RecruitingNCT04849806

Sympathetic Nerve Activity Predictors in Patients With Chronic Obstructive Pulmonary Disease

Dissecting the Nature and Determinants of Sympathetic Nerve Activity in Patients With COPD

Sponsor

RWTH Aachen University

Enrollment

135 participants

Start Date

May 10, 2022

Study Type

OBSERVATIONAL

Conditions

COPD Sympathetic Nervous System Diseases Catecholamine; Overproduction

Summary

The project will be pursued in our respiratory, autonomic nervous system physiology laboratory (Respiratory, autonomic nervous system physiology laboratory, Department of Pneumology and Intensive Care Medicine, RWTH Aachen University Hospital; Head of Department: Professor Michael Dreher). Overactivity of the sympathetic nerve activity (SNA) axis with "centrally" increased heart rate and peripheral vasoconstriction is a known phenomenon in patients with systolic heart failure (HF) and has recently been described in patients with primary lung disease as seen in chronic obstructive pulmonary disease (COPD). However, systematic analyses on this clinically relevant topic are currently lacking. Thus, using a comprehensive, multimodal approach and state-of-the-art technology, this research project is designed to determine the extent and nature of increased SNA in COPD (AIM 1) and evaluate the underlying mechanisms (AIM 2). The project will address the following hypotheses: 1. In COPD, concomitant obstructive sleep apnea is independently associated with increased SNA. 2. Precapillary pulmonary hypertension (PH), inspiratory muscle dysfunction and systemic inflammation describe a COPD phenotype characterised by increased SNA with a different subtype.

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at how the nervous system affects the heart and lungs in people who have COPD (chronic obstructive pulmonary disease), a lung condition that makes it hard to breathe. **You may be eligible if...** - You are 18 years or older - You are willing and able to give consent to participate **You may NOT be eligible if...** - You have atrial fibrillation (an irregular heart rhythm) - You have a cardiac pacemaker that controls your heart rate completely - You have been diagnosed with high blood pressure or heart failure - You were hospitalized in the last 4 weeks before the study exam Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTAssessments of the sympathetic nerve activity axis

For assessment sympathovagal balance (SVB), HRV and dBPV will be analysed using a 3-lead electrocardiogram (sampling rate 1000Hz) and a continuous non-invasive arterial blood pressure signal (CNAP® technology, sampling rate 100Hz). HRV (ms2 based on continuously recorded variability in RR intervals) and (diastolic) BPV (expressed as mmHg2 based on continuously recorded variability in diastolic BP) will be computed by time domain analysis and by frequency domain analysis and presented as the high frequency component (HF; 0.15-0.4 Hz), low frequency component (LF; 0.04-0.15 Hz), their relative ratio (LF/HF), and the very low frequency component (VLF; 0.0-0.04 Hz) for both HRV and dBPV . Muscle SNA will be recorded via a tungsten microelectrode carefully placed in the peroneal nerve. Plasma catecholamines will also be assessed.

DIAGNOSTIC_TESTOSA severity

OSA is defined as apnoea-hypopnoea index \[AHI\] \>15/h and obstructive apnoea index \[OAI\] \>5/h) and sleep architecture

DIAGNOSTIC_TESTDetermination of PH and right HF severity

(defined as tricuspid annular plane systolic excursion ≤14 mm) and pulmonary arterial pressure (PAsys) using transthoracic echocardiography

DIAGNOSTIC_TESTComprehensive lung function and inspiratory muscle function testing.

Respiratory Muscle strength and function testing as previously established by our group and Assessment of daytime hypoxia (PaO2 \<55 mmHg) and hypercapnia (PaCO2 \>45 mmHg) using capillary blood gas analysis.

DIAGNOSTIC_TESTAssessment of systemic inflammation

Based on blood samples taken.