Asthma is a chronic disease that affects about 300 million people worldwide.
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Asthma is a heterogeneous disease, defined by variable expiratory airflow limitation
and history of respiratory symptoms such as wheeze, shortness of breath, chest tightness,
and cough.
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The cardinal feature of asthma is excessive narrowing of the lower airways. Excessive
airway narrowing accounts for the morbidity and mortality of asthma and it makes breathing
difficult or, in the extreme, impossible.
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Despite the advances in pharmacological treatment options, a large fraction of asthma
sufferers has poor asthma control.
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For example, in Canada, it is estimated that asthma is not well-controlled in 90%
of asthmatics.
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The presence of nocturnal symptoms is an important marker of poor asthma control.
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Indeed, 50% to 68% of asthma attacks that led to death occur during night.
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However, the mechanisms accounting for nocturnal worsening of asthma remain unclear.
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It is well known that sleep changes respiratory mechanics, including reductions in
respiratory drive, pharyngeal dilator muscle tone, and lung volume.
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However, the changes in respiratory mechanics during sleep do not account for all
the nocturnal increases in airflow resistance in asthma. For example, maintaining
lung volumes similar to the wakefulness values by continuous negative pressure applied
to the chest during sleep does not prevent the overnight increase in airway resistance.
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Moreover, whether awake or asleep, airway resistance increases overnight and doubles
with sleep.
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This shows independent contribution of sleep over circadian effects.
Recent evidences show that rostral fluid shift from the legs to the thorax during
supine posture
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and fluid overloading
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are potential contributors to poor asthma control and nocturnal worsening of asthma
symptoms. Fluid accumulation in the thorax may cause a cascade of events that exacerbate
airway narrowing.
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These events include increased blood volume and blood pressure in the bronchial circulation.
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As a result, the pressure gradient from blood to interstitium increases, drives more
fluid leak, and causes increased airway wall edema,
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and peribronchial fluid cuffing.
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These events can lead to the excessive airway narrowing
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and airway hyper-responsiveness
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that contribute to asthma severity and fatality.
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Our group has been investigating the effects of rostral fluid shift on lower airway
narrowing in asthma.
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In order to control for the confounding effects of sleep on airway resistance, we
performed a daytime study in healthy controls and patients with asthma.
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We simulated nocturnal rostral fluid shift by applying lower body positive pressure
with inflatable trousers. After 30 minutes, lower body positive pressure moved similar
amount of fluid out of the legs to that which happens overnight. We found that despite
similar amount of fluid moving to the thorax in healthy controls and asthmatics with
lower body positive pressure: (1) only in asthmatics, fluid accumulation in the thorax
increased lower airway narrowing
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; (2) changes in lower airway resistance were directly related to the amount of fluid
moving to the thorax
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; and (3) the effects of fluid shift were larger in women than in men.
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Airway resistance is inversely related to the forth power of airway diameter. For
similar amount of fluid accumulating in the airway wall, airway wall becomes thicker
in smaller airways than larger airways. Thus, airway lumen narrows more and its resistance
increases more in patients with narrower airways at baseline. Women have narrower
airways than men even at similar lung volumes
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and women are at higher risk of nocturnal asthma than men.
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Thus, rostral fluid shift may have larger effects in airway narrowing in asthmatics
with smaller airways, such as women, obese patients, and those with more severe asthma.
Kantor et al
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investigated the relationship between fluid overload and asthma exacerbation. In children
admitted for asthma exacerbation, they performed a large retrospective cohort study
over 7 years to evaluate fluid balance and clinical outcomes. In particular, they
investigated length of in-hospital stay and duration of administration of beta agonist
and supplemental oxygen.
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They calculated the percentage of fluid overload as the difference between fluid intake
and fluid output normalized by the admission weight in the first 72 hours of hospitalization.
They found that peak fluid overload ≥7% was associated with worse clinical outcomes,
such as longer length of hospital stay, longer treatment duration, and increased risk
of supplemental oxygen use.
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Kantor et al validated their results in a sample of subjects with multiple hospitalizations,
finding similar results in matched sample.
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The same study
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investigated the physiological mechanisms that may contribute to worse clinical outcomes
in patients with asthma and fluid overload. In a prospective observational cohort,
they showed that patients with peak fluid overload ≥7% had more negative swings in
inspiratory intrapleural pressure and evidence of extravascular lung water, as assessed,
respectively, by the variation in peak aortic velocity and the cumulative number of
B-lines in ultrasound images of lung.
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Their findings were in agreement with their hypothesis that during asthma exacerbation,
the excessive airway narrowing increases the negative pleural pressure which pulls
part of the extra fluid to the lungs and increases extravascular lung water.
The findings from Bhatawadekar et al
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and Kantor et al
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have important clinical implications, especially for the patients with difficult-to-treat
asthma. So far, the recognized risk factors for asthma exacerbation include severe
nasal sinus disease, gastroesophageal reflux, recurrent respiratory infection control,
physiological dysfunctioning (such as depression and anxiety), and obstructive sleep
apnea (OSA).
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Among the recognized risk factors for asthma exacerbation, OSA is one with unclear
pathophysiological mechanism. Asthma and OSA coexist in up to 30% of patients with
either disorder.
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Moreover, in patients with difficult-to-control asthma, prevalence of OSA is about
90%.
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Interestingly, previous studies have shown that overnight rostral fluid shift is associated
with worsening of OSA by increasing fluid accumulation in the neck that narrows the
pharynx, increasing its resistance and collapsibility.
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During OSA, the pharynx collapses; causing strong inspiratory efforts against the
occluded pharynx to resume inspiration. The result is large negative (subatmospheric)
intrapleural pressures that increase venous return. The OSA events associated with
the overnight rostral fluid shift may increase even more the accumulation of fluid
in the chest, aggravating the airway narrowing and hyper-responsiveness. Indeed, OSA
is associated with up to 7 times greater risk of having severe asthma
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and 3.4 times increased risk of asthma exacerbations.
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However, the overlap between asthma and OSA is poorly recognized. Thus, both patients
and physicians may not attribute sleep problems and poor asthma control to the OSA.
Recognizing fluid accumulation in the thorax as a risk factor for poor asthma control,
difficult-to-treat asthma, and worse clinical outcomes in asthma has the potential
to reveal new treatments to improve asthma control and change the clinical management
of asthma. Asthma patients may benefit from simple treatments to reduce fluid retention
in the legs such as wearing compression stockings or physical exercise. In fact a
recent systematic review from our group showed that physical exercise improves nocturnal
asthma in children and adults by reducing the prevalence and frequency of nocturnal
symptoms.
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In our review, we could not determine the mechanisms by which physical exercise could
improve nocturnal asthma. However, the reduction of rostral fluid shift by reducing
fluid retention in the legs may be one of the mechanisms related with the improvements
in nocturnal asthma.
While rostral fluid shift occurs in everyone during sleep, it is likely to exert detrimental
effects on airway narrowing in other high-risk populations including: (i) pregnant
women, postoperative patients, and patients with heart or renal failure; (ii) individuals
with limited mobility or sedentary lifestyle; and (iii) the elderly who have stiffer
arteries and/or compromised cardiac function. Finally and importantly, in patients
with asthma exacerbation, controlling the fluid balance to avoid fluid overload can
potentially improve the clinical outcomes, reducing the risks and costs associated
with long-term hospitalization.
In conclusion, in asthma, fluid overload and fluid accumulation in the thorax can
be potential contributing factors for worsening of asthma symptoms and poor clinical
outcomes. More studies are needed to understand the mechanism of asthma worsening
due to fluid accumulation in the thorax and to identify the specific asthma phenotypes
in adults and children who are at higher risk of asthma worsening due to the fluid
accumulation in the thorax. A better understanding of these mechanisms has the potential
to facilitate development of new treatments and prevent the pernicious effects of
asthma exacerbations.
Acknowledgments
Supported by Canadian Respiratory Research Network, Allergen NCE and Ontario Lung
Association.
Conflicts of interest
The authors declare no conflicts of interest.