Using Both Genetic And Mathematical Modelling To Better Understand Lung Disease
Researchers at the University of Auckland are pioneering a new approach to the understanding of Chronic Obstructive Pulmonary Disease (COPD), combining world-leading research into genetic modelling of the disease with mathematical modelling of lung structure-function.
COPD is the term used for
a group of lung conditions that cause breathing
difficulties, including emphysema which is the result of
damage to the air sacs in the lungs, and chronic bronchitis,
the long-term inflammation of the airways.
COPD can make
normal activities difficult. It typically gets worse over
time, and is a leading cause of death for New Zealanders,
with Māori and Pacific people being disproportionately
affected.
The research is being led by Professors Merryn
Tawhai and Justin O’Sullivan, who are respectively the
deputy directors of the Auckland Bioengineering Institute
(ABI) and the Liggins Institute.
Support from the Dines
Family Foundation has enabled them to combine Dr
O’Sullivan’s expertise in the genetic analysis of the
formation of and susceptibility to COPD, with Dr Tawhai’s
research into quantitative analysis and computational
modelling of normal and COPD lungs.
Most cases of COPD
are caused by smoking, yet some individuals are more
susceptible to the disease than others, and some people are
more responsive to different treatments than others. Dr
Tawhai says “we do expect that over the next ten or 20
years that smoking-related COPD might start to decline in
some countries, in line with the reduction in smoking. But
now we have vaping, and it’s quite possible that a person
who is a lifetime vaper will develop something that is very
similar to COPD.
“We know vaping causes inflammation,
and we know that’s bad. We’re potentially creating a new
COPD epidemic. Kids who might not have smoked are vaping,
and vaping more than they might have smoked, because they
think there’s nothing wrong with it.”
Drs Tawhai and
O’Sullivan aim to develop an approach that will help
identify how both disease and treatment affects people at a
personalised level. “Everyone has their own genetic
profile, and the way they respond to disease such as COPD is
different,” says Dr O’Sullivan. While numerous studies
have investigated the genetic basis of COPD and why some
people respond better to treatment than others, this
collaboration will allow the team to revisit earlier
studies, combining genetic modelling with mathematical
modelling, to advance understanding of individual patient
differences.
It will involve investigating the disease at
myriad scales and levels, including DNA sequence, the way
the DNA folds, the cells involved, the way the cells
interact in the tissue, the proteins in those cells, the
distribution of tissue damage within the lung, and
more.
“So this will help us predict the trajectory of
the disease at a very personalised and individualised
level,” says Dr Tawhai.
She notes that people know they
shouldn’t smoke, but don’t always follow that advice. If
people could be shown their personal risk of developing a
disease, the impact on their lungs, the personalised
trajectory of their disease, they might be more motivated to
look after their health.
That is, by not smoking, or
vaping.
“If you can show people their personal risk
profile, if they vape or smoke, then that, from a public
health perspective, could make a difference. We hope that
this will be one of the outcomes – that we can work out a
way to refine what we do to allow for more personalised
prediction. Prevention is much better than waiting for
treatment.”