Noradrenergic and Stress-Related Etiologies of Chronic Fatigue Syndrome

Vanderbilt University Medical Center55 enrolled

Overview

The objective of this study is to measure sympathetic nervous system function and stress responses in patients with clinically documented and self-reported chronic fatigue that is worsened by stress, compared to healthy controls. Baseline norepinephrine (NE) levels and stress-induced NE levels in patients who fulfill criteria for Chronic Fatigue Syndrome (CFS) and who self-identify with stress induced worsening fatigue, will be compared to data from normal individuals pre and post-stress.

Symptoms of Chronic Fatigue Syndrome (CFS) are critically important to study as patients report that these symptoms are often profoundly debilitating and an impediment to effective daily functioning as well as effective vocational and social functioning, while also contributing to a significantly increased risk of psychiatric illness and diminished quality of life. Previous Phenome-Wide Association (PheWAS) studies revealed a link between a norepinephrine transporter (NET) genetic variant and CFS. Based on the potential function of the variant and published literature, elevated norepinephrine (NE) levels may underlie at least some cluster of fatigue symptoms. Some patients may experience chronic fatigue that is due to an excess of circulating NE, and fatigue symptoms are reported by our patient population to be commonly exacerbated by stress. This study will test the hypothesis that in a subset of people with severely debilitating fatigue of long duration (\>6 months) that is worsened by stress identified through the Vanderbilt electronic health record phenotyping study, have chronic over-release of the hormone NE into the bloodstream/periphery over time that results in an overload of NE. This overload of NE causes a compensatory but deleterious effect on the brain and nervous system, including sympathetic effects and dysregulated physiologic response to stress. Thus, while numerous currently approved therapies that target NET inhibit the transporter, a drug with the opposite mechanism of action, a NET activator that would decrease circulating NE, may have efficacy in treating underlying pathophysiology of chronic fatigue. Baseline NE levels and stress-induced NE levels in patients who fulfill criteria for CFS and who self-identify with stress induced worsening fatigue, will be compared to data from normal individuals pre and post-stress. After all inclusion criteria has been confirmed, an IV will be placed for blood collection, a continuous electrocardiographic trace and blood pressure cuff will be placed on the subject's arm and finger. Subjects will undergo a posture study, autonomic reflex testing, and Stroop stress testing each followed by blood specimen collection. An optional blood draw for DNA analysis will occur after patients have been provided lunch. Questionnaires will be completed after study procedures and patients have been provided lunch. Study blood collection will total up to 28 milliliters (mL): 5 mL for cytokines, 20 mL for catecholamines, and optional 3 mL for DNA.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Chronic Fatigue Syndrome

Interventions

Posture Study, Autonomic Function Tests, and a Stress TestOTHER

Participants will undergo a Posture Study, Autonomic Function Tests, and a Stress Test. Participants' blood will be drawn to measure markers of sympathetic nervous system function at baseline, in three postural positions, after autonomic tests, and after a stress test.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Chronic Fatigue Participants: Inclusion Criteria: * Confirmed chronic fatigue with severity \>50 on a scale of 1 to 100 that is not improving over time * Meet The Centers for Disease Control and Prevention (CDC) diagnostic criteria of CFS (self-reported persistent or relapsing fatigue lasting 6 or more consecutive months) Exclusion Criteria: * Male and female subjects \<18 or \>60 years * Obesity, defined as a BMI of 30 or more * Presence of other medical or psychiatric conditions known to cause fatigue (alcohol/drug abuse, anorexia nervosa, bipolar disorder, bulimia nervosa, dementia, major depression, psychotic/delusional disorders, schizophrenia) * Presence of sleep disorder/disruption known to cause fatigue (sleep apnea, narcolepsy) * Cardiovascular, pulmonary, hepatic, or hematological disease by history or prior testing defined as significant by investigator (including but not limited to chronic hepatitis, chronic kidney disease, cirrhosis, emphysema, heart failure, HIV, lupus, multiple sclerosis, myasthenia gravis, rheumatoid arthritis) * History of hypertension defined as supine resting BP\>145/95 mmHg off medications or needing antihypertensive medication * Patients taking medications that can affect autonomic function or plasma catecholamines (vasoactive drugs), stimulants, and/or are sedatives * Other factors which in the opinion of the investigator could potentially impact the study outcomes (e.g., underlying disease, medications, history)\* or prevent the participant from completing the protocol (poor compliance or unpredictable schedule) * Inability to stand unassisted for 10 minutes * Patients who are bedridden or chair-ridden * Patients who are colorblind * Inability or refusal to give informed consent for any reason including a diagnosis of dementia or cognitive impairment * Patients who are pregnant or breastfeeding Healthy Control Participants: * Participant with no significant reported conditions or medications. Exclusion Criteria: * Male and female subjects \<18 or \>60 years * Obesity, defined as a BMI of 30 or more * Presence of any serious or chronic disease, or prescription medication as deemed by investigator including hypertension as defined by supine resting BP \>145/95 mmHg off medications or needing antihypertensive medication * Other factors which in the investigator's opinion would prevent the participant from completing the protocol, including poor compliance during previous studies or an unpredictable schedule * Inability to stand unassisted for 10 minutes * Patients who are bedridden or chair-ridden * Patients who are colorblind * Inability or refusal to give informed consent for any reason including a diagnosis of dementia or cognitive impairment * Patients who are pregnant or breastfeeding * Stress Overload Score above 66

Locations (1)

Vanderbilt University Medical Center

Nashville, Tennessee, United States

Outcomes

Primary Outcomes

dihydroxyphenylglycol (DHPG)/norepinephrine (NE) Ratio (post stress)

Change in DHPG/NE Ratio from Baseline to post stress compared across arms

Time frame: Change from Baseline to post stress test (approximately 100 minutes post-baseline blood collection)

Secondary Outcomes

DHPG/NE Ratio (post Autonomic Function test)

Change in DHPG/NE Ratio from Baseline to post Autonomic Function test compared across arms

Time frame: Change from Baseline to post Autonomic Function test (approximately 30 minutes post-baseline blood collection)

DHPG/NE Ratio (post Standing position)

Change in DHPG/NE Ratio from Baseline to post Standing position compared across arms

Time frame: Change from Baseline to post Standing position (approximately 40 minutes post-baseline blood collection)

DHPG/NE Ratio (post Sitting position)

Change in DHPG/NE Ratio from Baseline to post Sitting position compared across arms

Time frame: Change from Baseline to post Sitting position (approximately 70 minutes post-baseline blood collection)

Absolute DHPG and NE Levels (post stress)

Change in absolute DHPG and NE Levels from Baseline to post stress compared across arms

Time frame: Change from Baseline to post stress test (approximately 100 minutes post-baseline blood collection)

Absolute DHPG and NE Levels (post Autonomic Function test)

Change in DHPG and NE levels from Baseline to post Autonomic Function test compared

Time frame: Change from Baseline to post Autonomic Function test (approximately 30 minutes post-baseline blood collection)

Data from ClinicalTrials.gov

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