The study, led by Andrew T Lovering, a professor of human physiology at the University of Oregon compared the lung function of adults born after fewer than 32 weeks to adults born full-term.
The study found premature infants are at increased risk for contracting bronchopulmonary dysplasia (BPD), a chronic respiratory condition mainly affecting infants born less than 28 weeks of age.
BPD primarily affects preterm infants who receive oxygen therapy to help them breathe.
Research has indicated that infants with BPD are at a higher risk for the subsequent development of chronic obstructive pulmonary disease, a progressive disease that makes it harder to breathe.
COPD, commonly known as smoker's lung, is a fairly common condition, affecting 329 million people worldwide.
The condition is most often the result of smoking or exposure to air pollution.
To study the lung capacity of adult survivors of preterm births, Lovering and colleagues looked at three groups: 20 adults born prematurely with BPD, 15 adults born prematurely without BPD and a control group of 20 healthy adults born full-term.
The study suggests that adults born prematurely without BPD, like their counterparts with BPD, show symptoms of a mild form of COPD in their mid-20s. Their lungs did not function as efficiently as the control group, which caused them to tire sooner.
"We were expecting more variation between the two preterm groups - with and without BPD. We didn't anticipate that they would share a similar lung profile," Lovering said.
Even if the rate of decline in their lung function remains normal throughout their life, adult preterm survivors with COPD will likely develop respiratory complications at a much younger age, Lovering said.
The study was published in the Annals of the American Thoracic Society.
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