The Exercise Response to Pharmacologic Cholinergic Stimulation in Myalgic Encephalomyelitis / Chronic Fatigue Syndrome
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- Change in Peak Oxygen Uptake (Peak VO2) Between the First and Second iCPET
研究概览
简要总结
Myalgic encephalomyelitis/Chronic fatigue syndrome (ME/CFS), otherwise known as Chronic fatigue syndrome (CFS) or myalgic encephalomyelitis (ME), is an under-recognized disorder whose cause is not yet understood. Suggested theories behind the pathophysiology of this condition include autoimmune causes, an inciting viral illness, and a dysfunctional autonomic nervous system caused by a small fiber polyneuropathy. Symptoms include fatigue, cognitive impairments, gastrointestinal changes, exertional dyspnea, and post-exertional malaise. The latter two symptoms are caused in part by abnormal cardiopulmonary hemodynamics during exercise thought to be due to a small fiber polyneuropathy. This manifests as low biventricular filling pressures throughout exercise seen in patients undergoing an invasive cardiopulmonary exercise test (iCPET) along with small nerve fiber atrophy seen on skin biopsy.
After diagnosis, patients are often treated with pyridostigmine (off-label use of this medication) to enhance cholinergic stimulation of norepinephrine release at the post-ganglionic synapse. This is thought to improve venoconstriction at the site of exercising muscles, leading to improved return of blood to the heart and increasing filling of the heart to more appropriate levels during peak exercise. Retrospective studies have shown that noninvasive measurements of exercise capacity, such as oxygen uptake, end-tidal carbon dioxide, and ventilatory efficiency, improve after treatment with pyridostigmine. To date, there are no studies that assess invasive hemodynamics after pyridostigmine administration.
It is estimated that four million people suffer from ME/CFS worldwide, a number that is thought to be a gross underestimate of disease prevalence. However, despite its potential for debilitating symptoms, loss of productivity, and worldwide burden, the pathophysiology behind ME/CFS remains unknown and its treatment unclear. By evaluating the exercise response to cholinergic stimulation, this study will shed further light on the link between the autonomic nervous system and cardiopulmonary hemodynamics, potentially leading to new therapeutic targets.
详细描述
The hypothesis of our study is that hemodynamic, ventilatory and oxygen exchange variables such biventricular filling pressures and systemic oxygen extraction can be improved by cholinergic stimulation in patients with ME/CFS.
The objective of this study is to examine the exercise response to pharmacologic cholinergic stimulation in ME/CFS patients already undergoing a clinically indicated invasive cardiopulmonary exercise test (iCPET). This will be achieved by inhibiting acetylcholinesterase with pyridostigmine, thus increasing acetylcholine levels, downstream levels of norepinephrine, and enhancing vascular regulation.
To test our hypothesis, we propose the following specific aims:
Define the response of peak oxygen uptake(VO2) to pyridostigmine. Define the gas exchange responses, such as end-tidal carbon dioxide(CO2) and ventilatory efficiency to pyridostigmine.
Define the hemodynamic responses, such as right atrial pressures, pulmonary artery pressure, pulmonary capillary wedge pressures, cardiac output, heart rate, stroke volume, pulmonary vascular resistance and systemic vascular resistance to pyridostigmine.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Meets the Institute of Medicine (IOM) criteria for ME/CFS
- •Completing the clinically indicated invasive cardiopulmonary exercise test (iCPET)
排除标准
- •Obesity (BMI > 30 kg/m2)
- •Non-controlled asthma
- •Anemia (Hb < 10 g/dl)
- •Active or treated cancer
- •History of interstitial lung disease (ILD)
- •Chronic obstructive pulmonary disease (COPD)
- •Pulmonary hypertension (PH)
- •Congestive heart failure (CHF)
- •Active arrhythmias
- •Valvular heart disease
- •Coronary artery disease (CAD)
- •Other conditions that could predict a limitation or not completion of the study.
- •Pregnancy
- •Submaximal testing in clinically indicated iCPET
- •Pulmonary mechanical limitation to exercise in clinically indicated iCPET.
- •Pulmonary arterial hypertension in clinically indicated iCPET.
- •Pulmonary venous hypertension in clinically indicated iCPET.
- •Exercise induced pulmonary arterial hypertension in clinically indicated iCPET.
- •Exercise induced pulmonary venous hypertension in clinically indicated iCPET.
- •Persistent hypotension during or after the clinically indicated iCPET.
- •Refractory arrhythmia during or after the clinically indicated level 3 CPET.
研究组 & 干预措施
Placebo
Placebo by mouth as a one time dose
干预措施: Placebo (Drug)
Study Drug - Pyridostigmine
Pyridostigmine 60 mg by mouth as a one time dose
干预措施: Pyridostigmine Bromide (Drug)
结局指标
主要结局
Change in Peak Oxygen Uptake (Peak VO2) Between the First and Second iCPET
时间窗: First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.
Define the response of oxygen uptake to pyridostigmine expressed both as mL/min and mL/min/kg. The difference in peak oxygen uptake from first iCPET to second iCPET. Research has shown that ME/CFS patients have inability to reproduce results on two consecutive cardiopulmonary exercise tests(CPET). Traditionally this is demonstrated with a two-day CPET protocol, but in this study we investigate the acute effects of pyridostigmine administration on the early stages of post exertional malaise(PEM).
次要结局
- Peak Right Atrial Pressure (RAP)(First iCPEt up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak-Rest Right Atrial Pressure (RAP)(First iCPEt up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Ventilatory Efficiency (VE/VCO2)(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Borg Fatigue Scale(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak-Rest Oxygen Uptake (VO2)(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak Cardiac Output (Qc)(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak (Ca-vO2)/[Hgb](First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak-Rest Cardiac Output (Qc)(First iCPET up to 30 min, 50 minutes rest, second iCPET up to 30 minutes)
- Peak Pulmonary Arterial Wedge Pressure (PAWP)(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Peak Stroke Volume (SV)(First iCPEt up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
- Borg Dyspnea Scale(First iCPET up to 30 minutes, 50 minutes rest, second iCPET up to 30 minutes.)
研究者
David Systrom
Principal Investigator; Director, Dyspnea Center; Associate Professor of Medicine
Brigham and Women's Hospital