Abstract

Cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) are chronic pulmonary diseases that affect ~70,000 and 251 million individuals worldwide, respectively. Although these two diseases have distinctly different pathophysiologies, both cause chronic respiratory insufficiency that erodes quality of life and causes significant morbidity and eventually death. In both CF and COPD, the respiratory microbiome plays a major contributing role in disease progression and morbidity. Pulmonary pathogens can differ dramatically during various stages of each disease and frequently cause acute worsening of lung function due to disease exacerbation. Despite some similarities, outcome and timing/type of exacerbation can also be quite different between CF and COPD. Given these clinical distinctions, both patients and physicians should be aware of emerging therapeutic options currently being offered or in development for the treatment of lung infections in individuals with CF and COPD. Although interventions are available that prolong life and mitigate morbidity, neither disorder is curable. Both acute and chronic pulmonary infections contribute to an inexorable downward course and may trigger exacerbations, culminating in loss of lung function or respiratory failure. Knowledge of the pulmonary pathogens causing these infections, their clinical presentation, consequences, and management are, therefore, critical. In this review, we compare and contrast CF and COPD, including underlying causes, general outcomes, features of the lung microbiome, and potential treatment strategies.

Highlights

  • Obstructive sleep apnea (OSA) is a frequent sleeprelated respiratory disease with frequent upper airway total or partial obstruction during sleep [1]

  • OSA patients showed significant enhancement of PTX-3 levels and Left ventricular diastolic dysfunction (LVDD). Both PTX-3 and LVDD were independently correlated with severity of OSA defined by apnea-hypopnea index (AHI)

  • Serum PTX-3 levels were positively correlated with LVDD in OSA patients

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Summary

Introduction

Obstructive sleep apnea (OSA) is a frequent sleeprelated respiratory disease with frequent upper airway total or partial obstruction during sleep [1]. Chronic intermittent hypoxia (CIH) and hypoxemia attributing to apnea provoke systemic effects and increase levels of biomarkers related to cardiovascular abnormality [2]. Left ventricular diastolic dysfunction (LVDD) is an early marker of cardiac function abnormality before clinically noticeable cardiovascular disease [3,4]. It is characterized by reducing and/or totally losing the relaxation and compliance of cardiomyocytes. Echocardiographic examination is used as a convenient and reliable method to measure left ventricular functions. Diagnosis and effective intervention of LVDD have become one of the most pressing problems in the cardiovascular field

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