This is an observational study to deeply phenotype the disorder of POTS using multiple testing modalities.
This comprehensive multimodality deep phenotyping will improve the diagnostic approach, inform the development of new treatments, and allow the targeting of therapies to specific POTS patients. The investigators will further identify the diagnostic tools, biomarkers, and clinical outcome measures most relevant to defining the disorder in clinical practice. The specific aim is to (1) Define clinical POTS classifications from multimodal clinical and laboratory data, (2) address exercise tolerance in POTS using metabolomic assessments, (3) evaluate novel POTS-specific patient outcome measures and (4) evaluate one year outcome data for POTS Specific research tests will include blood work (for immunophenotyping and neurohormonal assessments), autonomic function testing, skin biopsy (to evaluate intraepidermal nerve fiber density), CO (Carbon Monoxide) rebreathing (for quantitative measurement of plasma volume and red blood cell mass), patient surveys (to characterize symptom profile and disease impact). Blood biosamples will be stored as a repository for future research questions.
Study Type
OBSERVATIONAL
Enrollment
350
Serological testing, cardiac MRI, skin biopsy, cardiovascular testing, blood volume measurements
UT Southwestern Medical Center
Dallas, Texas, United States
RECRUITINGPhenotyping POTS
Assignment of participant to a phenotypic group(s) based on analysis of multimodal data
Time frame: 2 weeks
Natural history
Patient reported functional and subjective change. Surveys including COMPASS31 (Composite Autonomic Symptom Score-31) on a score of 0-100. Higher scores indicate more severe autonomic symptoms
Time frame: 1 year
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