World lung health study allows scientists to predict your chance of developing deadly disease

Posted by pt91 at Feb 06, 2017 04:02 PM |
Breakthrough advance offers the potential to defuse a ‘ticking timebomb’ for serious lung disease, including for over 1billion smokers worldwide

Issued by University of Leicester Press Office on 6 February 2017

Key Facts:

  • World’s biggest study of genetics of lung health and disease – participants from 13 countries
  • Scientists compared 24 million genetic differences in individuals to develop a model for more accurately predicting your chances of developing COPD
  • COPD is a deadly lung disease – third biggest killer in the world
  • Study helps predict the chances of smokers developing the disease
  • By quitting smoking in early adulthood, COPD can be reduced in 5 out of 10 people at high genetic risk

The world’s biggest study into an individual’s genetic make-up and the risk of developing lung disease could allow scientists to more accurately ‘predict’ - based on genes and smoking - your chance of developing COPD, a deadly disease which is the third commonest cause of death in the world.

By comparing 24 million genetic variants - genetic differences between people - in each participant with measures of lung health, the scientists from 14 countries, led by a team from the University of Leicester and University of Nottingham, were able to group people based on genetic variants to show their risk of developing COPD.

They discovered that those in the highest risk group were at 3.7 times the risk of developing COPD than those in the lowest risk group. Because smokers are already at higher risk of developing COPD, this could mean that 72 of 100 smokers in the genetically high-risk group will develop COPD in later life.

Through this study, the researchers almost doubled the number of genetic variants known to be associated with lung health and COPD. These advances could help to explain why and how COPD develops and one day could help personalise treatments based on an individual’s genetic make-up.

The breakthrough advance could help defuse a ‘ticking timebomb’ for serious lung disease, with over 1 billion smokers worldwide at risk.

Chronic obstructive pulmonary disease (COPD) is a lung disease which makes it difficult to breathe and is the third commonest cause of death worldwide. In the UK there are around 900,000 people living with COPD, costing the NHS over £800m annually and costing the economy £3.8 billion in lost productivity.

Smoking is a strong risk factor for COPD, but not all people affected by COPD are smokers and not all smokers develop the disease. In large part, this is due to one’s genetic make-up. The new research aimed to discover genetic variation in the DNA content of cells between individuals that is associated with the risk of developing lung disease.

At present there are no drug treatments for COPD that alter the course of the disease. But this study led by the scientists at the University of Leicester and University of Nottingham has identified many new genetic variants which are associated with enhanced or worsened lung function in both smokers and non-smokers. It paves the way for the development of new treatments.

The study, published by Nature Genetics, was funded by the Medical Research Council (MRC) using detailed genetic data provided by UK Biobank and data provided by other countries, and supported by the Wellcome Trust. Led by the Universities of Leicester and Nottingham, the four-year study involved over 100 scientists and 350,000 people from 13 countries. It is spurring new collaborations with pharmaceutical company partners aimed at developing new medicines for COPD.

Professor Martin Tobin from the University of Leicester who co-led the study said: “Our findings point to proteins that will help guide the development of new drugs and to proteins that are targets for drugs already tested for different diseases. This indicates that repurposing drugs already tested for different diseases could be one way to improve treatments for COPD.

“As a result of this work, we can now better predict who will develop COPD – opening up the possibility of using this information in prevention (such as for targeting smoking cessation services).

“This genetic information guides future treatments including the development of new drugs as well as the repurposing of drugs already tested for different diseases.”

Professor Ian Hall from the University of Nottingham who co-led the study said: “Given how common COPD is, we know surprisingly little about the reasons why one individual develops the condition whilst another does not. The study of genetic variation between individuals provides a powerful way to understand these mechanisms which underlie disease risk, which in turn will provide a stimulus for drug development.”

Dr Louise Wain, Associate Professor in Genetic Epidemiology who led the team of analysts at the University of Leicester added: “The research shows the value of the UK Biobank study and of ‘big data’ for making discoveries that will improve health. The discoveries were the result of bringing together these very large datasets, highly skilled analysts and the outstanding high performance computing facilities at the University of Leicester.”

Apart from help in developing new drug treatments for COPD, the study is important for understanding whether there may be distinct subtypes of COPD in which patients respond differently to treatment. This means some patients may benefit from particular treatments whereas in others these treatments may be ineffective or harmful (precision medicine).

The research is also important for understanding risk of COPD in smokers and in non-smokers, giving the potential to offer better advice and preventive strategies.

Professor Tobin added: “I’d like to thank the UK Biobank participants who have contributed to these studies and the junior scientists who have shown sustained dedication throughout the project. I’m very proud of the 10 Leicester researchers who have undertaken analyses and contributed to the paper and delighted that this has transformed our knowledge of the genetics of lung health and disease.”

Professor Hall added: “The research represents the culmination of almost a decade of strategic collaboration between the Universities of Nottingham and Leicester. We are delighted that East Midlands-led genomic studies have made such an impact on our knowledge of lung health and COPD, paving the way for improving treatment for COPD in the future.”

Ian Jarrold, Head of Research at the British Lung Foundation, said: “COPD has a devastating effect on the lives of people who live with it, and on their loved ones and carers. Understanding how COPD develops and progresses is key to the discovery of new effective treatments and for using existing treatments more effectively. This work represents an important step towards this, and may also lead to better prevention, earlier diagnosis and earlier treatment of COPD.”

  • The same group of researchers also co-authored another paper published in the same issue of Nature Genetics. The research described in the parallel paper was led by Harvard University and the University of Groningen. It corroborates that many genetic variants that affect lung health in general populations also affect the risk of COPD. It also shows some overlap between the genetic causes of COPD and those of the less common but severe disease, idiopathic pulmonary fibrosis. This study was part-funded by the National Heart, Lung, and Blood Institute
  • The DOI for this paper will be 10.1038/ng.3787. Once the paper is published electronically, the DOI can be used to retrieve the abstract and full text by adding it to the following url: http://dx.doi.org/

Ends

NOTES TO EDITORS:

Contact for more information:

Professor Martin Tobin

Email: mt47@le.ac.uk

Professor Ian Hall: email: ian.hall@nottingham.ac.uk

  • The researchers led the first genetic study in UK Biobank (UK BiLEVE), published in the Lancet Respiratory Medicine in October 2015.
  • Precision medicine will provide early and accurate diagnosis and identify the best treatment and disease management for patients. It will move therapy away from a trial-and-error approach to one that selects the most appropriate prevention or treatment based on quality science, clinical evidence and economic value. It encompasses the development and use of genomic diagnostics (underpinned by research evidence of the kind generated by this study) and other diagnostic tools to guide clinicians in identifying the predisposition to disease, and selecting the best treatment and care for patients. More positive clinical outcomes will occur with earlier detection coupled with appropriate treatment of disease. In this way genomics supports both the health of the nation but also the wealth of the nation, enabling more effective and cost effective treatment provision by NHS, ensuring that patients are able to return to normal life and the national workforce sooner, attraction of research investment to the UK, creation of innovative life science companies and the diagnostic industry thereby increasing national employment and overseas exports.
  • The researchers undertaking this work were from 14 countries including the UK, Canada, Malta, Finland, Australia, Germany, Switzerland, Sweden, Croatia, USA, Norway, Netherlands, Iceland and China.
  • The study participants originated from 13 countries including the UK, Canada, USA, Iceland, Netherlands, Norway, China, Australia, Sweden, Germany, Switzerland, Finland, Croatia.
  • About Leicester Precision Medicine Institute
    • The Leicester Precision Medicine Institute is a partnership between the University of Leicester and the NHS, particularly the University Hospitals of Leicester NHS Trust. As a Centre of Excellence, it will develop, evaluate and implement treatments and patient care pathways that are based on the characteristics of individuals and subgroups of the population to provide more targeted, effective and safer healthcare that will improve health outcomes.
    • Advice on quitting smoking: https://www.nhs.uk/smokefree

ABOUT MRC

The Medical Research Council is at the forefront of scientific discovery to improve human health. Founded in 1913 to tackle tuberculosis, the MRC now invests taxpayers’ money in some of the best medical research in the world across every area of health. Thirty-one MRC-funded researchers have won Nobel prizes in a wide range of disciplines, and MRC scientists have been behind such diverse discoveries as vitamins, the structure of DNA and the link between smoking and cancer, as well as achievements such as pioneering the use of randomised controlled trials, the invention of MRI scanning, and the development of a group of antibodies used in the making of some of the most successful drugs ever developed. Today, MRC-funded scientists tackle some of the greatest health problems facing humanity in the 21st century, from the rising tide of chronic diseases associated with ageing to the threats posed by rapidly mutating micro-organisms. www.mrc.ac.uk

About Wellcome

Wellcome exists to improve health for everyone by helping great ideas to thrive. We’re a global charitable foundation, both politically and financially independent. We support scientists and researchers, take on big problems, fuel imaginations and spark debate.

About the British Lung Foundation

The British Lung Foundation is the only UK charity fighting to help the 1 in 5 people in the UK affected by lung disease, by researching new treatments, campaigning for better awareness and services, and providing support and advice for patients, carers and family members. For further information, please visit www.blf.org.uk. For help and support, call the BLF Helpline on 03000 030 555.To donate £5 to help the BLF fight lung disease, please text LUNGS to 70500.

University of Leicester

The University of Leicester is led by discovery and innovation – an international centre for excellence renowned for research, teaching and broadening access to higher education. The University of Leicester is ranked among the top one per cent of universities in the world by the THE World University Rankings and also among the top 100 leading international universities in the world. It is among the top 25 universities in the Times Higher Education REF Research Power rankings with 75% of research adjudged to be internationally excellent with wide-ranging impacts on society, health, culture, and the environment.

Find out more: http://le.ac.uk/about-us

University of Nottingham

Notes to editors: The University of Nottingham has 43,000 students and is ‘the nearest Britain has to a truly global university, with a “distinct” approach to internationalisation, which rests on those full-scale campuses in China and Malaysia, as well as a large presence in its home city.’ (Times Good University Guide 2016). It is also one of the most popular universities in the UK among graduate employers and was named University of the Year for Graduate Employment in the 2017 The Times and The Sunday Times Good University Guide. It is ranked in the world’s top 75 by the QS World University Rankings 2015/16, and 8th in the UK by research power according to the Research Excellence Framework 2014. It has been voted the world’s greenest campus for four years running, according to Greenmetrics Ranking of World Universities.

Impact: The Nottingham Campaign, its biggest-ever fundraising campaign, is delivering the University’s vision to change lives, tackle global issues and shape the future. More news…

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