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Active NON-SBIR/STTR RPGS NIH (US)

Airway distensibility and lung inflation effects on the maximal expiratory flow volume curve in elderly adults

$2.35M USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization Washington State University
Country United States
Start Date Sep 01, 2024
End Date Jun 30, 2026
Duration 667 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10988957
Grant Description

PROJECT SUMMARY Both the total number of elderly persons and the incidence of lung disease will increase in the coming decades. It is vital that we define the normal physiological changes that take place in the aging respiratory system. Peak lung function occurs in early adulthood and progressively declines with age. The decreased lung function is

readily apparent in the maximal expiratory flow volume curve (MEFV), depicting decreases in maximal expiratory airflow (MEF) at all lung volumes in elderly adults. Clinically, the reduced MEF is attributed to a concomitant, progressive loss of lung elastic recoil. However, in young-to-middle aged adults, the inhalation to total lung

capacity that precedes a maximal forced expiration causes a transient airway dilation. The deep inflation-induced airway dilation results in higher MEF than can be achieved in the absence of the deep inflation (DI). The effects of normal aging on the dynamic interaction between a DI and MEF is not known. This is problematic, since the

MEFV curve is interpreted assuming that the airway response to a DI is equal across the aging spectrum. We hypothesize that one cause of the decreased MEF with aging is a blunted airway dilatory effect of a DI. If this hypothesis is true, it would indicate that the MEFV curve exaggerates the reduced MEF in elderly adults. Three

specific aims will test our hypothesis. Aim 1 will compare the effect of a DI on the MEFV curve in young and elderly adults. We hypothesize that a DI will increase MEF in young adults whereas it will decrease MEF in elderly adults. The effect of a DI on airway caliber will be quantified by comparing MEF after a DI with MEF during

a forced expiration begun at normal end-inspiratory lung volume (maximal:partial [M:P]). All M:P measurements will be analyzed at 40% of vital capacity. Aim 2 will determine the effect of aging on the bronchodilatory effect of a DI. In young adults, a DI exerts a bronchodilatory effect on airways that have been constricted by inhaled

methacholine (airway smooth muscle agonist). We hypothesize that the bronchodilatory effect of a DI will be reduced in elderly adults. Inhaled methacholine will be used to cause bronchoconstriction. M:P measurements will be used to determine the magnitude of DI-induced bronchodilation (as in SA1). If findings support our

hypothesis, they will provide evidence that aging is associated with the loss of an essential mechanism for preserving airway function. Aim 3 will compare airway distensibility in young and elderly adults. We hypothesize that airway distensibility will be lower in elderly adults than young adults. Using impulse oscillometry, airway

distensibility will be quantified as the change in airway conductance relative to the change in lung volume

(∆Grs/∆VL), [l·cmH2O-1·s-1·l-1]). These experiments will generate insight into the effects of aging on the strength of coupling between the airways and the surrounding elastic tissues. This proposal will generate novel data that addresses the question: Is interpretation of the MEFV curve inaccurate in elderly patients? The

findings will lend insight into the mechanisms for the maladaptive changes to lung function with aging and might significantly impact clinical interpretation of spirometry in elderly adults.

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Washington State University

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