Phenotyping Mitochondrial and Immune Dysfunction in POTS With Targeted Clinical Intervention.
Phenotyping Mitochondrial and Immune Dysfunction in POTS With Targeted Clinical Intervention.
The mechanisms underlying POTS are not well understood. Though heterogeneous in nature, patients often present with symptoms that include fatigue, orthostatic lightheadedness and tachycardia, "brain fog", shortness of breath, and sleep disruption. The central mediator that links observations in disease entities similar to POTS is energy use and balance driven by mitochondrial health. Mitochondrial dysfunction (i.e. respiration defects, reactive oxygen species (ROS) generation, and structural abnormalities) are hallmarks of currently defined syndromes that resemble POTS symptomatology. Many patients with POTS have underlying immune system dysfunction, which, when treated, may improve the patient's overall health. Though autoimmunity has been demonstrated in POTS, overall immune dysregulation may be broader and include immune cell exhaustion and persistent inflammatory cytokine responses. Immune dysfunction including cellular exhaustion and persistent inflammation has been linked to mitochondrial function. Therefore, we hypothesize that a unifying feature of POTS results from latent or continued mitochondrial/immune dysfunction which then impacts multi-organ energy imbalance and immune homeostasis. Understanding and targeting mitochondria utilizing established, novel, and directed approaches including time-restricted eating (TRE) will help to unravel common etiologies and help us to better diagnose, manage, and treat POTS.
Inclusion Criteria:
Age: 18-70 years old
POTS, as defined by the presence of any of the following criteria:
Baseline eating period > 12-hour window
Exclusion Criteria:
Taking insulin within the last 6 months.
Manifest diabetes, defined as HbA1c > 7.0% given a 0.3% margin of error in lab readings, or diagnosis of diabetes.
Known inflammatory and/or rheumatologic disease.
Active tobacco abuse or illicit drug use or history of treatment for alcohol abuse.
Pregnant or breast-feeding women.
Shift workers with variable (e.g. nocturnal) hours.
Caregivers for dependents requiring frequent nocturnal care/sleep interruptions.
Planned travel to a time zone with greater than a 3-hour difference during study period.
History of a major adverse cardiovascular event within the past 1 year (acute coronary syndrome (ACS), percutaneous coronary intervention, coronary artery bypass graft surgery, hospitalization for congestive heart failure, stroke/transient ischemic attack (TIA)).
Uncontrolled arrhythmia (i.e. rate-controlled atrial fibrillation/atrial flutter are not exclusion criteria).
History of thyroid disease requiring dose titration of thyroid replacement medication(s) within the past 3 months (i.e. hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion).
History of adrenal disease.
History of malignancy undergoing active treatment, except non-melanoma skin cancer.
Known history of type I diabetes.
History of eating disorder.
History of cirrhosis.
History of stage 4 or 5 chronic kidney disease or requiring dialysis.
History of HIV/AIDS.
Currently enrolled in a weight-loss or weight-management program.
On a special or prescribed diet for other reasons (e.g. Celiac disease).
Currently taking any medication that is meant for, or has known effect on, appetite.
Any history of surgical intervention for weight management.
Uncontrolled psychiatric disorder (including history of hospitalization for psychiatric illness).
A score of >16 on the Epworth Sleepiness Scale (ESS).
Depression determined by the Beck Depression Inventory (BDI-II) (unless previously diagnosed and well-controlled)
Failure to use the smartphone app for documentation (defined as <2 meals/day for ≥3 days during baseline).