Anti-Cholinergic Receptors Antibodies, Autonomic Profile and Dysautonomia Symptoms in PAF, ALS and POTS (DISAUT-AB) (DISAUT-AB)
Primary Purpose
Pure Autonomic Failure, Amyotrophic Lateral Sclerosis, Postural Orthostatic Tachycardia Syndrome
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Immunoabsorption/plasmapheresis procedure
Sponsored by
About this trial
This is an interventional supportive care trial for Pure Autonomic Failure focused on measuring Neural control of circulation and respiration, Anti-Cholinergic receptors antibodies, Power Spectrum Analysis
Eligibility Criteria
Inclusion Criteria:
• Patients, older than 18 years affected by PAF, ALS and POTS, with dysautonomia symptoms assessed by clinical evaluation and by the Composite Autonomic Scoring Scale (CASS)
Exclusion Criteria:
- Hepatic, renal, heart and other secondary causes of autonomic dysfunction
- History/familiarity with seizures
- Atrial fibrillation and other relevant cardiac rhythm disturbances
- Diabetes
- Other neurological or psychiatric diseases
- Pacemakers or other electronic implants inserted into the body
- Coronary disorders, elevated intracranial blood pressure
- Assumption of drugs facilitating seizures, psychiatric drugs, alcohol abuse
Sites / Locations
- Humanitas Research Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Anti-AChRs Abs positive patients
Arm Description
Immunoabsorption
Outcomes
Primary Outcome Measures
Prevalence of plasma anti-AChR Abs in PAF, ALS and POTS
Number of patients with plasma anti-AChR Abs
Effects of anti-AChR Abs removal on dysautonomic symptoms
COMPASS31 scores (range 0-100; 0 best -100 worst)
Time course of dysautonomia symptoms
COMPASS31 scores (range: 0-100; 0 best-100 worst)
Time course of orthostatic tolerance
Orthostatic tolerance (minutes)
Secondary Outcome Measures
Full Information
NCT ID
NCT04875949
First Posted
January 12, 2021
Last Updated
May 3, 2021
Sponsor
Istituto Clinico Humanitas
Collaborators
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, Fondazione Salvatore Maugeri
1. Study Identification
Unique Protocol Identification Number
NCT04875949
Brief Title
Anti-Cholinergic Receptors Antibodies, Autonomic Profile and Dysautonomia Symptoms in PAF, ALS and POTS (DISAUT-AB)
Acronym
DISAUT-AB
Official Title
Anti-Cholinergic Receptors Antibodies and Dysautonomia Symptoms Relationships in Pure Autonomic Failure, Amyotrophic Lateral Sclerosis, Postural Orthostatic Tachycardia Syndrome: a Pathophysiology Based Therapeutic New Strategy.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
April 2016 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
April 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Clinico Humanitas
Collaborators
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, Fondazione Salvatore Maugeri
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Anti alfa-3 and alfa-7 ganglionic cholinergic receptors (anti-AChRs) antibodies (Abs) plasma removal by plasmapheresis (1,2) acutely improved dysautonomia symptoms in case reports with Pure Autonomic Failure (PAF) (3). We shall assess the prevalence of anti-AChRs Ab and the relationship among Ab titer, cardiovascular autonomic profile and symptoms in neurodegenerative diseases characterized by similar dysautonomia symptoms such as PAF, Amyotrophic Lateral Sclerosis (ALS) and Postural Orthostatic Tachycardia Syndrome (POTS) (4). Ab positive patients will undergo selective immunoabsorption once a week up to achievement of Ab titer lower than 65% of baseline followed by immunosuppressive therapy with prednisone. Both Ab positive and negative groups will undergo anti-AChR Abs, autonomic profile and dysautonomia symptoms assessment, every 4 months up to 3 years. Evidence of correlation among reduced Ab titer and autonomic profile and symptoms improvement may result in new effective therapy.
Detailed Description
PAF is a rare neurodegenerative disorder characterized by symptoms due to sympathetic failure, such as orthostatic hypotension and syncope, and deficient parasympathetic activity such as constipation, urinary retention and decreased salivation (3). Plasma anti-AChRs Abs were found in PAF (1, 2, 5) and in POTS (6), raising the possibility that Ab mediated alterations in the ganglionic cholinergic function might induce autonomic abnormalities and related symptoms. Anti-AchRs Abs removal by plasmapheresis was associated with acute improvement of orthostatic tolerance in PAF single case report (2).
There is no data on the medium/long term clinical follow-up of these patients. Nothing is known about the time course of the relationships among Abs plasma titer, neural autonomic profile and symptoms if a selective immunoabsorption procedure is combined with drug immunosoppression (Prednisone) to lower Ab levels and potentially ameliorate ganglionic function.
Finally, it is unknown whether a neurodegenerative disease with concomitant dysautonomia symptoms such as the Amyotrophic Lateral Sclerosis (ALS) may share an analogous anti-AChRs Ab profile. Variations in cholinergic receptor subunits 3 and 4 were observed in ALS but no plasma anti-AChRs Abs were searched for (7). Abs removal by immunoabsorption technique combined with drug immunosoppression might represent a new effective therapy for dysautonomia symptoms in ALS as well as in POTS and PAF.
Hyphotesis and Significance:
Changes in anti-AChR Abs plasma titer may be mirrored by modifications in the cardiovascular autonomic profile, as assessed by spectrum analysis of RR and arterial pressure variability, and be related to fluctuations in the magnitude of dysautonomia symptoms in PAF, ALS and POTS patients.
Plasma anti-AChR Abs might underlie dysautonomia symptoms associated to neurodegenerative disorders such as ASL and POTS
Plasma anti-AChR Abs removal by selective immunoabsorption techniques may improve ganglionic transmission leading to clinical amelioration and represent a new effective etiologic therapy for these diseases.
Specific Aim:
Aim 1: To evaluate the prevalence of plasma anti-AChR Abs in patients affected by PAF, ALS and POTS .
Aim 2: To address the time course and relationships of anti-AChR Abs plasma titers, cardiovascular autonomic profile and dysautonomia symptoms before and after anti-AChR Abs plasma removal by selective immunoabsorption technique in PAF, ALS and POTS patients. The core laboratory of the Neuroimmunology Unit of Istituto Neurologico Besta will provide expertise and facilities for assessing plasma anti-AChR Abs. The clinical laboratory of Clinica Medica Syncope Unit (Humanitas) will provide the know-how and facilities for patients neural autonomic assessment.
Aim 3:To set up a new therapeutic strategy based on selective immunoabsorption technique sessions combined with drug immunosuppression (Prednisone) in patients with anti-AChR Abs.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pure Autonomic Failure, Amyotrophic Lateral Sclerosis, Postural Orthostatic Tachycardia Syndrome, Anti-Cholinergic Receptors Antibodies
Keywords
Neural control of circulation and respiration, Anti-Cholinergic receptors antibodies, Power Spectrum Analysis
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
75 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Anti-AChRs Abs positive patients
Arm Type
Experimental
Arm Description
Immunoabsorption
Intervention Type
Procedure
Intervention Name(s)
Immunoabsorption/plasmapheresis procedure
Primary Outcome Measure Information:
Title
Prevalence of plasma anti-AChR Abs in PAF, ALS and POTS
Description
Number of patients with plasma anti-AChR Abs
Time Frame
3 years
Title
Effects of anti-AChR Abs removal on dysautonomic symptoms
Description
COMPASS31 scores (range 0-100; 0 best -100 worst)
Time Frame
3 years
Title
Time course of dysautonomia symptoms
Description
COMPASS31 scores (range: 0-100; 0 best-100 worst)
Time Frame
3 years
Title
Time course of orthostatic tolerance
Description
Orthostatic tolerance (minutes)
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• Patients, older than 18 years affected by PAF, ALS and POTS, with dysautonomia symptoms assessed by clinical evaluation and by the Composite Autonomic Scoring Scale (CASS)
Exclusion Criteria:
Hepatic, renal, heart and other secondary causes of autonomic dysfunction
History/familiarity with seizures
Atrial fibrillation and other relevant cardiac rhythm disturbances
Diabetes
Other neurological or psychiatric diseases
Pacemakers or other electronic implants inserted into the body
Coronary disorders, elevated intracranial blood pressure
Assumption of drugs facilitating seizures, psychiatric drugs, alcohol abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raffaello Furlan, Prof.
Organizational Affiliation
Humanitas Research Hospital, Humanitas University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Franca Barbic, MD
Organizational Affiliation
Humanitas Research Hospital, Humanitas University, Rozzano
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Raffaello Furlan, Prof.
Organizational Affiliation
Humanitas Research Hospital, Humanitas University
Official's Role
Study Director
Facility Information:
Facility Name
Humanitas Research Hospital
City
Rozzano
ZIP/Postal Code
20089
Country
Italy
12. IPD Sharing Statement
Citations:
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10995864
Citation
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Anti-Cholinergic Receptors Antibodies, Autonomic Profile and Dysautonomia Symptoms in PAF, ALS and POTS (DISAUT-AB)
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