Exercise Prescription in Cardiac Rehabilitation Mediated by Autonomic Function
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 入组人数
- 90
- 试验地点
- 2
- 主要终点
- Normalization Factor for Sympathetic Activation Derived from Multimodal Autonomic Assessment
研究概览
简要总结
Cardiac rehabilitation (CR) is an essential secondary prevention component in the treatment of cardiovascular diseases and one of the most cost- effective clinical interventions. Exercise training (ET) in CR programs (CRP) has unequivocal benefits in the reduction of cardiovascular adverse events, by decreasing the overactivated sympathetic tone. This ET added value can be measured by variables that express autonomic control using indirect (standard) or direct (experimental) methodologies. Direct autonomic assessment (ex. Microneurography) is accurate but unusable in daily practice, whereas standard indirect autonomic assessment using clinical parameters is imprecise, resulting in underprescription to safeguard patient safety, with less benefit to the patients. In this project, we aim to apply Machine Learning models to a set of indirect and direct variables, to make a multivariate correlation analysis and so define a normalization factor for exercise prescription.
详细描述
Cardiac rehabilitation (CR) has proved to be an essential secondary prevention component of the continuum in the treatment of Cardiovascular diseases (CVD), being a Class I recommendation with level of evidence A and B on the European Society of Cardiology (ESC) and American Heart Association and American College of Cardiology (AHA/ACC) Guidelines. CR is also one of the most cost-effective clinical interventions in the treatment of CVD. These diseases, namely coronary artery disease (CAD) and heart failure (HF), are associated with autonomic dysfunction, particularly an overactivation of the autonomic sympathetic system (ASS), leading to coronary vasoconstriction, myocardial remodeling, and increased basal oxygen consumption. The main component of the CR programs (CRP) is Exercise training (ET), one of the central pillars of non- pharmacological treatment in CVD, thus preventing the above- mentioned progression of deleterious effects. The role of ET in CRP has been increasingly emphasized; however, it is still not clear, among the variety of existing training programs, which is the optimal combination and type of exercise (aerobic/anaerobic or both), frequency and duration of the sessions, whose prescription should be customized considering the patient's clinical history and the pre-CRP exam results. This limitation is pointed out as a major drawback in obtaining optimized results on CRP. The absence of a methodology that can more precisely assess and hence better quantify the effect of the prescription, safely optimizing the training plan, is one of the central problems regarding CR, and will be addressed in this research proposal putting the autonomic modulation of CV system in the center of the rational to prescribe ET in CRP. The main objective of this research plan is to draw an objective and individualized protocol to prescribe ET in CRPs based on the Autonomic output.
After careful ponderation, two important but different pathologies with clearly demonstrated ASS overactivation were considered: "non- ischemic HF with reduced ejection fraction" (NIHFrEF) and "CAD without HF" (CADnonHF). The following secondary objectives contribute to the achievement of this central goal, and define the majority of the associated tasks:
- Evaluation of the basal sympathetic activation pattern in patients with NIHFrEF and CADnonHF (Task2);
- Definition of a normalization factor regarding sympathetic activation for ET prescription purposes in the context of CRPs (Task3)
- Definition of an exercise training program for CRPs with prescription guided by the autonomic response (Task 4); In Task 2 the basal activation level of the Autonomic nervous system (ANS) will be characterized for each of the two identified conditions (NIHFrEF and CADnonHF) using a sample of 30 patients for each one to ensure a good approximation of the sampling distribution of the mean using the central limit theorem, and the participants will be enrolled at the CR consultation in Centro Hospitalar de Leiria (CHL) Cardiology department. The CHL CR Unit is accreditated by the European Association of Preventive Cardiology (EAPC) since 2022. Classical indirect measures of ANS which are relatively imprecise, such as heart rate variability (HRV) and derived indexes will be obtained with a 24h Holter and a "long duration EKG", as well as the first minute HR recovery with a Cardiopulmonary Exercise Test (CPET) and also serum catecholamines in blood and urine samples. Besides these indirect measures, a direct recording of the SNS obtained by microneurography (MSNA) will be conducted, being available at the host research institution (ciTechCare). The set of variables (autonomic and its derivatives), together with the metabolic biomarkers, will allow a multivariate correlation analysis followed by the use of the Machine Learning algorithm "Principal Component analysis" (PCA) to reduce the dimensionality of the data set, and so define a normalization factor for exercise prescription purposes, which corresponds to the main goal associated with Task 3. This normalization factor will be key to establish the individual pattern of sympathetic activation, establishing the same starting point for initial prescription of exercise and an unbiased follow up of patient's performance. Regarding Task 4, training plans (aerobic/anaerobic load) will be carried out in conjunction with the levels defined for the classification model (one of the derivable of the previous Task), and will be developed by the candidate along with the Physiatrist of the CRP Team, by setting a combined (aerobic and resistance) and stratified (with various levels of intensity, frequency, stages and duration) training program. This protocol will be evaluated by the due health ethics committees (Task 1), and all legal issues regarding safety and data protection will be respected.
Regarding risks and strategies to mitigate them, the main risk is related to data assessment. In that case other hospitals may be contacted to increase the number of participants. Another risk is related to task dependency. In this case, the experience of the mentors and the integration of this project in a team with expertise in CRP and familiar with artificial intelligence applications in Medicine will be determinant.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with Coronary artery disease and no heart failure criteria
- •Patients with non ischaemic heart failure and reduced left ventricle ejection fraction
排除标准
- •patients with ongoing acute coronary syndrome
- •patients with ongoing acute decompensated heart failure
- •Severe valvular heart disease that might confound the relationship between exercise and autonomic function.
- •Severe arrhythmias (e.g., sustained ventricular tachycardia, atrial fibrillation with a rapid ventricular rate) that are symptomatic or untreated
- •Severe uncontrolled hypertension (e.g., systolic BP > 180 mmHg or diastolic BP > 110 mmHg)
- •Active infectious diseases or other significant acute medical illnesses (e.g., sepsis, active malignancy, acute kidney injury)
- •Pregnancy or lactation (to ensure safety during exercise interventions)
- •Significant cognitive impairment or mental illness (e.g., dementia, schizophrenia) that would impair the ability to follow exercise protocols or understand study instructions
- •nability to comply with study procedures due to any reason (e.g., language barriers, lack of informed consent)
- •Chronically immunocompromised states (e.g., HIV with CD4 count < 200 cells/µL or on immunosuppressive therapy)
- •Presence of significant comorbidities such as advanced chronic obstructive pulmonary disease (COPD), kidney disease (e.g., stage 4-5 chronic kidney disease), or uncontrolled diabetes that would make exercise unsafe or confound the study outcomes
- •Critical limb ischemia, or severely symptomatic peripheral artery disease or claudication limiting functional capacity and response to exercise
- •Advanced chronic kidney disease (stage 4 or 5), due to contraindications with exercise
- •Severe anemia (hemoglobin < 8 g/dL) or other blood disorders that affect exercise capacity
- •Inability to tolerate exercise due to other comorbidities or debility
- •individuals with known autonomic neuropathy (such as poorly controlled diabetes or neurodegenerative disorders)
- •Specific Exclusion Criteria for Coronary Artery Disease (CAD) without Heart Failure Group:
- •Left ventricular ejection fraction (LVEF) < 50%
- •Clinical/echocardiographic criteria of heart failure with oreserved ejection fraction.
- •Specific Exclusion Criteria for Non-Ischemic Heart Failure with Reduced LVEF Group:
- •Ischemic heart disease or previous myocardial infarction
- •LVEF > 40%
- •End-stage heart failure (e.g., patients on a heart transplant list, those with imminent need for mechanical circulatory support like LVAD).
- •Severe fluid overload that cannot be corrected
结局指标
主要结局
Normalization Factor for Sympathetic Activation Derived from Multimodal Autonomic Assessment
时间窗: Baseline (before initiation of cardiac rehabilitation program)
A composite autonomic normalization factor will be generated using Principal Component Analysis (PCA) applied to multimodal autonomic and metabolic biomarkers (including microneurography-derived MSNA, heart rate variability indices from 24-hour Holter, CPET first-minute heart rate recovery, and serum/urinary catecholamines). This factor will quantify the individual degree of sympathetic activation and will serve as the basis for personalized exercise training prescription (Units of mesaure: unitless)
次要结局
- LF/HF Ratio (Heart Rate Variability) obtained from 24-hour Holter ECG(Baseline)
- Urinary 3-methoxytyramine(Baseline)
- Basal Sympathetic Nervous System Activity (MSNA burst frequency)(Baseline)
- SDNN (Heart Rate Variability) obtained from 24-hour Holter ECG and long-duration ECG(Baseline)
- RMSSD (Heart Rate Variability) obtained from 24-hour Holter ECG and long duration ECG(Baseline)
- LF Power (Heart Rate Variability) Low-frequency spectral power obtained from 24-hour Holter ECG(Baseline)
- Plasma epinephrine concentration(Baseline)
- Plasma norepinephrine concentration(Baseline)
- Plasma dopamine concentration(Baseline)
- Urinary metanephrine(Baseline)
- Urinary normetanephrine(Baseline)
- CPET First-Minute Heart Rate Recovery(Baseline)
研究者
Alexandre Antunes
Medical Doctor (MD), Cardiologist, Coordinator of the Cardiac Rehabilitation Unit of Hospital Santo André
Instituto Politécnico de Leiria