral endothelial dysfunction, the microcirculation of the forearm skin will be studied using iontophoresis with acetylcholine delivery, and heat delivery, both coupled with blood flow measurement using laser Doppler. An intravital capillaroscopy of the phalanx skin will be performed. The serum levels of CRP, ICAM-1, VCAM-1, VEGF, angiopoietin 2 and endostatin will also be measured.

Study Timeline

• Study First Submitted: 2010-03-31
• Study First Submitted QC: 2010-03-31
• Study First Posted: 2010-04-01
• Study Start: 2011-01
• Primary Completion: 2011-07
• Study Completion: 2011-07
• Status Verified: 2012-07
• Last Update Submitted: 2012-07-02
• Last Update Posted: 2012-07-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 38

Inclusion Criteria

• For diabetic patients :

  • age between 20 and 60
  • type 1 diabetes mellitus
  • diabetes duration of more than 5 years
  • no diabetic retinopathy on fundus examination or fundus photographs
  • no systemic hypertension (defined as systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg)

• For control subjects :

  • sex and age matching with the diabetic patients
  • no diabetes, no familial or personal history of elevated blood sugar
  • Non-diabetic subjects, criteria defined by a fasting glucose <1.10 g / l and an HbA1c <6.5% (according to Lariboisière biochemistry laboratory HbA1c)
  • no systemic hypertension (defined as systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg)
  • Subject with a normal ophthalmologic examination

• For both diabetic patients and control subjects :

  • Subject that has signed informed consent
  • Subject affiliated to a social security
  • Subject available for a period of 4 months

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Exclusion Criteria

• For both diabetic patients and control subjects :

  • presence of cataract or history of cataract surgery
  • intraocular pressure of more than 21 mmHg
  • treatment with vasoactive drugs
  • tobacco consumption of more than 20 cigarettes a day
  • Contraindications to trinitrin administration: hypersensitivity to trinitrin, treatment by sildenafil, heart disease, severe arterial hypotension, bradycardia, intracranial hypertension
  • Clinical Raynaud syndrome
  • Pregnant or breast-feeding subject
  • Subject whose age is <18 and> 60 years on the day of inclusion
  • Subject with cardiac disease, severe hypotension (BP <80/50 mmHg), a resting heart rate below 50 beats / minute
  • Subject intracranial hypertension
  • Subject with a current consumption of drugs or drugs that may impact vasomotion (antiglaucoma eye drops, vasodilators, antihypertensive drugs). Vasoactive drug use will be prohibited within 24 hours preceding the study.
  • Subject has not signed an informed consent
  • Subject not affiliated to a social security
  • Subject not available for a period of 4 months

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Patients with type 1 diabetes	Trinitrin	Diabetes duration \>= 5 years, age \>= 18 and \<= 60 years old, patients with no visible diabetic retinopathy, and no arterial hypertension
Patients with type 1 diabetes	Neosynephrine 10% collyrium	Diabetes duration \>= 5 years, age \>= 18 and \<= 60 years old, patients with no visible diabetic retinopathy, and no arterial hypertension
Patients with type 1 diabetes	Iontophoresis with acetylcholine delivery	Diabetes duration \>= 5 years, age \>= 18 and \<= 60 years old, patients with no visible diabetic retinopathy, and no arterial hypertension
Patients with type 1 diabetes	Dynamic Vessel Analyzer	Diabetes duration \>= 5 years, age \>= 18 and \<= 60 years old, patients with no visible diabetic retinopathy, and no arterial hypertension
Healthy subjects	Trinitrin	Sex and age-matched control healthy subjects
Healthy subjects	Neosynephrine 10% collyrium	Sex and age-matched control healthy subjects
Healthy subjects	Dynamic Vessel Analyzer	Sex and age-matched control healthy subjects
Healthy subjects	Iontophoresis with acetylcholine delivery	Sex and age-matched control healthy subjects

Primary Outcome Measures

Name	Time	Method
Evaluation of the presence of a retinal endothelial dysfunction in patients with type 1 diabetes mellitus with Dynamic vessel analyser(assessment study visit)	up to 4 months

Secondary Outcome Measures

Name	Time	Method
Presence of a peripheral endothelial dysfunction	up to 4 months
Correlation between retinal and peripheral endothelial dysfunction (assessment study visit)	up to 4 months
Serum concentration of: CRP, ICAM-1, VCAM-1, VEGF, angiopoietin 2 and endostatin.	up to 4 months

Trial Locations

Locations (1)

Hôpital LARIBOISIERE Service d'Ophtalmologie; 🇫🇷 Paris, France