Validation of a Non Invasive Blood Marker of SIDS and Vagal Disorders
NCT01358461 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 240
Last updated 2017-09-08
Summary
Context
The investigators recently demonstrated a highly significant increase in muscarinic receptor density in the myocardium of infants deceased from sudden infant death syndrome (SIDS) compared to those of infants deceased from identified causes 1. Muscarinic receptor overexpression was found in all SIDS samples studied to date. It was associated with an average increase in acetylcholinesterase activity, appearing as a compensatory mechanism to oppose the cardiac muscarinic receptor overexpression. Similar vago-cardiac abnormalities were detected in a rabbit model of vagal hyperreactivity that the investigators first described some years ago2. In these hyperreactive animals, expression of muscarinic receptors was also enhanced in blood white cells. Noticeably, the pattern of changes in these cells paralleled the pattern of changes in the heart. Thus, muscarinic abnormalities in cardiac tissues could be inferred with high confidence from those measured in lymphocytes.This was the first report of a vago-cardiac abnormality in sudden infant death syndrome. The investigators findings also provided original and important perspectives for the identification and therapeutic management of infants at risk of sudden death. As such, the publication of the investigators work raised a major interest from the population and from the scientific and medical communities, in particular cardio-pediatricians. ObjectivesThe objective of the present clinical project is to validate, in human lymphocytes, muscarinic receptor expression level (assessed by quantitative RT-PCR) as a circulating biomarker of autonomic nervous system dysfunction and more specifically, of vagal hyperactivity and of risk of sudden death. The project will include 2 major items, conducted in parallel:1. evaluation of the muscarinic receptor expression in lymphocytes from adults with vagal syncopes (n=60 patients from an existing file versus 60 controls) (Cardiology unit + Clinical Investigation Centre (CIC) + Laboratory of Neurobiology and Cardiovascular Pharmacology); 2. evaluation of the muscarinic receptor expression in lymphocytes from children with vagal syncopes (n=60 versus 60 controls) (Pediatry unit + Clinical Investigation Centre + Laboratory of Neurobiology and Cardiovascular Pharmacology).PerspectivesThis project represents the first step of validation of a circulating marker of vagal hyperactivity and of risk of SIDS in human. Once this step is completed, the investigators will start with the prospective study " muscarinic receptor expression in lymphocytes and SIDS " (cord blood collected at birth and follow up of the new-borns) (Maternity ward + CIC + Laboratory of Neurobiology and Cardiovascular Pharmacology). Then therapeutic preventive management becomes a realistic objective. A therapeutic clinical study will then be started with atropinic drugs, in order to test their potential protective action against sudden death. The final objective of the investigators research is the prevention of SIDS through i) identification - as soon as birth - of new-borns at high risk and ii) appropriate prophylactic therapy. The investigators work also opens exciting perspectives in the field of the still poorly understood vagal disorders in children and adults such as vagal pauses.1 Livolsi et coll, Plos One 5, e9464, 2010 ; 2 Livolsi et coll, Circulation 106, 2301-2304, 2002
Conditions
- Vagal Syncope
Interventions
- BIOLOGICAL
-
Blood sampling
Blood sampling
- OTHER
-
ECG-Holter 24 h tape and sino-carotid stimulation test
ECG-Holter 24 h tape and sino-carotid stimulation test
Sponsors & Collaborators
-
University Hospital, Strasbourg, France
lead OTHER
Principal Investigators
-
Angelo LIVOLSI · Hôpitaux Universitaires de Strasbourg
Eligibility
- Min Age
- 1 Month
- Max Age
- 51 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-03-31
- Primary Completion
- 2015-05-31
- Completion
- 2015-05-31
Countries
- France
Study Locations
More Related Trials
-
The Effect of CPC on Aborting Tilt Induced Syncope in Patients With a History of Vasovagal Syncope or Near Syncope
NCT04972123 ·Status: COMPLETED ·Phase: PHASE2
-
Observational Prospective Study Measuring the Impact of the Use of a Hypnotic Script Associated With Virtual Reality on the Pain of the Child's Sickle Cell During a Vaso-occlusive Crisis
NCT04917120 ·Status: COMPLETED ·Phase: NA
-
Mechanism-based Therapy of Hypotensive Syncope
NCT06513650 ·Status: RECRUITING
-
Effect of Dietary Salt Supplemantation in Vasovagal Syncope Prophylaxis: A Clinical Trial
NCT00465946 ·Status: UNKNOWN ·Phase: NA
-
Cord Blood for Neonatal Hypoxic-ischemic Encephalopathy
NCT00593242 ·Status: COMPLETED ·Phase: PHASE1
-
The Benefit of Prophylactic Anticonvulsant in Post Cardiac Arrest Syndrome With Induced Mild Hypothermia
NCT01083784 ·Status: UNKNOWN ·Phase: PHASE4
-
Creation of a Syncope Channel for Patients Admitted to the Emergency Department for Loss of Consciousness and Not Hospitalized: Etiological Predictivity (Before/After Study)
NCT06503653 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Safety of Intravenous Milrinone for the Treatment of Subarachnoid Hemorrhage-induced Vasospasm
NCT03517670 ·Status: COMPLETED
-
Continuous Neurophysiological Monitoring Detection of Cerebral Vasospasm in Aneurysmal Subarachnoid Hemorrhage Subjects
NCT01343537 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
Permanent Cerebral Oxymetry Monitoring for Early Diagnosis and Treatment of Delayed Vasospasm After Subarachnoid Hemorrhage
NCT04042571 ·Status: COMPLETED ·Phase: NA
-
Impact of Intranasal Insulin on Sympathetic Activity and Cerebral Vasodilation
NCT05153395 ·Status: SUSPENDED ·Phase: EARLY_PHASE1
-
Stop Vasodepressor Drugs in Reflex Syncope
NCT02137278 ·Status: COMPLETED ·Phase: PHASE3
-
Whole Body Cooling Using Phase Changing Material
NCT01138176 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Prevention of Low Blood Pressure in Persons With Tetraplegia
NCT00237770 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
SW-RCT Implementation of Canadian Syncope Risk Score Based Practice Recommendations
NCT04972071 ·Status: RECRUITING ·Phase: NA
-
Northera Improves Postural Tachycardia Syndrome (POTS) and Postural Vasovagal Syncope (VVS)
NCT02558972 ·Status: TERMINATED ·Phase: PHASE2
-
In Hospital 24 Hour Observation of Syncope Patients
NCT06472375 ·Status: RECRUITING
-
Vasospasm in Pediatric Traumatic Brain Injury
NCT01461902 ·Status: COMPLETED
-
Prolonged Vasospasm in Subarachnoid Hemorrhage
NCT04193124 ·Status: COMPLETED
-
Predictive Value of Mean Flow Velocity by TCD in Early Cerebral Vasospasm in Aneurysmal Subarachnoid Hemorrhage
NCT04329208 ·Status: COMPLETED
-
Cervical Sympathetic Block in Patients With Cerebral Vasospasm
NCT05230134 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Role of Adenosine in the Control of Choroidal Blood Flow During Changes in Ocular Perfusion Pressure.
NCT00712764 ·Status: COMPLETED ·Phase: NA
-
Normal Values of Brain Oxygenation
NCT00512447 ·Status: COMPLETED
-
Blood Pressure and Brain Blood Flow Regulation After Midodrine Administration in Those With Spinal Cord Injury
NCT01498809 ·Status: COMPLETED
-
Evaluation of Cerebral Spinal Fluid and Blood in Patients With Subarachnoid Hemorrhage
NCT00593268 ·Status: ACTIVE_NOT_RECRUITING