Three-quarters of COPD cases are linked to childhood risk factors that are exacerbated in adulthood
Press release issued: 5 April 2018
Three-quarters of chronic obstructive pulmonary disease (COPD) cases have their origins in poor lung function pathways beginning in childhood. These pathways are associated with exposures in childhood, and amplified by factors in adulthood, according to a cohort study published in The Lancet Respiratory Medicine journal.
While smoking remains the biggest risk factor for COPD, the study demonstrates that childhood illnesses (such as asthma, bronchitis, pneumonia, allergic rhinitis, eczema) and exposures to parental smoking are also linked to the disease.
A second study in the journal, involving University of Bristol researchers, also suggests that there could be a window of opportunity during childhood to reduce the risk of poor lung function in later life.
Both studies identified pathways of how lung function changes over life, which are associated with different risk factors and disease risk in later life. The authors say that these insights are important for lung disease prediction, prevention, and treatment.
"These findings highlight the importance of preventing both early life adverse exposures that could lead to poorer lung growth, and adult risk factors contributing to accelerated lung decline. COPD is expected to be the third largest cause of death globally by 2030, and it is important that we identify its key causes so that this burden can be reduced," says study author Professor Shyamali Dharmage, School of Population and Global Health, The University of Melbourne, Australia. "Reduction of maternal smoke exposure and personal smoking and promotion of immunisation are identified as public health targets to prevent poor lung function pathways. Doctors and patients with asthma should be made aware of the potential long-term implications of non-optimal asthma control throughout life, and this should be investigated in future research."
In the first study, 2,438 participants from the Tasmanian Longitudinal Health Study (Australia) were tracked from childhood to the age of 53 – making it the largest and longest-running study of its kind. Lung function was measured at the ages of seven, 13, 18, 45, 50 and 53 years old, and participants’ exposure to various risk factors was also recorded.
The authors identified six distinct pathways describing how lung function changes with age. Three of these pathways were associated with COPD – the group with below average lung function in early life and a quick decline in lung function in later life, those with persistently low lung function, and those with below average lung function. Combined, these three pathways were linked to an estimated three-quarters of all cases of COPD occurring at the age of 53 (75.2 per cent overall). For moderate-to-severe COPD, all cases only arose from these three trajectories.
These three pathways were also linked to childhood asthma, bronchitis, pneumonia, allergic rhinitis, eczema, parents having asthma or smoking, and the participants themselves smoking or having asthma.
The authors suggest that the childhood risk factors are important indicators of COPD risk, that are aggravated by smoking and having asthma in adulthood. This amplifies the damage already caused by childhood risk factors, and may result in a more rapid decline in lung function.
As a result, the authors say that it will be important to reduce parental smoking, encourage immunisation, and avoid smoking to promote healthy lung function pathways and minimise COPD risk, especially for people who had low childhood lung function or whose parents smoked. In addition, ensuring all people with asthma have appropriate treatment may be vital to preserve lung function.
The authors note some limitations, including that the last measurement in their study is at the age of 53, when COPD is just starting to emerge, but most patients are diagnosed in their sixties. Therefore, tracking these lung function pathways later into life may give a clearer picture of COPD risk in later life.
In the second study, using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), also known as Children of the 90s, 2,632 participants were tracked from birth to 24 years old and their lung function was measured. The authors found that around three-quarters of infants aged one to six months with poor lung function improved throughout their childhood, indicating a window of opportunity to increase lung function and potentially reduce risk of COPD in later life. They suggest that interventions to maximise lung growth in early childhood might modify the risk of COPD in older age.
Writing in a linked Comment, Professor Erika von Mutius, Dr von Hauner Children’s Hospital, Ludwig Maximilians University, Germany, said: "Chronic obstructive pulmonary disease (COPD) is a common condition in adults, with high morbidity and mortality. COPD has been mainly attributed to active smoking in adulthood, but some patients are diagnosed with COPD in the absence of a smoking history and only 20–25% of smokers develop COPD. Taken together, these findings clearly point towards the importance of early life for the development of COPD. Importantly, maternal smoking and childhood asthma not only adversely affected early lung function, but predisposed children to more rapid lung function decline if they still suffered from asthma or actively smoked as adults."
The first study was funded by National Health and Medical Research Council of Australia, European Union’s Horizon 2020, The University of Melbourne, Clifford Craig Medical Research Trust of Tasmania, The Victorian, Queensland & Tasmanian Asthma Foundations, The Royal Hobart Hospital, Helen MacPherson Smith Trust, and GlaxoSmithKline. It was conducted by researchers from The University of Melbourne, National Institute of Fundamental Studies, University of Tasmania, The Alfred Hospital, Monash Health, Monash University, Flinders University, Sir Charles Gairdner Hospital, University of New South Wales, Imperial College London, University of Bergen, Royal Brisbane and Women’s Hospital, University of Queensland, Gold Coast Hospital, Cancer Council Victoria.
The second study had no funding, and was conducted by researchers from Imperial College London, Bristol Medical School, University of Bristol, University of Aberdeen, University of Manchester, Manchester Academic Health Science Centre, University of Western Australia.
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 A group with below average lung function in early age and a quick decline in function in later life (4%, 97/2438 people), persistently low lung function (6%, 136/2438 people), a group with low lung function in early age followed by rapid improvement and normal decline in function later in life (8%, 196/2438 people), persistently high lung function (12%, 293/2438 people), below average lung function (32%, 772/2438 people) and average lung function (39%, 944/2438 people).