Assessment of Antibodies and Inflammatory Markers in Postural Tachycardia Syndrome

Postural Orthostatic Tachycardia Syndrome Clinical Trial

Official title: Assessment of Antibodies and Inflammatory Markers in Postural Tachycardia Syndrome

Status Active, not recruiting

Clinical Trial Summary

In this pilot study, the investigators will test the hypothesis that patients with postural tachycardia syndrome will have an elevated percentage of functional antibodies to adrenergic receptors compared with control subjects without POTS. The investigators further hypothesize that the percentage of POTS patients with antibodies will be higher in those patients with a viral infection at the onset of their illness than in those patients with other or undefined illness onsets.

Clinical Trial Description

Postural orthostatic tachycardia syndrome is poorly understood. Many of these patients have elevated levels of plasma norepinephrine, particularly when upright One subgroup of patients has a primary hyperadrenergic state. The majority of patients have a marked deficit in plasma blood volume compared to healthy control subjects. The investigators have previously reported that some patients suffer paradoxically from a partial dysautonomia affecting the lower limbs. Most patients seem to suffer from either a primary or secondary increase in central sympathetic nervous system drive. Recent data have shown that patients with postural orthostatic tachycardia syndrome have a lower cardiac stroke volume than their healthy counterparts and this low stroke volume may drive their orthostatic tachycardia.

The investigators plan to do the following:

The physical examination will include (at minimum):

• Height

• Weight

• Orthostatic vital signs (heart rate and blood pressure) Supine and Standing for up to 10 minutes

• Beighton Criteria for Joint Hypermobility Syndrome (Ehlers-Danlos III)

• Dependent acrocyanosis (during stand test)

Continuous Heart Rate and Blood Pressure Recording A subset of subjects will be given the opportunity to also have continuous recordings of heart rate and blood pressure for 5-10 minutes while lying down quietly. They will be instrumented with EKG patches on their body and a finger blood pressure cuff, and these data will be digitally sampled and acquired on a dedicated laptop computer for later offline analysis.

There will be an optional rider on the consent form to allow the patient to consent to this portion of the study.

Blood work

Blood will be drawn for future assay and analysis of the following tests:

• Antibodies regulating cardiovascular function

o The clinical significance of these antibodies is unknown. The investigators will share the results of the antibody panel with the subject, but with the caveat that no clinical interpretation or comment on significance can be made.

• Inflammatory markers

The total amount of blood drawn for this project will be less than 15 ml.

Questionnaires

• RAND-36

• Health Thermometer

• Chandler Fatigue Scale

• Daily diary of Fatigue Symptoms - Fibromyalgia

• Pain Detect Questionnaire

• Orthostatic Grading Scale

• COMPASS-31

• Structured History (including some of the elements from section 6.1)

These questionnaires will be completed directly online (web-based interface) using a personalized link that will be provided to the subjects after they give their informed consent. These will be created in a REDCap-Survey environment, with the data collected and stored on a password-protected, HIPAA-compliant, secure computer server. ;

Related Conditions & MeSH terms

• Postural Orthostatic Tachycardia Syndrome
• Syndrome
• Tachycardia

• NCT number: NCT02196376
• Study type: Observational
• Source: Vanderbilt University Medical Center
• Status: Active, not recruiting
• Start date: July 2014
• Completion date: July 2025